US20030036001A1

US20030036001A1 - Electrical energy devices

Info

Publication number: US20030036001A1
Application number: US10/179,906
Authority: US
Inventors: David James; Daniel Allison; John Kelley; James Doe
Original assignee: Individual
Current assignee: Individual
Priority date: 1995-09-29
Filing date: 2002-06-24
Publication date: 2003-02-20
Also published as: EP0868757A1; KR19990063787A; JPH11512869A; CN1996656A; AU702715B2; EP0868757A4; ATE268058T1; CN1263185C; ES2224177T3; AU7248696A; DK0868757T3; US6451485B1; DE69632594D1; US5766789A; DE69632594T2; WO1997012410A1; AR043512A2; CA2233337A1; EP0868757B1; CN1199509A

Abstract

The performance of electrochemical energy devices such as batteries, fuel cells, capacitors and sensors is enhanced by the use of electrically conducting ceramic materials in the form of fibers, powder, chips and substrates.

Description

Priority is claimed to provisional application No. 60/004,553, filed Sep. 29, 1995.[0001]

FIELD OF THE INVENTION

The present invention relates to electrochemical devices such as batteries, fuel cells, capacitors and sensors which employ electrically conductive ceramic materials, fibers, powder, chips and substrates therein to improve the performance of the electrochemical device.

BACKGROUND OF THE INVENTION

There are numerous applications which involve the transfer of electrical current in environments which are highly corrosive or otherwise degrading to metallic conductors. Most notably are electrochemical devices operating under highly corrosive conditions and high temperatures. Examples of such applications are the use of electrodes for the chlor-alkali cell to make chlorine gas, electrodes for metal recovery, electrodes in hydrogen/oxygen fuel cells, electrodes for producing ozone, electrolysis of water and electrodes in high temperature solid oxide fuel cells. Most of these applications involve the contact of an electrode with an electrolyte under conditions which render the electrode ineffective during prolonged use. The loss of effectiveness can be gradual, such loss being manifested by reduced current-carrying capacity of the electrode. Exemplary types of conditions which render electrodes ineffective as they are used in current-carrying applications are described below.

One such condition involves chemical attack of the electrode by corrosive gas which is evolved from the electrolyte as it is decomposed during use. For example, the evolution of chlorine gas, a highly corrosive material, from an aqueous chloride-containing electrolyte such as, in the chlor-alkali cell is exemplary.

Another type of condition involves passivation of the electrode as it combines with the anions from the electrolyte to form an insoluble layer on its surface. This passivation condition occurs when the product from the electrochemical reaction can not diffuse from the electrode surface and this produces a blocking of the electrochemical sites and/or pores. The end result is a diminishing of the electrode current carrying capacity. An example of this passivation is the lead dioxide electrode in an aqueous sulfuric acid solution.

Another type of condition which renders electrodes ineffective involves the dissolution of the electrode by the electrolyte. The use of a zinc electrode in an aqueous potassium hydroxide solution is exemplary.

Various types of batteries such as secondary(rechargeable) batteries: lead-acid(Pb/PbO ₂), NaS, Ni/Cd, NiMH(metal hydride), Ni/Zn, Zn/AgO, Zn/MnO₂, Zn/Br₂; and primary(non-rechargeable) batteries: Zn/MnO₂, AgCl/Mg, Zn/HgO, Al/Air(O₂), Zn/Air(O₂), Li/SO₂, Li/Ag₂CrO₄and Li/MnO₂exist.

Although a variety of batteries are available, the lead-acid battery remains favored for uses such as starting internal combustion engines, electric vehicle motive power, as well as portable and emergency power for industrial and military applications.

Lead-acid batteries include a cathode comprising a lead alloy grid (active material support structure and electrical network structure contact with the battery terminals) having PbO ₂active material thereon; and an anode comprising sponge lead on a grid. The active material on a grid is called the plate and electrically, the anode (Pb) plate is negative and the cathode (PbO₂) plate is positive. A separator, either glass fibers or porous plastic, is used to separate the cathode and anode from direct contact when the plates are in sulfuric acid electrolyte. For the lead-acid battery, the rated capacity (ampere-hours) depends on the total amount of electrochemically active material in the battery plates, the concentration and amount of sulfuric acid electrolyte, the discharge rate and the percent utilization (conversion of active material into ampere-hours)for the active materials (the cathode or PbO₂usually being the limiting factor).

During discharge of a lead-acid battery, the lead and lead dioxide active materials are converted to lead sulfate. The lead sulfate can form an undesirable, insulating layer or passivation around the cathode active material particles which reduces the active material utilization during discharge. This passivating layer can be the result of improper battery charging, low temperature operation, and/or excessive (high current) discharge rates. In order to increase the cathode active material utilization, which is desirable for battery performance, means to increase the cathode active material porosity which increases the amount of active material contact with the sulfuric acid and/or active material conductivity which minimizes resistance and electrical isolation of the active material particles are useful. However, raising the cathode active material porosity tends to increase the tendency for a loosening and possible loss of active material from the plate as well as electrical isolation of the active material from the grid structure. Wrapping the cathode plate with a glass mat holds the loosened active material tightly to the plate and minimizes the tendency for active material sediment (electrochemically lost cathode material) in the bottom of the battery container. The addition of conductive materials (carbon, petroleum coke, graphite) to increase the conductivity of the cathode active material is well-known, but these materials are degraded rapidly from the oxygen generated at the cathode during charging.

Since the lead-acid battery anode is very conductive, the additives for the sponge lead active material have concentrated on improving low temperature battery performance and cycle life. The fundamental additive to the anode is the expander which is comprised of lampblack, barium sulfate and lignosulfonic acid mixed with the lead oxide (PbO) carrier agent. The expander addition to the sponge lead inhibits densification or decrease in the sponge lead porosity. If the anode active material becomes too dense, it is unable to operate at low temperatures and can no longer sustain practical current discharges.

In the manufacture of lead-acid batteries, cathode electrodes are usually prepared from lead alloy grids which are filled with an active paste that contains sulfated lead oxide. This sulfated lead oxide is then later converted or formed into sponge lead for the anode and lead dioxide for the cathode. In an alternative construction, known as tubular cathode plates, the cathode active material is a sulfated lead oxide powder that is poured into a non-conductive tube (braided or woven glass or polyethylene) containing a protruding lead alloy rod or spine. Several of these tubes make up the grid structure and electrical connections are made to the terminals by the protruding lead alloy rods. The tubular cathodes and the usual plate anodes are then assembled into elements and these are then placed in a battery container. The cells are filled with electrolyte and the battery is subjected to the formation process. See details on lead-acid batteries, by Doe in Kirk-Othmer: Encyclopedia of Chemical Technology, Volume 3 (1978), page 640-663.

During lead-acid battery formation, active material particles in contact with the grid are formed first and particles further away from the grid are formed later. This tends to reduce the efficiency of formation. An apparent solution to this problem is addition of a conductive material to the active material paste. The additive should be electrochemically stable in the lead-acid system both with respect to oxidation and reduction at the potentials experienced during charge and discharge of the cell, as well as to chemical attack by the sulfuric acid solution. The use of barium metaplumbate and other ceramic perovskite powder and plating additives to the lead-acid battery anode and cathode are reported to enhance the formation of lead-acid batteries. See U.S. Pat. No. 5,045,170 by Bullock and Kao. However, these additives are limited to the lead-acid battery system and require up to a 50 weight percent addition to be effective.

For other battery systems, the cathode materials such as, MoO ₃, V₂O₅, Ag₂CrO₄and (CF_x)_nthat are used in primary lithium batteries are typically mixed with carbon, metal or graphite powder to improve the overall cathode electrical conductivity and therefore, the utilization of the cathode material. Depending on the battery design, the current collector is either the cathode material itself or a nickel screen pressed into the cathode material. The current collector for the anode (lithium) is a nickel screen pressed into the lithium metal. The separator between the lithium battery cathode and anode is typically a non-woven polypropylene, Teflon or polyvinyl chloride membrane. The electrolyte for the lithium battery is an organic solvent such as propylene carbonate, dimethyl sulphoxide, dimethylformamide, tetrahydrofuran to which some inorganic salt such as, LIClO₄, LiCl, LiBr, LiAsF₆has been added to improve the solution ionic conductivity. Hughes, Hampson and Karunathilaka (J. Power Sources, 12 (1984), pages 83-144)) discuss the enhancement techniques used for improving the cathode electrical conductivity for lithium anode cells. While the addition of the materials to improve the cathode conductivity and utilization are feasible, the amount of additive material required means that much less electrochemical active cathode material that will be available, and in some lithium battery designs, because of volume limitations, that can be critical.

Other battery systems requiring that the cathode have improved conductivity and thereby, improved cathode (NiOOH/Ni(OH) ₂) active material utilization are secondary nickel batteries such as, Ni/Cd, Ni/Zn and Ni/MH (metal hydride). The electrolyte for the nickel battery system is usually potassium hydroxide solution and the separator between the anode and cathode is non-woven polypropylene. To enhance the cathode conductivity, graphite is added but this material is not long lasting as it is gradually oxidized to carbon dioxide. In addition to the degradation of the graphite, there is a gradual build-up of carbonate ions which reduces the conductivity of the electrolyte. See discussion on nickel batteries in “Maintenance-Free Batteries” by Berndt.

A sodium-sulfur battery comprises molten sulfur or molten sodium polysulfide as a cathode, molten sodium as an anode, and a non-porous solid electrolyte made of beta alumina that permits only sodium ions to pass. The sulfur or sodium polysulfide in the cathode has an inferior electrical conductivity in itself. The art has attempted to address this problem by adding conductive fibers such as metal fiber or carbon fiber to the molten sulfur or molten sodium polysulfide. For general information, see U.S. Pat. Nos. 3, 932,195 and 4,649,022. These types of fibers however, are prone to corrosion in the electrochemical environment of a sodium-sulfur battery. A need therefore continues for sodium-sulfur batteries which employ chemically stable conductive ceramic materials therein.

Another type of electrical energy generating device, as is known in the art, is the fuel cell such as acid fuel cells, molten carbonate fuel cells, solid polymer electrolyte fuel cells and solid oxide fuel cells. A fuel cell is an apparatus for continually producing electric current by electrochemical reaction of a fuel with an oxidizing agent. More specifically, a fuel cell is a galvanic energy conversion device that chemically converts a fuel such as hydrogen or a hydrocarbon and an oxidant that catalytically react at electrodes to produce a DC electrical output. In one type of fuel cell, the cathode material defines passageways for the oxidant and the anode material defines passageways for fuel. An electrolyte separates the cathode material from the anode material. The fuel and oxidant, typically as gases, are continuously passed through the cell passageways for reaction. The essential difference between a fuel cell and a battery is that there is a continuous supply of fuel and oxidant from outside the fuel cell. Fuel cells produce voltage outputs that are less than ideal and decrease with increasing load (current density). Such decreased output is in part due to the ohmic losses within the fuel cell, including electronic impedances through the electrodes, contacts and current collectors. A need therefore exists for fuel cells which have reduced ohmic losses. The graphite current collectors used in phosphoric acid and solid polymer electrolyte fuel cells, to the cathode metal oxides such as, praseodymium oxide, indium oxide used in solid oxide fuel cells and to the nickel oxide cathode used in molten carbonate fuel cells are examples of a need for conductive additives. See generally, “Handbook of Batteries and Fuel Cells”, Edited by Linden.

Multilayer surface mount ceramic chip capacitors which store electrical energy are used extensively by the electronics industry on circuit boards. A typical multilayer surface mount chip capacitor is comprised of alternating multilayers of dielectric (ceramics such as BaTiO ₃) electrodes (metals such as Pd or Pd—Ag). The end caps or terminations of the capacitor are typically a metallic (Ag/Pd) in combination with a conductive glass. This termination is the means of contact to the internal electrodes of the multilayer ceramic capacitor. The development of other electrodes such as nickel and copper to reduce costs and the use of low cost conductive additives to the glass are actively being sought. See generally, Sheppard (American Ceramic Society Bulletin, Vol. 72, pages 45-57, 1993) and Selcuker and Johnson (American Ceramic Society Bulletin, 72, pages 88-93, 1993).

An ultra-capacitor, sometimes referred to as a super capacitor, is a hybrid encompassing performance elements of both capacitors and batteries. Various types of ultra-capacitors are shown in “Ultracapacitors, Friendly Competitors and Helpmates for Batteries,” A. F. Burke, Idaho National Engineer Laboratory, February 1994. A problem associated with an ultracapacitor is high cost of manufacture.

Sensors, as are known in the art, generate an electrical potential in response to a stimulus. For example, gas sensors such as oxygen sensors generate an electrical potential due to interaction of oxygen with material of the sensor. An example of an oxygen sensor is that described by Takami (Ceramic Bulletin, 67, pages 1956-1960, 1988). In this design, the sensor material, titania (TiO ₂), is coated on an alumina (Al₂O₃) substrate with individual lead connections for the substrate and the titania components. The development of higher electrical conductive titania to improve the oxygen sensor response is an on-going process. Another sensor, humidity, is based upon the electrical conductivity of MgCr₂O₄—TiO₂porous ceramics is discussed by Nitta et al. (J. American Ceramic Society, 63, pages 295-300, 1980). For humidity sensing, leads are placed on both sides of the porous ceramic plaque and the sensor is then placed in the air-moisture stream for resistivity (inverse of electrical conductivity) measurements. The relative humidity value is then related to the measured resistivity value. With this design, the porous ceramic resistivity value, as low as possible, is critical because of the need for a rapid measurement response time (seconds) that can be related to an accurate relative humidity value.

Another type of electrical device, as is known in the art, is a bipolar battery. Such a battery typically comprises an electrode pair constructed such that cathode and anode active materials are disposed on opposite sides of an electrically conductive plate, that is, a bipolar plate. The cells that have this electrode pair are configured such that the cell-to-cell discharge path is comparatively shorter and dispersed over a large cross-sectional area, thus providing lower ohmic resistance and improved power capabilities compared to unipolar batteries such as automobile batteries. The bipolar electrodes are stacked into a multicell battery such that the electrolyte and separators lie between adjacent bipolar plates. The Lead-acid batteries are attractive candidates for bipolar construction because of the high power capabilities, known chemistry, excellent thermal characteristics, safe operation and widespread use. However, such lead-acid batteries with bipolar construction often fail due to the corrosion of the electrically conductive plate when in contact with the active material. A need therefore exists for bipolar batteries which have improved corrosion resistance, low resistivity and reduced weight. For general information on bipolar batteries, see Bullock (J. Electrochemical Society, 142, pages 1726-1731, 1995 and U.S. Pat. No. 5,045,170) and U.S. Pat. No. 4,353,969.

Although the devices of the prior art are capable of generating and storing electrical energy, and acting as oxygen and relative humidity sensors, there is a need for improved materials of construction for reasons of diminished corrosion, higher capacity and/or higher electrical conductivity which overcome the disadvantages of the prior art.

In addition to the previously mentioned materials used in the above applications, there are several U.S. Patents which delineate the electrochemical use of electrically conductive ceramics such as the sub-oxides of titanium which are formed from the reduction of titanium dioxide in hydrogen or carbon monoxide reducing gases at high temperatures (1000° C. or greater). For example, U.S. Pat. No. 5,126,218 discusses the use of TiO _x(where x=1.55 to 1.95) as a support structure (grids, walls, conductive-pin separators), as a conductive paint on battery electrodes and as powder in a plate for the lead-acid battery. A similar discussion occurs in U.S. Pat. No. 4,422,917 which teaches that an electrochemical cell electrode is best made from bulk material where the TiO_xhas its x vary from 1.67 to 1.85, 1.7 to 1.8, 1.67 to 1.8, and 1.67 to 1.9.

The said mentioned electrode materials are suitable for electrocatalytically active surfaces when it includes material from the platinum group metals, platinum group metal alloys, platinum group metal oxides, lead and lead dioxide. The electrodes are also suitable for metal plating, electrowinning, cathodic protection, bipolar electrodes for chlorine cells, tile construction, and electrochemical synthesis of inorganic and organic compounds.

Oxides of titanium are discussed in U.S. Pat. No. 5,173,215 which teaches that the ideal shapes for the Magneli phases (Ti _nO_2n-1where n is 4 or greater) are particles that have a diameter of about one micron (1 micron (denoted μ) is 10⁻⁶meter (denoted m)) or more and a surface area of 0.2 m²/g or less.

The U.S. Pat. No. 5,281,496 delineates the use of the Magneli phase compounds) in powder form for use in electrochemical cells. The use of powder is intended for the electrode structure only.

U.S. Pat. No. 4,931,213 discusses a powder containing the conductive Magneli phase sub-oxides of titanium and a metal such as copper, nickel, platinum, chromium, tantalum, zinc, magnesium, ruthenium, iridium, niobium or vanadium or a mixture of two of more of these metals.

SUMMARY OF THE INVENTION

The invention is directed to solving the problems of the prior art by improving electrochemical devices such as batteries, fuel cells, capacitors, sensors and other electrochemical devices as follows: (1) In batteries for example, there will be an improved discharge rate, increased electrochemically active material utilization, improved charging efficiency, reduced electrical energy during the formation of electrochemically active materials and decreased electrical resistance of the electrochemically active material matrix; (2) In fuel cells, for example, there will be decreased electrical resistance of the current collectors and cathode materials as well as increased electrical chemical efficiency of the reactants; (3) In capacitors, for example, there will be development of less expensive electrodes and conductive glass; (4) In sensors, there will be the development of lower resistive titanium dioxide for oxygen sensors and lower resistive binary compounds containing titanium dioxide for relative humidity sensors; and (5) In other electrochemical devices, for example, there will be the development of more corrosion resistant and current efficient electrodes for electrolysis, electrosynthesis.

As used herein, conductive ceramic materials include conductive ceramic compositions such as solids, plaques, sheets (solid and porous), fibers, powders, chips and substrates (grids, electrodes, current collectors, separators, foam, honeycomb, complex shapes for use in components such as grids made by known methods such as weaving, knitting, braiding, felting, forming into paper-like materials, extrusion, tape casting or slip casting) made from conductive ceramic compositions having metal containing additives and metallic coatings thereon, or made from non-conductive ceramic compositions having metal containing additives and metallic coatings dispersed thereon.

The electrically conductive ceramic materials for use in the invention, when in the form of fibers, powders, chips or substrate, are inert, light weight, have high surface area per unit weight, have suitable electrical conductivity, as well as high corrosion resistance. Typically, the electrically conductive ceramic fibers, powders, chips or substrate herein have an electrical conductivity of 0.1 (ohm-cm) ⁻¹or more.

Electrically conductive ceramic fibers, powder, chips or substrate useful in the invention include an electrically conductive or non-electrically conductive ceramic matrix, preferably with a metal containing additive and/or metallic coating. Ceramic matrix materials which may be employed include, the oxides of the metals titanium, and vanadium and the oxides of zirconium, and aluminum. The reduced oxides of titanium and vanadium have a certain amount of intrinsic electrical conductivity and the oxides of zirconium and aluminum are intrinsically insulators. All mentioned ceramic oxides have different chemical and physical attributes and these materials cover a wide range of applicability. Either ceramic metal oxide can have the electrical conductivity increased by the addition or plating or coating or deposition of singly or a mixture thereof of metallic d-block transition elements (Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au), Lanthanides (Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu) and/or by the addition or plating or coating or deposition singly or a mixture thereof of selected main-group elements (B, Al, Ga, In, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te) and/or the oxides, halides, carbides, nitrides and borides of the aforementioned elements. Chemical reduction processes for the selected mixtures reduce the ceramic to its final electrically conductivity form. Similarly, chemical oxidation processes may be used to form superstoichiometric titanium oxide in which the atomic oxygen to titanium ratio is slightly above 2.

The electrically conductive ceramic materials, fibers, powders, and chips mentioned in this invention can be used to enhance the electrical conductivity and thereby, the utilization of the electrochemically active materials in cathode for the following primary and secondary battery systems: lithium batteries, zinc air batteries, aluminum air batteries, alkaline batteries, Leclanche batteries, nickel batteries, lead-acid batteries, and sodium-sulfur. The electrically conductive ceramic substrate as mentioned in this invention would be suitable for fuel cell electrodes and current collectors and bipolar plate batteries. In addition, the electrically conductive ceramic materials, fibers, powders, chips and substrate according to this invention would be suitable for oxygen and humidity sensors as well as multilayer chip capacitors and ultracapacitors. The electrode made from this invention can also be useful as an anode or cathode, whichever is applicable, in electrochemical devices including batteries and in an electrolytic cell generating ozone, chlorine gas, or sodium, recovering metals from wastewater and purification of metals by electrolysis.

The electrically conductive ceramic materials, fibers, powders, chips and/or substrates therein may impart superior battery discharge and charging performance, battery cycle life, battery charge retention, battery weight reduction, deep battery discharge recovery, as well as battery structure vibration and shock resistance. Batteries such as lead-acid batteries which employ electrically conductive ceramic materials, fiber, powder, chips and/or substrates therein advantageously may require reduced electrical energy during formation. Fuel cells utilizing electrically conductive ceramic materials, fibers, powder and/or substrate for the current collector and the electrodes may have longer operating life because of superior corrosion resistance and enhanced performance because of superior electrical conductivity. The use of electrically conductive ceramic materials, fibers, powder, chips and substrates from this invention may impart low cost manufacturing, superior electrical resistivity performance in oxygen and humidity sensors, multilayer chip capacitors, and ultracapacitors.

Other advantages of the present invention will become apparent as a fuller understanding of the invention is gained from the detailed description to follow.

DETAILED DESCRIPTION OF THE INVENTION

In accordance with the invention, electrically conductive ceramic materials, fibers, powders, chips and substrates are either added to components or used to construct components for electrochemical devices such as batteries, fuel cells, capacitors, sensors, and other electrochemical devices. The type of conductive ceramic material used depends on the type of chemical, electropotential and electrochemical environments to which the conductive ceramic materials will be subjected. [0035]

Preferred Ceramic Materials

The preferred starting materials for electrically conductive sub-oxide titanium ceramics according to this invention are the following: TiO[0036] ₂(preferably rutile), Ti, Ti₂O₃, Ti₃O₅, metal (chromium, copper, nickel, platinum, tantalum, zinc, magnesium, ruthenium, iridium, niobium, and vanadium or a mixture of two or more of the aforementioned metals)-containing intercalated graphite, graphite and carbon. Also possible, the addition of singly or a mixture thereof metallic d-block transition elements (Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au), Lanthanides (Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu) and by the addition singly or a mixture thereof selected main-group elements (B, Al, In, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te) and/or the oxides, halides, carbides, nitrides and borides of the aforementioned elements. All materials used should have a purity level that excludes deleterious substances for this process as well as the projected use.
The preferred starting materials for electrically conductive sub-oxide vanadium ceramics according to this invention are the following: V[0037] ₂O₅, V₂O₃, VO₂, V, metal (chromium, copper, nickel, platinum, tantalum, zinc, magnesium, ruthenium, iridium, niobium, and vanadium or a mixture of two or more of the aforementioned metals)-containing intercalated graphite, graphite, and carbon. Also possible, the addition of singly or a mixture thereof metallic d-block transition elements (Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au), Lanthanides (Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu) and by the addition singly or a mixture thereof selected main-group elements (B, Al, In, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te) and/or the oxides, halides, carbides, nitrides and borides of the aforementioned elements. All materials used should have a purity level that excludes deleterious substances for this process as well as the projected use.
The teachings of U.S. Pat. No. 4,422,917 state that the conductive materials of choice for the sub-oxides of titanium should consistent essentially of Ti[0038] ₄O₇and Ti₅O₉in order to maximize the conductivity. This concept was further extended by the teachings of U.S. Pat. No. 5,173,215 which stated that it is more proper to speak of the appropriate conductive sub-oxides of titanium as Magneli phases with the general formula Ti_nO_2n-1where n=4 or greater. TiO is never considered in either patent as an important component because of reported instability and less than desirable resistance to chemical attack. For the sub-oxides of titanium, Ti₄O₇has been measured with a conductivity value of 1585 (ohm-cm)⁻¹, Ti₅O₉has been measured with an electrical conductivity value of 553 (ohm-cm)⁻¹, and the electrical conductivity of TiO has been measured to be 3060 (ohm-cm)⁻¹. This TiO value is almost twice that of the Magneli phase Ti₄O₇. With this invention, the TiO is considered to be an important component of the over-all electrical conductivity. Through judicious selection of the sub-oxide titanium reduction process conditions to make a well-defined TiO structure and with the aforementioned metal compound additions to the starting materials for the titanium oxides, a synergism effect occurs during processing and results in a stable and chemical resistance TiO structure within the ceramic matrix of the sub-oxides of titanium. Separately, the '917 and '215 patents do not teach super-oxides of titanium (superstoichiometric “TiO₂”) in which the atomic oxygen to titanium ratio is slightly above 2.

A preferred composition of matter for the electrically conductive ceramic material, fibers, powders, chips and substrates of the sub-oxides of titanium with additives is as follows:



	Constituent	Weight Percent (%)

	Ti_nO_2n−1where n = 4 or greater	80-90
	TiO	0-10
	Ti₂O₃and Ti₃O₅	>>>1
	M oxides, and/or borides, and/or carbides,	0-10

and/or nitrides and/or free metal, wherein the sum of the above percentages is less than or equal to 100% and wherein M=Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, B, Al, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te. [0040]
Another composition of matter for the electrically conductive ceramic material, fibers, powders, chips and substrates of the sub-oxides of titanium, if there were no metal compound additives, and if the starting materials were only TiO[0041] ₂(preferably rutile) and metal-containing intercalated graphite, is:

Constituent Weight Percent (%)

Ti_nO_2n−1where n = 4 or greater 90-100

M oxides and/or free metal 0-10

Where M = Cr, Cu, Ni, Pt, Ta, Zn, Mg, Ru,

Ir, Nb, V.
A preferred composition of matter for the electrically conductive ceramic material, fibers, powders, chips and substrates of the sub-oxides of vanadium with additives is as follows: [0042]

Constituent Weight Percent (%)

VOx (x = 1 to 2.5) 50-90

M oxides, and/or borides, and/or carbides, 10-50

and/or nitrides and/or free metal
wherein the sum of the above-noted weight percents is less than or equal to 100 and wherein M=Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, b, Al, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te. [0043]
Another composition of matter for the electrically conductive ceramic material, fibers, powders, chips, and substrates of the sub-oxides of vanadium, if there were no metal compound additives, and if the starting materials were only V[0044] ₂O₃and metal-containing intercalated graphite, is:

Constituent Weight Percent (%)

VOx (x = 1 to 2.5) 90-100
M oxides and/or free metal [0045]
Where M=Cr, Cu, Ni, Pt, Ta, Zn, Mg, Ru, [0046]
Ir, Nb, V either singly or mixtures thereof. 0 . . 10 [0047]
For electrically conductive ceramics made by plating, coatings, and deposition of metals and/or conductive ceramic, the composition of matters are as follows: [0048]

Constituent Weight Percent (%)

Al₂O₃ 85-90

M oxides and/or free metal 5-15
Where M=Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, In, Tl, Sn, Pb, Sb, Bi, Se, Te either singly or mixtures thereof. [0049]

Constituent Weight Percent (%)

ZrO₂ 85-95

M oxides and/or free metal 5-15
Where M=Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, B, Al, Ti, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te singly or mixtures thereof. [0050]

Constituent Weight Percent (%)

Al₂O₃ 40-48

ZrO₂ 40-48

M oxides and/or free metal 4-20
Where M=Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, B, Al, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te, singly or mixtures thereof. [0051]
Examples of applications in which the conductive ceramic materials of the present invention can be used are the following: (1) the use of fibers, powder, or chips in the cathode active materials of the lead-acid, lithium, nickel, Zn, and metal air batteries; (2) the use of fibers, powder or chips to make substrates for use as current collectors and electrodes and the use of fiber, powder, and chips in electrodes for fuel cells; (3) the use of fibers, powders or chips to make substrates for use as electrodes for electrosynthesis, cathodic protection, electrocatalysis, electrolysis, and metal recovery; (4) the use of fibers, powder and chips to make substrates which can act as bipolar electrode construction for lead-acid batteries; (5) the use fibers, powders and chips to make substrates for use as electrodes and the use of fibers and powder in glass for capacitors; (6) the use of fibers, powders, chips to make a substrate which can act as an electrode in sensors. If so desired, the electrodes fabricated from this invention can be plated, coated, or deposited with metals to enhance their electrochemical properties. [0052]

Forming of Shaped Materials

Electrically conductive ceramic materials and fibers can be formed from the oxides of titanium or vanadium material that may or may not have metal containing additives and “in situ” reduction agents dispersed therein. Shaping may be done on either electrically-conducting or electrically non-conducting materials. In the latter case, activation of the oxide to a conducting state is done on the shaped material. For titanium or vanadium materials, this activation may be done by chemical reduction. Normally non-conducting oxides such as Al[0053] ₂O₃or ZrO₂are made conducting by plating of conducting materials, as is discussed below. In the following, various possible shapes are discussed.

Fibers

These ceramic matrixes are made into fibers by known fiber-making processes such as the viscous suspension spinning process (Cass, Ceramic Bulletin, Vol. 70, pages 424-429, 1991) with and without metal-containing intercalated graphite, or by the sol-gel process (Klein, Sol-Gel Technology for Thin Films, Fibers, Preforms, Electronics, and Speciality Shapes, Noyes Publications, pages 154-161), and or by either the slurry or solution extrusion process (Schwartz,Handbook of Structural ceramics, page 4.55, 1992). The procedures for sample slurry or slip preparation, drawing or extruding material as well as the appropriate drying to remove water, heating to burn off organics, and sintering are discussed in detail in these articles. After the sintering operation at 1000-2000° C., these ceramic fiber materials are made electrically conductive through reduction in a furnace at 1000-2000° C. whose atmosphere is either hydrogen, carbon monoxide or mixtures of these gases. In addition, depending on the metal containing additives in the starting ceramic matrix, “in situ” reduction and/or decomposition processes occur during the drying, heating, sintering and reduction cycles via the use of “in situ” reduction materials such as carbon, metal-containing intercalated graphite, graphite, and metal powders incorporated either singly or mixtures thereof into the ceramic matrix. Once after the reduction process has ended, the fibers are cooled in a dry atmosphere and stored until use. At this point, the electrically conductive ceramic fibers are now ready for use. All initial starting materials are in powdery form and the ceramic matrix powders have been mixed to obtain a homogeneous mixture of materials before preparing the slurry or slip prior to the fiber making process. For enhanced ceramic matrix reactivity, it is preferred that the particle size of the powders be in the range of 40 to 150 microns. Preferably, the electrically conductive ceramic fibers have an aspect ratio of greater than 1 and an electrical conductivity value of 0.1 (ohm-cm)[0054] ⁻¹or greater.
Non-electrically conductive ceramic fibers are formed from alumina (Al[0055] ₂O₃) or zirconia (ZrO₂) or zirconia-alumina material with no metal containing additives or “in situ” reduction agents. These ceramic matrixes are then made into fibers by the previously mentioned viscous suspension spinning process, or by the sol-gel process, and/or by either the slurry or solution process. The sample slurry or slip preparation, drawing or extruding material as well as the appropriate drying to remove water, heating to burn off organics, sintering and storage conditions are the same as discussed for the electrically conductive ceramics matrixes. All the initial starting materials are in powdered form and are mixed to obtain a homogeneous mixture before slurry or slip preparation prior to the fiber-making process. It is preferred that the particle size of the starting powders be in the range of 40 to 150 microns. The ceramic fibers so obtained are considered to be insulators or non-electrically conductive.
Details of Spinning and Sintering to Make Fibers [0056]
In forming the conductive ceramic fibers by solution spinning and sintering, a suspension of particles of ceramic material in a solution of destructible carrier dissolved in a solvent is prepared. The fibers then are wet or dry spun from the suspension, dryed and fired to drive off the carrier and sinter the fiber. Preferably, the particle size is 5 microns or less, and polyvinyl alcohol/water system may be used as a carrier/solvent. [0057]
After the aforementioned components have been mixed at a certain compositional ratio characteristic of the desired ceramic material, the resulting mixture is dispersed or dissolved in a polymer compound solution. Thus, a spinning solution is obtained. Optionally, the aforementioned mixture may be roasted at an elevated temperature such as 900-1,100° C. for about 1-5 hours before it is dispersed or dissolved in the polymer compound-containing solution. [0058]
Examples of polymer compounds which may be used in the present invention include polyacrylonitrile, polyethylene, polypropylene, polyamide, polyester, polyvinyl alcohol polymers (“PVA”), cellulose derivatives (e.g., methyl cellulose, hydroxyethyl cellulose, hydroxyethylmethyl cellulose, etc.), polyvinylpyrrolidone, polyacrylamide, polyethylene glycol, etc. [0059]
Generally, the degree of saponification of the aforementioned PVA polymer may be 70-100 mol %, more preferably 85-100 mol %, most preferably 95-100 mol %. The degree of polymerization of the polymer may be 500-20,000, preferably 1,000-15,000. [0060]
Polyvinyl alcohol polymers which may be employed include ordinary unmodified polyvinyl alcohol as well as modified polyvinyl alcohols can also be used. As modified polyvinyl alcohols, a saponified copolymer of vinyl acetate and a copolymerizable comonomer may be used. Examples of these comonomers include vinyl esters such as vinyl propionate, vinyl stearate, vinyl benzoate, vinyl saturated branched fatty acid salts, etc., unsaturated monocarboxylic acids such as acrylic acid, methacrylic acid, crontonic acid, etc. and their alkyl esters, unsaturated polycarboxylic acids such as maleic acid, maleic anhydride, fumaric acid, itaconic acid, etc. and their partial esters or total esters, acrylonitrile, methacrylonitrile, acrylamide, methacrylamide, olefinsulfonic acids such as ethylenesulfonic acid, allylsulfonic acid, methacrylsulfonic acid, etc. and their salts, α-olefins such as ethylene, propylene, butene, α-octene, α-dodecene, α-octadecene, etc., vinyl ether, silane-containing monomers, etc. The concentrations of the aforementioned comonomers with respect to the copolymer may be less than 20 mol %. [0061]
As other modified polyvinyl alcohols, products obtained by modifying a vinyl acetate homopolymer or the aforementioned saponified copolymer can be used. Examples of modifying reactions include acetylation, urethanation, phosphoric acid esterification, sulfuric acid esterification, sulfonic acid esterification, etc. [0062]
A useful spinning solution for forming fibers for use in the present invention may be obtained by dispersing or dissolving a ceramic material or a substance which can be converted to a conductive ceramic material by heat treatment (preferably a fiber) in the aforementioned polymer compound solution. [0063]
As the solvents of the polymer compound solution, water or other solvents which can solubilize polymer compounds may be used. [0064]
Examples of solvents other than water include alcohols, ketones, ethers, aromatic compounds, amides, amines, sulfones, etc. These solvents may be mixed with water at certain ratios. [0065]
Polyvinyl alcohol polymers may be employed as the polymer compound. The solvents such as water, dimethyl sulfoxide, glycerin, ethylene glycol, diethylene glycol, N-methylpyrrolidone, dimethylformamide, and their mixtures can be advantageously used. [0066]
In the present invention, dry spinning may be employed to produce fibers for use in the claimed invention. As is known in the art, dry spinning entails spinning a solution drawn into air or another gas from a die or in a die-free state. The spinning draft typically is about 0.1-2.0. Subsequently, the resulting precursor fiber is heat-treated. The precursor fiber may be stretched before heat treatment. In a typical heat treatment, the fiber is baked for several minutes to several hours in a desired atmosphere to achieve a desired level of conductivity in the fiber. Then, the fiber is cooled. [0067]
There are no special restrictions on the diameter of the conductive fiber obtained. Typically, the diameter is about 200 μm or less, preferably 100 μm or less, more preferably 50 μm or less, most preferably 20 μm or less. There are no special restrictions on the lower limit. [0068]
In the aforementioned spinning solution, the weight ratio of the polymer compound with respect to the conductive ceramic material or substance which can be converted to conductive ceramic material by heat treatment is about 15 wt % or less and 3 wt % or more, preferably 10 wt % or less and 3 wt % or more, respectively. [0069]
When the aforementioned spinning solution is prepared, a dispersant for the conductive ceramic material or substance which can be converted to conductive ceramic material by heat treatment can also be used. Examples of dispersants include anionic emulsifiers, nonionic emulsifiers, and cationic emulsifiers such as polyoxyethylene (10) octylphenyl ether and sodium dodecylsulfate. Moreover, polyacrylic acid and its salts, polystyrene, neutralized maleic anhydride copolymers, maleic anhydride-isobutene copolymer, and other polymer dispersion stabilizers may be used. [0070]
There are no special restrictions on the total solid content of the aforementioned spinning solution. Generally speaking, however, the solid content is about 20-70 wt %. After the spinning solution has been dry-spun, it is dried. Thus, a continuous precursor fiber is obtained. [0071]
Sintering of mixtures of ceramic powders, optionally with metals, may also be employed to manufacture conductive ceramic fibers. In the manufacture of conductive ceramic materials by sintering, ceramic matrix material and metal additive are combined with a binder, and subjected to elevated temperatures in a selected atmosphere. The specific temperatures and the atmosphere depend on the composition to be sintered. See for example, U.S. Pat. No. 4,931,213 directed to sintering of substoichiometric TiO[0072] ₂having Cu therein. Metal containing additives which may be incorporated into the ceramic matrix by sintering have a relatively high melting point and a low vapor pressure to minimize loss of the metal containing additive. Metals which may be included in ceramic matrices to provide conductive ceramic material for use in the invention include Cu, Ni, Co, Ag, Pt, Ta, Zn, Mg, Ru, Ir, Nb, V, Sn, SnO, SnO₂, Pb, and alloys thereof, as well as other metals which are stable in the electrochemical system of the device. For example, conductive ceramic fibers formed of non-stoichiometric TiO₂such as Ti₄O₇and/or Ti₅O₉matrix having Cu therein may be employed.
Coating of Fibers [0073]
The conductive ceramic fibers employed in the invention may be coated with a metal such as Cu, Ni, Co, Ag, Pt, Ta, Zn, Mg, Ru, Ir, Nb, V, W, Sn, SnO, SnO[0074] ₂, Pb, as well as alloys thereof. Choice of metal coating on the conductive ceramic materials and fibers depends on the active material, and/or the component in which the coated conductive ceramic fibers are employed. For example, in lead-acid batteries, especially useful metal coatings include Sn—Pb alloys wherein Sn may be up to 90%, remainder Pb in thicknesses of about 0.1-1.0 mil on a conductive ceramic fiber material of either Ti₄O₇and/or Ti₅O₉.
In alkaline batteries such as NiCd, NiMH, Ni—Fe, Ni—Zn and MnO[0075] ₂—Zn, especially useful metal coatings include Ni, Ag and Cu in thicknesses of about 0.1-1.0 mil on a conductive ceramic fiber matrix of substoichiometric TiO₂such as Ti₄O₇and/or Ti₅O₉intercalated with Cu.
In Li batteries such as Li—MnO[0076] ₂, especially useful coatings include Ni, Ag, Cu, Li, and SnO₂in thicknesses of about 0.1-1.0 mil on a conductive ceramic fiber matrix of substoichiometric TiO₂such as Ti₄O₇and/or Ti₅O₉.
In Ni batteries such as NiCd, and NiMH, especially useful metal coatings include Co, Ni, NiCo alloys on a ceramic matrix of Ti[0077] ₄O₇and/or Ti₅O₉, each of which optionally may have Cu therein. In sensors such as gas sensors, especially useful coatings include SnO₂on, for example, Ti₄O₇and/or Ti₅O₉ceramic matrix, each of which may have Cu therein.
In capacitors such as TiO[0078] ₂on Ti₄O₇and/or Ti₅O₉carbon or graphite on Ti₄O₇and/or Ti₅O₉, especially useful coatings include Cu on a ceramic matrix of Ti₄O₇and/or Ti₅O₉.
The specific choice of conductive ceramic matrix material and metal containing additive therein, as well as the composition of metal coating thereon, may be determined by the art skilled in accordance with the specific electrochemical system of the device in which the fibers or other conductive ceramic materials are employed. The primary requirements are that the fiber or other conductive ceramic materials and metal coating be compatible with the electrochemistry of the battery. Accordingly, the choice of metal coating on the conductive ceramic fiber or material will vary depending on the electrochemistry of the device, the adherence of the metal coating to the ceramic matrix of the conductive ceramic fiber or material. Generally, the metal coating should not be attacked by the electrolyte in the device. [0079]
The thickness of the metal coating on the conductive ceramic fiber or other conductive ceramic materials similarly depends on the device in which the conductive ceramic fibers or other conductive ceramic materials are employed. Generally, the thickness of the applied metal coating should be sufficient to provide a pore free coating. For example, lead-acid batteries which employ conductive ceramic fibers formed of Ti[0080] ₄O₇and/or Ti₅O₉having SnO₂therein may have about a 0.001 inch thick coating of Pb, Sn, or Sb thereon. Similarly, alkaline batteries such as NiCd which employ conductive ceramic fibers formed of a Ti₄O₇and/or Ti₅O₉matrix having Ni, Co, Cn, or NiCo alloys therein may have a 0.001 inch thick coating of Ni thereon. In Li batteries such as LiMnO₂which employ conductive ceramic fibers formed of a Ti₄O₇and/or Ti₅O₉matrix having Li, Ni or Mn therein may have about a 0.001 inch thick coating of Cu thereon. In Ni batteries which employ conductive ceramic fibers formed of a Ti₄O₇and/or Ti₅O₉matrix having Ni or Co therein may have about a 0.001 inch thick coating of Co thereon.
Well known methods such as chemical vapor deposition, plasma spraying, laser deposition, and solution dipping may be employed to apply a metal coating onto the conductive ceramic fibers or other conductive ceramic materials, provided that hat method does not attack the underlying substrate. For example, tin, lead and alloys thereof can be applied by immersion dipping to provide a coating thickness on the order of microns to mils. [0081]

In a further aspect of the invention, the conductive ceramic fibers or other conductive ceramic materials may be coated with alternating metal layers of differing compositions. Useful combinations of conductive ceramic fibers or other conductive ceramic materials having metal coatings thereon are shown in Table 1.

TABLE 1


	Metal
	containing
	additive	FIRST	SECOND
	dispersed in	METAL	METAL
CERAMIC MATRIX	ceramic matrix	COATING	COATING

Ti₄O₇	Cu	Cu	NONE
Ti₄O₇	Sn	Sn	NONE
Ti₄O₇	Pb	Pb	NONE
Ti₄O₇	Cu	Sn	Pb
Ti₄O₇	Sn	Pb	NONE
Ti₄O₇	Ag	Sn—Pb alloy	—
Ti₄O₇	Sb	Pb	—
Ti₄O₇	W	—	—
Ti₄O₇	Ni	Ni	Co
Ti₄O₇	Co	Ni	—
Ti₄O₇	Ni—Co	Ni—Co	Ni
Ti₄O₇	Li	Cu	—
Ti₄O₇	Zn	Cu
Ti₄O₇	Pb—Sn	Pb—Sn
Ti₄O₇	SnO2	Pb
Ti₅O₉	Cu	Cu	NONE
Ti₅O₉	Sn	Sn	NONE
Ti₅O₉	Pb	Pb	NONE
Ti₅O₉	Cu	Sn	Pb
Ti₅O₉	Sn	Pb	NONE
Ti₅O₉	Ag	Sn—Pb alloy	—
Ti₅O₉	Sb	Pb	—
Ti₅O₉	W	—	—
Ti₅O₉	Ni	Ni	Co
Ti₅O₉	Co	Ni	—
Ti₅O₉	Ni—Co	Ni—Co	Ni
Ti₅O₉	Li	Cu	—
Ti₅O₉	Zn	Cu
Ti₅O₉	Pb—Sn	Pb—Sn
Ti₅O₉	SnO2	Pb
SiC	Li	Cu
ZrB	Li	Cu

Active pastes which employ conductive ceramic fibers or other conductive ceramic materials therein typically have about 0.1-30% of the active paste, preferably about 5-20%, as conductive ceramic fibers depending on the conductivity of the conductive ceramic fiber composition. In an active paste, the size of the fibers is sufficient to provide uniform distribution of the ceramic fiber material throughout the paste. Useful sizes of conductive ceramic fibers may vary from about 2-10 microns diameter. [0083]
Examples of components in which conductive ceramic fibers or other conductive ceramic materials may be employed include the grids of electrodes for batteries. The conductive ceramic fibers may be present in a grid in an amount of about 80 to 100% by weight of the grid. [0084]
In capacitors such as double layer capacitors and ultracapacitors, materials and components which may employ conductive ceramic fibers or other conductive ceramic materials such as Ti[0085] ₄O₇and Ti₅O₉wherein the fibers are present in amounts of about 30 to 100% based on the total weight of the plates of the capacitor.
In fuel cells, materials and components which may employ conductive ceramic fibers or other conductive ceramic materials and molded products such as electrodes formed of those fibers or other conductive ceramic materials include H[0086] ₂and O₂electrodes.
In sensors such as O[0087] ₂gas or organic vapor sensors, materials and components which may employ conductive ceramic fibers or other conductive ceramic materials include electrodes.
In bipolar batteries such as lead-acid bipolar batteries, materials and components which may employ conductive ceramic fibers or other conductive ceramic materials include for example, the active material. [0088]
Conductive ceramic fibers or other conductive ceramic materials may be formed into complex shapes suitable for use in components such as grids by known methods such as weaving, knitting, braiding, extrusion, and slip casting. The conductive ceramic fibers or other conductive ceramic materials may be formed into porous paper-like materials by known methods. The choice of method depends on the porosity and strength desired in the grid. For example, a grid formed by felting of a liquid slurry of conductive ceramic fibers has a surface area greater than that obtainable by processes such as weaving. [0089]
When forming the components by extrusion, a blend of conductive ceramic precursor material and a binder is formed by mixing. The amounts of conductive ceramic precursor material and binder may vary within wide limits depending on the shape to be extruded as well as the specific ceramic material and binder compositions. Useful binder compositions include those commonly employed in the manufacture of extruded ceramic products. Examples of useful binders include organic binders such as polyethylene, polypropylene, stearates, celluloses such as hydroxy propyl cellulose, polyesters and the like. Typically, greater amounts of binder materials are employed when forming intricately shaped articles. The specific amounts and composition of binder for use with a specific conductive ceramic precursor material to provide a blend suitable for extrusion can readily be determined by those skilled in the art. The extruded product then is dried and fired to produce the desired component such as a plaque or a bipolar electrode. [0090]
In slip casting, as is generally known in the art, a slurry of a conductive ceramic precursor material and a liquid vehicle such as water, optionally with an organic binder and surfactants, is cast into a mold to provide the desired shaped article. The specific amounts of ceramic material, organic binder and liquid vehicle can be varied depending on the density desired in the cast product. The resulting cast product is dried and fired by conventional techniques known in the art. [0091]
Felting of conductive ceramic fibers or other conductive ceramic materials also may be employed to produce components such as grids for use in electrochemical devices such as batteries. Felting can be performed as shown in the John Badger patent directed to glass mat separators. Green fibers, as well as certain sintered fibers, of the ceramic materials may be employed in well known weaving processes to produce components such as grids which then are fired for use in electrochemical devices such as batteries. [0092]
Fiber Requirements [0093]
The conductive ceramic fibers for use in the invention have a diameter and a length consistent with the processing requirements of the paste or other component in which the conductive ceramic fiber is to be employed. Generally, preferred fibers have lengths of 10 to 10,000μ and length to diameter ratios of 1 to 100. Typically, when conductive ceramic fibers are employed in active pastes, the fibers are about 0.125 inches (3,175μ) to 0.250 inches (6,350μ) long and about 0.002 to 0.007 inches diameter. The fibers, moreover, should be capable of withstanding substantial levels of shear stress. The fibers are mixed into the active material paste by conventional mixers. [0094]
The grid for use in an electrode of a device such as a battery or fuel cell may include varying amounts of ceramic fibers or other conductive device depending on the type of device. For example, in a lead acid battery, the current collector may be formed of about fifty percent, up to one hundred percent of conductive ceramic fiber material such as Ti[0095] ₄O₇or Ti₅O₉having therein an oxide which is conductive, stable to sulfuric acid and capable of nucleating PbO₂. Such oxides include SnO₂, WO₃, (TiO and Ti₄O₇and/or Ti₅O₉). Similarly, in alkaline batteries such as NiCd, about 0.1-20% conductive ceramic fibers of (TiO and (Ti₄O₇) and/or Ti₄O₇) having Ni therein may be employed.
When the ceramic fibers are formed into a grid by deposition of the fibers from a liquid slurry, the diameter of the fibers may be about 0.002-0.007 inches and have a length of about 0.125 to about 0.250 inches. Generally, the conductive ceramic fibers should be long enough to yield intersecting joints and/or span the width of the mesh size of a grid to yield a conductive pathway. Specific fiber diameters and lengths can therefore be determined by the art skilled for a specific application for a given fiber composition. [0096]
Conductive ceramic fibers may be mixed with active materials such as PbO or PbSO[0097] ₄to provide improved active material pastes. The conductive ceramic fibers are uniformly distributed throughout the active material paste to provide low resistance paths for flow of electrons between the active material particles and the grid. These low resistance paths may function to reduce the internal resistance of the device in which the active material is employed, especially at low states of charge.
Conductive ceramic fibers or other conductive ceramic materials may be employed in various devices such as batteries, fuel cells, capacitors, and sensors. Batteries may be classified according to the shape of the electrodes. These classifications include paste type electrodes and tubular electrodes. Paste type electrodes have a grid of lead or lead alloy, or a grid formed of woven, knitted, or braided conductive ceramic fibers. Tubular electrodes are made by inserting a cylindrical tube of braided fibers such as glass fibers and polyester fibers around a grid, and then filling the tube with active material. Tubular type electrodes typically are employed as positive electrodes, whereas paste type electrodes are typically positive or negative electrodes. In accordance with the invention, it is contemplated that conductive ceramic fibers or other conductive ceramic materials may be employed in paste and tubular electrodes. [0098]

The conductive ceramic fibers or other conductive ceramic materials may be admixed with additional fibers and the resulting blend employed in the active paste and current collector of a battery. The amount of additional fiber in the paste or current collector may vary depending on the physical properties desired. Useful blends are contemplated to include Ti ₄O₇and/or Ti₅O₉having SnO₂, Cu, Ni, Co, and the like therein with any of carbon fibers, nickel fibers, stainless steel fibers, olefin fibers such as polyethylene, polypropylene, cellulosic fiber, polyesters such as Dacron, and composite fibers such as lead-coated glass fibers. The amount of additional fibers may vary from about 1 to 30% based on the total weight of active material. These additional fibers may be employed to impart additional mechanical strength and corrosion resistance to components formed of the conductive ceramic fibers. Examples of useful blends are given in Table II.

TABLE II


	Ceramic
Example	Conductive	Metal	Olefin
No.	Fiber %	Fiber %	Fiber %

1	Ti₄O₇ ¹	Ni 60-20%	Polypropylene
	30-70%		10%
2	Ti₅O₉ ¹	Stainless	Polypropylene
	30-70%	Steel 60-70%	10-20%
3	SnO₂90%	—	Polypropylene
			10%
4	Ti₄O₇	—	Polypropylene
	90%		10%
5	Ti₄O₇	—	Polyester
	50-90%		10-50%

The conductive ceramic fibers or other conductive ceramic materials employed in the invention typically have conductivity sufficient to provide an increase in conductivity of the active material but yet are sufficiently porous and provide enhanced electrochemical utilization of the active material. The active material paste to which the conductive ceramic fibers are added may influence the amount of conductive ceramic fibers employed therein. For instance, in a lead-acid battery where the active paste material of the cathode is PbO[0100] ₂having about 5-10% conductive ceramic fiber of Ti₄O₇, and/or Ti₅O₉matrix, having about 0.5-1.8% metal containing SnO₂therein may be used in the cathode. In alkaline batteries such as Zn—MnO₂wherein the less conductive MnO₂material is used as the active paste material, about 1-30% conductive ceramic fiber of matrix of Ti₄O₇and/or Ti₅O₉having Cu therein may be employed in the active material. In lithium containing batteries such as Li—MnO₂, about 1-10% conductive ceramic fiber or other conductive ceramic materials of matrix Ti₄O₇and/or Ti₅O₉having Cu therein may be employed. In nickel containing batteries such as NiMH, about 1-10% conductive ceramic fiber of matrix Ti₄O₇and/or Ti₅O₉having Co therein may be employed. Typically, conductive ceramic fibers may be used as the additive in the active material in amounts of about 0.1% to 40% by weight of active material.
The diameter and length of the conductive ceramic fiber for use in devices such as batteries, fuel cells, sensors, and capacitors may vary according to the material and component to be formed therefrom, as well as the conductivity desired in the component or paste material in which the fiber is to be employed. The method used to make the specific material or component in which the conductive ceramic fiber is employed is also a factor in determining the diameter and length of the conductive ceramic fiber. [0101]
In forming an active paste which includes conductive ceramic fibers, the fibers should have dimensions sufficient to be processable with the active material of the paste. Typically, the size of the conductive ceramic fibers may vary from about 0.125-0.250 inches long and a diameter of about 0.001-0.005 inches, i.e. dimensions sufficient to retain the fibrous form within the active paste material. [0102]
Various batteries may be improved by using conductive ceramic fibers. For example, in NiCd batteries, the Ni foam electrode may be pasted with an active material of Ni(OH)[0103] ₂having about 10% conductive ceramic fibers of Ti₄O₇and/or Ti₅O₉having Ni therein. In NiMH batteries, a conductive ceramic fiber of Ti₄O₇and/or Ti₅O₉having Ni or Cu therein can be added to both the cathode of NiOH and anode formed of mischmetal hydride. In NiZn batteries, a conductive ceramic fiber of Ti₄O₇and/or Ti₅O₉having Cu therein may be added to a paste of ZnO.
Nickel electrodes also may employ conductive ceramic fibers by adding the fibers to the electrode material, principally NiOOH. [0104]
In a nickel-cadmium alkaline cell, porous nickel plates are used in both the positive and negative electrodes. The active material for the positive and negative electrodes is contained within the nickel plates. The positive plate contains nickel hydroxide while the negative plate contains cadmium hydroxide. To form improved electrodes for use in a Ni—Cd cell, a blend of NiOH, CdOH and 0.5-5% of conductive ceramic fiber of Ti[0105] ₄O₇and/or Ti₅O₉, each having Cu, Ni therein, is mixed with about 0.5-5% organic polymeric binder such as carboxy methylcellulose in aqueous solution sufficient to provide an active material paste.
In lithium containing batteries such as Li—AgV[0106] ₂O₅, Li—CF, Li—CuO, Li—FeS, Li—FeS₂, Li—I₂, Li—MnO₂, Li—MoS₂, Li—V₂O₅, Li—SOCl₂, and Li—SO₂, especially useful ceramic conductive fibers include Li, Co, Cu or Ni in a ceramic matrix of Ti₄O₇and/or Ti₅O₉. Ceramic conductive fibers or other conductive ceramic materials such as Ti₄O₇or Ti₄O₉having Co or Cu therein can be manufactured using the viscous suspension spinning process described by Cass in Ceramic Bulletin, No. 70, pages 424-429, 1991 or by other processes described herein.
In batteries in which a lithium compound of lithium thermodynamic activity less than that of lithium metal is the anode material (one example of which is lithium intercalated into graphite or petroleum coke, see J. M. Tarascon and D. Guyomard, Electrochimica Acta, 38: 1221-1231 (1992)) and the cathode material is selected from the group containing AgV[0107] ₂O₅, CF_x, CuO, MnO₂, FeS, FeS₂, TiS₂, MoS₂, V₂O₅, SOCl₂, SO₂, and I₂, and lithium-containing materials derived therefrom (including those cathode materials suitable for “rocking chair” batteries as described by Michel Armand in “Materials for Advanced Batteries”, eds. D. W. Murphy, J. Broadhead, and B. C. H. Steele, Plenum Press, New York, at page 160 and as described by J. M. Tarascon and D. Guyomard, Electrochimica Acta 38: 1221-1231 (1992)), ceramic conductive fibers may be added to the cathode material to enhance current collection. Especially useful ceramic conductive fibers include Ni, Co, Cu and NiCo alloy in a ceramic matrix of Ti₄O₇and/or Ti₅O₉with or without TiO. Ceramic conductive fibers such as Ti₄O₇—Ni, Ti₅O₉—Cu are available from ACI.
While the present invention has been described with respect to various specific embodiments and examples it is to be understood that the invention is not limited thereto and that it can be variously practiced within the scope of the following claims. [0108]

Powders

Electrically conductive ceramic powders are formed from the oxides of titanium or vanadium material that may or may not have metal containing additives and “in situ” reduction agents such as carbon, metal-containing intercalated graphite, graphite, and metal powders incorporated singly or mixtures dispersed therein. All materials for making electrically conductive ceramic powders are in powdery form and mixed to obtain a homogeneous mixture. For enhanced ceramic matrix reactivity, it is preferred that the particle size of the powders be in the range of 40 to 150 microns. This powder mixture is placed in a furnace at 300° C. to burn off the organics and then heated up to 1000-2000° C. in a reducing atmosphere of hydrogen or carbon monoxide or mixtures of these gases. In general, the reduced powdered mixture needs to be ground up to meet the particle size requires for an aspect ratio of 1. [0109]

Chips

Electrically conductive chips are made from the oxides of titanium or vanadium material that may or may not have metal containing additives and “in situ” reduction agents such as carbon, metal-containing graphite, graphite, and metal powders incorporated singly or mixtures dispersed therein. All materials for making electrically conductive ceramic chips are in powdery form and mixed to obtain a homogeneous mixture. A slip is made from this mixture and used in a tape casting process (See Mistler, Tape Casting Chapter in Engineered Materials Handbook, Vol. 4, 1992) which makes a dried or “green” (unfired) tape of the ceramic matrix. This dried tape is then cut into ceramic chips with a pasta or like cutting machine. The chips are then placed in a furnace in air at 300° C. to burn off the organics, then the furnace temperature is raised to 1000-2000° C. for sintering and after this the furnace atmosphere, but not the temperature, is changed to a reducing gas such as hydrogen or carbon monoxide or a mixture of both gases. For some electrochemical device applications, the dried tape can be thermally processed and reduced without cutting into chips for use as electrodes or layers in a multilayer chip capacitor. After thermally processing and reducing, the chips are roughly rectangular in size and the aspect ratio (aerodynamic definition (long dimension/short dimension)) is 8 or less. The hot chips are cooled in a dry, inert atmosphere and stored in a sealed container. At this point, the electrically conductive ceramic chips are ready to use. [0110]
Non-electrically conductive ceramic chips are made from alumina (Al[0111] ₂O₃) or zirconia (ZrO₂) or zirconia-alumina material with no metal-containing additives or “in situ” reduction agents. All materials for making non-electrically conductive ceramic chips are in powdered form and are mixed to obtain a homogeneous mixture. A slip is made from this mixture and used in tape casting to make a dried tape of the ceramic matrix. This dried tape is then cut into ceramic chips with a pasta or like cutting machine. The chips are then placed in a furnace in air at 300° C. to burn off the organics, then the furnace temperature is raised to 1000-2000° C. for sintering and after this the furnace atmosphere, but not the temperature, is changed to a reducing gas such as hydrogen or carbon monoxide or a mixture of both gases. For some electrochemical device applications, the dried tape can be thermally processed without cutting into chips. The dried tape can then be cut into electrodes and coated with a metal or metals. for a particular application. After thermally processing, the chips are roughly rectangular in size and the aspect ratio (aerodynamic definition (long dimension/short dimension)) is 8 or less. The hot chips are cooled in a dry, inert atmosphere and stored in sealed containers. At this point, the non-electrically conductive ceramic chips are ready to be coated, plated, or deposited with a metal or metals to make them electrically conductive and/or catalytically active.

Substrates

For substrate (grids, electrodes, current collectors, separators, porous sheets, foam, honey-comb sheets, solid sheets) fabrication, the electrically conductive ceramic materials, fibers, powders and chips can be mixed with a suitable binding agent and filler and the resulting mixture molded in a ram press or extruded into the desired shape. The shape is then vitrified in a non-oxidizing atmosphere at 1000-2000° C. to inhibit the oxidation of the sub-oxides of the titanium or vanadium. After this vitrification process, the cooled substrates are ready for use. The ceramic foam can be made by the Scotfoam process (Selee Corporation). [0112]
Activation of Non-Electrically Conducting Materials [0113]
Since the electrically conducting ceramic fibers, powders, chips and substrates have their own intrinsic electrical conductivity developed by metal compound additives and/or by a reduction of the metal sub-oxide, it only remains for the non-electrically conducting ceramic fibers, powders, chips and substrates to be made electrically conductive. The increase in electrical conductivity for the non-electrically conductive ceramic materials as well as electrically conductive substrates is done by plating or coating or deposition of singly or a mixture thereof metallic d-block transition elements (Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Lanthanides (Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu) and by the addition or plating or coating or deposition singly or a mixture thereof selected main-group elements (In, Tl, Sn, Pb, Sb, Bi, Se, Te). All materials used should have a purity level that excludes deleterious substances for this process as well as the projected use. There are several metal plating, metal deposition and ceramic coating techniques that can be used to treat the non-electrically conductive material and they are as follows: (1) electroless plating for non-conductors using a reducing solution of either formaldehyde or hydrazine to plate out the desired metal or metals (see Lowenheim, Electroplating, pages 387-425, 1978 and 1994 Products Finishing Directory, page 112-130); (2) thermal metal spraying (See Thorp, Chemical Engineering Progress, pages 54-57, 1991) of the desired metal or metals and electrically conductive ceramic; and (3) layer-by-layer deposition:ion beam sputtering and laser deposition (Beardsley, Scientific American, pages 32-33, 1995 and Wasa, et al., Science and Technology of Thin Film Superconductors-2, pages 1-2) to deposit electrically conductive ceramic materials as defined in this invention, and any other method to provide suitable plating, coating or deposition of the desired metal. Once the non-electrically conductive ceramics have been interacted with metal, metals or electrically conductive ceramic, they are now ready for use. [0114]

Claims

1. An electrical energy device having at least one component having conductive ceramic fibers therein, said fibers having a length of about 10 to about 10,000μ (1μ=10⁻⁶m) and a length to diameter ratio of about 1 to about 20.

2. The device of claim 1 wherein said conductive ceramic fibers have a ceramic matrix and metal containing additive dispersed within said ceramic matrix.

3. The device of claim 2 wherein said device is capable of at least one of either generating electrical energy or storing electrical energy.

4. The device of claim 3 wherein said device is at least one of batteries, fuel cells, capacitors, and sensors.

5. The device of claim 4 wherein said device is a battery.

6. The device of claim 5 wherein said battery is at least one of lead-acid batteries, alkaline batteries, sulfur containing batteries, lithium containing batteries, and nickel containing batteries.

7. The device of claim 2 wherein said conductive ceramic fibers have at least one metal coating thereon.

8. The device of claim 7 wherein said metal coating is substantially the same composition as said metal containing additive in said fibers.

9. The device of claim 6 wherein said battery is a lead acid battery.

10. The device of claim 6 wherein said battery is an alkaline battery.

11. The device of claim 10 wherein said alkaline battery is any of Zn—AgO₂, Zn—AgO, Zn—AgNO₂, Zn—Ag₂PbO₂, Zn—HgO, Zn—MnO₂.

12. The device of claim 11 wherein said alkaline battery includes at least one conductive ceramic fiber selected from the group of titanium suboxides and titanium superoxides.

13. The device of claim 6 wherein said sulfur containing battery is a sodium-sulfur battery.

14. The device of claim 13 wherein said sodium-sulfur battery includes at least one conductive ceramic fiber comprising TiO and an oxide selected from the group of Ti₄O₇, Ti₅O₉, copper-intercalated Ti₄O₇and copper-intercalated Ti₅O₉.

15. The device of claim 6 wherein said device is a lithium containing battery of any of Li—AgV₂O₅, Li—CF, Li—CuO, Li—FeS, Li—FeS₂, Li—I, Li—MnO₂, Li—MoS₂, Li—V₂O₅, Li—TiS₂, Li—SOCl₂, Li—SO₂.

16. The device of claim 15 wherein said lithium containing battery includes at least one conductive ceramic fiber selected from the group of substoichiometric titanium and superstoichiometric titanium dioxide.

17. The device of claim 6 wherein said device is a Ni containing battery of any one of Ni—Cd, Ni—H₂, Ni—Zn, Ni—MH and Ni—Fe.

18. The Ni containing battery of claim 17 wherein said battery includes at least one conductive ceramic fiber selected from the group of Ti₄O₇intercalated with Cu, and Ti₅O₉intercalated with Cu.

19. The device of claim 3 wherein said device is a fuel cell.

20. The device of claim 3 wherein said device includes at least one electrode having conductive ceramic fibers therein, said electrode having at least one of a current collector and active material.

21. The device of claim 20 wherein said conductive ceramic fibers are present in at least one of said current collector or said material.

22. The device of claim 19 wherein said fibers are present in said collector in an amount of about 50 to 100% by weight of said collector.

23. The device of claim 20 wherein said fibers are present in said paste in an amount of about to % by weight of said paste.

24. The device of claim 21 wherein said matrix material is selected from the group of oxides, carbides, nitrides, and borides.

25. The device of claim 24 wherein said oxide is selected from the group of substoichiometric titanium dioxides, superstoichiometric titanium dioxides, and perovskite oxides.

26. The device of claim 25 wherein said perovskite oxide is tungsten oxide.

27. The device of claim 24 wherein said metal containing additive is selected from the group of Cu, Ni, Co, Ag, Pt, Ta, Zn, Mg, Ru, Ir, Nb, V, Sn, SnO, SnO₂, Pb, Pd, Ir and alloys thereof.

28. The device of claim 27 wherein said oxide is substoichiometric titanium dioxides and said metal containing additive is selected from the group of Sn, SnO, and SnO₂.

29. The device of claim 3 wherein said device is in the form of a capacitor.

30. The device of claim 29 wherein said capacitor includes conductive ceramic fiber therein.

31. The device of claim 30 wherein said conductive ceramic fibers are selected from the group of titanium suboxide and titanium superoxides.

32. The device of claim 3 wherein said sensors include at least one of thermal sensors and chemical sensors.

33. The device of claim 32 wherein said thermal sensor is in the form of single fibers or bundles of conductive, doped ceramic fibers.

34. The device of claim 33 wherein said chemical sensor is in the form of a sheet, paper, nonwoven or woven mat, and composed principally of conductive ceramic fibers.

35. A lead-acid battery having a plurality of electrodes therein, said electrode comprising an active material composition and a current collector, wherein conductive ceramic fibers are included in at least one said active material and said current collector.

36. The lead acid battery of claim 35 wherein said active material composition is lead dioxide and said conductive ceramic fibers have a substoichiometric titanium dioxide matrix and a Sn—Pb alloy dispersed throughout said matrix.

37. The lead acid battery of claim 36 wherein said current collector comprises conductive ceramic fibers from the group of substoichiometric titanium and superstoichiometric titanium.

38. The lead acid battery of claim 37 wherein said conductive ceramic fiber is a ceramic matrix of substoichiometric titanium dioxide having Sn—Pb alloy therein.

39. The lead acid battery of claim 38 wherein said substoichiometric titanium dioxide is Ti₄O₇.

40. The device of claim 5 wherein the anode compartment comprises a lithium material of thermodynamic activity less than that of lithium metal.

41. The device of claim 40 wherein the cathode compartment comprises a material containing manganese.

42. The device of claim 40 wherein the electrolyte material comprises an organic polymer.

43. The device of claim 40 wherein the anode compartment comprises a carbon material selected from the group containing graphite and petroleum coke.

44. The device of claim 5 wherein the battery is of bipolar design.

45. A battery which comprises an electrically conducting ceramic comprising an electrically conducting vanadium oxide.

46. A battery which comprises an electrically conducting ceramic comprising an oxide selected from the group of Al₂O₃and ZrO₂coated with a metal.

47. An electrically conductive composition comprising, about 80 to about 90% Ti_nO_(2n-1)where n=4 or greater,

up to about 10% TiO,

at least 1% (Ti₂O₃and Ti₃O₅), and

up to about 10% of an additive selected from the group consisting of M oxides, M borides, M carbides, M nitrides, and M metal, or mixtures thereof,

wherein M is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu. Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, B, Al, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te.

48. An electrically conductive ceramic composition comprising, at least about 90% Ti_nO_(2n-1)where n is at least 4, and up to about 10% of an additive selected from the group consisting of M oxides, M metal or mixtures thereof,

wherein M is selected from the group consisting of Cr, Cu, Ni, Pt, Ta, Zn, Mg, Ru, Ir, Nb and V.

49. An electrically conductive composition comprising,

about 50% to about 90% VO_x(x=l-2.5),

about 10% to about 50% of an additive selected from the group consisting of M oxides, M borides, M carbides, M nitrides, and M metal,

wherein M is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, B, Al, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te.

50. The electrically conductive composition of claim 49 wherein said VO_x(x=1-2.5) is present in an amount of about 90% to about 100%,

said additive is selected from the group consisting of M oxides, M metal, or mixtures thereof,

wherein M is selected from the group consisting of Cr, Cu, Ni, Pt, Ta, Zn, Mg, Ru, Ir, Nb, V or mixtures thereof.

51. A composition comprising,

Al₂O₃and a component selected from the group consisting of N oxides, N metal or mixtures thereof,

wherein N is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, In, Tl, Sn, Pb, Sb, Bi, Se, Te or mixtures thereof.

52. The composition of claim 51 wherein said Al₂O₃is present in an amount of about 85% to about 90% based on total weight of said composition.

53. The composition of claim 52 wherein said component is present in an amount of about 5 to about 15%, based on total weight of said compositions.

54. A composition comprising ZrO₂and a component selected from the group consisting of N oxides, N metal or mixtures thereof,

where M is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, In, Tl, Sn, Pb, Sb, Bi, Se, Te or mixtures thereof.

55. The composition of claim 54 wherein said ZrO₂is present in an amount of about 85% to about 95% based on total weight of said composition, and said component is present in an amount of about 5% to about 15% of said composition.

56. A composition comprising Al₂O₃, ZrO₂and a component selected from the group consisting of M oxides, N metal or mixtures thereof,

where N is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, In, Tl, Sn, Pb, Sb, Bi, Se, Te or mixtures thereof.

57. The composition of claim 56 wherein said Al₂O₃is present in an amount of about 40% to about 48%,

said ZrO₂is present in an amount of about 40% to about 48%, and

said component is present in an amount of about 4% to about 20%.

58. A cathode having an electrically conductive ceramic composition.

59. The cathode of claim 58 wherein said composition comprises,

Ti_nO_(2n-1)where n=4 or greater, TiO, (Ti₂O₃and Ti₃O₅) and a component selected from the group consisting of [N] M oxides, N borides, M carbides, N nitrides, and N metal, or mixtures of said N oxides, N borides, N carbides, N nitrides, and N metal,

wherein N is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, B, Al, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te.

60. The cathode of claim 59 wherein said Ti_nO_(2n-1)is present in an amount of about 80 to about 90% based on total weight of the composition, said TiO is present in an amount of up to about 10% based on total weight of the composition, said (Ti₂O₃and Ti₃O₅)is present in an amount of at least about 1%, and said component is present in an amount of up to about 10%.

61. A cathode having a composition comprising,

at least about 90% Ti_nO_(2n-1)where n is at least 4, and

up to about 10% of a component selected from the group of M oxides, M metal or mixtures thereof,

where M is selected from the group consisting of Cr, Cu, Ni, Pt, Ta, Zn, Mg, Ru, Ir, Nb and V.

62. A cathode having a composition comprising VO_x(x=l-2.5), and

a component selected from the group consisting of M oxides, N borides, M carbides, N nitrides, and M metal

63. The cathode of claim 62 wherein said VO_x(x=l-2.5) is present in an amount of about 50 to about 90%, and

said component is present in an amount of about 10% to about 50%.

64. A cathode having a ceramic composition and a metallic coating on said ceramic composition.

65. The cathode of claim 64 wherein said composition comprises Al₂O₃and a component selected from the group consisting of N oxides, N metal or mixtures thereof,

66. The cathode of claim 65 wherein said Al₂O₃is present in an amount of about 85% to about 90%, and

said component is present in an amount of about 5% to about 15%.

67. The cathode of claim 64 wherein said composition comprises,

ZrO₂and a component selected from the group consisting of M oxides, metal or mixtures thereof,

68. The cathode of claim 67 wherein said ZrO₂is present in an amount of about 85% to about 95%, and

said component is present in an amount of about 5 to about 15%.

69. The cathode of claim 64 wherein said composition comprises Al₂O₃, ZrO₂and a component selected from the group consisting of M oxides, N metal or mixtures thereof, where M is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, In, Tl, Sn, Pb, Sb, Bi, Se, Te or mixtures thereof.

70. The cathode of claim 69 wherein said Al₂O₃is present in an amount of about 40% to about 48%,

said ZrO₂is present in an amount of about 40% to about 48%, and

said component is present in an amount of about 4 to about

71. A battery having a cathode according to claim 70.

72. The battery of claim 71 wherein said battery is a lithium battery.

73. The battery of claim 71 wherein said battery is a Zn air battery.

74. The battery of claim 71 wherein said battery is an Al air battery.

75. The battery of claim 71 wherein said battery is a Leclanche battery.

76. The battery of claim 71 wherein said battery is a sodium sulphur battery.

77. The battery of claim 71 wherein said battery is a Nickel battery.

78. The battery of claim 71 wherein said battery is a lead acid battery.

79. A fuel cell electrode comprising an electrically conductive ceramic composition.

80. The electrode of claim 79 wherein said composition comprises Ti_nO_(2n-1)where n=4 or greater, TiO, (Ti₂O₃and Ti₃O₅) and a component selected from the group of M oxides, M borides, M carbides, M nitrides, and M metal, or mixtures thereof,

81. The electrode of claim 80 wherein said Ti_nO_(2n-1)where n=4 or greater is present in an amount of about 80% to about 90%,

said TiO is present in an amount of up to about 10%,

said (Ti₂O₃and Ti₃O₅) is present in an amount of at least 1%, and

said component is present in an amount of up to about 10%.

82. The electrode of claim 79 wherein said composition comprises Ti_nO_(2n-1)where n is at least 4, and a component selected from the group of M oxides, M metal or mixtures thereof,

83. The electrode of claim 82 wherein said Ti_nO_(2n-1)where n is at least 4 is present in an amount of at least about 90%, and

said component is present in an amount of up to about 10%.

84. The electrode of claim 79 wherein said composition comprises VO_x(x=1-2.5), and a component selected from the group consisting of M oxides, M borides, M carbides, M nitrides, and M metal,

wherein N is selected from the group consisting of Sc, Ti, V, Cr. Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, B, Al, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te.

85. The electrode of claim 84 wherein said VO_x(x=l-2.5) is present in an amount of about 50% to about 90%, and

said component is present in an amount of about 10% to about 50%.

86. A fuel cell electrode having a ceramic composition and a metallic coating on said ceramic composition.

87. The electrode of claim 86 wherein said composition comprises Al₂O₃and a component selected from the group consisting of N oxides, M metal or mixtures thereof,

88. The electrode of claim 86 wherein said Al₂O₃is present in an amount of about 85% to about 90%, and

said component is present in an amount of about 5 to about 15%.

89. The electrode of claim 86 wherein said composition comprises ZrO₂and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

90. The electrode of claim 89 wherein said ZrO₂is present in an amount of about 85% to about 95%, and said component is present in an amount of about 5% to about 15%.

91. The electrode of claim 86 wherein said composition comprises Al₂O₃, ZrO₂and a component selected from the group consisting of N oxides, N metal or mixtures thereof,

92. The electrode of claim 91 wherein said Al₂O₃is present in said composition an amount of about 40% to about 48%, said ZrO₂is present in said composition an amount of about 40% to about 48%, and said component is present in said composition in an amount of about 4% to about 20%.

93. A fuel cell having an electrode according to claim 92.

94. A current collector having an electrically conductive ceramic composition.

95. The current collector of claim 94 wherein said composition comprises Ti_nO_(2n-1)where n=4 or greater, TiO, (Ti₂O₃and Ti₃O₅) and a component selected from the group consisting of N oxides, M borides, N carbides, N nitrides, and N metal, or mixtures thereof,

96. The current collector of claim 95 wherein said Ti_nO_(2n-1)is present in said composition in an amount of about 80% to about 90%,

said TiO is present in an amount of up to about 10%,

said (Ti₂O₃and Ti₃O₅) is present in an amount of at least 1%, and

said component is present in an amount of up to about 10%.

97. The current collector of claim 94 wherein said composition comprises Ti_nO_(2n-1)where n is at least 4, and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

98. The current collector of claim 97 wherein said Ti_nO_(2n-1)is present in said composition an amount of at least about 90%, and said component is present in an amount up to about 10%.

99. The current collector of claim 94 wherein said composition comprises VO_x(x=l-2.5), and a component selected from the group consisting of M oxides, M borides, M carbides, M nitrides, and M metal,

100. The current collector of claim 99 wherein said VO_x(x=1-2.5) is present in said composition an amount of about 50% to about 90%, and

said component is present in said composition in an amount of about 10-50%.

101. A current collector having a ceramic composition and a metallic coating on said ceramic composition.

102. The current collector of claim 101 wherein said composition comprises Al₂O₃and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

103. The current collector of claim 102 wherein said Al₂O₃is present in said composition an amount of about 85% to about 90%, and said component is present in said composition in an amount of about 5 to about 15%.

104. The current collector of claim 101 wherein said composition comprises ZrO₂and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

105. The current collector of claim 104 wherein said ZrO₂is present in said composition in an amount of about 85 to about 95%,

and said component is present in said composition in an amount of about 5% to about 15%.

106. The current collector of claim 101 wherein said composition comprises Al₂O₃, ZrO₂and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

107. The current collector of claim 106 wherein said Al₂O₃is present in said composition an amount of about 40% to about 48%,

said ZrO₂is present in said composition in an amount of about 40% to about 48% ZrO₂, and

said component is present in said composition in an amount of about 4% to about 20%.

108. A bipolar electrode having an electrically conductive ceramic composition.

109. The bipolar electrode of claim 108 wherein said composition comprises Ti_nO_(2n-1)where n=4 or greater, TiO, (Ti₂O₃and Ti₃O₅) and a component selected from the group consisting of N oxides, M borides, M carbides, M nitrides, and M metal, or mixtures thereof,

110. The bipolar electrode of claim 109 wherein said Ti_nO_(2n-1)where n=4 or greater is present in said composition in an amount of about 80% to about 90%, said TiO is present in said composition in an amount of up to about 1%, and

said (Ti₂O₃and Ti₃O₅) is present in said composition in an amount at least 1%, and

said component is present in an amount of up to about 10%,

111. The bipolar electrode of claim 108 wherein said composition comprises at least about 90% Ti_nO_(2n-1)where n is at least 4, and up to about 10% of said component, and

112. The bipolar electrode of claim 108 wherein said composition comprises VO_x(x=l-2.5), and a component selected from the group consisting of N oxides, N borides, M carbides, N nitrides, and M metal,

wherein N is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, B, Al, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te and mixtures thereof.

113. The bipolar electrode of claim 112 wherein said VO_x(x=1-2.5) is present in said composition in an amount of about 50% to about 90% and said component is present in said composition in an amount of about 10% to about 50%.

114. A bipolar electrode having a ceramic composition and a metallic coating on said ceramic composition.

115. The bipolar electrode of claim 114 wherein said composition comprises Al₂O₃and a component selected from the group consisting of M oxides, N metal or mixtures thereof,

116. The bipolar electrode of claim 115 wherein said composition comprises about 85-90% Al₂O₃and about 5% to about 15% of said component.

117. The bipolar electrode of claim 114 wherein said composition comprises ZrO₂and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

118. The bipolar electrode of claim 117 wherein said composition comprises about 85-95% ZrO₂and about 5% to about 15% of said component.

119. The bipolar electrode of claim 114 wherein said composition comprises Al₂O₃, ZrO₂and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

120. The bipolar electrode of claim 119 wherein said Al₂O₃is present in said composition in an amount of about 40% to about 48%,

121. A lead acid battery having the bipolar electrode of claim 120.

122. A capacitor having an electrically conductive ceramic composition.

123. The capacitor of claim 122 wherein said composition comprises Ti_nO_(2n-1)where n=4 or greater, TiO, (Ti₂O₃and Ti₃O₅) and a component selected from the group consisting of M oxides, M borides, M carbides, M nitrides, and M metal, or mixtures thereof,

124. The capacitor of claim 123 wherein said composition comprises about 80 to about 90% Ti_nO_(2n-1) _{where n=}4 or greater, up to about 10% TiO, at least 1% (Ti₂O₃and Ti₃O₅) and up to about 10% of said component.

125. The capacitor of claim 123 wherein said composition comprises Ti_nO_(2n-1)where n is at least 4, and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

126. The capacitor of claim 125 wherein said composition. comprises at least about 90% Ti_nO_(2n-1)where n is at least 4, and up to about 10% of said component.

127. The capacitor of claim 122 wherein said composition comprises VO_x(x=l-2.5), and a component selected from the group consisting of M oxides, M borides, M carbides, M nitrides, M metal and mixtures thereof,

wherein M is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Gs, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, B, Al, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te.

128. The capacitor of claim 127 wherein said composition comprises about 50% to about 90% VO_x(x=l2.5), and about 10 to about 50% of said component.

129. A capacitor having a ceramic composition and a metallic coating on said ceramic composition.

130. The capacitor of claim 129 wherein said composition comprises Al₂O₃and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

131. The capacitor of claim 130 wherein said composition comprises about 85% to about 90% Al₂O₃and about 5% to about 15% of said component.

132. The capacitor of claim 129 wherein said composition comprises ZrO₂and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

133. The capacitor of claim 132 wherein said composition comprises about 85% to about 95% ZrO₂and about 5% to about 15% of said component.

134. The capacitor of claim 129 wherein said composition comprises Al₂O₃, ZrO₂and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

where M is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu. Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, In, Tl, Sn, Pb, Sb, Bi, Se, Te or mixtures thereof.

135. The capacitor of claim 134 wherein said composition comprises about 40% to about 48% Al₂O₃, about 40% to about 48% ZrO₂, and about 4% to about 20% of said component.

136. A sensor having an electrically conductive ceramic composition.

137. The sensor of claim 136 wherein said composition comprises Ti_nO_(2n-1)where n=4 or greater, TiO, (Ti₂O₃and Ti₃O₅) and a component selected from the group consisting of M oxides, M borides, M carbides, M nitrides, and M metal, or mixtures of said M oxides, M borides, M carbides, M nitrides, and M metal, wherein M is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, B, Al, Tl, Si, Ge, Sn, Pb, As, Sb, Bi, Se, Te.

138. The sensor of claim 137 wherein said composition comprises about 80 to about 90% Ti_nO_(2n-1)where n=4 or greater, up to about 10% TiO, at least 1% (Ti₂O₃and Ti₃O₅) and up to about 10% of said component.

139. The sensor of claim 136 wherein said composition comprises Ti_nO_(2n-1)where n is at least 4, and a component selected from the group consisting of M oxides, M metal or mixtures thereof,

140. The sensor of claim 139 wherein said composition comprises at least about 90% Ti_nO_(2n-1)where n is at least 4, and up to about 10% of said component.

141. The sensor of claim 136 wherein said composition comprises about 50 to about 90% VO_x(x=1-2.5), and about 10-50% of a component selected from the group consisting of M oxides, M borides, M carbides, M nitrides, and M metal,

142. A sensor having a ceramic composition and a metallic coating on said ceramic composition.

143. The sensor of claim 142 wherein said composition comprises about 85-90% Al₂O₃and about 5% to about 15% of a component of a selected from the group consisting of M oxides, M metal or mixtures thereof,

144. The sensor of claim 142 wherein said composition comprises about 85-95% ZrO₂and about 5% to about 15% of a second component selected from the group consisting of M oxides, M metal or mixtures thereof,

where M is selected from the group consisting of Sc, Ti, V, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Tm, Yb, Lu, In, Tl, Sn, Pb, Sb, Bi, Se, Te or mixtures thereof.

145. The sensor of claim 142 wherein said composition comprises about 40-48% Al₂O₃, about 40-48% ZrO₂and about 4 to about 20% of a second component selected from the group consisting of M oxides, M metal or mixtures thereof,

where M is selected from the group consisting of Sc, Ti, V, Cr. Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, In, Tl, Sn, Pb, Sb, Bi, Se, Te or mixtures thereof.

146. The sensor of claim 142 wherein said sensor is an oxygen sensor.

147. The sensor of claim 142 wherein said sensor is a humidity sensor.

148. An active paste having conductive ceramic fibers, said fibers having a length of about 10 microns to about 10,000 microns and a length to diameter ratio of about 1 to about 100.

149. The active paste of claim 148 having conductive ceramic fibers,

said fibers having a length of about 3,175 microns to about 6,350 microns and a diameter of about 0.002 inches to about 0.007 inches.

150. The active paste of claim 148 wherein said active paste comprises a material selected from the group consisting of PbO and PbSO₄.

151. The active paste of claim 150 wherein said fiber comprises Ti₄O₇, Ti₅O₉, Ti₄O₇having an additive selected from the group consisting of SnO₂, Cu, Ni, and Co, Ti₅O₉having an additive selected from the group consisting of SnO₂, Cu, Ni, and Co therein, and

mixtures thereof and a second fiber selected from the group consisting of carbon fibers, nickel fibers, stainless steel fibers, olefin fibers, and cellulosic fibers, polyester fibers, and composite fibers.

152. The active paste of claim 151 wherein said second fiber is present in said paste in an amount of about 1% to about 30%.

153. The active paste of claim 152 wherein said olefin fibers are selected from the group consisting of polyethylene and polypropylene.

154. The active paste of claim 151 wherein said composite fibers are lead coated glass fibers.

155. A conductive composition comprising ceramic conductive fiber, metal fiber and olefin fiber.

156. The composition of claim 155 wherein said conductive fiber comprises Ti₄O₇, said metal fiber is Ni, and said olefin fiber is polypropylene.

157. The composition of claim 156 wherein said conductive ceramic fiber is present in said composition in an about 30% to about 70%,

said metal fiber is present in said composition an amount about 20%, and

said olefin fiber is present in said composition an amount of about 10%.

158. The composition of claim 155 wherein said conductive fiber comprises Ti₅O₉intercalated with Nb, said metal fiber is stainless steel, said olefin fiber is polypropylene.

159. The composition of claim 158 wherein said conductive ceramic fiber is present in said composition in an amount of about 30% to about 70%,

said metal fiber is present in said composition an amount of about 60% to about 70%, and

said olefin fiber is present in said composition an amount of about 10% to about 20%.

160. A conductive composition comprising a conductive ceramic fiber and an organic fiber selected from the group consisting of polyolefins and polyesters.

161. The composition of claim 160 wherein said fiber is SnO₂and said olefin is polypropylene.

162. The composition of claim 161 wherein said fiber is present in said composition an amount of about 90% and said polypropylene is present in an amount of about 10%.

163. The composition of claim 160 wherein said fiber is Ti₄O₇, intercalated with Cu, and said olefin is polypropylene.

164. The composition of claim 163 wherein said fiber is present in said composition in an amount of about 90% and said polypropylene is present in an amount of about 10%.

165. The composition of claim 160 wherein said fiber is Ti₄O₇and said organic fiber is polyester.

166. The composition of claim 165 wherein said fiber is present in said composition an amount of about 50% to about 90% and said polyester is present in said composition in an amount of about 10% to about 50%.

167. A current collector for a lead acid battery, said collector having from about 50% to about 100% of a conductive ceramic fiber selected from the group consisting of Ti₄O₇, Ti₅O₉, having an oxide selected from the group consisting of SnO₂, WO₃, (TiO and Ti₄O₇) and (TiO and Ti₅O₉).

168. An active paste comprising an electrically conductive ceramic composition.

169. The active paste of claim 168 wherein said composition comprises about 80% to about 90% Ti_nO_(2n-1)where n=4 or greater, up to about 10% TiO, at least 1% (Ti₂O₃and Ti₃O₅) and up to about 10% of a component selected from the group consisting of M oxides, M borides, M carbides, M nitrides, and M metal, or mixtures thereof,

170. The active paste of claim 169 wherein said composition comprises at least about 90% Ti_nO_(2n-1)where n is at least 4, and

up to about 10% of a second component selected from the group consisting of M oxides, M metal or mixtures thereof,

where M is selected from the group consisting of Cr, Cu, Ni, Pt, Ta, Zn, Mg, Ru, Nb and V.

171. The active paste of claim 168 wherein said composition comprises about 50% to about 90% VO_x(x=1-2.5), and about 10% to about 50% of a second component selected from the group consisting of M oxides, M borides, M carbides, M nitrides, and N metal,

172. An active paste having a ceramic composition and a metallic coating on said ceramic composition.

173. The active paste of claim 172 wherein said composition comprises about 85%-90% Al₂O₃and about 5% to about 15% of a second component selected from the group consisting of M oxides, M metal or mixtures thereof,

174. The active paste of claim 172 wherein said composition comprises about 85% to about 95% ZrO₂and about 5% to about 15% of a component selected from the group consisting of N oxides, M metal or mixtures thereof,

175. The active paste of claim 172 wherein said composition comprises about 40% to about 48% Al₂O₃, about 40% to about 48% ZrO₂, and about 4% to about 20% of a second component selected from the group consisting of N oxides, N metal or mixtures thereof,

where N is selected from the group consisting of Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu. Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, La, Hf, Ta, W, Re, Os, Ir, Pt, Au, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Tm, Yb, Lu, In, Tl, Sn, Pb, Sb, Bi, Se, Te or mixtures thereof.

176. The capacitor of claim 122 wherein said capacitor is a multi layer chip capacitor.

177. The capacitor of claim 122 wherein said capacitor is an ultra capacitor.

178. A fiber comprising a composition of claim 47.

179. The fiber of claim 178 wherein said fiber has a diameter of less than about 200 microns.

180. The fiber of claim 179 wherein said fiber has a diameter less than about 100 microns.

181. The fiber of claim 180 wherein said fiber has a diameter less than about 50 microns.

182. The fiber of claim 181 wherein said fiber has a diameter less than about 20 microns.

183. A metal coated ceramic fiber comprising a ceramic fiber and a metallic coating thereon, said metallic coating selected from the group consisting of Cu, Ni, Co, Ag, Pt, Ta, Zn, Mg, Ru, Ir, Nb, V, W, Sn, SnO, SnO₂, Pb, and alloys thereof.

184. The metal coated ceramic fiber of claim 183 wherein said metallic coating is a Sn—Pb alloy.

185. The metal coated ceramic fiber of claim 184 wherein said metallic coating is an Sn—Pb alloy having up to about 90% Sn, remainder Pb.

186. The metal coated ceramic fiber of claim 184 wherein said metallic coating is an Sn—Pb alloy having a thickness of about 0.1 mil to about 1.0 mil.

187. The metal coated ceramic fiber of claim 183 wherein said ceramic fiber comprises at least one of Ti₄O₇, Ti₅O₉, or mixtures thereof.

188. The metal coated ceramic fiber of claim 187 wherein said metallic coating comprises Ni, Ag and Cu.

189. The metal coated ceramic fiber of claim 188 wherein metallic coating has a thickness of about 0.1 mil to about 1.0 mil.

190. The metal coated ceramic fiber of claim 183 wherein said ceramic fiber comprises at least one of Ti₄O₇, Ti₅O₉, Ti₄O₇intercalated with Cu, Ti₅O₉intercalated with Cu, or mixtures thereof.

191. The metal coated ceramic fiber of claim 190 wherein said metallic coating is selected from the group consisting of Ni, Ag, Cu, Li and SnO₂and mixtures thereof.

192. The metal coated ceramic fiber of claim 191 wherein said metallic coating has a thickness of about 0.1 mil to about 1.0 mil.

193. The metal coated ceramic fiber of claim 183 wherein said ceramic fiber comprises at least one of Ti₄O₇, Ti₅O₉, or mixtures thereof.

194. The metal coated ceramic fiber of claim 193 wherein said metallic coating is selected from the group consisting of Ni, Co, NiCo alloys, and mixtures thereof.

195. The metal coated ceramic fiber of claim 193 wherein said metallic coating is SnO₂.

196. The metal coated ceramic fiber of claim 183 wherein said ceramic fiber comprises at least one of Ti₄O₇, Ti₅O₉, Ti₄O₇having Cu therein, Ti₅O₉having Cu therein, or mixtures thereof.

197. The metal coated ceramic fiber of claim 195 wherein said metallic coating is Cu.

198. A NiCd battery having about 0.1 to about 20% conductive ceramic fibers selected from the group consisting of Ti₄O₇, and mixtures of TiO and Ti₄O₇, said ceramic fibers having Ni therein.

199. An alkaline battery having the metal coated fiber of claim 183.

200. The alkaline battery of claim 199 wherein said alkaline battery is a NiCd battery.

201. The alkaline battery of claim 199 wherein said alkaline battery is a NiMH battery.

202. The alkaline battery of claim 199 wherein said alkaline battery is a NiFe battery.

203. The alkaline battery of claim 199 wherein said alkaline battery is Ni—Zn battery.

204. The alkaline battery of claim 203 wherein said alkaline battery is a MnO₂—Zn battery.

205. A Li battery having the metal coated fiber of claim 183.

206. The Li battery of claim 205 wherein said Li battery is a Li—MnO₂battery.

207. A Ni battery having the metal coated fiber of claim 183.

208. The Ni battery of claim 207 wherein said Ni battery is a NiCd battery.

209. The Ni battery of claim 207 wherein said Ni battery is a NiMH battery.

210. A sensor having the metal coated fiber of claim 183.

211. The sensor of claim 210 wherein said sensor is a gas sensor.

212. A capacitor having the metal coated fiber of claim 183.

213. The capacitor of claim 212 wherein said capacitor is TiO₂on Ti₄O₇, Ti₅O₉or mixtures thereof.

214. The capacitor of claim 212 wherein said capacitor is carbon or graphite on Ti₄O₇, Ti₅O₉or mixtures thereof.

215. A lead acid battery having a ceramic fiber having a metal coating thereon, said fiber selected from the group consisting of Ti₄O₇, Ti₅O₉, Ti₄O₇having SnO₂therein, Ti₅O₉having SnO₂therein, or mixtures thereof.

216. The lead acid battery of claim 215 wherein said metal is selected from the group consisting of Pb, Sn, Sb or alloys thereof.

217. The lead acid battery of claim 216 wherein said metal coating is about 0.001 inch thick.

218. A Li battery having a ceramic fiber having metal coating thereon, said fiber selected from the group consisting of Ti₄O₇, Ti₅O₉, Ti₄O₇having a metal selected from the group consisting of Li, Ni or Mn therein, and Ti₅O₉having a metal selected from the group consisting of Li, Ni or Mn.

219. The Li battery of claim 218 wherein said metal coating is about 0.001 inch thick.

220. A Ni battery having a ceramic fiber having metal coating thereon, said fiber selected from the group consisting of Ti₄O₇, Ti₅O₉, Ti₄O₇having therein a metal selected from the group consisting of Ni or Co, and Ti₅O₉having therein a metal selected from the group consisting of Ni or Co.

221. The Ni battery of claim 220 wherein said metal coating is about 0.001 inch thick.

222. A ceramic fiber having a plurality of metal coatings thereon,

said ceramic fiber comprising Ti₄O₇having therein a first metal selected from the group consisting of Cu, Ni, Ni—Co,

a first coating having a second metal selected from the group consisting of Sn, Ni, and Ni—Co and

a second coating having a third metal selected from the group consisting of Pb, Co, and Ni.

223. The ceramic fiber of claim 222 wherein said first metal is Cu, said second metal is Sn, and said third metal is Pb.

224. The ceramic fiber of claim 222 wherein said first metal is Ni, said second metal is Ni, and said third metal is Co.

225. The ceramic fiber of claim 222 wherein said first metal is Ni—Co, said second metal is Ni—Co, and said third metal is Ni.

226. A ceramic fiber having a plurality of metal coatings thereon,

said ceramic fiber comprising Ti₅O₉having therein a first metal selected from the group consisting of Ni and Ni—Co,

a first coating having a second metal selected from the group consisting of Ni and Ni—Co, and

a second coating having a third metal selected from the group consisting of Co and Ni.

227. The ceramic fiber of claim 226 wherein said first metal is Ni, said second metal is Ni, and said third metal is Co.

228. The ceramic fiber of claim 226 wherein said first metal is Ni—Co, said second metal is Ni—Co, and said third metal is Ni.

229. An alkaline battery having a ceramic fiber having metal coating thereon,

said fiber selected from the group consisting of Ti₄O₇, Ti₅O₉, Ti₄O₇having a metal therein, Ti₅O₉having a metal therein,

or mixtures thereof, said metal selected from the group consisting of Ni, Co, Cu, NiCo alloys, or mixtures thereof.

230. The alkaline battery of claim 229 wherein said metal coating is Ni.

231. The alkaline battery of claim 230 wherein said metal coating is about 0.001 inch thick.

232. A lead acid battery having a cathode, said cathode having an active paste material wherein the active paste material comprises PbO₂and about 5% to about 10% conductive ceramic fiber.

233. The battery of claim 232 wherein said ceramic fiber is selected from the group consisting of Ti₄O₇having SnO₂therein, and Ti₅O₉having SnO₂therein.

234. The battery of claim 233 wherein said SnO₂is present in said fiber an amount of about 0.5% to about 1.8%.

235. A Zn-MnO₂battery having an active paste comprising MnO₂; and about 1-30% conductive ceramic fibers selected from the group consisting of Ti₄O₇having Cu therein, and Ti₅O₉having Cu therein.

236. A Li—MnO₂battery having about 1-10% conductive ceramic fibers selected from the group consisting of Ti₄O₇having Cu therein, and Ti₅O₉having Cu therein.

237. A NiMH battery having about 1-10% conductive ceramic fibers selected from the group consisting of Ti₄O₇having Co therein, and Ti₅O₉having Co therein.

238. A NiCd battery having a Ni foam electrode, said electrode pasted with an active material comprising Ni(OH)₂and conductive ceramic fibers.

239. The battery of claim 238 wherein said ceramic fibers are selected from the group consisting of Ti₄O₇, having Ni therein and Ti₅O₉having Ni therein.

240. The battery of claim 239 wherein said conductive ceramic fibers are present in an amount of 10%.

241. A NiMH battery having a cathode of NiOH and an anode comprising mishmetal hydride,

said cathode having a conductive ceramic fiber comprising Ti₄O₇, Ti₅O₉, Ti₄O₇having Cu therein, Ti₅O₉having Cu therein, Ti₄O₇having Ni therein, Ti₅O₉having Ni therein, and mixtures thereof.

242. The NiMH battery of claim 241 wherein said anode comprises a conductive ceramic fiber selected from the group consisting of Ti₄O₇, Ti₅O₉, Ti₄O₇having Cu therein, Ti₅O₉having Cu therein, Ti₄O₇having Ni therein, Ti₅O₉having Ni therein, and mixtures thereof.

243. A NiZn battery having an active paste comprising ZnO, said paste having a conductive ceramic fiber selected from the group consisting of Ti₄O₇, Ti₅O₉, Ti₄O₇having Cu therein, Ti₅O₉having Cu therein, and mixtures thereof.

244. A Ni-Cd alkaline cell having an electrode comprising an active material paste, said paste comprising NiOH, CdOH, and conductive ceramic fiber.

245. The cell of claim 244 wherein said conductive fiber is present in said active paste in an amount of about 0.5% to about 5% by weight, based on the weight of the active paste.

246. The cell of claim 245 wherein said conductive fiber is selected from the group consisting of Ti₄O₇, Ti₅O₉, Ti₄O₇having Cu therein, Ti₅O₉having Cu therein, Ti₄O₇having Ni therein, Ti₅O₉having Ni therein, Ti₄O₇having Cu and Ni therein, Ti₅O₉having Cu and Ni therein, and mixtures thereof.

247. The cell of claim 246 wherein said active paste further comprises an organic polymeric binder.

248. The cell of claim 247 wherein said polymeric binder is carboxy methylcellulose.

249. The cell of claim 248 wherein said carboxy methylcellulose is present in said active paste in an amount of about 0.5-5%.

250. A Li containing battery having a conductive ceramic fiber selected from the group consisting of Ti₄O₇, Ti₅O₉, Ti₄O₇having Li therein, Ti₅O₉having Li therein, Ti₄O₇having Co therein, Ti₅O₉having Co therein, Ti₄O₇having Cu therein, Ti₅O₉having Cu therein, Ti₄O₇having Ni therein, Ti₅O₉having Ni therein, and mixtures thereof.

251. The battery of claim 250 wherein said battery is a Li—AgV₂O₅battery.

252. The battery of claim 251 wherein said battery is a Li—CF_xbattery.

253. The battery of claim 252 wherein said battery is a Li—CuO battery.

254. The battery of claim 250 wherein said battery is a LiFeS battery.

255. The battery of claim 253 wherein said battery is a Li—FeS₂battery.

256. The battery of claim 250 wherein said battery is a Li—I₂battery.

257. The battery of claim 256 wherein said battery is a Li—MnO₂battery.

258. The battery of claim 250 wherein said battery is a Li—MoS₂battery.

259. The battery of claim 250 wherein said battery is a Li—V₂O₅battery.

260. The battery of claim 250 wherein said battery is a Li—SOCl₂battery.

261. The battery of claim 250 wherein said battery is a Li—SO₂battery.

262. A Li containing battery having an anode comprising Li and a cathode comprising ceramic conductive fibers.

263. The Li containing battery of claim 263 wherein said cathode comprises a compound selected from the group consisting of AgV₂O₅CF_x, CuO, MnO₂, FeS, FeS₂, TiS₂, MoS₂, V₂O, SOCl₂, SO₂, and I₂.

264. The Li containing battery of claim 263 wherein said ceramic conductive fibers are selected from the group consisting of Ti₄O₇, Ti₅O₉, Ti₄O₇having Ni therein, Ti₅O₉having Co therein, Ti₄O₇having Cu therein, Ti₅O₉having Cu therein, Ti₄O₇having NiCo alloy therein, Ti₅O₉having NiCo alloy therein, and mixtures thereof.

265. A method of manufacture of electrically conductive ceramic product comprising forming a mixture of a ceramic oxide and organic binder, heat treating said mixture to burn off the binder, and sintering in a reducing atmosphere to form an electrically conductive ceramic powder.

266. The method of claim 265 wherein said ceramic oxide is selected from the group consisting of titanium oxides and vanadium oxides.

267. The method of claim 266 wherein said ceramic oxides have a particle size of about 40 microns to about 150 microns.

268. The method of claim 266 wherein said mixture further comprises metal containing additives.

269. The method of claim 266 wherein said mixture further comprises a reducing agent selected from the group consisting of intercalated graphite, graphite, and carbon.

270. The method of claim 265 wherein said heat treating is performed at a temperature of about 300° C.

271. The method of claim 270 wherein said sintering is performed at a temperature of about 1000-2000° C.

272. The method of claim 271 wherein said reducing atmosphere is selected from the group consisting of H, CO or mixtures thereof.

273. The method of claim 272 further comprising cooling in an inert atmosphere.

274. The method of claim 265 wherein said product is a ceramic chip.

275. A method of producing a metal coated, electrically conductive ceramic chip comprising, providing an oxide selected from the group of Al₂O₃, ZrO₂, ZrO₂—Al₂O₃or mixtures thereof, an organic binder, forming a mixture of said oxide and said binder, sintering said mixture in a reducing atmosphere to provide a sintered product, and applying a metallic coating to said sintered product.

276. The method of claim 275 wherein said reducing atmosphere is selected from the group consisting of H, CO and mixtures thereof.

277. The method of claim 276 wherein said sintering is performed at about 1000° C. to about 2000° C.

278. The method of claim 277 further comprising cooling within an inert atmosphere.

279. A method of forming a ceramic product having conductive ceramic material therein comprising,

providing a slurry comprising conductive ceramic material therein, casting said slurry to provide a shaped product, and firing said shaped product to provide said ceramic product having conductive ceramic material.

280. The method of claim 279 further comprising an organic binder.

281. A substrate comprising an electrically conductive ceramic material.

282. The substrate of claim 279 wherein said substrate is a grid.

283. The substrate of claim 279 wherein said substrate is an electrode.

284. The substrate of claim 279 wherein said substrate is a current collector.

285. The substrate of claim 279 wherein said substrate is a foam.

286. The substrate of claim 279 wherein said substrate is a honey-comb.

287. The substrate of claim 281 wherein said substrate is a solid sheet.

288. A method of making a substrate having conductive ceramic material therein comprising,

forming a mixture having conductive ceramic material therein,

molding said mixture into a preform, and firing said preform in a non-oxidizing atmosphere to yield said substrate.

289. The method of claim 288 wherein said substrate is a grid.

290. The method of claim 289 wherein said conductive ceramic material comprises sub-oxides of an element selected from the group consisting of Ti and V.

291. The method of claim 289 wherein said conductive ceramic material comprises the composition of any one of claims 47-57.

292. The method of claim 288 wherein said substrate is an electrode.

293. The method of claim 292 wherein said conductive ceramic material comprises sub-oxides of an element selected from the group consisting of Ti and V.

294. The method of claim 292 wherein said conductive fibers comprise the composition of any one of claims 47-57.

295. The of method claim 288 wherein said substrate is a current collector.

296. The method of claim 295 wherein said conductive ceramic material comprises sub-oxides of an element selected from the group consisting of Ti and V.

297. The method of claim 295 wherein said conductive ceramic material comprises the composition of claim 47.

298. The method of claim 288 wherein said substrate is a foam.

299. The method of claim 298 wherein said conductive ceramic material comprises sub-oxides of an element selected from the group consisting of Ti and V.

300. The method of claim 298 wherein said conductive ceramic material comprises the composition of claim 47.

301. The method of claim 288 wherein said substrate is a honey-comb.

302. The method of claim 301 wherein said conductive material comprises sub-oxides of an element selected from the group consisting of Ti and V.

303. The method of claim 302 wherein said conductive ceramic material comprises the composition of claim 47.

304. The method of claim 288 wherein said substrate is a solid sheet.

305. The method of claim 304 wherein said conductive ceramic material comprises sub-oxides of an element selected from the group consisting of Ti and V.

306. The method of claim 304 wherein said conductive ceramic material comprises the composition of any one of claims 47-57.

307. A method of making a substrate having a conductive ceramic material therein comprising,

forming a mixture having conductive ceramic material therein,

308. The method of claim 307 wherein said substrate is a grid.

309. The method of claim 308 wherein said conductive material comprises sub-oxides of an element selected from the group consisting of Ti and V.

310. The method of claim 308 wherein said conductive material comprises the composition of claim 47.

311. The method of claim 309 wherein said material is at least one of powders or chips.

312. The method of claim 310 wherein said material is at least one of powders and chips.

313. The method of claim 307 wherein said substrate is an electrode.

314. The method of claim 313 wherein said conductive material comprises sub-oxides of an element selected from the group consisting of Ti and V.

315. The method of claim 313 wherein said conductive material comprises the composition of claim 47.

316. The method of claim 313 wherein said material is at least one of powders and chips.

317. The method of claim 314 wherein said material is at least one of powders and chips.

318. The of method claim 307 wherein said substrate is a current collector.

319. The method of claim 318 wherein said conductive material comprises sub-oxides of an element selected from the group consisting of Ti and V.

320. The method of claim 318 wherein said conductive material comprises the composition of any one of claims 47-57.

321. The method of claim 319 wherein said material is at least one of powders and chips.

322. The method of claim 319 wherein said material is at least one of powders and chips.

323. The method of claim 307 wherein said substrate is a foam.

324. The method of claim 323 wherein said conductive material comprises sub-oxides of an element selected from the group consisting of Ti and V.

325. The method of claim 323 wherein said conductive material comprises the composition of claim 47.

326. The method of claim 324 wherein said material is at least one of powders and chips.

327. The method of claim 324 wherein said material is at least one of powders and chips.

328. The method of claim 307 wherein said substrate is a honey-comb.

329. The method of claim 328 wherein said conductive material comprises sub-oxides of an element selected from the group consisting of Ti and V.

330. The method of claim 328 wherein said conductive material comprises the composition of claim 47.

331. The method of claim 329 wherein said material is at least one of powders and chips.

332. The method of claim 329 wherein said material is at least one of powders and chips.

333. The method of claim 307 wherein said substrate is a solid sheet.

334. The method of claim 333 wherein said conductive material comprises sub-oxides of an element selected from the group consisting of Ti and V.

335. The method of claim 333 wherein said conductive material comprises the composition of claim 47.

336. The method of claim 334 wherein said material is at least one of powders and chips.

337. The method of claim 335 wherein said material is at least one of powders and chips.

338. The method of claim 288 wherein said sintering is performed in a nonoxidizing atmosphere.

339. The method of claim 338 wherein said sintering is performed at about 1000-2000° C.

340. The method of claim 290 wherein said sintering is performed in a non-oxidizing atmosphere.

341. The method of claim 340 wherein said sintering is performed at about 1000° C. to about 2000° C.

342. The method of claim 299 wherein said sintering is performed in a non-oxidizing atmosphere.

343. The method of claim 342 wherein said sintering is performed at about 1000° C. to about 2000° C.

344. The method of claim 297 wherein said sintering is performed in a non-oxidizing atmosphere.

345. The method of claim 344 wherein said sintering is performed at about 1000° C. to about 2000° C.

346. The method of claim 300 wherein said sintering is performed in a non-oxidizing atmosphere.

347. The method of claim 346 wherein said sintering is performed at about 1000° C. to about 2000° C.

348. The method of claim 303 wherein said sintering is performed in a non-oxidizing atmosphere.

349. The method of claim 348 wherein said sintering is performed at about 1000° C. to about 2000° C.

350. The method of claim 306 wherein said sintering is performed in a non-oxidizing atmosphere.

351. The method of claim 350 wherein said sintering is performed at about 1000° C. to about 2000° C.

352. The method of claim 310 wherein said sintering is performed in a non-oxidizing atmosphere.

353. The method of claim 352 wherein said sintering is performed at about 1000° C. to about 2000° C.

354. The method of claim 312 wherein said sintering is performed in a non-oxidizing atmosphere.

355. The method of claim 354 wherein said sintering is performed at about 1000° C. to about 2000° C.

356. The method of claim 320 wherein said sintering is performed in a non-oxidizing atmosphere.

357. The method of claim 336 wherein said sintering is performed at about 1000° C. to about 2000° C.

358. The method of claim 325 wherein said sintering is performed in a non-oxidizing atmosphere.

359. The method of claim 358 wherein said sintering is performed at about 1000° C. to about 2000° C.

360. The method of claim 327 wherein said sintering is performed in a non-oxidizing atmosphere.

361. The method of claim 360 wherein said sintering is performed at about 1000° C. to about 2000° C.

362. The method of claim 330 wherein said sintering is performed in a non-oxidizing atmosphere.

363. The method of claim 362 wherein said sintering is performed at about 1000° C. to about 2000° C.

364. The method of claim 332 wherein said sintering is performed in a non-oxidizing atmosphere.

365. The method of claim 364 wherein said sintering is performed at about 1000° C. to about 2000° C.

366. The method of claim 335 wherein said sintering is performed in a non-oxidizing atmosphere.

367. The method of claim 366 wherein said sintering is performed at about 1000° C. to about 2000° C.

368. The method of claim 337 wherein said sintering is performed in a non-oxidizing atmosphere.

369. An electrical energy device having at least one component having a conductive ceramic material therein.

370. The device of claim 369 wherein said material is at least one of conductive ceramic powder, conductive ceramic chips, and conductive ceramic foam.

371. The device of claim 370 wherein said material comprises the composition of claim 47.

372. The device of claim 370 wherein said conductive ceramic material comprises a ceramic matrix and metal containing additive dispersed within said ceramic matrix.

373. The device of claim 372 wherein said matrix material is selected from the group of oxides, carbides, nitrides, and borides.

374. The device of claim 373 wherein said oxide is selected from the group of substoichiometric titanium dioxides, superstoichometric titanium dioxides, and perovskite oxides.

375. The device of claim 374 wherein said perovskite oxide is tungsten oxide.

376. The device of claim 372 wherein said metal containing additive is selected from the group of Cu, Ni, Co, Ag, Pt, Ta, Zn, Mg, Ru, Ir, Nb, V, Sn, SnO, SnO₂, Pb, Pd, and alloys thereof.

377. The device of claim 372 wherein said conductive ceramic powder comprises at least one metal coating on said ceramic matrix.

378. The device of claim 377 wherein said metal coating is substantially the same composition as said metal containing. additive.

379. The device of claim 370 wherein said device is at least one of batteries, fuel cells, capacitors, and sensors.

380. The device of claim 379 wherein said device is a battery.

381. The device of claim 379 wherein said battery is at least one of lead-acid batteries, alkaline batteries, sulfur containing batteries, lithium containing batteries and nickel containing batteries.

382. The device of claim 381 wherein said battery is a lead acid battery.

383. The device of claim 381 wherein said battery is an alkaline battery.

384. The device of claim 383 wherein said alkaline battery is any of Zn—AgO₂, Zn—AgO, Zn—AgNO₂, Zn—Ag₂PbO₂, Zn—HgO, Zn—Br₂, Zn—Air(O₂) and Zn—MnO₂.

385. The device of claim 384 wherein in said alkaline battery said conductive ceramic material comprises the composition of any one of claims 47-57.

386. The device of claim 381 wherein said sulfur containing battery is a sodium-sulfur battery.

387. The device of claim 386 wherein in said sulfur containing battery said conductive ceramic material comprises the composition of claim 47.

388. The device of claim 381 wherein said device is a lithium containing battery of any of Li—AgV₂O₅, Li—CF_x, Li—CuO, Li—FeS, LI—FeS₂, Li—I₂, Li—MnO₂, Li—MoS₂, Li—V₂O₅, Li—TiS₂, Li—SOCl₂and Li—SO₂.

389. The device of claim 381 wherein in said lithium containing battery said conductive ceramic material comprises the composition of claim 47.

390. The device of claim 381 wherein said device is a Ni containing battery of any one of Ni—Cd, Ni—H₂, Ni—Zn Ni—MH and Ni—Fe.

391. The Ni containing battery of claim 389 wherein in said battery said conductive ceramic material comprises the composition of claim 47.

392. The device of claim 381 wherein said battery is a bipolar battery.

393. The device of claim 391 in said bi-polar battery said conductive ceramic material comprises the composition of claim 47.

394. A lead-acid battery having a plurality of electrodes therein, said electrode comprising an active material composition and a current collector.

wherein conductive ceramic material is present in at least one of said active material and said current collector,

said active material comprising at least one of conductive ceramic powder, conductive ceramic chips, and conductive ceramic foam.

395. The lead acid battery of claim 394 wherein said conductive ceramic material comprises the composition of claim 47.

396. The lead acid battery of claim 395 wherein said conductive ceramic material is present in said current collector and wherein in said conductive ceramic material comprises conductive ceramic powder.

397. The device of claim 381 wherein said battery comprises an anode component having a lithium containing material having thermodynamic activity less than that of lithium metal.

398. The device of claim 395 wherein said battery comprises a cathode component having a material comprising an oxide of manganese.

399. The device of claim 398 wherein said battery comprises an electrolyte comprising an organic polymer.

400. The device of claim 397 wherein said anode component compartment comprises a carbon material selected from the group containing graphite and petroleum coke.

401. A battery which comprises an electrically conducting ceramic material comprising electrically conducting vanadium oxide, wherein said material is any of ceramic conductive chips, ceramic conductive powder, and ceramic conductive foam.

402. A battery which comprises an electrically conducting ceramic material comprising an oxide selected from the group of Al₂O₃coated with metal and ZrO₂coated with a metal, wherein said material is any of conductive ceramic chips, conductive ceramic powder, and conductive foam.

403. The device of claim 379 wherein said device is a fuel cell.

404. The device of claim 403 wherein said fuel cell comprises an electrode having at least one of a current collector and an active paste therein.

405. The device of claim 404 wherein said conductive ceramic material is present in said current collector.

406. The device of claim 405 wherein said conductive ceramic material is present in said collector in an amount of about 50% to about 100% by weight of said collector.

407. The device of claim 406 wherein said material is at least conductive ceramic powder, conductive ceramic chips, and conductive ceramic foam.

408. The device of claim 407 wherein in said fuel cell said conductive ceramic material comprises the composition of claim 47.

409. The device of claim 404 wherein said conductive ceramic material is present in said active paste.

410. The device of claim 408 wherein said material is at least conductive ceramic powder, conductive ceramic chips, and conductive ceramic foam.

411. The device of claim 410 wherein in said fuel cell said conductive ceramic material comprises the composition of claim 47.

412. The device of claim 379 wherein said device is a capacitor.

413. The device of claim 412 wherein said capacitor is any of multi-layer and ultra capacitors.

414. The device of claim 413 wherein in said capacitor said conductive ceramic material comprises the composition of claim 47.

415. The device of claim 378 wherein said sensor is any of thermal sensors and chemical sensors.

416. The device of claim 415 wherein said sensor is a thermal sensor comprising conductive ceramic material, said material present as at least one of conductive ceramic powder, conductive ceramic chips, and conductive ceramic foam.

417. The device of claim 416 wherein said material comprises the composition of claim 47.

418. The device of claim 416 wherein said sensor is any of sheets, paper, non woven mat, and woven mat.

419. The device of claim 415 wherein said sensor is a chemical sensor comprising conductive ceramic material, said material present as at least one of conductive ceramic powder, conductive ceramic chips and conductive ceramic foam.

420. The device of claim 419 wherein said material comprises the Composition of claim 47.

421. The device of claim 420 wherein said sensor is any of sheets, paper, non woven mat, and woven mat.

422. An electrical energy device capable of at least one of generating electrical energy or storing electrical energy having at least one electrode having conductive ceramic fibers therein, said electrode having a current collector and active material, said fibers having a length of about 10 to about 10,000μ (1μ=10⁻⁶m) and a length to diameter ratio of about 1 to about 20 wherein said conductive fibers include a metal containing additive, wherein said fibers are present in said active material in an amount of about 0.1 to 30% by weight of said active material.

423. The electrical energy device of claim 422 wherein said fibers are present in said active material in an amount of about 5 to 20% by weight of said active material.

424. A battery comprising a cathode, an anode, a current collector, the anode comprising a lithium composition having a lithium thermodynamic activity less than lithium metal.