JP5992198B2 - Method for producing negative electrode active material for nonaqueous electrolyte secondary battery and negative electrode active material for nonaqueous electrolyte battery obtained thereby - Google Patents

Description

  The present invention relates to a method for producing a negative electrode active material for a non-aqueous electrolyte secondary battery with an improved negative electrode active material, and a negative electrode active material for a non-aqueous electrolyte secondary battery obtained thereby.

  In recent years, various portable electronic devices are becoming widespread due to rapid development of miniaturization technology of electronic devices. Further, miniaturization is also required for batteries that are power sources of these portable electronic devices, and non-aqueous electrolyte secondary batteries having high energy density are attracting attention.

Nonaqueous electrolyte secondary batteries using metallic lithium as the negative electrode active material have a very high energy density, but the dendritic crystals called dendrites are deposited on the negative electrode during charging, so the battery life is short, and There was also a problem in safety, such as growing up to reach the positive electrode and causing an internal short circuit. Therefore, carbon materials that absorb and desorb lithium, particularly graphitic carbon, have been used as negative electrode active materials instead of lithium metal. However, there is a problem that the capacity of graphitic carbon is smaller than that of lithium metal, lithium alloy, etc., and the large current characteristics are low. Therefore, attempts have been made to use a substance having a large lithium storage capacity and a high density, such as an element that forms an alloy with lithium such as silicon and tin, and an amorphous chalcogen compound.
Among them, silicon can occlude lithium up to a ratio of 4.4 lithium atoms to 1 silicon atom, and the negative electrode capacity per weight is about 10 times that of graphitic carbon. However, silicon has a problem in cycle life, such as a large change in volume accompanying lithium insertion / desorption in a charge / discharge cycle, such as pulverization of active material particles.

Conventionally, an attempt has been made to solve the above-mentioned problems by coating the negative electrode material of Si particles with carbon (see Patent Document 1). Such a patent document describes that SiO ₂ may also be contained as an impurity.

  However, the Si powder, which is a starting material for the negative electrode material of this known example, is a large one of 0.1 μm or more, and it is difficult to prevent the active material from being pulverized or cracked in a normal charge / discharge cycle. For example, in the examples, Wako Pure Chemical's reagent grade silicon powder is used as the starting material Si. This is a powdered crystalline silicon, and Si (220) in the powder X-ray diffraction measurement of the negative electrode material. The diffraction peak of the surface has a very low value of 0.1 ° C. or less. With such a negative electrode active material, it has been difficult to realize a battery with higher capacity and higher cycle characteristics.

That is, as a result of intensive experiments, the present inventors have found that only a certain improvement can be expected even if the cycle characteristics are improved by dispersing Si in the carbonaceous material of the negative electrode active material. As for the cause, it has been found that there is a causal relationship between the size of the dispersed Si crystal and the bonding property with the substrate around Si, and the microcrystalline Si is included in SiO ₂ that is firmly bonded to Si. It has been found that high capacity and improved cycle characteristics can be achieved by dispersing the carbonaceous material in a retained state, and the present invention has been completed.

JP 2000-215887 A

  The conventional negative electrode active material of a non-aqueous electrolyte secondary battery has a problem that it can provide only a non-aqueous electrolyte secondary battery that can be expected only to have a certain capacity increase even by addition of Si.

  The present invention was made in view of the solution of the above problems, and has a negative electrode active material for a non-aqueous electrolyte secondary battery that can achieve higher capacity and higher cycle characteristics than a battery that has been conventionally realized by adding Si, and It is an object to provide a non-aqueous electrolyte secondary battery.

The negative electrode for a non-aqueous electrolyte secondary battery according to the present embodiment is composed of three phases of Si, SiO ₂ and a carbonaceous material, and the SiO ₂ phase is bonded to and includes the Si phase, and these are combined. In the negative electrode for a non-aqueous electrolyte secondary battery using the composite as a negative electrode active material, the thickness of the negative electrode active material layer formed of the negative electrode active material, the conductive material, and the binder on the current collector is 10 μm or more and 150 μm The negative electrode active material has a particle size of 5 μm or more and 100 μm or less, a specific surface area of 0.5 m ² / g or more and 15.0 m ² / g or less, and the Si (220) XRD peak of the negative electrode active material The full width at half maximum is 1.5 ° or more and 8 ° or less .

Another embodiment is a nonaqueous electrolyte secondary battery comprising the negative electrode for a nonaqueous electrolyte secondary battery described in the above embodiment.

  ADVANTAGE OF THE INVENTION According to this invention, the negative electrode active material of the high capacity | capacitance nonaqueous electrolyte secondary battery can be provided, and a higher capacity | capacitance nonaqueous electrolyte secondary battery can be provided.

The fragmentary sectional view which shows the cylindrical nonaqueous electrolyte secondary battery which is an example of the nonaqueous electrolyte secondary battery concerning this invention.

  Hereinafter, the details of the negative electrode active material of the present invention will be described.

A desirable embodiment of the negative electrode active material of the present invention is composed of three phases of Si, SiO ₂ and a carbonaceous material, and these are finely combined. The Si phase inserts and desorbs a large amount of lithium, greatly increasing the capacity of the negative electrode active material. The expansion and contraction due to the insertion and desorption of a large amount of lithium into and from the Si phase is mitigated by dispersing the Si phase in the other two phases to prevent the active material particles from being pulverized, and the carbonaceous material phase is a negative electrode active material. The SiO ₂ phase has a great effect in maintaining the particle structure as a buffer that holds the refined Si firmly bonded to Si.

  The Si phase has a large expansion and contraction when occluding and releasing lithium, and it is preferable that the Si phase be dispersed as finely as possible in order to alleviate this stress. Specifically, it is preferably dispersed from a cluster of several nm to a size of 300 nm or less at the maximum.

The SiO ₂ phase can adopt an amorphous structure, a crystalline structure, or the like, but it is preferable that the SiO ₂ phase is uniformly distributed in the active material particles so as to bind to and include or hold the Si phase.

The carbonaceous material may be graphite, hard carbon, soft carbon, amorphous carbon, acetylene black or the like, and may be composed of one or several kinds, and preferably a mixture of graphite and hard carbon or soft carbon. Graphite is preferable in terms of enhancing the conductivity of the active material, and hard carbon and soft carbon have a large effect of covering the entire active material and relaxing expansion and contraction. The carbonaceous material preferably has a shape that includes a Si phase and a SiO ₂ phase.

The particle size of the negative electrode active material is preferably 5 μm or more and 100 μm or less, and the specific surface area is preferably 0.5 m ² / g or more and 15.0 m ² / g or less. The particle size and specific surface area of the active material affect the rate of lithium insertion and desorption reaction, and have a great influence on the negative electrode characteristics. However, values within this range can stably exhibit the characteristics.

  In addition, the half width of the diffraction peak of the Si (220) plane in the powder X-ray diffraction measurement of the active material needs to be 1.5 ° or more and 8.0 ° or less. The diffraction peak half-width of the Si (220) surface becomes smaller as the Si phase crystal grains grow, and when the Si phase crystal grains grow larger, the active material particles crack and the like due to expansion and contraction accompanying lithium insertion and desorption. However, if the half width is in the range of 1.5 ° or more and 8.0 ° or less, it is possible to avoid such a problem from appearing on the surface.

As for the ratio of the Si phase, SiO ₂ phase, and carbonaceous material phase, the molar ratio of Si and carbon is preferably in the range of 0.2 ≦ Si / carbon ≦ 2. The quantitative relationship between the Si phase and the SiO ₂ phase is preferably such that the molar ratio is 0.6 ≦ Si / SiO ₂ ≦ 1.5 because a large capacity and good cycle characteristics can be obtained as the negative electrode active material.

  Next, the manufacturing method of the negative electrode active material for nonaqueous secondary batteries of this Embodiment is demonstrated.

It is preferable to use SiOx (0.8 ≦ X ≦ 1.5) as the Si raw material. In particular, it is desirable to use SiO (x≈1) in order to obtain a preferable ratio of the quantitative relationship between the Si phase and the SiO ₂ phase. The shape is powder and the particle size is preferably 1 μm or more and 50 μm or less. SiOx is separated into a fine Si phase and a SiO ₂ phase in a baking step described later, but it is preferable that the particle size be as small as possible in order to ensure conductivity to the finely dispersed Si phase. This is because when the particle size is large, the Si phase is thickly covered with the SiO ₂ phase of the insulator at the center of the particle, and the function of insertion / extraction of lithium as an active material is hindered. Accordingly, the particle size of SiOx is preferably 50 μm or less. However, the surface of SiOx that comes into contact with the atmosphere is oxidized to become SiO _2, and therefore, when the particle size is extremely reduced, the surface area becomes larger and the surface becomes SiO ₂ , resulting in an unstable composition. Accordingly, the particle size is preferably 1 μm or more.

  As materials for carbonaceous materials, in addition to carbonized materials such as graphite, acetylene black, carbon black, and hard carbon, those that become carbonaceous materials when heated in an inert atmosphere, such as pitch, resin, and polymer, should be used. I can do it. As the carbonaceous material, it is preferable to use a combination of a material having high electrical conductivity such as graphite and acetylene black and a non-carbonized material such as polymer and pitch. The material such as pitch and polymer can be made into a shape in which SiOx is included in the carbonaceous material by melting or polymerizing with SiOx in a stage before firing. The carbonization firing temperature in the production method of the present invention is a relatively low temperature of 800 ° C. to 1400 ° C., so graphitization of carbonized pitch or polymer is not high, and graphite and acetylene black are used to increase the conductivity of the active material. Etc. are necessary.

  The precursor before carbonization is prepared by mixing SiOx and carbonaceous material. When pitch is used as the carbonaceous material, SiOx and graphite are mixed in the molten pitch, solidified by cooling, and then pulverized to oxidize and infusibilize the surface. And then subjected to carbonization firing. When a polymer is used, a polymerized and solidified polymer in a state where graphite or the like and SiOx are dispersed in a monomer is subjected to carbonization firing.

The carbonization firing is performed in an inert atmosphere such as in Ar. In the carbonization firing, the polymer or pitch is carbonized, and SiOx is separated into two phases of Si and SiO ₂ by a disproportionation reaction. When x = 1, the reaction is represented by the following formula (1).

2SiO → Si + SiO ₂ (1)
This disproportionation reaction proceeds at a temperature higher than 800 ° C., and is separated into a fine Si phase and a SiO ₂ phase. The higher the reaction temperature, the larger the Si phase crystals and the smaller the half width of the Si (220) peak. The firing temperature at which a half width in the preferred range is obtained is in the range of 850 ° C to 1600 ° C. Moreover, Si produced | generated by disproportionation reaction reacts with carbon at a temperature higher than 1400 degreeC, and changes to SiC. Since SiC is completely inactive with respect to insertion of lithium, the capacity of the active material decreases when SiC is generated. Therefore, it is preferable that the temperature of carbonization baking is 850 degreeC or more and 1400 degrees C or less, More preferably, it is 900 degreeC or more and 1100 degrees C or less. The firing time is preferably in the range of 3 hours to 12 hours.

  The negative electrode active material of the present invention can be obtained by the synthesis method as described above. The product after the carbonization firing is used as an active material by adjusting the particle size, specific surface area and the like using various mills, pulverizers, grinders and the like.

Hereinafter, the production of a nonaqueous electrolyte secondary battery using the negative electrode active material of the present invention will be described in detail.
1) Positive electrode The positive electrode has a structure in which a positive electrode active material layer containing an active material is supported on one or both surfaces of a positive electrode current collector.

The thickness of one surface of the positive electrode active material layer is preferably in the range of 10 μm to 150 μm from the viewpoint of maintaining the large current discharge characteristics and cycle life of the battery. Therefore, when the positive electrode current collector is supported on both surfaces, the total thickness of the positive electrode active material layer is desirably in the range of 20 μm to 300 μm. A more preferable range on one side is 30 μm to 120 μm. Within this range, large current discharge characteristics and cycle life are improved.

  The positive electrode active material layer may contain a conductive agent in addition to the positive electrode active material.

  The positive electrode active material layer may include a binder that binds the positive electrode materials to each other.

Examples of the positive electrode active material include various oxides such as manganese dioxide, lithium manganese composite oxide, lithium-containing nickel cobalt oxide (for example, LiCOO ₂ ), lithium-containing nickel cobalt oxide (for example, LiNi _0.8 CO _0.2 O). ₂ ) and a lithium manganese composite oxide (for example, LiMn ₂ O ₄ , LiMnO ₂ ) are preferable because a high voltage can be obtained.

  Examples of the conductive agent include acetylene black, carbon black, and graphite.

  Specific examples of the binder include polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVdF), ethylene-propylene-diene copolymer (EPDM), styrene-butadiene rubber (SBR), and the like. .

  It is preferable that the positive electrode active material, the conductive agent and the binder are mixed in a range of 80 to 95% by weight of the positive electrode active material, 3 to 20% of the conductive agent, and 2 to 7% by weight of the binder. It is preferable because discharge characteristics and cycle life can be obtained.

As the current collector, a conductive substrate having a porous structure or a non-porous conductive substrate can be used. The thickness of the current collector is preferably 5 to 20 μm. This is because within this range, the electrode strength and weight reduction can be balanced.
2) Negative electrode The negative electrode has a structure in which a negative electrode active material containing a negative electrode material is supported on one side or both sides of a negative electrode current collector.

The thickness of the negative electrode active material layer is preferably in the range of 10 to 150 μm. Therefore, when the negative electrode current collector is supported on both surfaces, the total thickness of the negative electrode active material layer is in the range of 20 to 300 μm. A more preferable range of the thickness of one side is 30 to 100 μm. Within this range, the large current discharge characteristics and cycle life are greatly improved.

  The negative electrode active material layer may include a binder that binds the negative electrode materials. As the binder, for example, polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVdF), ethylene-propylene-diene copolymer (EPDM), styrene-butadiene rubber (SBR), or the like can be used.

  The negative electrode active material layer may contain a conductive agent. Examples of the conductive agent include acetylene black, carbon black, and graphite.

As the current collector, a conductive substrate having a porous structure or a nonporous conductive substrate can be used. These conductive substrates can be formed from, for example, copper, stainless steel, or nickel. The thickness of the current collector is preferably 5 to 20 μm. This is because within this range, the electrode strength and weight reduction can be balanced.
3) Electrolyte As the electrolyte, a non-aqueous electrolyte, an electrolyte-impregnated polymer electrolyte, a polymer electrolyte, or an inorganic solid electrolyte can be used.

  The non-aqueous electrolyte is a liquid electrolyte prepared by dissolving an electrolyte in a non-aqueous solvent, and is held in the voids in the electrode group.

  As the non-aqueous solvent, a non-aqueous solvent mainly composed of a mixed solvent of propylene carbonate (PC) or ethylene carbonate (EC) and a non-aqueous solvent having a viscosity lower than that of PC or EC (hereinafter referred to as a second solvent) is used. It is preferable.

  As the second solvent, for example, chain carbon is preferable, among which dimethyl carbonate (DMC), methyl ethyl carbonate (MEC), diethyl carbonate (DEC), ethyl propionate, methyl propionate, γ-butyrolactone (BL), acetonitrile ( AN), ethyl acetate (EA), toluene, xylene or methyl acetate (MA). These second solvents can be used alone or in the form of a mixture of two or more. In particular, the second solvent preferably has a donor number of 16.5 or less.

  The viscosity of the second solvent is preferably 2.8 cmp or less at 25 ° C. The blending amount of ethylene carbonate or propylene carbonate in the mixed solvent is preferably 1.0% to 80% by volume ratio. The blending amount of ethylene carbonate or propylene carbonate is more preferably 20% to 75% by volume ratio.

Examples of the electrolyte contained in the non-aqueous electrolyte include lithium perchlorate (LiClO ₄ ), lithium hexafluorophosphate (LiPF ₆ ), lithium borofluoride (LiBF ₄ ), and lithium arsenic hexafluoride (LiAsF ₆ ). And lithium salts (electrolytes) such as lithium trifluorometasulfonate (LiCF ₃ SO ₃ ) and lithium bistrifluoromethylsulfonylimide [LiN (CF ₃ SO ₂ ) ₂ ]. Of these, LiPF ₆ and LiBF ₄ are preferably used.

The amount of electrolyte dissolved in the non-aqueous solvent is preferably 0.5 to 2.0 mol / L.
3) Separator A separator can be used when a non-aqueous electrolyte is used and when an electrolyte-impregnated polymer electrolyte is used. A porous separator is used as the separator. As a material for the separator, for example, a porous film containing polyethylene, polypropylene, or polyvinylidene fluoride (PVdF), a synthetic resin nonwoven fabric, or the like can be used. Among these, a porous film made of polyethylene, polypropylene, or both is preferable because it can improve the safety of the secondary battery.

  The thickness of the separator is preferably 30 μm or less. If the thickness exceeds 30 μm, the distance between the positive and negative electrodes may be increased and the internal resistance may be increased. Further, the lower limit value of the thickness is preferably 5 μm. If the thickness is less than 5 μm, the strength of the separator is remarkably lowered and an internal short circuit is likely to occur. The upper limit value of the thickness is more preferably 25 μm, and the lower limit value is more preferably 1.0 μm.

  The separator preferably has a heat shrinkage rate of 20% or less when kept at 120 ° C. for 1 hour. If the heat shrinkage rate exceeds 20%, the possibility of a short circuit due to heating increases. The thermal shrinkage rate is more preferably 15% or less.

  The separator preferably has a porosity in the range of 30 to 70%. This is due to the following reason. If the porosity is less than 30%, it may be difficult to obtain high electrolyte retention in the separator. On the other hand, if the porosity exceeds 60%, sufficient separator strength may not be obtained. A more preferable range of the porosity is 35 to 70%.

The separator preferably has an air permeability of 500 seconds / 1.00 cm ³ or less. If the air permeability exceeds 500 seconds / 1.00 cm ³ , it may be difficult to obtain high lithium ion mobility in the separator. The lower limit of the air permeability is 30 seconds / 1.00 cm ³ . This is because if the air permeability is less than 30 seconds / 1.00 cm ³ , sufficient separator strength may not be obtained.

The upper limit value of the air permeability is more preferably 300 seconds / 1.00 cm ³ , and the lower limit value is more preferably 50 seconds / 1.00 cm ³ .

  A cylindrical nonaqueous electrolyte secondary battery which is an example of a nonaqueous electrolyte secondary battery according to the present invention will be described in detail with reference to FIG.

For example, a bottomed cylindrical container 1 made of stainless steel has an insulator 2 disposed at the bottom. The electrode group 3 is housed in the container 1. The electrode group 3 has a structure in which a belt-like material in which the positive electrode 4, the separator 5, the negative electrode 6, and the separator 5 are laminated is wound in a spiral shape so that the separator 5 is located outside.
An electrolytic solution is accommodated in the container 1. The insulating paper 7 having an open center is disposed above the electrode group 3 in the container 1. The insulating sealing plate 8 is disposed in the upper opening of the container 1, and the sealing plate 8 is fixed to the container 1 by caulking the vicinity of the upper opening. The positive terminal 9 is fitted in the center of the insulating sealing plate 8. One end of the positive electrode lead 1.0 is connected to the positive electrode 4, and the other end is connected to the positive electrode terminal 9. The negative electrode 6 is connected to the container 1 which is a negative electrode terminal via a negative electrode lead (not shown).
In addition, in FIG. 1 mentioned above, although the example applied to the cylindrical nonaqueous electrolyte secondary battery was demonstrated, it can apply similarly to a square type nonaqueous electrolyte secondary battery. The electrode group housed in the battery container is not limited to the spiral system, and a plurality of positive electrodes, separators, and negative electrodes may be stacked in this order.

Moreover, in FIG. 1 mentioned above, although the example applied to the nonaqueous electrolyte secondary battery using the exterior body which consists of metal cans was demonstrated, the nonaqueous electrolyte secondary battery using the exterior body which consists of film materials is also demonstrated. The same can be applied. As the film material, a laminate film including a thermoplastic resin and an aluminum layer is preferable.
The negative electrode active material for a non-aqueous electrolyte secondary battery according to the present invention described above is a compound containing three phases of Si, SiO ₂ and a carbonaceous material.
Since such a negative electrode active material can simultaneously achieve a high charge / discharge capacity and a long cycle life, a long-life nonaqueous electrolyte secondary battery with an improved discharge capacity can be realized.

  Hereinafter, specific examples of the present invention will be given and the effects thereof will be described. However, the present invention is not limited to the examples.

  As raw materials, amorphous SiO having an average particle diameter of 30 μm was used as SiOx, and graphite and furfuryl alcohol having an average particle diameter of 6 μm were used as carbonaceous materials. The mixing ratio of SiO: graphite: furfuryl alcohol was 3: 0.5: 5 by weight. 1/10 weight of water was added to furfuryl alcohol, graphite and then SiO were added, and each was stirred. Thereafter, 1/10 weight of furfuryl alcohol was added to dilute hydrochloric acid, and the mixture was allowed to stand after stirring to polymerize and solidify.

  The obtained solid was fired in Ar at the temperature and time shown in Table 1, cooled to room temperature, pulverized by a pulverizer, and sieved with a 30 μm diameter to obtain an active material. This active material was subjected to the X-ray diffraction test described later. Moreover, the charging / discharging test mentioned later was done as a negative electrode active material about the obtained active material.

(Charge / discharge test)
Acetylene black 5 wt% and polytetrafluoroethylene 3 wt% were added to the obtained sample to form a sheet, pressure-bonded to a stainless steel mesh, and vacuum dried at 150 ° C. to obtain a test electrode. A battery having a counter electrode and a reference electrode made of metallic Li and an electrolytic solution of 1M LiPF ₆ in EC / MEC (volume ratio 1: 2) was prepared in an argon atmosphere and subjected to a charge / discharge test. Conditions of the charge and discharge test, between the reference electrode test electrode potential charging at a current density of 1 mA / cm ² to 0.01 V, further subjected to constant-voltage charging for 8 hours at 0.01 V, discharge of 1 mA / cm ² The current density was up to 3V.
(X-ray diffraction measurement)
Powder X-ray diffraction measurement was performed on the obtained powder sample, and the half width of the peak of the Si (220) plane was measured. The measurement was performed under the following conditions using an X-ray diffractometer (model M18XHF22) manufactured by Mac Science Co., Ltd.

Counter cathode: Cu
Tube voltage: 50 kv
Tube current: 300mA
Scanning speed: 1 ° (2θ) / min
Time constant: 1 sec
Receiving slit: 0.15mm
Divergent slit: 0.5 °
Scattering slit: 0.5 °
From the diffraction pattern, the half-value width (° (2θ)) of the peak of the Si surface index (220) appearing at d = 1.92 ° (2θ = 47.2 °) was measured. Moreover, when the peak of Si (220) overlapped with the peaks of other substances contained in the active material, the peak was isolated and the half width was measured.
(Comparative Example 3)
The SiO in Example 2 was made into Si powder having an average particle diameter of 0.5 μm, and Si: graphite: furfuryl alcohol was synthesized in a weight ratio of 1: 0.5: 5 in the same manner as in the example. At this time, the firing temperature was 1000 ° C. The obtained sample was subjected to a charge / discharge test and X-ray diffraction measurement. A counter electrode Li test battery using the obtained material as a negative electrode active material was formed in the same manner as in the example.

  Table 2 shows the discharge capacity at the first cycle in the charge / discharge test, the discharge capacity retention after 50 cycles, and the half width of the Si (220) peak obtained from powder X-ray diffraction.

From the results listed in Table 2, it is understood that the negative electrode active material of the present invention has a large discharge capacity and good cycle characteristics. That is, in Comparative Example 1, since the firing temperature was set to 700 ° C., SiO was not separated into Si and SiO 2, and thus capacity and cycle characteristics were also lowered. In Comparative Example 2, since the firing temperature was set to 1400 ° C., the half width of the Si (220) peak was reduced, the cycle characteristics were lowered, and the generated Si reacted with C to become SiC that did not occlude Li, so the capacity was greatly increased. Declined. In Comparative Example 3, the Si characteristics were large and the half width was small, and since no SiO ₂ was present, the cycle characteristics were greatly deteriorated.

1 ... exterior body,
3 ... Electrode group,
4 ... positive electrode,
5 ... Separator,
6 ... negative electrode,
8: Sealing plate,
9: Positive terminal.

Claims (3)

A non-aqueous electrolyte secondary comprising a three-phase structure of Si, SiO ₂ and a carbonaceous material, wherein the SiO ₂ phase is bonded to and includes the Si phase, and a composite of these is combined as a negative electrode active material In the negative electrode for a battery, the thickness of the negative electrode active material layer formed of the negative electrode active material, the conductive material, and the binder on the current collector is 10 μm or more and 150 μm or less, and the particle size of the negative electrode active material is 5 μm or more and 100 μm. The specific surface area is 0.5 m ² / g or more and 15.0 m ² / g or less, and the half width of the Si (220) XRD peak of the negative electrode active material is 1.5 ° or more and 8 ° or less. There is a negative electrode for a non-aqueous electrolyte secondary battery. The negative electrode for a non-aqueous electrolyte secondary battery according to claim 1,
A negative electrode for a non-aqueous electrolyte secondary battery, wherein the negative electrode current collector is a porous substrate or a nonporous copper, stainless steel, or nickel conductive substrate, and has a thickness of 5 μm or more and 20 μm or less. Non-aqueous electrolyte secondary battery characterized by having a negative electrode according to claim 1 or 2.