US20060261485A1 - Combined barrier layer and seed layer - Google Patents
Combined barrier layer and seed layer Download PDFInfo
- Publication number
- US20060261485A1 US20060261485A1 US11/492,261 US49226106A US2006261485A1 US 20060261485 A1 US20060261485 A1 US 20060261485A1 US 49226106 A US49226106 A US 49226106A US 2006261485 A1 US2006261485 A1 US 2006261485A1
- Authority
- US
- United States
- Prior art keywords
- dual
- layer
- tungsten
- substrate
- conductive interconnect
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 230000004888 barrier function Effects 0.000 title abstract description 20
- 239000004065 semiconductor Substances 0.000 claims abstract description 46
- 239000000758 substrate Substances 0.000 claims description 72
- 239000010949 copper Substances 0.000 claims description 36
- 229910052802 copper Inorganic materials 0.000 claims description 35
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 34
- 229910052721 tungsten Inorganic materials 0.000 claims description 34
- 239000010937 tungsten Substances 0.000 claims description 34
- 230000015654 memory Effects 0.000 claims description 32
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 27
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 11
- 229910052710 silicon Inorganic materials 0.000 claims description 11
- 239000010703 silicon Substances 0.000 claims description 11
- -1 tungsten nitride Chemical class 0.000 claims description 8
- 229910052581 Si3N4 Inorganic materials 0.000 claims description 7
- WNUPENMBHHEARK-UHFFFAOYSA-N silicon tungsten Chemical compound [Si].[W] WNUPENMBHHEARK-UHFFFAOYSA-N 0.000 claims description 7
- 229910000881 Cu alloy Inorganic materials 0.000 claims description 5
- 229910045601 alloy Inorganic materials 0.000 claims description 3
- 239000000956 alloy Substances 0.000 claims description 3
- 239000012212 insulator Substances 0.000 claims description 3
- 229910052594 sapphire Inorganic materials 0.000 claims description 2
- 239000010980 sapphire Substances 0.000 claims description 2
- 235000012431 wafers Nutrition 0.000 abstract description 24
- 238000012545 processing Methods 0.000 abstract description 6
- 239000010410 layer Substances 0.000 description 122
- 239000003792 electrolyte Substances 0.000 description 90
- 239000000463 material Substances 0.000 description 81
- 238000000034 method Methods 0.000 description 39
- 238000006722 reduction reaction Methods 0.000 description 30
- 150000001768 cations Chemical class 0.000 description 28
- 238000000151 deposition Methods 0.000 description 26
- 230000009467 reduction Effects 0.000 description 22
- 238000003487 electrochemical reaction Methods 0.000 description 21
- 230000008021 deposition Effects 0.000 description 17
- 230000008569 process Effects 0.000 description 17
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 238000004070 electrodeposition Methods 0.000 description 12
- 230000003647 oxidation Effects 0.000 description 12
- 238000007254 oxidation reaction Methods 0.000 description 12
- 239000008139 complexing agent Substances 0.000 description 11
- 229910052782 aluminium Inorganic materials 0.000 description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 238000010586 diagram Methods 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 238000000137 annealing Methods 0.000 description 5
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 5
- 230000006870 function Effects 0.000 description 5
- 229910000838 Al alloy Inorganic materials 0.000 description 4
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 4
- 238000005229 chemical vapour deposition Methods 0.000 description 4
- 238000004891 communication Methods 0.000 description 4
- 229910000365 copper sulfate Inorganic materials 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 229940021013 electrolyte solution Drugs 0.000 description 4
- 239000008151 electrolyte solution Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 238000001465 metallisation Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229910052697 platinum Inorganic materials 0.000 description 4
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- 229910052719 titanium Inorganic materials 0.000 description 4
- ZNOKGRXACCSDPY-UHFFFAOYSA-N tungsten trioxide Chemical compound O=[W](=O)=O ZNOKGRXACCSDPY-UHFFFAOYSA-N 0.000 description 4
- DZKDPOPGYFUOGI-UHFFFAOYSA-N tungsten(iv) oxide Chemical compound O=[W]=O DZKDPOPGYFUOGI-UHFFFAOYSA-N 0.000 description 4
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000004020 conductor Substances 0.000 description 3
- 238000007599 discharging Methods 0.000 description 3
- 229940071106 ethylenediaminetetraacetate Drugs 0.000 description 3
- 238000005755 formation reaction Methods 0.000 description 3
- 238000005240 physical vapour deposition Methods 0.000 description 3
- 238000011946 reduction process Methods 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 230000001360 synchronised effect Effects 0.000 description 3
- 229910001930 tungsten oxide Inorganic materials 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 230000006978 adaptation Effects 0.000 description 2
- 230000002146 bilateral effect Effects 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 229910001431 copper ion Inorganic materials 0.000 description 2
- 238000005137 deposition process Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- VVRQVWSVLMGPRN-UHFFFAOYSA-N oxotungsten Chemical class [W]=O VVRQVWSVLMGPRN-UHFFFAOYSA-N 0.000 description 2
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 229910052715 tantalum Inorganic materials 0.000 description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 2
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- NXHILIPIEUBEPD-UHFFFAOYSA-H tungsten hexafluoride Chemical compound F[W](F)(F)(F)(F)F NXHILIPIEUBEPD-UHFFFAOYSA-H 0.000 description 2
- 229910001934 tungsten pentoxide Inorganic materials 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 229910000676 Si alloy Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000002457 bidirectional effect Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 235000019994 cava Nutrition 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 230000005496 eutectics Effects 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000005468 ion implantation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004518 low pressure chemical vapour deposition Methods 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- DCKVFVYPWDKYDN-UHFFFAOYSA-L oxygen(2-);titanium(4+);sulfate Chemical compound [O-2].[Ti+4].[O-]S([O-])(=O)=O DCKVFVYPWDKYDN-UHFFFAOYSA-L 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000003870 refractory metal Substances 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910000348 titanium sulfate Inorganic materials 0.000 description 1
- UBZYKBZMAMTNKW-UHFFFAOYSA-J titanium tetrabromide Chemical compound Br[Ti](Br)(Br)Br UBZYKBZMAMTNKW-UHFFFAOYSA-J 0.000 description 1
- XROWMBWRMNHXMF-UHFFFAOYSA-J titanium tetrafluoride Chemical compound [F-].[F-].[F-].[F-].[Ti+4] XROWMBWRMNHXMF-UHFFFAOYSA-J 0.000 description 1
- NLLZTRMHNHVXJJ-UHFFFAOYSA-J titanium tetraiodide Chemical compound I[Ti](I)(I)I NLLZTRMHNHVXJJ-UHFFFAOYSA-J 0.000 description 1
- SOBXOQKKUVQETK-UHFFFAOYSA-H titanium(3+);trisulfate Chemical compound [Ti+3].[Ti+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O SOBXOQKKUVQETK-UHFFFAOYSA-H 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/288—Deposition of conductive or insulating materials for electrodes conducting electric current from a liquid, e.g. electrolytic deposition
- H01L21/2885—Deposition of conductive or insulating materials for electrodes conducting electric current from a liquid, e.g. electrolytic deposition using an external electrical current, i.e. electro-deposition
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76843—Barrier, adhesion or liner layers formed in openings in a dielectric
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76853—Barrier, adhesion or liner layers characterized by particular after-treatment steps
- H01L21/76861—Post-treatment or after-treatment not introducing additional chemical elements into the layer
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76871—Layers specifically deposited to enhance or enable the nucleation of further layers, i.e. seed layers
- H01L21/76873—Layers specifically deposited to enhance or enable the nucleation of further layers, i.e. seed layers for electroplating
Definitions
- the present invention relates generally to the fabrication of semiconductor devices. More particularly, the present invention relates to the formation of dual-purpose layers that serve as both barrier and seed layers for electrochemical deposition of conductive interconnect materials.
- the performance of semiconductor chips is limited by the electrical conductivity of the metal interconnects that electrically connect the various components that form the integrated circuits on the semiconductor chip. Therefore, in order to take full advantage of transistors that are capable of operating at faster speeds, the electrical interconnects must be highly conductive, yet low in resistance.
- Aluminum or an aluminum alloy was widely used as the preferred material for forming conductive interconnects by a process known as “metallization”.
- Metallization is a term used in the semiconductor industry to describe the process of wiring together the components of an integrated circuit, and typically occurs by the process of electrochemical deposition.
- Aluminum emerged as the preferred metal for metallization because it has a relatively low resistivity, good current-carrying density, and superior adhesion to silicon dioxide. In addition, aluminum is available in high purity and has a natural low contact resistance with silicon.
- aluminum and aluminum alloys present some disadvantages when used to make interconnects.
- aluminum has a resistance that can be tolerated by most integrated circuits, it is difficult to deposit in a high aspect ratio.
- aluminum and aluminum alloys suffer from eutectic formations, thermally induced voiding, and electromigration when used in very large scale integration (VLSI) and ultra large scale integration (ULSI) semiconductor chips.
- VLSI very large scale integration
- ULSI ultra large scale integration
- Copper metal has begun to replace aluminum and aluminum-silicon alloys in VLSI and ULSI metallization processes. Copper has better conductivity and is more reliable than aluminum or aluminum alloys. The use of copper for making semiconductor chip interconnects is appealing because of the low cost, high throughput, excellent via-filling capabilities, and high quality of the deposited copper film. In contrast to aluminum, copper is capable of being deposited with high aspect ratios. Copper is also a much better conductor than aluminum, provides good step coverage, is more resistant to electromigration and can be electrochemically deposited at low temperatures.
- tantalum is generally not suitable to serve as the cathode during the electrochemical deposition process.
- a seed layer is typically formed on top of the barrier layer to provide the desired resistivity.
- the seed layer is often a layer of PVD copper.
- formation of the seed layer overlying the barrier layer necessarily adds a discrete process step.
- FIG. 1 illustrates cross-sectional view of a metallized workpiece according to the prior art.
- FIG. 2 illustrates an embodiment of the present invention.
- FIG. 3 is an illustration an electrochemical reaction cell.
- FIG. 4 is a block diagram of one embodiment of an integrated circuit memory device.
- FIG. 5 is an elevation view of one embodiment of a wafer containing semiconductor dies.
- FIG. 6 is a block diagram of one embodiment of an exemplary circuit module.
- FIG. 7 is a block diagram of one embodiment of an exemplary memory module.
- FIG. 8 is a block diagram of one embodiment of an exemplary electronic system.
- FIG. 9 is a block diagram of one embodiment of an exemplary memory system.
- FIG. 10 is a block diagram of one embodiment of an exemplary computer system.
- substrate used in the following description refers to any structure having an exposed surface onto which structures of the present invention are to be formed.
- the term substrate includes any structure onto which a barrier layer may be effectively deposited.
- the term substrate should be understood as including silicon-on-sapphire (SOS) technology, silicon-on-insulator (SOI) technology, thin film transistor (TFT) technology, doped and undoped semiconductors, epitaxial layers of a silicon supported by a base semiconductor structure, as well as other semiconductor structures well known to one skilled in the art.
- SOS silicon-on-sapphire
- SOI silicon-on-insulator
- TFT thin film transistor
- doped and undoped semiconductors epitaxial layers of a silicon supported by a base semiconductor structure, as well as other semiconductor structures well known to one skilled in the art.
- wafer or substrate include the underlying layers containing such regions/junctions.
- substrate is understood to include semiconductor wafers.
- workpiece will also refer to semiconductor structures during processing, and may include other layers that have been fabricated thereupon.
- conductor is understood to include semiconductors, and the term insulator is defined to include any material that is less electrically conductive than the materials referred to as conductors. The following detailed description is, therefore, not to be taken in a limiting sense.
- Embodiments of the present invention reduce the number of necessary processing steps to form interconnects by removing the need to employ a separate seed layer interposed between the barrier layer and the conductive interconnect layer. This is accomplished in part through the utilization of a barrier material that can be metallized without the need for a seed layer.
- the present invention is a semiconductor comprising a conductive interconnect layer electrochemically deposited onto a dual-purpose layer.
- dual-purpose layer it is meant that the dual-purpose layer functions as both a barrier layer and a seed layer.
- Dual-purpose layers of the present invention reduce diffusion of conductive interconnect material sufficiently to serve as a barrier layer.
- Dual-purpose layers of the present invention also exhibit a resistivity sufficiently low to serve as a seed layer, allowing effective electrochemical deposition of the conductive interconnect layer onto the dual-purpose layer.
- the material comprising the dual-purpose layer contains tungsten.
- a method for metallizing a silicon wafer is provided.
- a dual-purpose layer is deposited on the surface of the silicon wafer.
- oxides on the dual-purpose layer are electrochemically reduced in an electrochemical reaction cell.
- a layer of conductive interconnect material is then electrochemically deposited onto the dual-purpose layer.
- Tungsten can be utilized to create a dual-purpose layer and copper can be used as the conductive interconnect material.
- tungsten interconnects are deposited onto tungsten.
- a first electrolyte is utilized to electrochemically reduce oxides on a dual-purpose layer and a second electrolyte is utilized to electrochemically deposit the conductive interconnect material onto the dual-purpose layer.
- the electrochemical deposition of the conductive interconnect material can be performed by discharging the first electrolyte from the electrochemical reaction cell after the electrochemical reduction of oxides and replacing it with the second electrolyte.
- the electrochemical deposition of the conductive interconnect material can be performed in a separate electrochemical reaction cell by transferring the substrate after the reduction of oxides to the separate electrochemical reaction cell.
- a single electrolyte is utilized in an electrochemical reaction cell to both electrochemically reduce the oxides on the dual-purpose layer and electrochemically deposit the conductive interconnect material onto the dual-purpose layer.
- the single electrolyte comprises the cation of the conductive interconnect material, a counterion, a complexing agent, and a pH control agent.
- conductive interconnects according to the present invention are advantageously utilized to produce articles such as semiconductor chips, memory devices, semiconductor dies, circuit modules, and electronic systems.
- FIG. 1 illustrates a cross-sectional view of a metallized workpiece 10 according to the prior art.
- the workpiece 10 includes a wafer 12 , an overlying dielectric layer 14 , a barrier layer 16 , a seed layer 18 , and a conductive interconnect layer 19 .
- the conductive interconnect layer 19 may be referred to as a metal layer.
- the workpiece 10 at this particular stage of manufacturing, may include a variety of integrated circuit components that were formed in earlier fabrication steps.
- the dielectric layer 14 is deposited on the surface of the wafer 12 using methods known in the art, such as chemical vapor deposition (CVD), plasma-enhanced chemical vapor deposition (PECVD), spin-on depositing or by thermal oxidation.
- CVD chemical vapor deposition
- PECVD plasma-enhanced chemical vapor deposition
- spin-on depositing or by thermal oxidation.
- the dielectric layer 14 can be selected from a variety of dielectric materials, but is preferably made from silicon dioxide or some variation of silicon dioxide. Once a dielectric layer 14 is deposited it typically is patterned using techniques known in the art such as etching. This patterning of the dielectric layer 14 creates what are generally referred to in the industry as trenches.
- the deposited and patterned dielectric layer 14 on the wafer 12 forms a substrate 15 .
- a barrier layer 16 is deposited on the substrate 15 using techniques known in the art.
- a seed layer 18 is deposited using techniques known in the art.
- the metal layer 19 is deposited utilizing techniques known in the art, filling the trenches.
- FIG. 2 illustrates an embodiment of the present invention.
- the dielectric layer 14 has been deposited onto the wafer 12 and patterned in the same manner as described in reference to FIG. 1 .
- a dual-purpose layer 22 is deposited on the substrate 15 .
- the dual-purpose layer 22 can be deposited utilizing the same techniques known in the art for depositing the barrier layer 16 . Oxides are removed from the dual-purpose layer 22 and the metal layer 19 is then deposited onto the dual-purpose layer 22 in accordance with methods of the present invention.
- a workpiece 10 of the prior art contains both a barrier layer 16 and a seed layer 18
- the present invention provides for only a single dual-purpose layer 22 .
- dual-purpose layer it is meant that the dual-purpose layer functions as both a barrier layer and a seed layer. Dual-purpose layers of the present invention reduce electromigration of conductive interconnect material sufficiently to serve as a barrier layer. Dual-purpose layers of the present invention also exhibit a resistivity sufficiently low to serve as a seed layer, allowing effective electrochemical deposition of the conductive interconnect layer onto the dual-purpose layer.
- dual-purpose materials Materials that can be used to make the dual-purpose layer are referred to herein as dual-purpose materials.
- Preferred dual-purpose materials can be deposited on substrates by techniques known in the art.
- the dual-purpose material contains tungsten.
- These tungsten-containing, dual-purpose materials include, for example, tungsten (W), tungsten nitride (WN X ), and tungsten-silicon nitride (WSiN X ).
- a preferred dual-purpose material is tungsten.
- Tungsten is a refractory metal that has a melting point of 3370° C. and a bulk resistivity of 52 ⁇ -cm at room temperature.
- a dual-purpose layer 22 of tungsten may be deposited on a silicon wafer 12 using several deposition techniques known in the art such as evaporation, ion-metal plasma (IMP), chemical vapor deposition (CVD), low pressure CVD, or physical vapor deposition (PVD).
- IMP ion-metal plasma
- CVD chemical vapor deposition
- PVD physical vapor deposition
- a frequently used method for the deposition of tungsten is the reduction of tungsten hexafluoride (WF 6 ) by hydrogen (H) or silane (SiH 4 ).
- Dual-purpose materials can be susceptible to oxidation, causing oxides to form on the surface of the dual-purpose layer. These oxides can inhibit the deposition of conductive interconnect material onto the surface of the dual-purpose layer. For example, when tungsten is exposed to air or moisture, it can be oxidized to tungsten dioxide (WO 2 ), tungsten trioxide (WO 3 ), or tungsten pentoxide (W 2 O 5 ). Tungsten oxides are not readily removed by rinsing or washing steps because they are not readily dissolved in acidic solutions such as are commonly used in the electrochemical deposition process. These oxides can inhibit the nucleation of copper, resulting in poor adhesion of copper as a conductive interconnect material.
- tungsten dioxide tungsten dioxide
- WO 3 tungsten trioxide
- W 2 O 5 tungsten pentoxide
- Tungsten oxides are not readily removed by rinsing or washing steps because they are not readily dissolved in acidic solutions such as are commonly used in the electrochemical
- an electrochemical reduction step is employed to remove oxides from the exposed surface of the dual-purpose layer.
- the electrochemical reduction of oxides on the surface of the dual-purpose layer requires the use of an electrochemical reaction cell.
- the basic design and operation of electrochemical reaction cells is well known in the art and includes various inlets and outlets for the introduction of gases and liquids, a cathode, an anode, a current source, and an electrolyte.
- the electrolyte is a medium capable of conducting electricity. Typically, the electrolyte is an aqueous solution.
- the electrolyte frequently contains metal ions or salts of metals.
- the cathode, the anode and the substrate are immersed in the electrolyte. A current is then provided to the electrolyte, by providing an electrical potential across the anode and the cathode.
- a first process for reducing oxides on the surface of a dual-purpose layer is performed utilizing one electrolyte and then a second process for depositing conductive interconnect material onto the dual-purpose layer is performed utilizing a second electrolyte.
- the two processes can be performed utilizing the same electrochemical reaction cell by changing electrolytes after the oxide reduction process and before deposition of the conductive interconnect material.
- the two processes can be performed using a single anode or two different anodes.
- the two processes can be preformed in two separate electrochemical reaction cells by performing the oxide reduction process in one cell and then transferring the workpiece to a second cell in which the deposition process is performed. The transferring of the workpiece is performed in a manner that does not allow oxides to reform on the surface of the workpiece.
- a single electrolyte is utilized for both the oxide reduction process and the copper deposition process.
- electrochemical reaction cells of the present invention comprise a power source, a substrate cathode, an anode, and an electrolyte.
- FIG. 3 illustrates a typical electrochemical reaction cell 30 according to the present invention.
- the reaction cell 30 in FIG. 3 comprises a cathode 32 , an anode 34 , an electrolyte supply 36 , and an electrolyte return 38 .
- the cathode and anode are electrically connected to an electrical power source in a manner that allows an electrical potential to be applied across the cathode and anode. Methods and apparatus for providing such an electrical connection are well understood in the art.
- wafer 40 is placed into the reaction cell 30 and an electrical potential is applied across the anode and the cathode.
- the application of the electrical potential may cause a reduction reaction to occur on the surface of the wafer 40 or the application of the electrical potential may cause a deposition reaction to occur on the surface of the wafer 40 .
- cations from the electrolyte are deposited onto the surface of the wafer 40 during a deposition reaction.
- the deposition reaction removes cations from the electrolyte.
- These cations removed from the electrolyte must be eventually replenished.
- the anode is made from the same material as the cations, then the cations can be replenished from the anode.
- FIG. 3 illustrates a mechanism for replenishing cations when they are not cations of the material from which the anode is made.
- FIG. 3 shows an electrolyte supply 36 containing a sufficient amount of cations. If the reaction cell 30 is used for deposition, the electrolyte exiting the cell at the electrolyte return 38 will have cations removed.
- the electrolyte can be transported to a cation source (not shown) to replenish the cations and then reintroduce into the reaction cell 30 through the electrolyte supply 36 .
- a substrate comprising a deposited dual-purpose layer is placed into an electrochemical reaction cell comprising a cathode, a first anode, and a second anode.
- the substrate will be a silicon wafer having been photolithographically etched and covered with a dual-purpose layer.
- the first anode is formed from a material that can be oxidized in the presence of the dual-purpose material. These materials can be readily identified by their oxidation potentials.
- Such a material will have an oxidation potential that is higher (i.e., more positive) than the oxidation potential of the dual-purpose material.
- Anodes useful in the present invention include anodes made from titanium, titanized platinum, platinum, and copper.
- the oxidation potential for the oxidation of tungsten to WO 3 is 0.09 volts and the oxidation potential for the oxidation of tungsten to WO 2 is 0.12 volts.
- the dual-purpose layer comprises tungsten
- the first anode is preferably formed from titanium or titanized platinum.
- the electrochemical reaction cell is charged with a first electrolyte.
- the first electrolyte is an aqueous solution comprising a metal salt M + X ⁇ , wherein M + is the cationic species of the material used to form the first anode and X ⁇ is a counterion.
- the first electrolyte solution can be titanium sulfate (Ti 2 (SO 4 ) 3 ), titanium bromide, titanium trichloride (TiCl 3 ), titanium iodide, titanium fluoride, or mixtures thereof.
- preferred first electrolyte solutions are titanium trichloride and titanium sulfate.
- the first electrolyte can be copper sulfate.
- the concentration of the metal salt in the first electrolyte will be from about 0.1 M to about 1 M.
- the concentration of the metal salt in the first electrolyte may vary depending on the specific metal salt utilized, but optimum concentration ranges can be determined by a practitioner of ordinary skill in the art without undue experimentation.
- the substrate is placed in the electrolyte and is electrically connected to an electrical circuit to form a cathode.
- the first anode is placed in the electrolyte solution and is also electrically connected to the electrical circuit.
- the electrical circuit is also equipped with a electrical power source.
- the power source, cathode, anode, and electrolyte form an electrical circuit as is known in the art.
- a first potential is applied to the electrical circuit.
- a first electrical potential between the first anode and the substrate cathode causes a reduction reaction to occur, reducing oxides on the dual-purpose layer surface.
- the first potential is applied with a magnitude and duration sufficient to reduce oxides on the surface of the dual-purpose layer.
- the magnitude of the first potential will be in the range of from about 0.1 V to about 1 V and will be applied for a time in the range of from about 1 second to about 60 seconds. These ranges may vary depending on the material used for the first anode and the specific composition of the electrolyte, but optimum ranges can be determined by a practitioner of ordinary skill in the art without undue experimentation.
- the first potential is no longer applied, and the first electrolyte is discharged from the electrochemical reaction cell.
- a second electrolyte is then introduced into the cell so that the substrate cathode and the second anode are placed in the second electrolyte.
- the discharging of the first electrolyte and the introduction of the second electrolyte should be done in a manner that does not expose the surface of the dual-purpose layer to conditions that would cause oxides to reform on the dual-purpose layer.
- One method for preventing the reformation of oxides is to keep the cell under a positive pressure of an inert gas such as nitrogen.
- the second electrolyte can be any electrolyte known in the art to be useful for depositing the conductive interconnect material.
- the second anode comprises the conductive interconnect material.
- the second electrolyte is an aqueous solution comprising a metal salt M + X ⁇ , wherein M + is the cationic species of the conductive interconnect material M that forms the second anode and that is to be electrochemically deposited on the surface of the dual-purpose layer and X ⁇ is a counterion.
- the pH of the second electrolyte will be less than about 1.
- the second anode typically is formed from copper and the second electrolyte solution preferably comprises copper sulfate (CuSO 4 ), hydrochloric acid (HCl), and sulfuric acid (H 2 SO 4 ).
- the second electrolyte can be an electrolyte of the present invention, such as those taught below in the detailed description of embodiments of the present invention that utilize the same electrolyte for both the oxide reduction step and the conductive interconnect deposition step.
- the substrate cathode and second anode are electrically connected in a manner allowing an electrical potential to be applied across the substrate cathode and the second anode.
- a second potential is applied to the resulting electrical circuit.
- Application of the second electrical potential between the second anode and the substrate cathode causes a deposition reaction to occur, depositing conductive interconnect material on the dual-purpose layer surface of the substrate.
- the conductive interconnect material is copper
- copper ions from the electrolyte are reduced and deposited on the surface of the dual-purpose layer.
- the copper ions from the electrolyte are deposited or plated on the substrate via electric migration and diffusion.
- the thickness of the conductive interconnect layer will be from about 2000 angstroms to about 20,000 angstroms. Preferably, the thickness of the conductive interconnect layer is from about 10,000 angstroms to about 12,000 angstroms.
- the amount of conductive interconnect material deposited over a period of time can be controlled by controlling the amount of current flowing through the electrolyte.
- the voltage and the period of time for applying the voltage is selected according to the depth of the layer of conductive interconnect material to be deposited on the surface of substrate.
- the voltage applied is typically at least abut 0.1 V and not more than about 1 V and is typically applied for a time period of from about 30 seconds to about 5 minutes.
- the resulting electrical current applied is typically from about 0.5 amps to about 10 amps and has a current density of from about 5 mA/cm 2 to about 25 mA/cm 2 . In some preferred embodiments, the current density will be from about 10 mA/cm 2 to about 15 mA/cm 2 . Additionally, in some embodiments a current density of about 12 mA/cm 2 is most preferred.
- two separate electrochemical reaction cells can be utilized.
- the reduction of oxides on the dual-purpose layer is performed in the first cell and the deposition of the conductive interconnect material is performed in the second cell.
- the same process parameters are used as described above, but instead of discharging the first electrolyte after the reduction of oxides and introducing the second electrolyte into the same cell, the substrate is transferred to the second cell containing the second electrolyte and second anode.
- the deposition of conductive interconnect material is performed in the second cell. It is important that the transfer of the substrate from the first cell to the second cell be done under conditions that does not allow for the reformation of oxides on the dual-purpose layer. Such conditions can be readily determined by a practitioner of ordinary skill in the art without undue experimentation.
- a single electrolyte can be utilized in a single electrochemical reaction cell containing a single anode.
- the composition of the electrolyte is chosen such that applying a potential across the anode and cathode first causes a reduction of oxides on the substrate cathode and then causes the deposition of the conductive interconnect material onto the substrate cathode.
- these electrolytes will be referred to as dual-purpose electrolytes since they can be utilized both for the reduction of oxides on the substrate and the deposition of the conductive interconnect material onto the substrate.
- dual-purpose electrolytes of the present invention may also be advantageously utilized in two electrolyte systems if so desired.
- dual-purpose electrolytes could be used to reduce the oxides on a substrate and then a second electrolyte could be used for the deposition of the conductive interconnect material onto the substrate.
- the second electrolyte could be any electrolyte known in the art for depositing conductive interconnect material onto a substrate.
- a dual-purpose electrolyte could be used to reduce the oxides on a substrate and deposit a thin layer of interconnect material and then a second electrolyte could be used to deposit additional interconnect material, thickening the layer of interconnect material to the resulting desired thickness.
- the second electrolyte could be any electrolyte known in the art for depositing conductive interconnect material onto a substrate.
- a first electrolyte could be used to reduce oxides on a substrate and then a dual-purpose electrolyte used for depositing conductive interconnect material onto a substrate.
- the deposition of conductive interconnect material occurs when the cation of the conductive interconnect material is reduced.
- Cu 2+ gets reduced, resulting in copper being deposited on the cathode.
- oxides on a substrate surface are removed via a reduction reaction.
- the reduction of conductive interconnect material cations has a lower oxidation potential (that is, a higher reduction potential) than the reduction of oxides (for example, tungsten oxide).
- oxides for example, tungsten oxide.
- the composition of the electrolyte can be chosen such that the reduction of oxides on the substrate cathode occurs before the reduction of conductive interconnect material cations.
- Electrolytes of this embodiment will also contain a cation of the conductive interconnect material along with a counterion like the second electrolyte described above.
- electrolytes of this embodiment will also contain a complexing agent and a pH control agent.
- the amount and type of complexing agent added should be sufficient to complex the conductive interconnect material cation so that the effective reduction potential of the conductive interconnect material cation is lower than the reduction potential of the oxides.
- complexing agents useful in the present invention include ethylene diamine tetra acetate (EDTA), boric acid, and malonic acid.
- EDTA ethylene diamine tetra acetate
- a preferred complexing agent is EDTA.
- the complexing agent will be present in a concentration of from about 0.01 M to about 1 M. Preferred concentrations of complexing agent used may depend on the precise complexing agent used, but can be determined by a practitioner of ordinary skill in the art without undue experimentation.
- the pH control agent is utilized to keep the pH of the electrolyte greater than or equal to about 7.
- the pH of the electrolyte is equal to or greater than about 10.
- the pH of the electrolyte is less than or equal to about 12.
- pH control agents include tetramethyl ammonium hydroxide (TMAH), ammonium hydroxide (NH 4 OH), and potassium hydroxide (KOH).
- the amount of complexing agent and the amount of pH control agent present should be sufficient to lower the reduction potential (that is, raise the oxidation potential) of the cation reduction reaction until it is lower than the reduction potential (higher than the oxidation potential) of the oxide reduction reaction.
- a substrate cathode comprising a dual-purpose layer is placed into an electrochemical reaction cell additionally comprising an anode and an electrolyte.
- the cations to be deposited are cations of the material from which the anode is made.
- the electrolyte could comprise copper sulfate, for example, and the anode could comprise copper.
- the copper cations that are deposited onto the surface of the dual-purpose layer can be replenished from the anode.
- the anode does not necessarily need to be made from the same material as the conductive interconnect material to be deposited.
- the anode comprises platinum.
- the cations in the electrolyte can be replenished as explained in the text referencing FIG. 3 .
- the electrolyte comprises cations of the conductive interconnect material, a counterion, a complexing agent, and a pH control agent.
- the substrate cathode and the anode are electrically connected to a power source and an electrical potential is applied across the substrate cathode and the anode.
- This potential causes a reduction reaction to occur at the substrate cathode, reducing oxides that may be present on the dual-purpose layer of the substrate. Once the oxides are reduced, or if no oxides are present, then the potential causes the reduction of conductive interconnect material cations in the electrolyte, resulting in conductive interconnect material being deposited on the dual-purpose layer of the substrate.
- conductive interconnect material can be deposited on a dual-purpose layer without having to first deposit a separate seed layer, without having to use two separate electrolytes, and without having to transfer a substrate from a first electrochemical reaction cell to a second electrochemical reaction cell.
- the process parameters are the same as described above for the two-electrolyte embodiments of the present invention.
- the thickness of the conductive interconnect layer can be controlled by controlling the amount of current flowing through the electrolyte.
- optimum process parameters can be determined by a practitioner having ordinary skill in the art without undue experimentation.
- copper is electrochemically deposited onto a substrate having a dual-purpose surface layer by utilizing a copper anode and an electrolyte comprising copper sulfate, a complexing agent, and a pH control agent.
- the dual-purpose surface layer may comprise tungsten.
- the conductive interconnect layer 19 has been electrochemically deposited on the surface of the substrate 15 with a dual-purpose layer 22 , it may be desirable for some integrated circuits to transform the conductive interconnect material into an alloy. For example, it may be desirable to transform a copper interconnect into a copper alloy. Copper alloys are more resistant to electromigration than regular copper, which can be useful in some applications.
- small traces of impurities are implanted on the copper conductive interconnect layer, using methods of ion implantation known in the art. Examples of impurities that may be implanted to create the copper alloy include materials such as magnesium, boron, tin and zirconium.
- the preferred implant dose is about 1 ⁇ 10 16 atoms/cm 2 .
- the resulting workpiece optionally may be subjected to an annealing process.
- the wafer crystal structure experiences lattice damage, damage cluster or vacancy-interstitial damage.
- Annealing may be necessary to correct the damage to the wafer crystal structure that may occur during processing.
- Methods of annealing silicon wafers to repair crystal damage are known in the art of semiconductor manufacturing. Restoration of the crystal structures that were damaged during processing can be achieved by a thermal heating step, which is commonly referred to as annealing.
- a workpiece optionally may be planarized using methods known in the art such as chemical mechanical polishing (CMP).
- the methods of the present invention are but a few of the steps performed in manufacturing a semiconductor device. Many other steps known in the art can be advantageously utilized in conjunction with the methods of the present invention by a practitioner of ordinary skill in the art to produce a wide variety of devices embodying the present invention.
- Semiconductors comprising dual-purpose layers and conductive interconnect layers may be advantageously produced in accordance with the present invention.
- semiconductor chips containing a dual-purpose layer comprising tungsten, tungsten nitride, or tungsten-silicon nitride and a conductive interconnect layer comprising copper may be manufactured in accordance with the present invention.
- FIG. 4 is a simplified block diagram of a memory device according to one embodiment of the invention.
- the memory device 500 includes an array of memory cells 502 , address decoder 504 , row access circuitry 506 , column access circuitry 508 , control circuitry 510 , and input/output circuitry 512 .
- the memory can be coupled to an external microprocessor 514 , or memory controller for memory accessing.
- the memory receives control signals from the processor 514 , such as WE*, RAN* and CAVES* signals.
- the memory is used to store data which is accessed via I/O lines. It will be appreciated by those skilled in the art that additional circuitry and control signals can be provided, and that the memory device of FIG. 4 has been simplified to help focus on the invention.
- Memory cells of the present invention have a conductive interconnect made in accordance with the present invention.
- DRAM Dynamic Random Access Memory
- SCRAM Synchronous Graphics Random Access Memory
- SCRAM Synchronous Dynamic Random Access Memory
- SCRAM II Synchronous Dynamic Random Access Memory
- DAR SCRAM Double Data Rate SCRAM
- memory devices of the type described herein are generally fabricated as an integrated circuit containing a variety of semiconductor devices.
- the integrated circuit is supported by a substrate.
- Integrated circuits are typically repeated multiple times on each substrate.
- the substrate is further processed to separate the integrated circuits into dies as is well known in the art.
- FIG. 5 illustrates another embodiment of the present invention.
- a semiconductor die 710 is produced from a wafer 700 .
- a die is an individual pattern, typically rectangular, on a substrate that contains circuitry, or integrated circuit devices, to perform a specific function.
- Semiconductor dies of the present invention comprise at least one integrated circuit device having a conductive interconnect made in accordance with the present invention.
- a semiconductor wafer will typically contain a repeated pattern of such dies containing the same functionality.
- die 710 may contain circuitry for the inventive memory device, as discussed above. Die 710 may further contain additional circuitry to extend to such complex devices as a monolithic processor with multiple functionality.
- Die 710 is typically packaged in a protective casing (not shown) with leads extending therefrom (not shown) providing access to the circuitry of the die for unilateral or bilateral communication and control.
- circuit module 800 may be a combination of dies 710 representing a variety of functions, or a combination of dies 710 containing the same functionality.
- Circuit modules of the present invention comprise one or more dies containing at least one conductive interconnect made in accordance with the present invention.
- Circuit modules include memory modules, device drivers, power modules, communication modems, processor modules and application-specific modules, and may include multilayer, multichip modules.
- Circuit module 800 may be a subcomponent of a variety of electronic systems, such as a clock, a television, a cell phone, a personal computer, an automobile, an industrial control system, an aircraft and others. Circuit module 800 will have a variety of leads 810 extending therefrom and coupled to the dies 710 providing unilateral or bilateral communication and control.
- FIG. 7 shows one embodiment of a circuit module as memory module 900 .
- Memory module 900 contains multiple memory devices 910 contained on support 915 , the number depending upon the desired bus width and the desire for parity.
- Memory module 900 accepts a command signal from an external controller (not shown) on a command link 920 and provides for data input and data output on data links 930 .
- the command link 920 and data links 930 are connected to leads 940 extending from the support 915 .
- Leads 940 are shown for conceptual purposes and are not limited to the positions shown in FIG. 7 .
- FIG. 8 shows an electronic system 1000 containing one or more circuit modules 800 .
- Electronic system 1000 generally contains a user interface 1010 .
- User interface 1010 provides a user of the electronic system 1000 with some form of control or observation of the results of the electronic system 1000 .
- Some examples of user interface 1010 include the keyboard, pointing device, monitor or printer of a personal computer; the tuning dial, display or speakers of a radio; the ignition switch, gauges or gas pedal of an automobile; and the card reader, keypad, display or currency dispenser of an automated teller machine.
- User interface 1010 may further describe access ports provided to electronic system 1000 . Access ports are used to connect an electronic system to the more tangible user interface components previously exemplified.
- circuit modules 800 may be a processor providing some form of manipulation, control or direction of inputs from or outputs to user interface 1010 , or of other information either preprogrammed into, or otherwise provided to, electronic system 1000 .
- electronic system 1000 will often contain certain mechanical components (not shown) in addition to circuit modules 800 and user interface 1010 . It will be appreciated that the one or more circuit modules 800 in electronic system 1000 can be replaced by a single integrated circuit. Furthermore, electronic system 1000 may be a subcomponent of a larger electronic system.
- FIG. 9 shows one embodiment of an electronic system as memory system 1100 .
- Memory system 1100 contains one or more memory modules 900 and a memory controller 1110 .
- Memory controller 1110 provides and controls a bidirectional interface between memory system 1100 and an external system bus 1120 .
- Memory system 1100 accepts a command signal from the external bus 1120 and relays it to the one or more memory modules 900 on a command link 1130 .
- Memory system 1100 provides for data input and data output between the one or more memory modules 900 and external system bus 1120 on data links 1140 .
- FIG. 10 shows a further embodiment of an electronic system as a computer system 1200 .
- Computer system 1200 contains a processor 1210 and a memory system 1100 housed in a computer unit 1205 .
- Computer system 1200 is but one example of an electronic system containing another electronic system, i.e., memory system 1100 , as a subcomponent.
- Computer system 1200 optionally contains user interface components. Depicted in FIG. 10 are a keyboard 1220 , a pointing device 1230 , a monitor 1240 , a printer 1250 and a bulk storage device 1260 . It will be appreciated that other components are often associated with computer system 1200 such as modems, device driver cards, additional storage devices, etc. It will further be appreciated that the processor 1210 and memory system 1100 of computer system 1200 can be incorporated on a single integrated circuit. Such single package processing units reduce the communication time between the processor and the memory circuit.
Landscapes
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Internal Circuitry In Semiconductor Integrated Circuit Devices (AREA)
- Electrodes Of Semiconductors (AREA)
Abstract
Apparatus with conductive interconnect layers disposed on a dual-purpose layer provide useful articles such as semiconductor wafers, semiconductor dies, memory devices, circuit modules, and electronic systems. The number of necessary processing steps to form such conductive interconnects are reduced by removing the need to employ a seed layer interposed between the barrier layer and the conductive interconnect layer.
Description
- This application is a Divisional of U.S. application Ser. No. 10/929,252, filed Aug. 30, 2004, which is a Divisional of U.S. application Ser. No. 09/838,493, filed Apr. 19, 2001, now U.S. Pat. No. 6,852,618, both of which are incorporated herein by reference.
- The present invention relates generally to the fabrication of semiconductor devices. More particularly, the present invention relates to the formation of dual-purpose layers that serve as both barrier and seed layers for electrochemical deposition of conductive interconnect materials.
- The need for high performance semiconductor chips has continued to increase over the past several years. As demand for better performance and faster semiconductor chips has grown, so have efforts to reduce semiconductor chip size. Reducing the size of individual integrated circuit components can dramatically increase the speed and performance of a semiconductor chip. For example, smaller gate lengths in MOS transistors dramatically increase their switching speed.
- The performance of semiconductor chips is limited by the electrical conductivity of the metal interconnects that electrically connect the various components that form the integrated circuits on the semiconductor chip. Therefore, in order to take full advantage of transistors that are capable of operating at faster speeds, the electrical interconnects must be highly conductive, yet low in resistance. Aluminum or an aluminum alloy was widely used as the preferred material for forming conductive interconnects by a process known as “metallization”. “Metallization” is a term used in the semiconductor industry to describe the process of wiring together the components of an integrated circuit, and typically occurs by the process of electrochemical deposition. Aluminum emerged as the preferred metal for metallization because it has a relatively low resistivity, good current-carrying density, and superior adhesion to silicon dioxide. In addition, aluminum is available in high purity and has a natural low contact resistance with silicon.
- However, aluminum and aluminum alloys present some disadvantages when used to make interconnects. For example, although aluminum has a resistance that can be tolerated by most integrated circuits, it is difficult to deposit in a high aspect ratio. In addition, aluminum and aluminum alloys suffer from eutectic formations, thermally induced voiding, and electromigration when used in very large scale integration (VLSI) and ultra large scale integration (ULSI) semiconductor chips.
- Recently, copper metal has begun to replace aluminum and aluminum-silicon alloys in VLSI and ULSI metallization processes. Copper has better conductivity and is more reliable than aluminum or aluminum alloys. The use of copper for making semiconductor chip interconnects is appealing because of the low cost, high throughput, excellent via-filling capabilities, and high quality of the deposited copper film. In contrast to aluminum, copper is capable of being deposited with high aspect ratios. Copper is also a much better conductor than aluminum, provides good step coverage, is more resistant to electromigration and can be electrochemically deposited at low temperatures.
- Because copper will diffuse into silicon if applied directly to a silicon-containing substrate, such as a silicon wafer, it is necessary to first apply a barrier layer between the substrate from which the semiconductor chip is fabricated and the copper layer. Additionally, the material must have a relatively low resistivity so that electrochemical deposition of copper on the surface of the barrier layer will occur. Unless the resistivity of the barrier material is relatively low, it will not function as a suitable surface for subsequent electrochemical deposition of the conductive interconnect material. Tantalum, for example, has a resistivity that is two orders of magnitude higher than copper. Accordingly, tantalum is generally not suitable to serve as the cathode during the electrochemical deposition process.
- To overcome this resistivity concern, a seed layer is typically formed on top of the barrier layer to provide the desired resistivity. For the electrochemical deposition of copper, the seed layer is often a layer of PVD copper. Unfortunately, formation of the seed layer overlying the barrier layer necessarily adds a discrete process step.
- Accordingly, there continues to be a need in the industry for improved methods and devices for forming conductive layers, such as used in device interconnects, onto barrier layers.
- The present invention is illustrated by way of example in the following drawings in which like references indicate similar elements. The following drawings disclose various embodiments of the present invention for purposes of illustration only and are not intended to limit the scope of the invention.
-
FIG. 1 illustrates cross-sectional view of a metallized workpiece according to the prior art. -
FIG. 2 illustrates an embodiment of the present invention. -
FIG. 3 is an illustration an electrochemical reaction cell. -
FIG. 4 is a block diagram of one embodiment of an integrated circuit memory device. -
FIG. 5 is an elevation view of one embodiment of a wafer containing semiconductor dies. -
FIG. 6 is a block diagram of one embodiment of an exemplary circuit module. -
FIG. 7 is a block diagram of one embodiment of an exemplary memory module. -
FIG. 8 is a block diagram of one embodiment of an exemplary electronic system. -
FIG. 9 is a block diagram of one embodiment of an exemplary memory system. -
FIG. 10 is a block diagram of one embodiment of an exemplary computer system. - In the following detailed description of the invention, reference is made to the accompanying drawings which form a part hereof, and in which is shown, by way of illustration, specific embodiments in which the invention may be practiced. These embodiments are described in sufficient detail to enable those skilled in the art to practice the invention. Other embodiments may be utilized and structural, logical, and electrical changes may be made without departing from the scope of the present invention.
- The term substrate used in the following description refers to any structure having an exposed surface onto which structures of the present invention are to be formed. For example, the term substrate includes any structure onto which a barrier layer may be effectively deposited. The term substrate should be understood as including silicon-on-sapphire (SOS) technology, silicon-on-insulator (SOI) technology, thin film transistor (TFT) technology, doped and undoped semiconductors, epitaxial layers of a silicon supported by a base semiconductor structure, as well as other semiconductor structures well known to one skilled in the art. Furthermore, when reference is made to a wafer or substrate in the following description, previous process steps may have been utilized to form regions/junctions in the base semiconductor structure, and terms wafer or substrate include the underlying layers containing such regions/junctions. The term substrate is understood to include semiconductor wafers. The term workpiece will also refer to semiconductor structures during processing, and may include other layers that have been fabricated thereupon. The term conductor is understood to include semiconductors, and the term insulator is defined to include any material that is less electrically conductive than the materials referred to as conductors. The following detailed description is, therefore, not to be taken in a limiting sense.
- Embodiments of the present invention reduce the number of necessary processing steps to form interconnects by removing the need to employ a separate seed layer interposed between the barrier layer and the conductive interconnect layer. This is accomplished in part through the utilization of a barrier material that can be metallized without the need for a seed layer.
- In one embodiment, the present invention is a semiconductor comprising a conductive interconnect layer electrochemically deposited onto a dual-purpose layer. By dual-purpose layer, it is meant that the dual-purpose layer functions as both a barrier layer and a seed layer. Dual-purpose layers of the present invention reduce diffusion of conductive interconnect material sufficiently to serve as a barrier layer. Dual-purpose layers of the present invention also exhibit a resistivity sufficiently low to serve as a seed layer, allowing effective electrochemical deposition of the conductive interconnect layer onto the dual-purpose layer. In one embodiment, the material comprising the dual-purpose layer contains tungsten.
- In one embodiment of the present invention, a method for metallizing a silicon wafer is provided. A dual-purpose layer is deposited on the surface of the silicon wafer. Next, oxides on the dual-purpose layer are electrochemically reduced in an electrochemical reaction cell. A layer of conductive interconnect material is then electrochemically deposited onto the dual-purpose layer. Tungsten can be utilized to create a dual-purpose layer and copper can be used as the conductive interconnect material. Thus, in one preferred embodiment of the present invention, tungsten interconnects are deposited onto tungsten.
- In another embodiment, a first electrolyte is utilized to electrochemically reduce oxides on a dual-purpose layer and a second electrolyte is utilized to electrochemically deposit the conductive interconnect material onto the dual-purpose layer. The electrochemical deposition of the conductive interconnect material can be performed by discharging the first electrolyte from the electrochemical reaction cell after the electrochemical reduction of oxides and replacing it with the second electrolyte. Alternatively, the electrochemical deposition of the conductive interconnect material can be performed in a separate electrochemical reaction cell by transferring the substrate after the reduction of oxides to the separate electrochemical reaction cell.
- In another embodiment, a single electrolyte is utilized in an electrochemical reaction cell to both electrochemically reduce the oxides on the dual-purpose layer and electrochemically deposit the conductive interconnect material onto the dual-purpose layer. The single electrolyte comprises the cation of the conductive interconnect material, a counterion, a complexing agent, and a pH control agent.
- In other embodiments of the present invention, conductive interconnects according to the present invention are advantageously utilized to produce articles such as semiconductor chips, memory devices, semiconductor dies, circuit modules, and electronic systems.
- Electroplating Methods
-
FIG. 1 illustrates a cross-sectional view of a metallizedworkpiece 10 according to the prior art. Theworkpiece 10 includes awafer 12, an overlyingdielectric layer 14, abarrier layer 16, aseed layer 18, and aconductive interconnect layer 19. Theconductive interconnect layer 19 may be referred to as a metal layer. As known in the art, theworkpiece 10, at this particular stage of manufacturing, may include a variety of integrated circuit components that were formed in earlier fabrication steps. Thedielectric layer 14 is deposited on the surface of thewafer 12 using methods known in the art, such as chemical vapor deposition (CVD), plasma-enhanced chemical vapor deposition (PECVD), spin-on depositing or by thermal oxidation. Thedielectric layer 14 can be selected from a variety of dielectric materials, but is preferably made from silicon dioxide or some variation of silicon dioxide. Once adielectric layer 14 is deposited it typically is patterned using techniques known in the art such as etching. This patterning of thedielectric layer 14 creates what are generally referred to in the industry as trenches. The deposited and patterneddielectric layer 14 on thewafer 12 forms asubstrate 15. Once adielectric layer 14 is deposited and patterned, abarrier layer 16 is deposited on thesubstrate 15 using techniques known in the art. Next aseed layer 18 is deposited using techniques known in the art. Finally, themetal layer 19 is deposited utilizing techniques known in the art, filling the trenches. -
FIG. 2 illustrates an embodiment of the present invention. InFIG. 2 , thedielectric layer 14 has been deposited onto thewafer 12 and patterned in the same manner as described in reference toFIG. 1 . Once thedielectric layer 14 has been deposited on thewafer 12 and patterned, a dual-purpose layer 22 is deposited on thesubstrate 15. The dual-purpose layer 22 can be deposited utilizing the same techniques known in the art for depositing thebarrier layer 16. Oxides are removed from the dual-purpose layer 22 and themetal layer 19 is then deposited onto the dual-purpose layer 22 in accordance with methods of the present invention. Thus, whereas aworkpiece 10 of the prior art contains both abarrier layer 16 and aseed layer 18, the present invention provides for only a single dual-purpose layer 22. - By dual-purpose layer, it is meant that the dual-purpose layer functions as both a barrier layer and a seed layer. Dual-purpose layers of the present invention reduce electromigration of conductive interconnect material sufficiently to serve as a barrier layer. Dual-purpose layers of the present invention also exhibit a resistivity sufficiently low to serve as a seed layer, allowing effective electrochemical deposition of the conductive interconnect layer onto the dual-purpose layer.
- Materials that can be used to make the dual-purpose layer are referred to herein as dual-purpose materials. Preferred dual-purpose materials can be deposited on substrates by techniques known in the art. In one embodiment of the present invention, the dual-purpose material contains tungsten. These tungsten-containing, dual-purpose materials include, for example, tungsten (W), tungsten nitride (WNX), and tungsten-silicon nitride (WSiNX). A preferred dual-purpose material is tungsten. Tungsten is a refractory metal that has a melting point of 3370° C. and a bulk resistivity of 52 μΩ-cm at room temperature. A dual-
purpose layer 22 of tungsten may be deposited on asilicon wafer 12 using several deposition techniques known in the art such as evaporation, ion-metal plasma (IMP), chemical vapor deposition (CVD), low pressure CVD, or physical vapor deposition (PVD). A frequently used method for the deposition of tungsten is the reduction of tungsten hexafluoride (WF6) by hydrogen (H) or silane (SiH4). - Dual-purpose materials can be susceptible to oxidation, causing oxides to form on the surface of the dual-purpose layer. These oxides can inhibit the deposition of conductive interconnect material onto the surface of the dual-purpose layer. For example, when tungsten is exposed to air or moisture, it can be oxidized to tungsten dioxide (WO2), tungsten trioxide (WO3), or tungsten pentoxide (W2O5). Tungsten oxides are not readily removed by rinsing or washing steps because they are not readily dissolved in acidic solutions such as are commonly used in the electrochemical deposition process. These oxides can inhibit the nucleation of copper, resulting in poor adhesion of copper as a conductive interconnect material.
- As indicated, conductive interconnect material may not adhere well to the exposed regions of the dual-purpose layer if oxides are present. Thus, according to the present invention, an electrochemical reduction step is employed to remove oxides from the exposed surface of the dual-purpose layer. The electrochemical reduction of oxides on the surface of the dual-purpose layer requires the use of an electrochemical reaction cell. The basic design and operation of electrochemical reaction cells is well known in the art and includes various inlets and outlets for the introduction of gases and liquids, a cathode, an anode, a current source, and an electrolyte. The electrolyte is a medium capable of conducting electricity. Typically, the electrolyte is an aqueous solution. The electrolyte frequently contains metal ions or salts of metals. The cathode, the anode and the substrate are immersed in the electrolyte. A current is then provided to the electrolyte, by providing an electrical potential across the anode and the cathode.
- In one embodiment of the present invention, a first process for reducing oxides on the surface of a dual-purpose layer is performed utilizing one electrolyte and then a second process for depositing conductive interconnect material onto the dual-purpose layer is performed utilizing a second electrolyte. The two processes can be performed utilizing the same electrochemical reaction cell by changing electrolytes after the oxide reduction process and before deposition of the conductive interconnect material. The two processes can be performed using a single anode or two different anodes. Alternatively, the two processes can be preformed in two separate electrochemical reaction cells by performing the oxide reduction process in one cell and then transferring the workpiece to a second cell in which the deposition process is performed. The transferring of the workpiece is performed in a manner that does not allow oxides to reform on the surface of the workpiece. In another embodiment of the present invention, a single electrolyte is utilized for both the oxide reduction process and the copper deposition process.
- Generally, electrochemical reaction cells of the present invention comprise a power source, a substrate cathode, an anode, and an electrolyte.
FIG. 3 illustrates a typicalelectrochemical reaction cell 30 according to the present invention. Thereaction cell 30 inFIG. 3 comprises acathode 32, ananode 34, anelectrolyte supply 36, and anelectrolyte return 38. It should be understood that in reaction cells of the present invention the cathode and anode are electrically connected to an electrical power source in a manner that allows an electrical potential to be applied across the cathode and anode. Methods and apparatus for providing such an electrical connection are well understood in the art. - According to the present invention,
wafer 40 is placed into thereaction cell 30 and an electrical potential is applied across the anode and the cathode. As explained in greater detail below, the application of the electrical potential may cause a reduction reaction to occur on the surface of thewafer 40 or the application of the electrical potential may cause a deposition reaction to occur on the surface of thewafer 40. - According to the present invention, cations from the electrolyte are deposited onto the surface of the
wafer 40 during a deposition reaction. Thus, the deposition reaction removes cations from the electrolyte. These cations removed from the electrolyte must be eventually replenished. If the anode is made from the same material as the cations, then the cations can be replenished from the anode.FIG. 3 illustrates a mechanism for replenishing cations when they are not cations of the material from which the anode is made.FIG. 3 shows anelectrolyte supply 36 containing a sufficient amount of cations. If thereaction cell 30 is used for deposition, the electrolyte exiting the cell at theelectrolyte return 38 will have cations removed. The electrolyte can be transported to a cation source (not shown) to replenish the cations and then reintroduce into thereaction cell 30 through theelectrolyte supply 36. - Two-Electrolyte, Single-Cell Embodiments
- Referring now to a two-electrolyte embodiment of the present invention, a substrate comprising a deposited dual-purpose layer is placed into an electrochemical reaction cell comprising a cathode, a first anode, and a second anode. Typically, the substrate will be a silicon wafer having been photolithographically etched and covered with a dual-purpose layer. Of course, the present invention contemplates that multiple substrates or workpieces may be simultaneously subjected to embodiments of the present invention. The first anode is formed from a material that can be oxidized in the presence of the dual-purpose material. These materials can be readily identified by their oxidation potentials. Such a material will have an oxidation potential that is higher (i.e., more positive) than the oxidation potential of the dual-purpose material. Anodes useful in the present invention include anodes made from titanium, titanized platinum, platinum, and copper. For example, the oxidation potential for the oxidation of tungsten to WO3 is 0.09 volts and the oxidation potential for the oxidation of tungsten to WO2 is 0.12 volts. When the dual-purpose layer comprises tungsten, then the first anode is preferably formed from titanium or titanized platinum.
- The electrochemical reaction cell is charged with a first electrolyte. Typically, the first electrolyte is an aqueous solution comprising a metal salt M+X−, wherein M+ is the cationic species of the material used to form the first anode and X− is a counterion. For example, when the first anode is formed from titanium, the first electrolyte solution can be titanium sulfate (Ti2(SO4)3), titanium bromide, titanium trichloride (TiCl3), titanium iodide, titanium fluoride, or mixtures thereof. When the first anode is formed from titanium, preferred first electrolyte solutions are titanium trichloride and titanium sulfate. Additionally, when the first anode is formed from copper, the first electrolyte can be copper sulfate.
- Generally, the concentration of the metal salt in the first electrolyte will be from about 0.1 M to about 1 M. The concentration of the metal salt in the first electrolyte may vary depending on the specific metal salt utilized, but optimum concentration ranges can be determined by a practitioner of ordinary skill in the art without undue experimentation.
- The substrate is placed in the electrolyte and is electrically connected to an electrical circuit to form a cathode. The first anode is placed in the electrolyte solution and is also electrically connected to the electrical circuit. The electrical circuit is also equipped with a electrical power source. Thus, the power source, cathode, anode, and electrolyte form an electrical circuit as is known in the art. A first potential is applied to the electrical circuit. A first electrical potential between the first anode and the substrate cathode causes a reduction reaction to occur, reducing oxides on the dual-purpose layer surface. The first potential is applied with a magnitude and duration sufficient to reduce oxides on the surface of the dual-purpose layer. Typically, the magnitude of the first potential will be in the range of from about 0.1 V to about 1 V and will be applied for a time in the range of from about 1 second to about 60 seconds. These ranges may vary depending on the material used for the first anode and the specific composition of the electrolyte, but optimum ranges can be determined by a practitioner of ordinary skill in the art without undue experimentation.
- After oxides on the surface of the dual-purpose layer are reduced, the first potential is no longer applied, and the first electrolyte is discharged from the electrochemical reaction cell. A second electrolyte is then introduced into the cell so that the substrate cathode and the second anode are placed in the second electrolyte. The discharging of the first electrolyte and the introduction of the second electrolyte should be done in a manner that does not expose the surface of the dual-purpose layer to conditions that would cause oxides to reform on the dual-purpose layer. One method for preventing the reformation of oxides is to keep the cell under a positive pressure of an inert gas such as nitrogen.
- The second electrolyte can be any electrolyte known in the art to be useful for depositing the conductive interconnect material. In one embodiment, the second anode comprises the conductive interconnect material. Typically, the second electrolyte is an aqueous solution comprising a metal salt M+X−, wherein M+ is the cationic species of the conductive interconnect material M that forms the second anode and that is to be electrochemically deposited on the surface of the dual-purpose layer and X− is a counterion. Generally, the pH of the second electrolyte will be less than about 1. For example, when the conductive interconnect material is copper, the second anode typically is formed from copper and the second electrolyte solution preferably comprises copper sulfate (CuSO4), hydrochloric acid (HCl), and sulfuric acid (H2SO4). Additionally, the second electrolyte can be an electrolyte of the present invention, such as those taught below in the detailed description of embodiments of the present invention that utilize the same electrolyte for both the oxide reduction step and the conductive interconnect deposition step.
- Methods for electrochemical deposition of conductive interconnect material are known in the art and can be utilized in conjunctive with the present invention. Generally, the substrate cathode and second anode are electrically connected in a manner allowing an electrical potential to be applied across the substrate cathode and the second anode. A second potential is applied to the resulting electrical circuit. Application of the second electrical potential between the second anode and the substrate cathode causes a deposition reaction to occur, depositing conductive interconnect material on the dual-purpose layer surface of the substrate. For example, when the conductive interconnect material is copper, copper ions from the electrolyte are reduced and deposited on the surface of the dual-purpose layer. The copper ions from the electrolyte are deposited or plated on the substrate via electric migration and diffusion.
- Generally, the thickness of the conductive interconnect layer will be from about 2000 angstroms to about 20,000 angstroms. Preferably, the thickness of the conductive interconnect layer is from about 10,000 angstroms to about 12,000 angstroms. The amount of conductive interconnect material deposited over a period of time (and therefore, the thickness) can be controlled by controlling the amount of current flowing through the electrolyte. The voltage and the period of time for applying the voltage is selected according to the depth of the layer of conductive interconnect material to be deposited on the surface of substrate. The voltage applied is typically at least abut 0.1 V and not more than about 1 V and is typically applied for a time period of from about 30 seconds to about 5 minutes. The resulting electrical current applied is typically from about 0.5 amps to about 10 amps and has a current density of from about 5 mA/cm2 to about 25 mA/cm2. In some preferred embodiments, the current density will be from about 10 mA/cm2 to about 15 mA/cm2. Additionally, in some embodiments a current density of about 12 mA/cm2 is most preferred.
- Two-Electrolyte, Two-Cell Embodiments
- In another embodiment of the present invention, two separate electrochemical reaction cells can be utilized. The reduction of oxides on the dual-purpose layer is performed in the first cell and the deposition of the conductive interconnect material is performed in the second cell. Generally, the same process parameters are used as described above, but instead of discharging the first electrolyte after the reduction of oxides and introducing the second electrolyte into the same cell, the substrate is transferred to the second cell containing the second electrolyte and second anode. The deposition of conductive interconnect material is performed in the second cell. It is important that the transfer of the substrate from the first cell to the second cell be done under conditions that does not allow for the reformation of oxides on the dual-purpose layer. Such conditions can be readily determined by a practitioner of ordinary skill in the art without undue experimentation.
- Single-Electrolyte, Single-Cell Embodiments
- In another embodiment of the present invention, a single electrolyte can be utilized in a single electrochemical reaction cell containing a single anode. In this embodiment, the composition of the electrolyte is chosen such that applying a potential across the anode and cathode first causes a reduction of oxides on the substrate cathode and then causes the deposition of the conductive interconnect material onto the substrate cathode. Accordingly, these electrolytes will be referred to as dual-purpose electrolytes since they can be utilized both for the reduction of oxides on the substrate and the deposition of the conductive interconnect material onto the substrate. However, it should be understood that dual-purpose electrolytes of the present invention may also be advantageously utilized in two electrolyte systems if so desired. For example, dual-purpose electrolytes could be used to reduce the oxides on a substrate and then a second electrolyte could be used for the deposition of the conductive interconnect material onto the substrate. The second electrolyte could be any electrolyte known in the art for depositing conductive interconnect material onto a substrate. Alternately, a dual-purpose electrolyte could be used to reduce the oxides on a substrate and deposit a thin layer of interconnect material and then a second electrolyte could be used to deposit additional interconnect material, thickening the layer of interconnect material to the resulting desired thickness. Again, the second electrolyte could be any electrolyte known in the art for depositing conductive interconnect material onto a substrate. Alternatively, a first electrolyte could be used to reduce oxides on a substrate and then a dual-purpose electrolyte used for depositing conductive interconnect material onto a substrate.
- The deposition of conductive interconnect material occurs when the cation of the conductive interconnect material is reduced. For example, the deposition of copper as a conductive interconnect material occurs according to the following reduction reaction:
Cu2++2e −=>Cu (1)
Thus, when a potential is applied across the anode and cathode, Cu2+ gets reduced, resulting in copper being deposited on the cathode. According to the present invention, oxides on a substrate surface are removed via a reduction reaction. For example, tungsten oxides can be removed according to the following reduction reaction:
WOX +e −=>W (2)
Generally in the prior art, the reduction of conductive interconnect material cations has a lower oxidation potential (that is, a higher reduction potential) than the reduction of oxides (for example, tungsten oxide). Thus, normally when a potential is applied across an anode and cathode in an electrochemical reaction cell where an electrolyte containing a conductive interconnect material cation is present, the reduction of the cation will occur before the reduction of any oxides. - However, according to the present invention, the composition of the electrolyte can be chosen such that the reduction of oxides on the substrate cathode occurs before the reduction of conductive interconnect material cations. Electrolytes of this embodiment will also contain a cation of the conductive interconnect material along with a counterion like the second electrolyte described above. In addition, electrolytes of this embodiment will also contain a complexing agent and a pH control agent.
- The amount and type of complexing agent added should be sufficient to complex the conductive interconnect material cation so that the effective reduction potential of the conductive interconnect material cation is lower than the reduction potential of the oxides. Examples of complexing agents useful in the present invention include ethylene diamine tetra acetate (EDTA), boric acid, and malonic acid. A preferred complexing agent is EDTA. Generally, the complexing agent will be present in a concentration of from about 0.01 M to about 1 M. Preferred concentrations of complexing agent used may depend on the precise complexing agent used, but can be determined by a practitioner of ordinary skill in the art without undue experimentation.
- The pH control agent is utilized to keep the pH of the electrolyte greater than or equal to about 7. Preferably, the pH of the electrolyte is equal to or greater than about 10. Preferably, the pH of the electrolyte is less than or equal to about 12. Examples of pH control agents include tetramethyl ammonium hydroxide (TMAH), ammonium hydroxide (NH4OH), and potassium hydroxide (KOH).
- The amount of complexing agent and the amount of pH control agent present should be sufficient to lower the reduction potential (that is, raise the oxidation potential) of the cation reduction reaction until it is lower than the reduction potential (higher than the oxidation potential) of the oxide reduction reaction. Thus, when a potential is applied across the anode and cathode, oxides on the substrate surface will reduce before the conductive interconnect material cation begins to reduce and be deposited on the substrate surface.
- Accordingly, in one embodiment of the present invention, a substrate cathode comprising a dual-purpose layer is placed into an electrochemical reaction cell additionally comprising an anode and an electrolyte. In one embodiment, the cations to be deposited are cations of the material from which the anode is made. For example, if it is desired to deposit a conductive interconnect material comprising copper, the electrolyte could comprise copper sulfate, for example, and the anode could comprise copper. In this manner, the copper cations that are deposited onto the surface of the dual-purpose layer can be replenished from the anode. However, the anode does not necessarily need to be made from the same material as the conductive interconnect material to be deposited. For example, in another embodiment, the anode comprises platinum. In embodiments where the cations are not comprised of the same material, the cations in the electrolyte can be replenished as explained in the text referencing
FIG. 3 . As indicated above, the electrolyte comprises cations of the conductive interconnect material, a counterion, a complexing agent, and a pH control agent. - The substrate cathode and the anode are electrically connected to a power source and an electrical potential is applied across the substrate cathode and the anode. This potential causes a reduction reaction to occur at the substrate cathode, reducing oxides that may be present on the dual-purpose layer of the substrate. Once the oxides are reduced, or if no oxides are present, then the potential causes the reduction of conductive interconnect material cations in the electrolyte, resulting in conductive interconnect material being deposited on the dual-purpose layer of the substrate. In this manner, conductive interconnect material can be deposited on a dual-purpose layer without having to first deposit a separate seed layer, without having to use two separate electrolytes, and without having to transfer a substrate from a first electrochemical reaction cell to a second electrochemical reaction cell.
- Generally, the process parameters (applied potential, current, and current density, for example) are the same as described above for the two-electrolyte embodiments of the present invention. Again, the thickness of the conductive interconnect layer can be controlled by controlling the amount of current flowing through the electrolyte. For specific embodiments of the present invention, optimum process parameters can be determined by a practitioner having ordinary skill in the art without undue experimentation.
- In one embodiment of the present invention, copper is electrochemically deposited onto a substrate having a dual-purpose surface layer by utilizing a copper anode and an electrolyte comprising copper sulfate, a complexing agent, and a pH control agent. The dual-purpose surface layer may comprise tungsten.
- Once the
conductive interconnect layer 19 has been electrochemically deposited on the surface of thesubstrate 15 with a dual-purpose layer 22, it may be desirable for some integrated circuits to transform the conductive interconnect material into an alloy. For example, it may be desirable to transform a copper interconnect into a copper alloy. Copper alloys are more resistant to electromigration than regular copper, which can be useful in some applications. In order to transform the copper into a copper alloy, small traces of impurities are implanted on the copper conductive interconnect layer, using methods of ion implantation known in the art. Examples of impurities that may be implanted to create the copper alloy include materials such as magnesium, boron, tin and zirconium. The preferred implant dose is about 1×1016 atoms/cm2. - After the both dual-purpose layer and the conductive interconnect layer have been deposited, the resulting workpiece optionally may be subjected to an annealing process. Sometimes during semiconductor manufacturing processes, the wafer crystal structure experiences lattice damage, damage cluster or vacancy-interstitial damage. Annealing may be necessary to correct the damage to the wafer crystal structure that may occur during processing. Methods of annealing silicon wafers to repair crystal damage are known in the art of semiconductor manufacturing. Restoration of the crystal structures that were damaged during processing can be achieved by a thermal heating step, which is commonly referred to as annealing. After any optional annealing processes are performed, a workpiece optionally may be planarized using methods known in the art such as chemical mechanical polishing (CMP).
- Typically, the methods of the present invention are but a few of the steps performed in manufacturing a semiconductor device. Many other steps known in the art can be advantageously utilized in conjunction with the methods of the present invention by a practitioner of ordinary skill in the art to produce a wide variety of devices embodying the present invention.
- Semiconductor Chip
- Semiconductors comprising dual-purpose layers and conductive interconnect layers may be advantageously produced in accordance with the present invention. For example, semiconductor chips containing a dual-purpose layer comprising tungsten, tungsten nitride, or tungsten-silicon nitride and a conductive interconnect layer comprising copper may be manufactured in accordance with the present invention.
- Memory Devices
-
FIG. 4 is a simplified block diagram of a memory device according to one embodiment of the invention. The memory device 500 includes an array of memory cells 502, address decoder 504, row access circuitry 506, column access circuitry 508, control circuitry 510, and input/output circuitry 512. The memory can be coupled to an external microprocessor 514, or memory controller for memory accessing. The memory receives control signals from the processor 514, such as WE*, RAN* and CAVES* signals. The memory is used to store data which is accessed via I/O lines. It will be appreciated by those skilled in the art that additional circuitry and control signals can be provided, and that the memory device ofFIG. 4 has been simplified to help focus on the invention. Memory cells of the present invention have a conductive interconnect made in accordance with the present invention. - It will be understood that the above description is that of a DRAM (Dynamic Random Access Memory) is intended to provide a general understanding of the memory and is not a complete description of all the elements and features of a DRAM. Further, the invention is equally applicable to any size and type of memory circuit and is not intended to be limited to the DRAM described above. Other alternative types of devices include SRAM (Static Random Access Memory) or Flash memories. Additionally, the DRAM could be a synchronous DRAM commonly referred to as SCRAM (Synchronous Graphics Random Access Memory), SCRAM (Synchronous Dynamic Random Access Memory), SCRAM II, and DAR SCRAM (Double Data Rate SCRAM), as well as Synchlink or Rambus DRAMs and other emerging DRAM technologies.
- As recognized by those skilled in the art, memory devices of the type described herein are generally fabricated as an integrated circuit containing a variety of semiconductor devices. The integrated circuit is supported by a substrate. Integrated circuits are typically repeated multiple times on each substrate. The substrate is further processed to separate the integrated circuits into dies as is well known in the art.
- Semiconductor Dies
-
FIG. 5 illustrates another embodiment of the present invention. InFIG. 5 , asemiconductor die 710 is produced from awafer 700. A die is an individual pattern, typically rectangular, on a substrate that contains circuitry, or integrated circuit devices, to perform a specific function. Semiconductor dies of the present invention comprise at least one integrated circuit device having a conductive interconnect made in accordance with the present invention. A semiconductor wafer will typically contain a repeated pattern of such dies containing the same functionality. For example, die 710 may contain circuitry for the inventive memory device, as discussed above.Die 710 may further contain additional circuitry to extend to such complex devices as a monolithic processor with multiple functionality.Die 710 is typically packaged in a protective casing (not shown) with leads extending therefrom (not shown) providing access to the circuitry of the die for unilateral or bilateral communication and control. - Circuit Modules
- As shown in
FIG. 6 , two or more dies 710 may be combined, with or without protective casing, into acircuit module 800 to enhance or extend the functionality of anindividual die 710.Circuit module 800 may be a combination of dies 710 representing a variety of functions, or a combination of dies 710 containing the same functionality. Circuit modules of the present invention comprise one or more dies containing at least one conductive interconnect made in accordance with the present invention. - Examples of circuit modules include memory modules, device drivers, power modules, communication modems, processor modules and application-specific modules, and may include multilayer, multichip modules.
Circuit module 800 may be a subcomponent of a variety of electronic systems, such as a clock, a television, a cell phone, a personal computer, an automobile, an industrial control system, an aircraft and others.Circuit module 800 will have a variety ofleads 810 extending therefrom and coupled to the dies 710 providing unilateral or bilateral communication and control. -
FIG. 7 shows one embodiment of a circuit module asmemory module 900.Memory module 900 containsmultiple memory devices 910 contained onsupport 915, the number depending upon the desired bus width and the desire for parity.Memory module 900 accepts a command signal from an external controller (not shown) on acommand link 920 and provides for data input and data output ondata links 930. Thecommand link 920 anddata links 930 are connected to leads 940 extending from thesupport 915.Leads 940 are shown for conceptual purposes and are not limited to the positions shown inFIG. 7 . - Electronic Systems
-
FIG. 8 shows anelectronic system 1000 containing one ormore circuit modules 800.Electronic system 1000 generally contains auser interface 1010.User interface 1010 provides a user of theelectronic system 1000 with some form of control or observation of the results of theelectronic system 1000. Some examples ofuser interface 1010 include the keyboard, pointing device, monitor or printer of a personal computer; the tuning dial, display or speakers of a radio; the ignition switch, gauges or gas pedal of an automobile; and the card reader, keypad, display or currency dispenser of an automated teller machine.User interface 1010 may further describe access ports provided toelectronic system 1000. Access ports are used to connect an electronic system to the more tangible user interface components previously exemplified. One or more of thecircuit modules 800 may be a processor providing some form of manipulation, control or direction of inputs from or outputs touser interface 1010, or of other information either preprogrammed into, or otherwise provided to,electronic system 1000. As will be apparent from the lists of examples previously given,electronic system 1000 will often contain certain mechanical components (not shown) in addition tocircuit modules 800 anduser interface 1010. It will be appreciated that the one ormore circuit modules 800 inelectronic system 1000 can be replaced by a single integrated circuit. Furthermore,electronic system 1000 may be a subcomponent of a larger electronic system. -
FIG. 9 shows one embodiment of an electronic system asmemory system 1100.Memory system 1100 contains one ormore memory modules 900 and amemory controller 1110.Memory controller 1110 provides and controls a bidirectional interface betweenmemory system 1100 and anexternal system bus 1120.Memory system 1100 accepts a command signal from theexternal bus 1120 and relays it to the one ormore memory modules 900 on acommand link 1130.Memory system 1100 provides for data input and data output between the one ormore memory modules 900 andexternal system bus 1120 ondata links 1140. -
FIG. 10 shows a further embodiment of an electronic system as acomputer system 1200.Computer system 1200 contains aprocessor 1210 and amemory system 1100 housed in acomputer unit 1205.Computer system 1200 is but one example of an electronic system containing another electronic system, i.e.,memory system 1100, as a subcomponent.Computer system 1200 optionally contains user interface components. Depicted inFIG. 10 are akeyboard 1220, apointing device 1230, amonitor 1240, aprinter 1250 and abulk storage device 1260. It will be appreciated that other components are often associated withcomputer system 1200 such as modems, device driver cards, additional storage devices, etc. It will further be appreciated that theprocessor 1210 andmemory system 1100 ofcomputer system 1200 can be incorporated on a single integrated circuit. Such single package processing units reduce the communication time between the processor and the memory circuit. - Although specific embodiments have been illustrated and described herein, it will be appreciated by those of ordinary skill in the art that any arrangement which is calculated to achieve the same purpose may be substituted for the specific embodiments shown. Many adaptations of the invention will be apparent to those of ordinary skill in the art. For example, other materials and shapes, as well as other deposition and removal processes, may be utilized in conjunction with the invention. Accordingly, this application is intended to cover any adaptations or variations of the invention. It is manifestly intended that this invention be limited only by the following claims and equivalents thereof.
Claims (26)
1. An electronic apparatus comprising:
a substrate;
a dual-purpose layer on the substrate; and
a conductive interconnect layer disposed on and contacting the dual-purpose layer.
2. The electronic apparatus of claim 1 , wherein the dual-purpose layer contains tungsten.
3. The electronic apparatus of claim 1 , wherein the dual-purpose layer is tungsten, tungsten nitride, or tungsten-silicon nitride.
4. The electronic apparatus of claim 1 , wherein the substrate includes silicon-on-sapphire.
5. The electronic apparatus of claim 1 , wherein the conductive interconnect layer includes copper.
6. The electronic apparatus of claim 1 , wherein the electronic apparatus includes a semiconductor wafer.
7. A semiconductor die comprising:
an individual pattern on a substrate, the individual pattern containing integrated circuit device, the integrated circuit device including:
a dual-purpose layer; and
a conductive interconnect layer electrochemically disposed on and contacting the dual-purpose layer.
8. The semiconductor die of claim 7 , wherein the dual-purpose layer contains tungsten.
9. The semiconductor die of claim 7 , wherein the dual-purpose layer is tungsten, tungsten nitride, or tungsten-silicon nitride.
10. The semiconductor die of claim 7 , wherein the substrate includes silicon-on-insulator.
11. The semiconductor die of claim 7 , wherein the conductive interconnect layer includes a conductive alloy.
12. A memory device, comprising:
an address decoder;
row access circuitry;
column access circuitry;
control circuitry;
an input output circuit; and
an array of memory cells, the array disposed on a substrate, wherein a memory cell includes:
a dual-purpose layer on the substrate; and
a conductive interconnect layer disposed on and contacting the dual-purpose layer.
13. The memory device of claim 12 , wherein the dual-purpose layer contains tungsten.
14. The memory device of claim 12 , wherein the dual-purpose layer is tungsten, tungsten nitride, or tungsten-silicon nitride.
15. The memory device of claim 12 , wherein the memory device includes a dielectric layer contacting the dual-purpose layer, the dielectric layer disposed between the dual-purpose layer and the substrate.
16. The memory device of claim 12 , wherein the conductive interconnect layer includes copper.
17. A circuit module comprising:
a plurality of semiconductor dies, wherein one or more of the semiconductor dies includes:
a substrate;
a dual-purpose layer on the substrate; and
a conductive interconnect layer disposed on and contacting the dual-purpose layer.
18. The circuit module of claim 17 , wherein the dual-purpose layer contains tungsten.
19. The circuit module of claim 17 , wherein the dual-purpose layer is tungsten, tungsten nitride, or tungsten-silicon nitride.
20. The circuit module of claim 17 , wherein the semiconductor die includes an insulating oxide layer contacting the dual-purpose layer, the insulating oxide layer disposed between the dual-purpose layer and the substrate.
21. The circuit module of claim 17 , wherein the conductive interconnect layer includes a copper alloy.
22. An electronic system comprising:
one or more circuit modules; and
a user interface coupled to one of the circuit modules, wherein at least one of the circuit modules having a semiconductor die, the semiconductor die including:
a substrate;
a dual-purpose layer on the substrate; and
a conductive interconnect layer disposed on and contacting the dual-purpose layer.
23. The electronic system of claim 22 , wherein the dual-purpose layer contains tungsten.
24. The electronic system of claim 22 , wherein the dual-purpose layer is tungsten, tungsten nitride, or tungsten-silicon nitride.
25. The electronic system of claim 22 , wherein the substrate includes a silicon substrate.
26. The electronic system of claim 22 , wherein the conductive interconnect layer includes a conductive alloy.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/492,261 US20060261485A1 (en) | 2001-04-19 | 2006-07-25 | Combined barrier layer and seed layer |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/838,493 US6852618B2 (en) | 2001-04-19 | 2001-04-19 | Combined barrier layer and seed layer |
US10/929,252 US7385290B2 (en) | 2001-04-19 | 2004-08-30 | Electrochemical reaction cell for a combined barrier layer and seed layer |
US11/492,261 US20060261485A1 (en) | 2001-04-19 | 2006-07-25 | Combined barrier layer and seed layer |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/929,252 Division US7385290B2 (en) | 2001-04-19 | 2004-08-30 | Electrochemical reaction cell for a combined barrier layer and seed layer |
Publications (1)
Publication Number | Publication Date |
---|---|
US20060261485A1 true US20060261485A1 (en) | 2006-11-23 |
Family
ID=25277216
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/838,493 Expired - Fee Related US6852618B2 (en) | 2001-04-19 | 2001-04-19 | Combined barrier layer and seed layer |
US10/929,252 Expired - Fee Related US7385290B2 (en) | 2001-04-19 | 2004-08-30 | Electrochemical reaction cell for a combined barrier layer and seed layer |
US11/492,261 Abandoned US20060261485A1 (en) | 2001-04-19 | 2006-07-25 | Combined barrier layer and seed layer |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/838,493 Expired - Fee Related US6852618B2 (en) | 2001-04-19 | 2001-04-19 | Combined barrier layer and seed layer |
US10/929,252 Expired - Fee Related US7385290B2 (en) | 2001-04-19 | 2004-08-30 | Electrochemical reaction cell for a combined barrier layer and seed layer |
Country Status (1)
Country | Link |
---|---|
US (3) | US6852618B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050023516A1 (en) * | 2001-04-19 | 2005-02-03 | Micron Technology, Inc. | Combined barrier layer and seed layer |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6511912B1 (en) * | 2000-08-22 | 2003-01-28 | Micron Technology, Inc. | Method of forming a non-conformal layer over and exposing a trench |
US20030207206A1 (en) * | 2002-04-22 | 2003-11-06 | General Electric Company | Limited play data storage media and method for limiting access to data thereon |
WO2004066381A1 (en) * | 2003-01-16 | 2004-08-05 | Infineon Technologies Ag | Method for the filling of contact holes or trenches in si semiconductor structures |
US20050085031A1 (en) * | 2003-10-15 | 2005-04-21 | Applied Materials, Inc. | Heterogeneous activation layers formed by ionic and electroless reactions used for IC interconnect capping layers |
US20050095830A1 (en) * | 2003-10-17 | 2005-05-05 | Applied Materials, Inc. | Selective self-initiating electroless capping of copper with cobalt-containing alloys |
US7205233B2 (en) * | 2003-11-07 | 2007-04-17 | Applied Materials, Inc. | Method for forming CoWRe alloys by electroless deposition |
US20050161338A1 (en) * | 2004-01-26 | 2005-07-28 | Applied Materials, Inc. | Electroless cobalt alloy deposition process |
US20050170650A1 (en) * | 2004-01-26 | 2005-08-04 | Hongbin Fang | Electroless palladium nitrate activation prior to cobalt-alloy deposition |
US20050258512A1 (en) * | 2004-05-21 | 2005-11-24 | Taiwan Semiconductor Manufacturing Co., Ltd. | Topographically elevated microelectronic capacitor structure |
US20060063379A1 (en) * | 2004-09-17 | 2006-03-23 | Dory Thomas S | Forming a combined copper diffusion barrier and seed layer |
US20060246699A1 (en) * | 2005-03-18 | 2006-11-02 | Weidman Timothy W | Process for electroless copper deposition on a ruthenium seed |
WO2006102318A2 (en) * | 2005-03-18 | 2006-09-28 | Applied Materials, Inc. | Electroless deposition process on a contact containing silicon or silicide |
US7651934B2 (en) | 2005-03-18 | 2010-01-26 | Applied Materials, Inc. | Process for electroless copper deposition |
TW200707640A (en) * | 2005-03-18 | 2007-02-16 | Applied Materials Inc | Contact metallization scheme using a barrier layer over a silicide layer |
US7217660B1 (en) | 2005-04-19 | 2007-05-15 | Spansion Llc | Method for manufacturing a semiconductor component that inhibits formation of wormholes |
US9202758B1 (en) | 2005-04-19 | 2015-12-01 | Globalfoundries Inc. | Method for manufacturing a contact for a semiconductor component and related structure |
WO2007035880A2 (en) * | 2005-09-21 | 2007-03-29 | Applied Materials, Inc. | Method and apparatus for forming device features in an integrated electroless deposition system |
US20070099806A1 (en) * | 2005-10-28 | 2007-05-03 | Stewart Michael P | Composition and method for selectively removing native oxide from silicon-containing surfaces |
US20130264214A1 (en) * | 2012-04-04 | 2013-10-10 | Rohm And Haas Electronic Materials Llc | Metal plating for ph sensitive applications |
US20140103534A1 (en) * | 2012-04-26 | 2014-04-17 | Applied Materials, Inc. | Electrochemical deposition on a workpiece having high sheet resistance |
KR101621852B1 (en) | 2014-12-05 | 2016-05-19 | 연세대학교 산학협력단 | Semiconductor device and method for manufacturing the same |
Citations (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3766037A (en) * | 1972-02-11 | 1973-10-16 | Andco Inc | Electrochemical processes for the removal of contaminants from aqueous media |
US4086149A (en) * | 1976-08-04 | 1978-04-25 | Ppg Industries, Inc. | Cathode electrocatalyst |
US4500405A (en) * | 1981-09-22 | 1985-02-19 | Permelec Electrode Ltd. | Cathode for electrolyzing acid solutions and process for producing the same |
US5151168A (en) * | 1990-09-24 | 1992-09-29 | Micron Technology, Inc. | Process for metallizing integrated circuits with electrolytically-deposited copper |
US5439562A (en) * | 1994-06-17 | 1995-08-08 | Westinghouse Electric Corporation | Electrochemical decontamination of radioactive metals by alkaline processing |
US5456819A (en) * | 1991-12-26 | 1995-10-10 | The United States Of America As Represented By The Secretary Of Commerce | Process for electrodepositing metal and metal alloys on tungsten, molybdenum and other difficult to plate metals |
US5804090A (en) * | 1995-03-20 | 1998-09-08 | Nissan Motor Co., Ltd. | Process for etching semiconductors using a hydrazine and metal hydroxide-containing etching solution |
US5877069A (en) * | 1996-09-16 | 1999-03-02 | Micron Technology, Inc. | Method for electrochemical local oxidation of silicon |
US5882502A (en) * | 1992-04-01 | 1999-03-16 | Rmg Services Pty Ltd. | Electrochemical system and method |
US5893966A (en) * | 1997-07-28 | 1999-04-13 | Micron Technology, Inc. | Method and apparatus for continuous processing of semiconductor wafers |
US5933758A (en) * | 1997-05-12 | 1999-08-03 | Motorola, Inc. | Method for preventing electroplating of copper on an exposed surface at the edge exclusion of a semiconductor wafer |
US5948558A (en) * | 1997-03-27 | 1999-09-07 | National Patent Development Corporation | High energy density boride batteries |
US20020100693A1 (en) * | 2001-02-01 | 2002-08-01 | Jiong-Ping Lu | Electrochemical reduction of copper seed for reducing ECD voids |
US6436257B1 (en) * | 1999-06-09 | 2002-08-20 | General Electric Company | Means for detecting and measuring the concentration of acetylene dissolved in a fluid |
US6436267B1 (en) * | 2000-08-29 | 2002-08-20 | Applied Materials, Inc. | Method for achieving copper fill of high aspect ratio interconnect features |
US6489235B2 (en) * | 1999-04-05 | 2002-12-03 | Micron Technology, Inc. | Method of forming a metal seed layer for subsequent plating |
US6545357B2 (en) * | 1999-08-27 | 2003-04-08 | Micron Technology, Inc. | Metal nitride barrier layer and electroplating seed layer with the same metal as the metal nitride layer |
US6555909B1 (en) * | 2001-01-11 | 2003-04-29 | Advanced Micro Devices, Inc. | Seedless barrier layers in integrated circuits and a method of manufacture therefor |
US6565729B2 (en) * | 1998-03-20 | 2003-05-20 | Semitool, Inc. | Method for electrochemically depositing metal on a semiconductor workpiece |
US6613671B1 (en) * | 2000-03-03 | 2003-09-02 | Micron Technology, Inc. | Conductive connection forming methods, oxidation reducing methods, and integrated circuits formed thereby |
US6632345B1 (en) * | 1998-03-20 | 2003-10-14 | Semitool, Inc. | Apparatus and method for electrolytically depositing a metal on a workpiece |
US6852618B2 (en) * | 2001-04-19 | 2005-02-08 | Micron Technology, Inc. | Combined barrier layer and seed layer |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0961972A (en) * | 1995-08-22 | 1997-03-07 | Konica Corp | Method for processing silver halide photographic sensitive material |
US5976344A (en) * | 1996-05-10 | 1999-11-02 | Lucent Technologies Inc. | Composition for electroplating palladium alloys and electroplating process using that composition |
US6017437A (en) | 1997-08-22 | 2000-01-25 | Cutek Research, Inc. | Process chamber and method for depositing and/or removing material on a substrate |
US6284652B1 (en) * | 1998-07-01 | 2001-09-04 | Advanced Technology Materials, Inc. | Adhesion promotion method for electro-chemical copper metallization in IC applications |
US6206756B1 (en) * | 1998-11-10 | 2001-03-27 | Micron Technology, Inc. | Tungsten chemical-mechanical polishing process using a fixed abrasive polishing pad and a tungsten layer chemical-mechanical polishing solution specifically adapted for chemical-mechanical polishing with a fixed abrasive pad |
JP2000351622A (en) * | 1999-06-14 | 2000-12-19 | Tokuyama Corp | Production of titanium (iii) sulfate |
US6261954B1 (en) * | 2000-02-10 | 2001-07-17 | Chartered Semiconductor Manufacturing, Ltd. | Method to deposit a copper layer |
US20020134684A1 (en) * | 2000-10-25 | 2002-09-26 | Shipley Company, L.L.C. | Seed layer processes |
-
2001
- 2001-04-19 US US09/838,493 patent/US6852618B2/en not_active Expired - Fee Related
-
2004
- 2004-08-30 US US10/929,252 patent/US7385290B2/en not_active Expired - Fee Related
-
2006
- 2006-07-25 US US11/492,261 patent/US20060261485A1/en not_active Abandoned
Patent Citations (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3766037A (en) * | 1972-02-11 | 1973-10-16 | Andco Inc | Electrochemical processes for the removal of contaminants from aqueous media |
US4086149A (en) * | 1976-08-04 | 1978-04-25 | Ppg Industries, Inc. | Cathode electrocatalyst |
US4500405A (en) * | 1981-09-22 | 1985-02-19 | Permelec Electrode Ltd. | Cathode for electrolyzing acid solutions and process for producing the same |
US5151168A (en) * | 1990-09-24 | 1992-09-29 | Micron Technology, Inc. | Process for metallizing integrated circuits with electrolytically-deposited copper |
US5456819A (en) * | 1991-12-26 | 1995-10-10 | The United States Of America As Represented By The Secretary Of Commerce | Process for electrodepositing metal and metal alloys on tungsten, molybdenum and other difficult to plate metals |
US5882502A (en) * | 1992-04-01 | 1999-03-16 | Rmg Services Pty Ltd. | Electrochemical system and method |
US5439562A (en) * | 1994-06-17 | 1995-08-08 | Westinghouse Electric Corporation | Electrochemical decontamination of radioactive metals by alkaline processing |
US5804090A (en) * | 1995-03-20 | 1998-09-08 | Nissan Motor Co., Ltd. | Process for etching semiconductors using a hydrazine and metal hydroxide-containing etching solution |
US5877069A (en) * | 1996-09-16 | 1999-03-02 | Micron Technology, Inc. | Method for electrochemical local oxidation of silicon |
US5948558A (en) * | 1997-03-27 | 1999-09-07 | National Patent Development Corporation | High energy density boride batteries |
US5933758A (en) * | 1997-05-12 | 1999-08-03 | Motorola, Inc. | Method for preventing electroplating of copper on an exposed surface at the edge exclusion of a semiconductor wafer |
US5893966A (en) * | 1997-07-28 | 1999-04-13 | Micron Technology, Inc. | Method and apparatus for continuous processing of semiconductor wafers |
US6565729B2 (en) * | 1998-03-20 | 2003-05-20 | Semitool, Inc. | Method for electrochemically depositing metal on a semiconductor workpiece |
US6632345B1 (en) * | 1998-03-20 | 2003-10-14 | Semitool, Inc. | Apparatus and method for electrolytically depositing a metal on a workpiece |
US6489235B2 (en) * | 1999-04-05 | 2002-12-03 | Micron Technology, Inc. | Method of forming a metal seed layer for subsequent plating |
US6436257B1 (en) * | 1999-06-09 | 2002-08-20 | General Electric Company | Means for detecting and measuring the concentration of acetylene dissolved in a fluid |
US6545357B2 (en) * | 1999-08-27 | 2003-04-08 | Micron Technology, Inc. | Metal nitride barrier layer and electroplating seed layer with the same metal as the metal nitride layer |
US6613671B1 (en) * | 2000-03-03 | 2003-09-02 | Micron Technology, Inc. | Conductive connection forming methods, oxidation reducing methods, and integrated circuits formed thereby |
US6436267B1 (en) * | 2000-08-29 | 2002-08-20 | Applied Materials, Inc. | Method for achieving copper fill of high aspect ratio interconnect features |
US6555909B1 (en) * | 2001-01-11 | 2003-04-29 | Advanced Micro Devices, Inc. | Seedless barrier layers in integrated circuits and a method of manufacture therefor |
US20020100693A1 (en) * | 2001-02-01 | 2002-08-01 | Jiong-Ping Lu | Electrochemical reduction of copper seed for reducing ECD voids |
US6852618B2 (en) * | 2001-04-19 | 2005-02-08 | Micron Technology, Inc. | Combined barrier layer and seed layer |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20050023516A1 (en) * | 2001-04-19 | 2005-02-03 | Micron Technology, Inc. | Combined barrier layer and seed layer |
US7385290B2 (en) | 2001-04-19 | 2008-06-10 | Micron Technology, Inc. | Electrochemical reaction cell for a combined barrier layer and seed layer |
Also Published As
Publication number | Publication date |
---|---|
US7385290B2 (en) | 2008-06-10 |
US6852618B2 (en) | 2005-02-08 |
US20050023516A1 (en) | 2005-02-03 |
US20020173137A1 (en) | 2002-11-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20060261485A1 (en) | Combined barrier layer and seed layer | |
US7479700B2 (en) | Semiconductor device featuring copper wiring layers of different widths having metal capping layers of different thickness formed thereon, and method for manufacturing the same | |
EP0982771B1 (en) | Process for semiconductor device fabrication having copper interconnects | |
US5275715A (en) | Electroplating process for enhancing the conformality of titanium and titanium nitride films in the manufacture of integrated circuits and structures produced thereby | |
US6181012B1 (en) | Copper interconnection structure incorporating a metal seed layer | |
US7008872B2 (en) | Use of conductive electrolessly deposited etch stop layers, liner layers and via plugs in interconnect structures | |
US6489235B2 (en) | Method of forming a metal seed layer for subsequent plating | |
US7220665B2 (en) | H2 plasma treatment | |
US8258057B2 (en) | Copper-filled trench contact for transistor performance improvement | |
US6429523B1 (en) | Method for forming interconnects on semiconductor substrates and structures formed | |
US7098128B2 (en) | Method for filling electrically different features | |
US20200083169A1 (en) | Metal interconnects | |
SG193501A1 (en) | Methods of forming at least one conductive element, methods of forming a semiconductor structure, methods of forming a memory cell and related semiconductor structures | |
US20090032958A1 (en) | Intermetallic conductors | |
US7205229B2 (en) | Interconnect alloys and methods and apparatus using same | |
US20090050471A1 (en) | Process of forming an electronic device including depositing layers within openings | |
US6955984B2 (en) | Surface treatment of metal interconnect lines | |
JP2003113494A (en) | IMPROVED METHOD FOR Cu ELECTROPLATING IN INTEGRATED CIRCUIT FABRICATION | |
US20060228934A1 (en) | Conductive materials for low resistance interconnects and methods of forming the same | |
KR100701673B1 (en) | METHOD FOR FORMING Cu WIRING OF SENICONDUCTOR DEVICE | |
US20200388524A1 (en) | Surface modified dielectric refill structure |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |