US20050153556A1 - Methods for polishing copper features of semiconductor devices structures - Google Patents
Methods for polishing copper features of semiconductor devices structures Download PDFInfo
- Publication number
- US20050153556A1 US20050153556A1 US11/011,363 US1136304A US2005153556A1 US 20050153556 A1 US20050153556 A1 US 20050153556A1 US 1136304 A US1136304 A US 1136304A US 2005153556 A1 US2005153556 A1 US 2005153556A1
- Authority
- US
- United States
- Prior art keywords
- copper
- slurry
- barrier layer
- polishing
- rate
- 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
- 239000010949 copper Substances 0.000 title claims abstract description 117
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims abstract description 116
- 229910052802 copper Inorganic materials 0.000 title claims abstract description 115
- 238000005498 polishing Methods 0.000 title claims abstract description 108
- 239000004065 semiconductor Substances 0.000 title claims abstract description 59
- 238000000034 method Methods 0.000 title claims abstract description 57
- 239000002002 slurry Substances 0.000 claims abstract description 122
- 230000004888 barrier function Effects 0.000 claims abstract description 80
- 239000000463 material Substances 0.000 claims abstract description 59
- 230000003647 oxidation Effects 0.000 claims abstract description 31
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 31
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 37
- 229910052721 tungsten Inorganic materials 0.000 claims description 37
- 239000010937 tungsten Substances 0.000 claims description 37
- 230000000694 effects Effects 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims 5
- 239000000758 substrate Substances 0.000 description 19
- 239000003082 abrasive agent Substances 0.000 description 11
- 239000003112 inhibitor Substances 0.000 description 11
- 239000007800 oxidant agent Substances 0.000 description 11
- 229910052715 tantalum Inorganic materials 0.000 description 11
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 11
- 239000008139 complexing agent Substances 0.000 description 8
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- -1 amine compounds Chemical class 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 235000012431 wafers Nutrition 0.000 description 4
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 3
- 239000005695 Ammonium acetate Substances 0.000 description 3
- 239000004254 Ammonium phosphate Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 235000019257 ammonium acetate Nutrition 0.000 description 3
- 229940043376 ammonium acetate Drugs 0.000 description 3
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 3
- 235000019289 ammonium phosphates Nutrition 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 2
- 239000004471 Glycine Substances 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 150000003868 ammonium compounds Chemical class 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000005380 borophosphosilicate glass Substances 0.000 description 2
- 239000005388 borosilicate glass Substances 0.000 description 2
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 description 2
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- CIYRLONPFMPRLH-UHFFFAOYSA-N copper tantalum Chemical compound [Cu].[Ta] CIYRLONPFMPRLH-UHFFFAOYSA-N 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000000635 electron micrograph Methods 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 description 2
- 150000002823 nitrates Chemical class 0.000 description 2
- 239000005360 phosphosilicate glass Substances 0.000 description 2
- 238000005240 physical vapour deposition Methods 0.000 description 2
- 238000007517 polishing process Methods 0.000 description 2
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
- JLKDVMWYMMLWTI-UHFFFAOYSA-M potassium iodate Chemical compound [K+].[O-]I(=O)=O JLKDVMWYMMLWTI-UHFFFAOYSA-M 0.000 description 2
- 239000001230 potassium iodate Substances 0.000 description 2
- 235000006666 potassium iodate Nutrition 0.000 description 2
- 229940093930 potassium iodate Drugs 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- YWYZEGXAUVWDED-UHFFFAOYSA-N triammonium citrate Chemical compound [NH4+].[NH4+].[NH4+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YWYZEGXAUVWDED-UHFFFAOYSA-N 0.000 description 2
- FFJCNSLCJOQHKM-CLFAGFIQSA-N (z)-1-[(z)-octadec-9-enoxy]octadec-9-ene Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCCCCCCC\C=C/CCCCCCCC FFJCNSLCJOQHKM-CLFAGFIQSA-N 0.000 description 1
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 description 1
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 1
- 206010010144 Completed suicide Diseases 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- GPXJNWSHGFTCBW-UHFFFAOYSA-N Indium phosphide Chemical compound [In]#P GPXJNWSHGFTCBW-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- BVCZEBOGSOYJJT-UHFFFAOYSA-N ammonium carbamate Chemical compound [NH4+].NC([O-])=O BVCZEBOGSOYJJT-UHFFFAOYSA-N 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 1
- 235000018660 ammonium molybdate Nutrition 0.000 description 1
- 239000011609 ammonium molybdate Substances 0.000 description 1
- 229940010552 ammonium molybdate Drugs 0.000 description 1
- VBIXEXWLHSRNKB-UHFFFAOYSA-N ammonium oxalate Chemical compound [NH4+].[NH4+].[O-]C(=O)C([O-])=O VBIXEXWLHSRNKB-UHFFFAOYSA-N 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000012217 deletion Methods 0.000 description 1
- 230000037430 deletion Effects 0.000 description 1
- YXVFQADLFFNVDS-UHFFFAOYSA-N diammonium citrate Chemical compound [NH4+].[NH4+].[O-]C(=O)CC(O)(C(=O)O)CC([O-])=O YXVFQADLFFNVDS-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 235000019837 monoammonium phosphate Nutrition 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 229940051841 polyoxyethylene ether Drugs 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- IWZKICVEHNUQTL-UHFFFAOYSA-M potassium hydrogen phthalate Chemical compound [K+].OC(=O)C1=CC=CC=C1C([O-])=O IWZKICVEHNUQTL-UHFFFAOYSA-M 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- WYXIGTJNYDDFFH-UHFFFAOYSA-Q triazanium;borate Chemical compound [NH4+].[NH4+].[NH4+].[O-]B([O-])[O-] WYXIGTJNYDDFFH-UHFFFAOYSA-Q 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/302—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to change their surface-physical characteristics or shape, e.g. etching, polishing, cutting
- H01L21/304—Mechanical treatment, e.g. grinding, polishing, cutting
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24B—MACHINES, DEVICES, OR PROCESSES FOR GRINDING OR POLISHING; DRESSING OR CONDITIONING OF ABRADING SURFACES; FEEDING OF GRINDING, POLISHING, OR LAPPING AGENTS
- B24B37/00—Lapping machines or devices; Accessories
- B24B37/005—Control means for lapping machines or devices
- B24B37/0056—Control means for lapping machines or devices taking regard of the pH-value of lapping agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24B—MACHINES, DEVICES, OR PROCESSES FOR GRINDING OR POLISHING; DRESSING OR CONDITIONING OF ABRADING SURFACES; FEEDING OF GRINDING, POLISHING, OR LAPPING AGENTS
- B24B37/00—Lapping machines or devices; Accessories
- B24B37/04—Lapping machines or devices; Accessories designed for working plane surfaces
-
- 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
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3205—Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
- H01L21/321—After treatment
- H01L21/32115—Planarisation
- H01L21/3212—Planarisation by chemical mechanical polishing [CMP]
Definitions
- the present invention relates generally to slurries that are useful in chemical-mechanical polishing or chemical-mechanical planarization processes and, more specifically, to slurries that are used to polish or planarize electrically conductive structures of semiconductor devices that include copper and an adjacent tungsten barrier.
- the present invention also relates to methods for substantially concurrently polishing or planarizing structures formed from copper and tungsten.
- Chemical-mechanical polishing and chemical-mechanical planarization are abrasive techniques that typically include the use of a combination of chemical and mechanical agents to planarize, or otherwise remove material from a surface of a semiconductor material substrate during the fabrication of devices thereon.
- a chemical component typically a slurry that includes one or more oxidizers, abrasives, complexing agents, and inhibitors, oxidizes the surface of one or more material layers that are being polished or planarized (i.e., at least partially removed).
- a polishing pad formed from a material such as polyurethane or acrylic is used with the slurry and, in combination with abrasives present in the slurry, effects mechanical removal of the layer or layers from the surface of the semiconductor device structure.
- abrasive-only polishing and planarization e.g., without the use of active chemical agents to effect material removal, are becoming more prevalent due to environmental concerns.
- CMP as used herein encompasses such abrasive-only (i.e., strictly mechanical) methods and apparatus.
- Conventional CMP pads are round, planar, and have larger dimensions than the semiconductor substrates (e.g., wafers or other substrates including silicon, gallium arsenide, indium phosphide, etc.) upon which the structures or layers to be planarized or otherwise polished have been formed.
- the substrate and the conventional CMP pad are rotated relative to one another, with the location of the substrate being moved continuously relative to the polishing surface of the pad so that different areas of the pad are used to polish one or more of the layers or structures formed on the substrate.
- polishing format is the so-called “web” format, wherein the pad has an elongated, planar configuration. The web is moved laterally from a supply reel to a take-up reel so as to provide “fresh” areas thereof for polishing one or more layers or structures formed on a semiconductor substrate.
- a similar, newer polishing format is the so-called “belt” format, wherein the pad is configured as a belt, or continuous loop, of polishing material.
- the semiconductor substrate is rotated or revolved upon being brought into contact with the pad. The pad is moved when a “fresh” polishing surface is needed or desired.
- a new type of polishing pad may be used to polish or planarize layers formed on a semiconductor substrate.
- Fixed-abrasive pads which may be embodied in the conventional, web, or belt formats, are typically formed from an acrylic material and embedded with particles of abrasive materials. The pad and embedded abrasives effect the mechanical part of CMP processes.
- the abrasive material is exposed at a polishing surface of the pad. Some of the abrasive material may also be leached out of the pad.
- the chemical slurries that are used to effect the chemical portion of chemical-mechanical polishing or chemical-mechanical planarization need not include the abrasives that are often required when conventional, abrasive-free pads are employed.
- a barrier layer is typically required between the copper and adjacent structures or layers.
- the barrier layer prevents diffusion of the copper into the adjacent layers or structures, as well as the formation of copper suicides, both of which may cause electrical shorts in semiconductor devices that include copper.
- Tantalum is an example of a material that is useful as a copper barrier.
- the semiconductor device including any features thereof into which copper is to be disposed (e.g., trenches), is lined with a layer of tantalum.
- the tantalum layer is then typically covered with a thin copper layer, often formed by physical vapor-deposition (“PVD”) processes.
- PVD physical vapor-deposition
- the thin copper layer then acts as a so-called “seed layer” for the formation of a copper structure, such as a conductive line, such as by electroplating processes.
- CMP processes are typically used to remove the tantalum and copper between the structures from over the active surface of the semiconductor device being fabricated.
- Slurries that are used in copper CMP processes typically have a pH of about 7.0. Many of these slurries include hydrogen peroxide (H 2 O 2 ) as an oxidizing agent. Since hydrogen peroxide readily generates hydroxy free radicals (OH.), hydrogen peroxide is a very strong oxidizing agent. Tantalum, however, is substantially chemically inert.
- the oxidizers of CMP slurries that remove copper do not effectively oxidize tantalum and, thus, do not adequately effect the removal of tantalum.
- slurries that are useful for removing tantalum by CMP processes are likewise not effective for removing copper.
- two separate slurries must be used.
- FIG. 1 illustrates a semiconductor device structure 10 that includes the portions of a copper layer 20 and an underlying tungsten barrier layer 18 disposed within a recess 14 formed in an active surface 16 of a substrate 12 of semiconductor device structure 10 following CMP thereof using an alumina fixed-abrasive polishing pad and a copper CMP slurry having a pH of about 7.
- barrier layer 18 was oxidized and dissolved at a faster rate than the adjacent copper of copper layer 20 , leaving a gap 21 between copper layer 20 and adjacent regions of substrate 12 , as well as undesirably permitting copper of copper layer 20 to contact and, possibly, diffuse into unprotected adjacent regions of substrate 12 .
- the inventors are not aware of a slurry that is useful in CMP processes and that effectively polishes or planarizes both copper and tungsten without causing oxidation or dissolution of the tungsten.
- the present invention includes a method for substantially simultaneously chemical-mechanical polishing a copper conductive structure and an adjacent barrier layer with a fixed-abrasive type polishing pad, as well as slurries that are useful with fixed-abrasive type polishing pads for substantially simultaneously polishing a copper conductive structure and a barrier layer adjacent thereto.
- the method of the present invention includes employing a fixed-abrasive type polishing pad along with a substantially abrasive-free liquid polishing formulation, which is referred to herein as a substantially abrasive-free slurry or, more simply, as a slurry.
- the slurry is formulated to oxidize copper and a material of the barrier layer, such as tungsten, at substantially the same rates.
- the oxidation energies of copper and the barrier material are substantially the same.
- the oxidation energy, or oxidation potential, of a barrier material is about 0.25 V greater to about 0.20 V less than an oxidation energy, or oxidation potential, of copper.
- a barrier material such as tungsten
- the barrier material is oxidized by the slurry at about the same rate as copper or at a slower rate than copper, use of a slurry so formulated to substantially simultaneously polish a copper conductive structure and an adjacent barrier layer prevents dissolution of the barrier layer.
- the slurry of the present invention removes a barrier material, such as tungsten, at a rate that is about the same as or up to about ten times slower than the rate at which the slurry removes copper and, preferably, at a rate that is about two to about four times slower than the rate at which the slurry removes copper.
- a barrier material such as tungsten
- Slurries that are useful in the method of the present invention include at least one oxidizer, at least one complexing agent, and at least one inhibitor.
- the relative amounts of at least the oxidizer, the pH control agent, and the inhibitor are balanced so as to facilitate substantially concurrent polishing of a copper structure and another structure adjacent thereto, such as a barrier layer formed from tungsten.
- the slurry is formulated such that the relative amounts of the oxidizer, the complexing agent, and the inhibitor oxidize copper and a barrier material, such as tungsten, at substantially the same rates, or such that the oxidation energies of copper and the barrier material are substantially the same in the slurry.
- the pH of the slurry may also be optimized so as to provide for oxidation of copper and a barrier material, such as tungsten, at substantially the same rates.
- the present invention also includes a system for substantially simultaneously polishing a copper conductive structure and an adjacent barrier layer of a semiconductor device.
- a system for substantially simultaneously polishing a copper conductive structure and an adjacent barrier layer of a semiconductor device includes a fixed-abrasive type polishing pad and a substantially abrasive-free slurry within which copper and the material of the barrier layer are oxidized at substantially the same rates, or have substantially the same oxidation energies.
- FIG. 1 is an electron micrograph illustrating the dissolution of regions of a tungsten barrier layer that underlie a copper structure of a semiconductor device structure when a conventional slurry is used to simultaneously remove the copper and tungsten;
- FIGS. 2-5 schematically illustrate an exemplary embodiment of a polishing method in which copper and a barrier material therefor are substantially simultaneously removed from a semiconductor device structure at substantially the same rates;
- FIG. 6 is a schematic representation of an exemplary embodiment of a system that employs a fixed-abrasive polishing pad and a slurry to effect the method of the present invention.
- FIGS. 2-5 A method incorporating teachings of the present invention is illustrated in FIGS. 2-5 .
- a semiconductor device structure 10 including a substrate 12 , which includes a recess 14 formed in an active surface 16 thereof is shown.
- a barrier layer 18 of a material, such as tungsten, that prevents copper from diffusing into adjacent insulative regions of semiconductor device structure 10 is located on active surface 16 and on the surfaces 15 of recess 14 .
- a copper layer 20 is formed over and contacts barrier layer 18 . Copper layer 20 also substantially fills recess 14 .
- substrate 12 may include various other structures beneath recess 14 , barrier layer 18 , and copper layer 20 , for purposes of simplicity, no additional structures are illustrated in the semiconductor device structure 10 shown in FIGS. 2-5 .
- a fixed-abrasive polishing pad 40 which may be embodied as a conventional polishing pad, a web-type polishing pad, a belt-type polishing pad, or in any other polishing pad format known in the art, is then brought into frictional contact (e.g., by rotation of semiconductor device structure 10 or polishing pad 40 ) with copper layer 20 to, along with slurry 30 , remove copper layer 20 .
- An inhibitor component 32 of slurry 30 fills recessed areas 22 of copper layer 20 , thereby preventing removal of material from recessed areas 22 until material of higher areas 24 of copper layer 20 has been removed.
- barrier layer 18 overlying active surface 16 are exposed through copper layer 20 , as shown in FIG. 4 .
- slurry 30 and fixed-abrasive polishing pad 40 remove the material or materials of barrier layer 18 and the copper of copper layer 20 at substantially the same rates.
- Barrier layer 18 is removed from active surface 16 by continued polishing with slurry 30 and fixed-abrasive polishing pad 40 . Once barrier layer 18 is substantially removed from active surface 16 and the surface 26 of the portion of copper layer 20 that remains within recess 14 is located substantially in the plane of active surface 16 , as depicted in FIG. 5 , the polishing process is terminated. As illustrated in FIG. 5 , the remaining portion of barrier layer 18 substantially lines recess 14 and separates the remaining portion of copper layer 20 from adjacent portions of substrate 12 .
- slurry 30 is formulated so as to oxidize copper and the material or materials of the adjacent barrier layer 18 at substantially the same rates.
- copper and the material or materials (e.g., tungsten) of the adjacent barrier layer 18 have substantially the same oxidation energies in slurry 30 .
- the material or materials of barrier layer 18 will not dissolve, or be removed from semiconductor device structure 10 , at a significantly greater rate than copper of copper layer 20 is dissolved or removed from semiconductor device structure 10 .
- the oxidation energy, or oxidation potential, of tungsten in slurry 30 is preferably about 0.25 V more to about 0.20 V less than the oxidation energy, or oxidation potential, of copper in slurry 30 .
- Slurry 30 preferably removes a barrier material, such as tungsten, at a rate that is about the same as or up to about ten times slower than the rate at which slurry 30 removes copper when a fixed-abrasive polishing pad is employed and, more preferably, at a rate that is about two to about four times slower than the rate at which slurry 30 removes copper.
- slurry 30 is intended to be used in conjunction with a fixed-abrasive polishing pad 40 , such as the acrylic fixed-abrasive polishing pads manufactured by 3M Company of St. Paul, Minn.
- a fixed-abrasive polishing pad 40 may be impregnated with particulate abrasives including, but not limited to, alumina (Al 2 O 3 ), titanium dioxide (TiO 2 ), silicon dioxide (SiO 2 ), and cerium dioxide (CeO 2 ).
- the abrasives in a fixed-abrasive polishing pad 40 are typically leached therefrom during polishing of a semiconductor device structure 10 .
- slurry 30 need not include abrasives and is preferably substantially free of abrasives.
- Slurry 30 includes an inhibitor component 32 , which prevents recessed, or lower, areas 22 of copper layer 20 from being removed until higher areas 24 of copper layer 20 have been removed down to substantially the same plane.
- Slurry 30 also includes an oxidizer component, which oxidizes both the copper of copper layer 20 and the material or materials (e.g., tungsten) of barrier layer 18 so as to chemically soften these materials and to thereby facilitate their mechanical removal from semiconductor device structure 10 by fixed-abrasive polishing pad 40 .
- slurry 30 includes one or more complexing agents, which complex with ions of the layers 18 , 20 being removed (e.g., copper ions from copper layer 20 ) so as to facilitate the dissolution of these reactant ions, allowing these reactant ions to be moved away from the locations at which layers 18 and 20 are being oxidized.
- complexing agents which complex with ions of the layers 18 , 20 being removed (e.g., copper ions from copper layer 20 ) so as to facilitate the dissolution of these reactant ions, allowing these reactant ions to be moved away from the locations at which layers 18 and 20 are being oxidized.
- oxidizers that are useful as the oxidizer component of slurry 30 include, without limitation, hydrogen peroxide, potassium iodate, potassium permanganate, ammonia, other amine compounds, ammonium compounds, nitrate compounds, and combinations thereof.
- exemplary ammonium compounds include, without limitation, ammonium persulfate and ammonium molybdate.
- exemplary nitrate compounds include, but are not limited to, ferric nitrate, nitric acid, and potassium nitrate.
- the oxidizer component preferably comprises about 0.1 to about 20%, by weight, of slurry 30 . It is preferred that slurry 30 include about 0.1 to about 5.0%, by weight, of the oxidizer component. Even more preferred is a potassium iodate oxidizer component that makes up about 3 to about 5% of the weight of slurry 30 .
- the one or more complexing agents of slurry 30 may include, but are not limited to, glycine, ammonium citrate, ammonium phosphate, ammonium acetate, and combinations thereof.
- Slurry 30 preferably includes about 1 to about 15% of the one or more complexing agents, by weight. It is more preferred that the one or more complexing agents make up about 3 to about 5% of the weight of slurry 30 .
- slurry 30 may include about 1% of the complexing agent glycine, including a concentration of 0.1 M (molar) polyethylene glycol (PEG), by weight of slurry 30 .
- PEG polyethylene glycol
- slurry 30 may include about 3% ammonium acetate, by weight.
- Inhibitor component 32 of slurry 30 prevents corrosion of copper during polishing.
- Inhibitor component 32 may include an azole, such as benzenetriazole (BTA), mercaptobenzothiazole, and tolytriazole, an amine, such as methylamine and diethylamine, a ring compound, such as pyridine, quinoline, and dicyclohexamine nitrate, as well as other compounds, such as potassium silicate, ammonium borate, ammonium phosphate, and potassium dichromate, or mixtures of any of these corrosion inhibitors.
- BTA benzenetriazole
- mercaptobenzothiazole mercaptobenzothiazole
- tolytriazole an amine, such as methylamine and diethylamine
- an amine such as methylamine and diethylamine
- a ring compound such as pyridine, quinoline, and dicyclohexamine nitrate
- other compounds such as
- inhibitor component 32 may make up about 0.05 to about 2% of the weight of slurry 30 , it is preferred the inhibitor component 32 comprise about 0.05 to about 0.2% of the weight of slurry 30 .
- slurry 30 may include about 0.1% BTA, by weight.
- Slurry 30 may have a pH in the range of about 2 to about 6, but the pH of slurry 30 is preferably in the range of about 3 to about 5 and, more preferably, is about 4.
- One or more buffers which are also referred to herein as pH control agents, may be used, as known in the art, to adjust the pH of slurry 30 to a desired level.
- Exemplary buffers that may be used in slurry 30 include, without limitation, potassium hydrogen phthalate, ammonium acetate, ammonium oxalate, ammonium carbamate, ammonium phosphate, ammonium hydrogen phosphate, ammonium dihydrogen phosphate, dibasic ammonium citrate, tribasic ammonium citrate, and mixtures thereof.
- Acetic acid, phosphoric acid, and sulfuric acid are examples of other pH control agents that may be used in a slurry 30 incorporating teachings of the present invention.
- the pH control agent will adjust the pH of slurry 30 to a desirable range or point without significantly etching the insulator (e.g., borophosphosilicate glass (BPSG), phosphosilicate glass (PSG), or borosilicate glass (BSG)) that underlies the layer or layers being polished.
- BPSG borophosphosilicate glass
- PSG phosphosilicate glass
- BSG borosilicate glass
- acetic acid is an example of a buffer that may be used to adjust the pH of slurry 30 and that will not etch an underlying glass insulator.
- slurry 30 may include a surfactant component, which may comprise from about 1% to about 15% of the volume of slurry 30 and, more preferably, about 1% to about 2% of the weight of slurry 30 .
- the surfactant component may include, for example, polyethylene glycol, polyoxyethylene ether, glycerol, polypropylene glycol, polyoxyethylene lauryl ether, polyoxyethylene cetyl ether, polyoxyethylene stearyl ether, polyoxyethylene oleyl ether, and mixtures thereof.
- Thickeners may also be included in slurry 30 to impart slurry 30 with a desired viscosity (e.g., about 10 to about 20 cps. at ambient temperature).
- exemplary thickeners that may be included in slurry 30 include, but are not limited to, POLYOX®, available from Union Carbide of Danbury, Conn., and CARBOPOL®, available from B.F. Goodrich of Cleveland, Ohio.
- Water may be used as the balance of slurry 30 .
- the specific amounts of the components of slurry 30 may be determined by identifying slurry 30 formulations in which copper gives up electrons at substantially the same rate as a barrier material, such as tungsten, of a barrier layer 18 to be polished substantially simultaneously with copper layer 20 .
- slurry 30 may be formulated so that copper and a barrier material therefor, such as tungsten, have the substantially same oxidation energies therein, or are oxidized at substantially the same rates therein.
- the oxidation energy of tungsten or another barrier material in slurry 30 is within the range of about 0.25 V more than to about 0.20 V less than the oxidation energy of copper in slurry 30 , the range including the end point values thereof.
- Slurry 30 formulations having these characteristics may be determined as known in the art, such as by measuring the open circuit potentials of copper and a barrier material, such as tungsten, in slurry 30 .
- Polishing system 50 includes a polishing apparatus 42 , which supports or carries a fixed-abrasive polishing pad 40 , and a substrate support 44 configured to hold a semiconductor device structure 10 , to bring the same into frictional contact with fixed-abrasive polishing pad 40 , and, preferably, to rotate semiconductor device structure 10 relative to fixed-abrasive polishing pad 40 .
- Polishing system 50 also includes a slurry applicator 47 .
- polishing apparatus 42 is illustrated in FIG. 6 as a web-type polishing apparatus, other known types of polishing apparatus, including, without limitation, belt-type and conventional rotational-type polishing apparatus, may alternatively be used in polishing systems incorporating teachings of the present invention.
- Any known CMP apparatus including conventional, rotary CMP apparatus, web format CMP apparatus, and belt format CMP apparatus, may comprise polishing apparatus 42 , substrate support 44 , and slurry applicator 47 of polishing system 50 .
- Fixed-abrasive polishing pad 40 may similarly include any known fixed-abrasive polishing pad, such as the acrylic fixed-abrasive polishing pads available from 3M Company, in any known pad format (e.g., conventional, web, or belt).
- one or more semiconductor device structures 10 having one or more layers thereon that are to be chemical-mechanical polished are secured to substrate support 44 .
- fixed-abrasive polishing pad 40 is also secured to polishing apparatus 42 .
- Slurry 30 is introduced by slurry applicator 47 onto one or both of semiconductor device structure 10 and fixed-abrasive polishing pad 40 .
- one or both of semiconductor device structure 10 and fixed-abrasive polishing pad 40 are substantially continuously laterally moved (e.g., rotated or vibrated or otherwise moved side-to-side) and brought into frictional contact with one another so as to effect the CMP process.
- the apparatus may precess semiconductor device structure 10 (i.e., rotate semiconductor device structure 10 around the axis of a support therefor), while the polishing pad remains substantially stationary.
- semiconductor device structure 10 is moved away from fixed-abrasive polishing pad 40 .
- Slurry 30 remaining on semiconductor device structure 10 is rinsed or otherwise removed therefrom by known processes.
- Subsequent fabrication processes may then be conducted on semiconductor device structure 10 , as known in the art.
- Polishing pad 40 may be incrementally moved to provide a fresh pad segment that was not utilized to polish semiconductor device structure 10 .
- Polishing pad 40 may be moved a distance that is less than the distance across (e.g., diameter) a semiconductor device structure 10 to be polished therewith.
- polishing pad 40 is moved a distance that is at most about 1% of the maximum distance across semiconductor device structure 10 so as to uniformly polish semiconductor device structures 10 and to maximize the useful life of polishing pad 40 .
- polishing pad 40 may be incrementally moved about a quarter of an inch (i.e., about 0.25 inches) between polishing each wafer or set of wafers.
- polishing in accordance with the present invention may be conducted at any suitable polishing temperature
- polishing with slurry 30 and a fixed-abrasive polishing pad 40 may be conducted at lower temperatures than those of conventional polishing processes.
- polishing methods that incorporate teachings of the present invention may be conducted at temperatures of about room temperature (e.g., about 23-27° C.) or cooler. It has been found that polishing causes fewer defects when conducted at cooler temperatures.
- the abrasive components of conventional slurries do not, however, remain soluble in or, thus, evenly dispersed throughout such slurries at cooler temperatures.
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Abstract
A method for substantially simultaneously polishing a copper conductive structure of a semiconductor device structure and an adjacent barrier layer includes use of a slurry that is formulated so as to oxidize copper at substantially the same rate as or at a faster rate than a material of the barrier layer is oxidized. Thus, copper and the barrier layer material have substantially the same oxidation energies in the slurry or the oxidation energy of the barrier layer material in the slurry may be greater than that of copper. The slurry may be configured for use with a fixed-abrasive type polishing pad and, therefore, may be substantially abrasive-free.
Description
- This application is a continuation of application Ser. No. 10/132,827, filed Apr. 25, 2002, now U.S. Pat. No. 6,830,500, issued Dec. 14, 2004, which is a divisional of application Ser. No. 09/651,808, filed Aug. 30, 2000, now U.S. Pat. No. 6,602,117, issued on Aug. 5, 2003.
- 1. Field of the Invention
- The present invention relates generally to slurries that are useful in chemical-mechanical polishing or chemical-mechanical planarization processes and, more specifically, to slurries that are used to polish or planarize electrically conductive structures of semiconductor devices that include copper and an adjacent tungsten barrier. The present invention also relates to methods for substantially concurrently polishing or planarizing structures formed from copper and tungsten.
- 2. Background of Related Art
- CMP
- Chemical-mechanical polishing and chemical-mechanical planarization, both of which are referred to in the art as “CMP,” are abrasive techniques that typically include the use of a combination of chemical and mechanical agents to planarize, or otherwise remove material from a surface of a semiconductor material substrate during the fabrication of devices thereon. A chemical component, typically a slurry that includes one or more oxidizers, abrasives, complexing agents, and inhibitors, oxidizes the surface of one or more material layers that are being polished or planarized (i.e., at least partially removed). A polishing pad formed from a material such as polyurethane or acrylic is used with the slurry and, in combination with abrasives present in the slurry, effects mechanical removal of the layer or layers from the surface of the semiconductor device structure. It should be noted that abrasive-only polishing and planarization, e.g., without the use of active chemical agents to effect material removal, are becoming more prevalent due to environmental concerns. Thus, the term “CMP” as used herein encompasses such abrasive-only (i.e., strictly mechanical) methods and apparatus.
- Conventional CMP pads are round, planar, and have larger dimensions than the semiconductor substrates (e.g., wafers or other substrates including silicon, gallium arsenide, indium phosphide, etc.) upon which the structures or layers to be planarized or otherwise polished have been formed. In polishing one or more layers or structures formed on a substrate, the substrate and the conventional CMP pad are rotated relative to one another, with the location of the substrate being moved continuously relative to the polishing surface of the pad so that different areas of the pad are used to polish one or more of the layers or structures formed on the substrate.
- Another polishing format is the so-called “web” format, wherein the pad has an elongated, planar configuration. The web is moved laterally from a supply reel to a take-up reel so as to provide “fresh” areas thereof for polishing one or more layers or structures formed on a semiconductor substrate. A similar, newer polishing format is the so-called “belt” format, wherein the pad is configured as a belt, or continuous loop, of polishing material. In both the “web” and “belt” formats, the semiconductor substrate is rotated or revolved upon being brought into contact with the pad. The pad is moved when a “fresh” polishing surface is needed or desired.
- A new type of polishing pad, known in the art as a fixed-abrasive pad, may be used to polish or planarize layers formed on a semiconductor substrate. Fixed-abrasive pads, which may be embodied in the conventional, web, or belt formats, are typically formed from an acrylic material and embedded with particles of abrasive materials. The pad and embedded abrasives effect the mechanical part of CMP processes. During use of the fixed-abrasive pad to planarize or polish one or more layers on the surface of a semiconductor device during fabrication thereof, the abrasive material is exposed at a polishing surface of the pad. Some of the abrasive material may also be leached out of the pad. As a result of the inclusion of abrasive particles in the pad, the chemical slurries that are used to effect the chemical portion of chemical-mechanical polishing or chemical-mechanical planarization need not include the abrasives that are often required when conventional, abrasive-free pads are employed.
- Copper Conductive Structures
- The use of copper as a conductive material in semiconductor devices is also ever-increasing. When copper is used in semiconductor devices, however, a barrier layer is typically required between the copper and adjacent structures or layers. The barrier layer prevents diffusion of the copper into the adjacent layers or structures, as well as the formation of copper suicides, both of which may cause electrical shorts in semiconductor devices that include copper. Tantalum is an example of a material that is useful as a copper barrier. When tantalum is used, the semiconductor device, including any features thereof into which copper is to be disposed (e.g., trenches), is lined with a layer of tantalum. The tantalum layer is then typically covered with a thin copper layer, often formed by physical vapor-deposition (“PVD”) processes. The thin copper layer then acts as a so-called “seed layer” for the formation of a copper structure, such as a conductive line, such as by electroplating processes.
- Once the tantalum and copper layers have been formed, it is necessary to isolate separate tantalum-copper conductive structures from one another. CMP processes are typically used to remove the tantalum and copper between the structures from over the active surface of the semiconductor device being fabricated. Slurries that are used in copper CMP processes typically have a pH of about 7.0. Many of these slurries include hydrogen peroxide (H2O2) as an oxidizing agent. Since hydrogen peroxide readily generates hydroxy free radicals (OH.), hydrogen peroxide is a very strong oxidizing agent. Tantalum, however, is substantially chemically inert. Thus, the oxidizers of CMP slurries that remove copper do not effectively oxidize tantalum and, thus, do not adequately effect the removal of tantalum. Likewise, slurries that are useful for removing tantalum by CMP processes are likewise not effective for removing copper. As a result, when conventional CMP processes are used to isolate the tantalum-copper conductive structures of a semiconductor device, two separate slurries must be used.
- It has been proposed that tungsten be used in place of tantalum in semiconductor devices as a barrier material for copper conductive structures. Nonetheless, when known copper CMP slurries are used to substantially simultaneously CMP tungsten and copper, the tungsten barrier layer may dissolve, or be removed, at a faster rate than the copper. This is at least partially because, as the following chemical equations illustrate, tungsten (W) is more readily oxidized than copper (Cu):
W+2H2O→4H++4e −+WO2 E 0=0.12;
Cu→Cu2++2e − E 0=−0.34.
Thus, in conventional slurries, although both copper and tungsten are simultaneously exposed to the same oxidants, the tungsten will typically be oxidized first. As a result, gaps may form in locations where the barrier material should be located between copper conductive structures and adjacent portions of the semiconductor device structure upon which the conductive structures are being fabricated. - This phenomenon is illustrated in the electron micrograph of
FIG. 1 , which illustrates asemiconductor device structure 10 that includes the portions of acopper layer 20 and an underlyingtungsten barrier layer 18 disposed within arecess 14 formed in anactive surface 16 of asubstrate 12 ofsemiconductor device structure 10 following CMP thereof using an alumina fixed-abrasive polishing pad and a copper CMP slurry having a pH of about 7. Once aninterface 19 betweenbarrier layer 18 andcopper layer 20 was exposed during the CMP process, tungsten ofbarrier layer 18 was oxidized and dissolved at a faster rate than the adjacent copper ofcopper layer 20, leaving agap 21 betweencopper layer 20 and adjacent regions ofsubstrate 12, as well as undesirably permitting copper ofcopper layer 20 to contact and, possibly, diffuse into unprotected adjacent regions ofsubstrate 12. - The inventors are not aware of a slurry that is useful in CMP processes and that effectively polishes or planarizes both copper and tungsten without causing oxidation or dissolution of the tungsten.
- The present invention includes a method for substantially simultaneously chemical-mechanical polishing a copper conductive structure and an adjacent barrier layer with a fixed-abrasive type polishing pad, as well as slurries that are useful with fixed-abrasive type polishing pads for substantially simultaneously polishing a copper conductive structure and a barrier layer adjacent thereto.
- The method of the present invention includes employing a fixed-abrasive type polishing pad along with a substantially abrasive-free liquid polishing formulation, which is referred to herein as a substantially abrasive-free slurry or, more simply, as a slurry. The slurry is formulated to oxidize copper and a material of the barrier layer, such as tungsten, at substantially the same rates. Thus, in a slurry incorporating teachings of the present invention, the oxidation energies of copper and the barrier material are substantially the same. Preferably, in the slurry, the oxidation energy, or oxidation potential, of a barrier material, such as tungsten, is about 0.25 V greater to about 0.20 V less than an oxidation energy, or oxidation potential, of copper. As the barrier material is oxidized by the slurry at about the same rate as copper or at a slower rate than copper, use of a slurry so formulated to substantially simultaneously polish a copper conductive structure and an adjacent barrier layer prevents dissolution of the barrier layer. When used with a fixed-abrasive polishing pad, the slurry of the present invention removes a barrier material, such as tungsten, at a rate that is about the same as or up to about ten times slower than the rate at which the slurry removes copper and, preferably, at a rate that is about two to about four times slower than the rate at which the slurry removes copper.
- Slurries that are useful in the method of the present invention include at least one oxidizer, at least one complexing agent, and at least one inhibitor. The relative amounts of at least the oxidizer, the pH control agent, and the inhibitor are balanced so as to facilitate substantially concurrent polishing of a copper structure and another structure adjacent thereto, such as a barrier layer formed from tungsten. Thus, the slurry is formulated such that the relative amounts of the oxidizer, the complexing agent, and the inhibitor oxidize copper and a barrier material, such as tungsten, at substantially the same rates, or such that the oxidation energies of copper and the barrier material are substantially the same in the slurry. The pH of the slurry may also be optimized so as to provide for oxidation of copper and a barrier material, such as tungsten, at substantially the same rates.
- The present invention also includes a system for substantially simultaneously polishing a copper conductive structure and an adjacent barrier layer of a semiconductor device. Such a system includes a fixed-abrasive type polishing pad and a substantially abrasive-free slurry within which copper and the material of the barrier layer are oxidized at substantially the same rates, or have substantially the same oxidation energies.
- Other features and advantages of the present invention will become apparent to those of ordinary skill in the art through consideration of the ensuing description, the accompanying drawings, and the appended claims.
-
FIG. 1 is an electron micrograph illustrating the dissolution of regions of a tungsten barrier layer that underlie a copper structure of a semiconductor device structure when a conventional slurry is used to simultaneously remove the copper and tungsten; -
FIGS. 2-5 schematically illustrate an exemplary embodiment of a polishing method in which copper and a barrier material therefor are substantially simultaneously removed from a semiconductor device structure at substantially the same rates; and -
FIG. 6 is a schematic representation of an exemplary embodiment of a system that employs a fixed-abrasive polishing pad and a slurry to effect the method of the present invention. - A method incorporating teachings of the present invention is illustrated in
FIGS. 2-5 . With reference toFIG. 2 , asemiconductor device structure 10 including asubstrate 12, which includes arecess 14 formed in anactive surface 16 thereof is shown. Abarrier layer 18 of a material, such as tungsten, that prevents copper from diffusing into adjacent insulative regions ofsemiconductor device structure 10 is located onactive surface 16 and on thesurfaces 15 ofrecess 14. Acopper layer 20 is formed over andcontacts barrier layer 18.Copper layer 20 also substantially fillsrecess 14. Althoughsubstrate 12 may include various other structures beneathrecess 14,barrier layer 18, andcopper layer 20, for purposes of simplicity, no additional structures are illustrated in thesemiconductor device structure 10 shown inFIGS. 2-5 . - In forming a conductive structure from
copper layer 20, portions ofcopper layer 20 and ofbarrier layer 18 that are not located withinrecess 14 must be removed fromsemiconductor device structure 10. As discussed previously herein, CMP processes are typically used to remove unwanted portions of copper layers. With reference toFIG. 3 , aslurry 30 is applied overcopper layer 20. A fixed-abrasive polishing pad 40, which may be embodied as a conventional polishing pad, a web-type polishing pad, a belt-type polishing pad, or in any other polishing pad format known in the art, is then brought into frictional contact (e.g., by rotation ofsemiconductor device structure 10 or polishing pad 40) withcopper layer 20 to, along withslurry 30, removecopper layer 20. Aninhibitor component 32 ofslurry 30 fills recessedareas 22 ofcopper layer 20, thereby preventing removal of material from recessedareas 22 until material ofhigher areas 24 ofcopper layer 20 has been removed. - Eventually, regions of
barrier layer 18 overlyingactive surface 16 are exposed throughcopper layer 20, as shown inFIG. 4 . At this point,slurry 30 and fixed-abrasive polishing pad 40 remove the material or materials ofbarrier layer 18 and the copper ofcopper layer 20 at substantially the same rates. -
Barrier layer 18 is removed fromactive surface 16 by continued polishing withslurry 30 and fixed-abrasive polishing pad 40. Oncebarrier layer 18 is substantially removed fromactive surface 16 and thesurface 26 of the portion ofcopper layer 20 that remains withinrecess 14 is located substantially in the plane ofactive surface 16, as depicted inFIG. 5 , the polishing process is terminated. As illustrated inFIG. 5 , the remaining portion ofbarrier layer 18 substantially linesrecess 14 and separates the remaining portion ofcopper layer 20 from adjacent portions ofsubstrate 12. - In order to effect removal of copper and the material or materials (e.g., tungsten) of an
adjacent barrier layer 18 or other structure by CMP at substantially the same rates,slurry 30 is formulated so as to oxidize copper and the material or materials of theadjacent barrier layer 18 at substantially the same rates. Stated another way, copper and the material or materials (e.g., tungsten) of theadjacent barrier layer 18 have substantially the same oxidation energies inslurry 30. As a result, as aninterface 19 betweenlayers slurry 30, the material or materials ofbarrier layer 18 will not dissolve, or be removed fromsemiconductor device structure 10, at a significantly greater rate than copper ofcopper layer 20 is dissolved or removed fromsemiconductor device structure 10. By way of example only, and not to limit the scope of the present invention, the oxidation energy, or oxidation potential, of tungsten inslurry 30 is preferably about 0.25 V more to about 0.20 V less than the oxidation energy, or oxidation potential, of copper inslurry 30.Slurry 30 preferably removes a barrier material, such as tungsten, at a rate that is about the same as or up to about ten times slower than the rate at whichslurry 30 removes copper when a fixed-abrasive polishing pad is employed and, more preferably, at a rate that is about two to about four times slower than the rate at whichslurry 30 removes copper. - With continued reference to
FIGS. 2-5 ,slurry 30 is intended to be used in conjunction with a fixed-abrasive polishing pad 40, such as the acrylic fixed-abrasive polishing pads manufactured by 3M Company of St. Paul, Minn. Such a fixed-abrasive polishing pad 40 may be impregnated with particulate abrasives including, but not limited to, alumina (Al2O3), titanium dioxide (TiO2), silicon dioxide (SiO2), and cerium dioxide (CeO2). The abrasives in a fixed-abrasive polishing pad 40 are typically leached therefrom during polishing of asemiconductor device structure 10. Thus,slurry 30 need not include abrasives and is preferably substantially free of abrasives.Slurry 30 includes aninhibitor component 32, which prevents recessed, or lower,areas 22 ofcopper layer 20 from being removed untilhigher areas 24 ofcopper layer 20 have been removed down to substantially the same plane.Slurry 30 also includes an oxidizer component, which oxidizes both the copper ofcopper layer 20 and the material or materials (e.g., tungsten) ofbarrier layer 18 so as to chemically soften these materials and to thereby facilitate their mechanical removal fromsemiconductor device structure 10 by fixed-abrasive polishing pad 40. In addition,slurry 30 includes one or more complexing agents, which complex with ions of thelayers material layers slurry 30 may occur at optimal rates and, thus, the rates at which the materials oflayers semiconductor device structure 10 may also be optimized. - Examples of oxidizers that are useful as the oxidizer component of
slurry 30 include, without limitation, hydrogen peroxide, potassium iodate, potassium permanganate, ammonia, other amine compounds, ammonium compounds, nitrate compounds, and combinations thereof. Exemplary ammonium compounds include, without limitation, ammonium persulfate and ammonium molybdate. Exemplary nitrate compounds include, but are not limited to, ferric nitrate, nitric acid, and potassium nitrate. The oxidizer component preferably comprises about 0.1 to about 20%, by weight, ofslurry 30. It is preferred thatslurry 30 include about 0.1 to about 5.0%, by weight, of the oxidizer component. Even more preferred is a potassium iodate oxidizer component that makes up about 3 to about 5% of the weight ofslurry 30. - The one or more complexing agents of
slurry 30 may include, but are not limited to, glycine, ammonium citrate, ammonium phosphate, ammonium acetate, and combinations thereof.Slurry 30 preferably includes about 1 to about 15% of the one or more complexing agents, by weight. It is more preferred that the one or more complexing agents make up about 3 to about 5% of the weight ofslurry 30. For example,slurry 30 may include about 1% of the complexing agent glycine, including a concentration of 0.1 M (molar) polyethylene glycol (PEG), by weight ofslurry 30. As another example,slurry 30 may include about 3% ammonium acetate, by weight. -
Inhibitor component 32 ofslurry 30 prevents corrosion of copper during polishing.Inhibitor component 32 may include an azole, such as benzenetriazole (BTA), mercaptobenzothiazole, and tolytriazole, an amine, such as methylamine and diethylamine, a ring compound, such as pyridine, quinoline, and dicyclohexamine nitrate, as well as other compounds, such as potassium silicate, ammonium borate, ammonium phosphate, and potassium dichromate, or mixtures of any of these corrosion inhibitors. Whileinhibitor component 32 may make up about 0.05 to about 2% of the weight ofslurry 30, it is preferred theinhibitor component 32 comprise about 0.05 to about 0.2% of the weight ofslurry 30. For example,slurry 30 may include about 0.1% BTA, by weight. -
Slurry 30 may have a pH in the range of about 2 to about 6, but the pH ofslurry 30 is preferably in the range of about 3 to about 5 and, more preferably, is about 4. One or more buffers, which are also referred to herein as pH control agents, may be used, as known in the art, to adjust the pH ofslurry 30 to a desired level. Exemplary buffers that may be used inslurry 30 include, without limitation, potassium hydrogen phthalate, ammonium acetate, ammonium oxalate, ammonium carbamate, ammonium phosphate, ammonium hydrogen phosphate, ammonium dihydrogen phosphate, dibasic ammonium citrate, tribasic ammonium citrate, and mixtures thereof. Acetic acid, phosphoric acid, and sulfuric acid are examples of other pH control agents that may be used in aslurry 30 incorporating teachings of the present invention. Preferably, the pH control agent will adjust the pH ofslurry 30 to a desirable range or point without significantly etching the insulator (e.g., borophosphosilicate glass (BPSG), phosphosilicate glass (PSG), or borosilicate glass (BSG)) that underlies the layer or layers being polished. Without limitation, acetic acid is an example of a buffer that may be used to adjust the pH ofslurry 30 and that will not etch an underlying glass insulator. - In addition,
slurry 30 may include a surfactant component, which may comprise from about 1% to about 15% of the volume ofslurry 30 and, more preferably, about 1% to about 2% of the weight ofslurry 30. The surfactant component may include, for example, polyethylene glycol, polyoxyethylene ether, glycerol, polypropylene glycol, polyoxyethylene lauryl ether, polyoxyethylene cetyl ether, polyoxyethylene stearyl ether, polyoxyethylene oleyl ether, and mixtures thereof. - Thickeners may also be included in
slurry 30 to impartslurry 30 with a desired viscosity (e.g., about 10 to about 20 cps. at ambient temperature). Exemplary thickeners that may be included inslurry 30 include, but are not limited to, POLYOX®, available from Union Carbide of Danbury, Conn., and CARBOPOL®, available from B.F. Goodrich of Cleveland, Ohio. - Water may be used as the balance of
slurry 30. - The specific amounts of the components of
slurry 30 may be determined by identifyingslurry 30 formulations in which copper gives up electrons at substantially the same rate as a barrier material, such as tungsten, of abarrier layer 18 to be polished substantially simultaneously withcopper layer 20. Stated another way,slurry 30 may be formulated so that copper and a barrier material therefor, such as tungsten, have the substantially same oxidation energies therein, or are oxidized at substantially the same rates therein. Preferably, the oxidation energy of tungsten or another barrier material inslurry 30 is within the range of about 0.25 V more than to about 0.20 V less than the oxidation energy of copper inslurry 30, the range including the end point values thereof. These formulations ofslurry 30 will facilitate the removal of copper and a barrier material, such as tungsten, from asemiconductor device structure 10 at substantially the same rates. -
Slurry 30 formulations having these characteristics may be determined as known in the art, such as by measuring the open circuit potentials of copper and a barrier material, such as tungsten, inslurry 30. - Referring now to
FIG. 6 , a polishingsystem 50 for effecting the substantially simultaneous polishing of copper and an adjacent barrier material in accordance with the method of the present invention is illustrated.Polishing system 50 includes a polishingapparatus 42, which supports or carries a fixed-abrasive polishing pad 40, and asubstrate support 44 configured to hold asemiconductor device structure 10, to bring the same into frictional contact with fixed-abrasive polishing pad 40, and, preferably, to rotatesemiconductor device structure 10 relative to fixed-abrasive polishing pad 40.Polishing system 50 also includes aslurry applicator 47. Although polishingapparatus 42 is illustrated inFIG. 6 as a web-type polishing apparatus, other known types of polishing apparatus, including, without limitation, belt-type and conventional rotational-type polishing apparatus, may alternatively be used in polishing systems incorporating teachings of the present invention. - Any known CMP apparatus, including conventional, rotary CMP apparatus, web format CMP apparatus, and belt format CMP apparatus, may comprise polishing
apparatus 42,substrate support 44, andslurry applicator 47 of polishingsystem 50. Fixed-abrasive polishing pad 40 may similarly include any known fixed-abrasive polishing pad, such as the acrylic fixed-abrasive polishing pads available from 3M Company, in any known pad format (e.g., conventional, web, or belt). - In use of polishing
system 50, one or moresemiconductor device structures 10 having one or more layers thereon that are to be chemical-mechanical polished are secured tosubstrate support 44. If necessary, fixed-abrasive polishing pad 40 is also secured to polishingapparatus 42.Slurry 30 is introduced byslurry applicator 47 onto one or both ofsemiconductor device structure 10 and fixed-abrasive polishing pad 40. Onceslurry 30 has been applied to fixed-abrasive polishing pad 40, one or both ofsemiconductor device structure 10 and fixed-abrasive polishing pad 40 are substantially continuously laterally moved (e.g., rotated or vibrated or otherwise moved side-to-side) and brought into frictional contact with one another so as to effect the CMP process. For example, when a web format or belt format polishing apparatus is employed, the apparatus may precess semiconductor device structure 10 (i.e., rotatesemiconductor device structure 10 around the axis of a support therefor), while the polishing pad remains substantially stationary. - Once the desired portions of one or
more layers 18, 20 (FIGS. 2-5 ) have been removed fromsemiconductor device structure 10,semiconductor device structure 10 is moved away from fixed-abrasive polishing pad 40.Slurry 30 remaining onsemiconductor device structure 10 is rinsed or otherwise removed therefrom by known processes. Subsequent fabrication processes may then be conducted onsemiconductor device structure 10, as known in the art.Polishing pad 40 may be incrementally moved to provide a fresh pad segment that was not utilized to polishsemiconductor device structure 10.Polishing pad 40 may be moved a distance that is less than the distance across (e.g., diameter) asemiconductor device structure 10 to be polished therewith. Preferably, polishingpad 40 is moved a distance that is at most about 1% of the maximum distance acrosssemiconductor device structure 10 so as to uniformly polishsemiconductor device structures 10 and to maximize the useful life of polishingpad 40. As an example, following the use of apolishing pad 40 to polish one or more 8 inch wafers, polishingpad 40 may be incrementally moved about a quarter of an inch (i.e., about 0.25 inches) between polishing each wafer or set of wafers. - While polishing in accordance with the present invention may be conducted at any suitable polishing temperature, polishing with
slurry 30 and a fixed-abrasive polishing pad 40 may be conducted at lower temperatures than those of conventional polishing processes. For example, polishing methods that incorporate teachings of the present invention may be conducted at temperatures of about room temperature (e.g., about 23-27° C.) or cooler. It has been found that polishing causes fewer defects when conducted at cooler temperatures. The abrasive components of conventional slurries do not, however, remain soluble in or, thus, evenly dispersed throughout such slurries at cooler temperatures. - Although the foregoing description contains many specifics, these should not be construed as limiting the scope of the present invention, but merely as providing illustrations of some of the presently preferred embodiments. Similarly, other embodiments of the invention may be devised which do not depart from the spirit or scope of the present invention. Features from different embodiments may be employed in combination. The scope of the invention is, therefore, indicated and limited only by the appended claims and their legal equivalents, rather than by the foregoing description. All additions, deletions and modifications to the invention as disclosed herein which fall within the meaning and scope of the claims are to be embraced thereby.
Claims (29)
1. A method for chemical-mechanical polishing a copper structure and an adjacent barrier layer of a semiconductor device structure, comprising:
providing a semiconductor device structure including at least one recess formed in a surface thereof, a barrier layer lining at least the at least one recess, and a conductive layer comprising copper at least partially filling the at least one recess; and
substantially concurrently polishing the conductive layer and the barrier layer without removing the barrier layer at a substantially greater rate than the copper is removed.
2. The method of claim 1 , wherein substantially concurrently polishing comprises employing a slurry formulated to effect an oxidation rate of the barrier layer substantially the same as or less than an oxidation rate of the copper.
3. The method of claim 1 , wherein substantially concurrently polishing comprises employing a slurry formulated to provide substantially similar oxidation energies of the barrier layer and the copper.
4. The method of claim 3 , wherein employing the slurry comprises employing a slurry in which an oxidation energy of the barrier layer is from about 0.25 V greater than to about 0.20 V less than an oxidation energy of the copper.
5. The method of claim 1 , wherein substantially concurrently polishing comprises employing a slurry in which a removal rate of the material of the barrier layer is up to about ten times slower than a removal rate of the copper.
6. The method of claim 1 , wherein substantially concurrently polishing comprises employing a slurry in which a removal rate of the material of the barrier layer is about two to about four times slower than a removal rate of the copper.
7. The method of claim 1 , wherein providing the semiconductor device structure comprises providing a semiconductor device structure with the barrier layer comprising tungsten.
8. The method of claim 1 , wherein substantially concurrently polishing is effected at ambient temperature or a cooler temperature.
9. A method for chemical-mechanical polishing a copper conductive structure and an adjacent barrier layer of a semiconductor device structure, comprising:
providing a semiconductor device structure including at least one recess formed in a surface thereof, a barrier layer lining at least the at least one recess, and a conductive layer comprising copper within the at least one recess; and
substantially concurrently polishing the barrier layer and the conductive layer without oxidizing a material of the barrier layer at a substantially greater rate than the copper is oxidized.
10. The method of claim 9 , wherein providing the semiconductor device structure comprises providing a semiconductor device structure with the barrier layer comprising tungsten.
11. The method of claim 9 , wherein substantially concurrently polishing comprises employing a polishing pad.
12. The method of claim 11 , wherein employing the polishing pad comprises employing a fixed-abrasive polishing pad.
13. The method of claim 9 , wherein substantially concurrently polishing comprises employing a slurry.
14. The method of claim 13 , wherein employing the slurry comprises employing a slurry formulated to oxidize the copper of the conductive layer at substantially the same rate as or a faster rate than the tungsten of the barrier layer is oxidized.
15. The method of claim 13 , wherein employing the slurry comprises employing a slurry formulated to provide substantially similar oxidation energies of the tungsten and the copper.
16. The method of claim 15 , wherein, in employing the slurry, the tungsten has an oxidation energy from about 0.25 V more to about 0.20 V less than the oxidation energy of the copper.
17. The method of claim 9 , wherein, during said substantially concurrently polishing, a material of the barrier layer is not removed at a substantially greater rate than the rate at which the copper is removed.
18. The method of claim 17 , wherein, during said substantially concurrently polishing, the material of the barrier layer is removed at a rate of as low as about one tenth the rate at which the copper is removed.
19. The method of claim 17 , wherein, during said substantially concurrently polishing, the material of the barrier layer is removed at a rate of about one fourth to about one half of the rate at which the copper is removed.
20. A method for polishing a surface of a semiconductor device structure, the surface including a conductive structure including copper and a barrier layer adjacent the conductive structure, the method comprising substantially concurrently oxidizing a material of the barrier layer at substantially the same rate as or at a slower rate than a rate at which the conductive structure is oxidized.
21. The method of claim 20 , wherein substantially concurrently oxidizing is effected with a slurry.
22. The method of claim 21 , wherein substantially concurrently oxidizing comprises employing a slurry that is substantially free of abrasive particles.
23. The method of claim 22 , further comprising employing a fixed abrasive polishing pad.
24. The method of claim 20 , wherein substantially concurrently oxidizing comprises employing a slurry in which the copper and the material of the barrier layer exhibit substantially the same oxidation energies.
25. The method of claim 24 , wherein employing the slurry comprises employing a slurry in which an oxidation energy of the material of the barrier layer is from about 0.25 V more to about 0.20 V less than an oxidation energy of the copper.
26. The method of claim 24 , wherein employing the slurry comprises employing a slurry in which a removal rate of the material of the barrier layer is as low as about one tenth a removal rate of the copper.
27. The method of claim 24 , wherein employing the slurry comprises employing a slurry in which a removal rate of the material of the barrier layer is about one fourth to about one half a removal rate of the copper.
28. The method of claim 20 , comprising providing a semiconductor device structure with a barrier layer comprising tungsten.
29. The method of claim 20 , wherein substantially concurrently polishing is effected without substantially dissolving a portion of the barrier layer located beneath a remaining portion of the conductive structure.
Priority Applications (1)
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US11/011,363 US20050153556A1 (en) | 2000-08-30 | 2004-12-14 | Methods for polishing copper features of semiconductor devices structures |
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Application Number | Priority Date | Filing Date | Title |
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US09/651,808 US6602117B1 (en) | 2000-08-30 | 2000-08-30 | Slurry for use with fixed-abrasive polishing pads in polishing semiconductor device conductive structures that include copper and tungsten and polishing methods |
US10/132,827 US6830500B2 (en) | 2000-08-30 | 2002-04-25 | Slurry for use with fixed-abrasive polishing pads in polishing semiconductor device conductive structures that include copper and tungsten and polishing methods |
US11/011,363 US20050153556A1 (en) | 2000-08-30 | 2004-12-14 | Methods for polishing copper features of semiconductor devices structures |
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US10/132,827 Continuation US6830500B2 (en) | 2000-08-30 | 2002-04-25 | Slurry for use with fixed-abrasive polishing pads in polishing semiconductor device conductive structures that include copper and tungsten and polishing methods |
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US10/132,827 Expired - Fee Related US6830500B2 (en) | 2000-08-30 | 2002-04-25 | Slurry for use with fixed-abrasive polishing pads in polishing semiconductor device conductive structures that include copper and tungsten and polishing methods |
US10/620,002 Abandoned US20040014318A1 (en) | 2000-08-30 | 2003-07-14 | Slurry for use with fixed-abrasive polishing pads in polishing semiconductor device conductive structures that include copper and tungsten |
US11/011,363 Abandoned US20050153556A1 (en) | 2000-08-30 | 2004-12-14 | Methods for polishing copper features of semiconductor devices structures |
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US10/132,827 Expired - Fee Related US6830500B2 (en) | 2000-08-30 | 2002-04-25 | Slurry for use with fixed-abrasive polishing pads in polishing semiconductor device conductive structures that include copper and tungsten and polishing methods |
US10/620,002 Abandoned US20040014318A1 (en) | 2000-08-30 | 2003-07-14 | Slurry for use with fixed-abrasive polishing pads in polishing semiconductor device conductive structures that include copper and tungsten |
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- 2001-08-30 AU AU2001288591A patent/AU2001288591A1/en not_active Abandoned
- 2001-08-30 EP EP01968338A patent/EP1314194A2/en not_active Ceased
- 2001-08-30 KR KR1020037003070A patent/KR100854258B1/en not_active IP Right Cessation
- 2001-08-30 JP JP2002523056A patent/JP2004507899A/en active Pending
- 2001-08-30 CN CNB018168264A patent/CN1291462C/en not_active Expired - Fee Related
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US20080096389A1 (en) * | 2006-10-20 | 2008-04-24 | Jian-Huei Feng | Copper damascene chemical mechanical polishing (CMP) for thin film head writer fabrication |
US7396768B2 (en) * | 2006-10-20 | 2008-07-08 | Hitachi Global Storage Technologies Netherlands B.V. | Copper damascene chemical mechanical polishing (CMP) for thin film head writer fabrication |
Also Published As
Publication number | Publication date |
---|---|
CN1291462C (en) | 2006-12-20 |
KR100869044B1 (en) | 2008-11-17 |
KR20070049690A (en) | 2007-05-11 |
US20020123299A1 (en) | 2002-09-05 |
EP1314194A2 (en) | 2003-05-28 |
US20040014318A1 (en) | 2004-01-22 |
JP2004507899A (en) | 2004-03-11 |
CN1468446A (en) | 2004-01-14 |
KR100854258B1 (en) | 2008-08-26 |
WO2002018099A3 (en) | 2002-10-31 |
WO2002018099A2 (en) | 2002-03-07 |
US6830500B2 (en) | 2004-12-14 |
AU2001288591A1 (en) | 2002-03-13 |
KR20030036740A (en) | 2003-05-09 |
US6602117B1 (en) | 2003-08-05 |
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