CN101313388A - Friction reducing aid for cmp - Google Patents
Friction reducing aid for cmp Download PDFInfo
- Publication number
- CN101313388A CN101313388A CNA2006800437962A CN200680043796A CN101313388A CN 101313388 A CN101313388 A CN 101313388A CN A2006800437962 A CNA2006800437962 A CN A2006800437962A CN 200680043796 A CN200680043796 A CN 200680043796A CN 101313388 A CN101313388 A CN 101313388A
- Authority
- CN
- China
- Prior art keywords
- polishing
- water
- polishing system
- substrate
- grinding agent
- 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.)
- Pending
Links
- 238000005498 polishing Methods 0.000 claims abstract description 235
- 239000000758 substrate Substances 0.000 claims abstract description 77
- -1 silicate compound Chemical class 0.000 claims abstract description 56
- 238000000034 method Methods 0.000 claims abstract description 50
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 31
- 239000007800 oxidant agent Substances 0.000 claims abstract description 29
- 239000003795 chemical substances by application Substances 0.000 claims description 45
- 238000000227 grinding Methods 0.000 claims description 38
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 claims description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 26
- 230000001590 oxidative effect Effects 0.000 claims description 26
- 229910052913 potassium silicate Inorganic materials 0.000 claims description 24
- 235000019353 potassium silicate Nutrition 0.000 claims description 23
- 239000004111 Potassium silicate Substances 0.000 claims description 21
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 claims description 20
- 229910052751 metal Inorganic materials 0.000 claims description 14
- 239000002184 metal Substances 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 14
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 13
- 239000000377 silicon dioxide Substances 0.000 claims description 12
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 10
- 235000012239 silicon dioxide Nutrition 0.000 claims description 10
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical group [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 9
- 229910052715 tantalum Inorganic materials 0.000 claims description 9
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 9
- 239000004115 Sodium Silicate Substances 0.000 claims description 8
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 8
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 8
- 102000004316 Oxidoreductases Human genes 0.000 claims description 7
- 108090000854 Oxidoreductases Proteins 0.000 claims description 7
- 235000019795 sodium metasilicate Nutrition 0.000 claims description 7
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 6
- 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 claims description 6
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 claims description 6
- 229910002651 NO3 Inorganic materials 0.000 claims description 5
- 239000011521 glass Substances 0.000 claims description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 4
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 claims description 4
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 4
- ICIWUVCWSCSTAQ-UHFFFAOYSA-M iodate Chemical compound [O-]I(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-M 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 claims description 3
- SASQRKZJTJRQFI-UHFFFAOYSA-N S(=O)(=O)(O)OO.S(=O)(=O)(O)O Chemical compound S(=O)(=O)(O)OO.S(=O)(=O)(O)O SASQRKZJTJRQFI-UHFFFAOYSA-N 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 85
- 238000002156 mixing Methods 0.000 description 15
- 239000002253 acid Substances 0.000 description 13
- 238000005260 corrosion Methods 0.000 description 13
- 230000007797 corrosion Effects 0.000 description 13
- 239000012530 fluid Substances 0.000 description 13
- 239000003112 inhibitor Substances 0.000 description 13
- 239000000243 solution Substances 0.000 description 13
- 239000000463 material Substances 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 8
- 239000012141 concentrate Substances 0.000 description 8
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 7
- 239000013530 defoamer Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 230000003115 biocidal effect Effects 0.000 description 5
- 239000003139 biocide Substances 0.000 description 5
- 230000003750 conditioning effect Effects 0.000 description 5
- 239000003989 dielectric material Substances 0.000 description 5
- 229910044991 metal oxide Inorganic materials 0.000 description 5
- 150000004706 metal oxides Chemical class 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- 239000006061 abrasive grain Substances 0.000 description 4
- 230000004888 barrier function Effects 0.000 description 4
- 238000007517 polishing process Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000004065 semiconductor Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 238000006073 displacement reaction Methods 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 229920000620 organic polymer Polymers 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 210000001138 tear Anatomy 0.000 description 3
- 150000000177 1,2,3-triazoles Chemical class 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 2
- 229930192627 Naphthoquinone Natural products 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 150000004054 benzoquinones Chemical class 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 238000011088 calibration curve Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
- 239000010432 diamond Substances 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910001092 metal group alloy Inorganic materials 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000004377 microelectronic Methods 0.000 description 2
- 150000002791 naphthoquinones Chemical class 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- LLYCMZGLHLKPPU-UHFFFAOYSA-M perbromate Chemical compound [O-]Br(=O)(=O)=O LLYCMZGLHLKPPU-UHFFFAOYSA-M 0.000 description 2
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 2
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 2
- 150000003009 phosphonic acids Chemical class 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- JLKDVMWYMMLWTI-UHFFFAOYSA-M potassium iodate Chemical group [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
- 230000001737 promoting effect Effects 0.000 description 2
- 239000005368 silicate glass Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- PFNQVRZLDWYSCW-UHFFFAOYSA-N (fluoren-9-ylideneamino) n-naphthalen-1-ylcarbamate Chemical compound C12=CC=CC=C2C2=CC=CC=C2C1=NOC(=O)NC1=CC=CC2=CC=CC=C12 PFNQVRZLDWYSCW-UHFFFAOYSA-N 0.000 description 1
- 150000004057 1,4-benzoquinones Chemical class 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 1
- 150000004416 2,5-dihydroxy-1,4-benzoquinones Chemical class 0.000 description 1
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 1
- OZTBHAGJSKTDGM-UHFFFAOYSA-N 9,10-dioxoanthracene-1,5-disulfonic acid Chemical compound O=C1C=2C(S(=O)(=O)O)=CC=CC=2C(=O)C2=C1C=CC=C2S(O)(=O)=O OZTBHAGJSKTDGM-UHFFFAOYSA-N 0.000 description 1
- IJNPIHLZSZCGOC-UHFFFAOYSA-N 9,10-dioxoanthracene-1,8-disulfonic acid Chemical compound O=C1C2=CC=CC(S(O)(=O)=O)=C2C(=O)C2=C1C=CC=C2S(=O)(=O)O IJNPIHLZSZCGOC-UHFFFAOYSA-N 0.000 description 1
- MMNWSHJJPDXKCH-UHFFFAOYSA-N 9,10-dioxoanthracene-2-sulfonic acid Chemical compound C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 MMNWSHJJPDXKCH-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 229910000684 Cobalt-chrome Inorganic materials 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical class OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 229910002601 GaN Inorganic materials 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- HMDDXIMCDZRSNE-UHFFFAOYSA-N [C].[Si] Chemical compound [C].[Si] HMDDXIMCDZRSNE-UHFFFAOYSA-N 0.000 description 1
- WAIPAZQMEIHHTJ-UHFFFAOYSA-N [Cr].[Co] Chemical compound [Cr].[Co] WAIPAZQMEIHHTJ-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229920001448 anionic polyelectrolyte Polymers 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- MSSUFHMGCXOVBZ-UHFFFAOYSA-N anthraquinone-2,6-disulfonic acid Chemical group OS(=O)(=O)C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 MSSUFHMGCXOVBZ-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009954 braiding Methods 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-N chloric acid Chemical compound OCl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-N 0.000 description 1
- 229940005991 chloric acid Drugs 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 239000010952 cobalt-chrome Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- WSALIDVQXCHFEG-UHFFFAOYSA-L disodium;4,8-diamino-1,5-dihydroxy-9,10-dioxoanthracene-2,6-disulfonate Chemical compound [Na+].[Na+].O=C1C2=C(N)C=C(S([O-])(=O)=O)C(O)=C2C(=O)C2=C1C(O)=C(S([O-])(=O)=O)C=C2N WSALIDVQXCHFEG-UHFFFAOYSA-L 0.000 description 1
- 238000001312 dry etching Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- PEYVWSJAZONVQK-UHFFFAOYSA-N hydroperoxy(oxo)borane Chemical compound OOB=O PEYVWSJAZONVQK-UHFFFAOYSA-N 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- XZWYZXLIPXDOLR-UHFFFAOYSA-N metformin Chemical compound CN(C)C(=N)NC(N)=N XZWYZXLIPXDOLR-UHFFFAOYSA-N 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- CMUOJBJRZUHRMU-UHFFFAOYSA-N nitrourea Chemical compound NC(=O)N[N+]([O-])=O CMUOJBJRZUHRMU-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000012285 osmium tetroxide Substances 0.000 description 1
- 229910000489 osmium tetroxide Inorganic materials 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- LLYCMZGLHLKPPU-UHFFFAOYSA-N perbromic acid Chemical compound OBr(=O)(=O)=O LLYCMZGLHLKPPU-UHFFFAOYSA-N 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920003209 poly(hydridosilsesquioxane) Polymers 0.000 description 1
- 229920000052 poly(p-xylylene) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229910001404 rare earth metal oxide Inorganic materials 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 150000005622 tetraalkylammonium hydroxides Chemical class 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910000314 transition metal oxide Inorganic materials 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- 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
- B24B29/00—Machines or devices for polishing surfaces on work by means of tools made of soft or flexible material with or without the application of solid or liquid polishing 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
- B24B37/042—Lapping machines or devices; Accessories designed for working plane surfaces operating processes therefor
-
- 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
- B24B57/00—Devices for feeding, applying, grading or recovering grinding, polishing or lapping agents
- B24B57/02—Devices for feeding, applying, grading or recovering grinding, polishing or lapping agents for feeding of fluid, sprayed, pulverised, or liquefied grinding, polishing or lapping agents
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Mechanical Treatment Of Semiconductor (AREA)
- Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)
Abstract
The invention provides a chemical-mechanical polishing system for polishing a substrate comprising a polishing component, a water-soluble silicate compound, an oxidizing agent, and water, wherein the pH of the polishing system is about 8 to about 12. The invention further provides a method of chemically-mechanically polishing a substrate with the aforementioned polishing system. The polishing system provides for reduced friction during polishing of substrates.
Description
Technical field
The friction reducing aid (frction reducing aid) of the present invention about being used for chemico-mechanical polishing.
Background technology
Integrated circuit by among millions of substrates that are formed at silicon wafer for example or on active device form.These active devices are connected in the substrate and by the use multilayer interconnection with chemistry and physics mode and are connected to each other to form functional circuit.In one manufacturing approach, by traditional dry etching method with the dielectric substrate patterning to be formed for vertically reaching the hole and the groove of horizontal interconnect.Patterned then surface randomly covers with diffusion impervious layer and/or adhesion promoting layer, and then depositing metal layers is to fill these grooves and hole.Use chemico-mechanical polishing (CMP) to reduce the thickness of metal layer thickness and diffusion impervious layer and/or adhesion promoting layer then, the dielectric layer below exposing forms circuit devcie thus.
In chemico-mechanical polishing, the polishing component of polishing pad (polishing component) contacts to make substrate surface and polishing composition for example reach.Polishing composition (being also referred to as polishing slurries) contains the grinding-material in the aqueous solution usually, and by making the surface and contacting with the saturated polishing pad of polishing composition and polishing composition is applied to the surface.The chemical composition of polishing composition is considered to the surfacing reaction with the substrate that is polishing, the derivative of more soft, the easier wearing and tearing by surfacing being converted into described material, then the mechanism by grinding-material and/or polishing pad removes described derivative, perhaps by dissolving the surfacing that removes via mechanism separately.In some applications, grinding agent can be fixed on the surface of polishing pad.
In polishing processing, the frictional force that relative motion caused by substrate surface that polishing composition is arranged therebetween and pad interface can be via destroying circuit by abrasive grains and/or polishing pad scratch substrate, and via the layering of superficial layer, thereby cause the defective of the device that just on substrate, forming from substrate.In addition, polishing pad can cause filling up premature failure at the frictional heat at pad/slurry interface place.The strategy that reduces friction, for example surfactant being joined in the polishing composition, use the polishing pad that is made of softer material or reducing to be applied to power on substrate/polishing pad interface causes the speed that removes of the material that polishing to reduce usually, this can cause increase process time, therefore reduces output and increases total unit cost.
In addition, for reduce the electric capacity between the conductive layer on the microelectronic component and therefore increase frequency or the speed that device can operate, using have permittivity ratio normally used based on the low material of the dielectric material of silicon dioxide so that the electric insulation between the circuit-line to be provided.The example of advanced low-k materials generally includes organic polymer material, inorganic and organic porous dielectric material, reaches blend or compound organic and inorganic material (it can be porous or non-porous).These materials mechanically than soft based on the dielectric material of silicon dioxide and in the manufacture process of device easier being damaged.Very desirable is that advanced low-k materials is incorporated in the semiconductor structure, still can utilize the surface of conventional chemico-mechanical polishing (CMP) system polishing obtained device simultaneously in the semiconductor wafer course of processing.
Therefore, exist the such chemical-mechanical polishing compositions and the needs of system, it demonstrates the friction that reduces between substrate and the polishing component.These and other advantage of the present invention, and other inventive features will become distinct from the embodiment of the present invention that this paper provided.
Summary of the invention
The invention provides a kind of chemical-mechanical polishing system that is used for polishing substrate, it comprises the polishing component that (a) is selected from polishing pad, grinding agent and combination thereof, and (b) water-soluble silicate compound presents in an amount at least sufficient to provide 0.1 weight % or more SiO
2, (c) oxidant of at least a portion of oxidase substrate reaches (d) water, and wherein the pH value of polishing system is 8 to 12.The present invention further provides a kind of method of chemical-mechanical polishing substrate, this method comprises: substrate is contacted with chemical-mechanical polishing system, this chemical-mechanical polishing system comprises: the polishing component that (a) is selected from polishing pad, grinding agent and combination thereof, (b) water-soluble silicate compound presents in an amount at least sufficient to provide 0.1 weight % or more SiO
2, (c) oxidant of at least a portion of oxidase substrate reaches (d) water; At least a portion that reaches the substrate that (ii) weares and teares is with polishing substrate, and wherein the pH value of polishing system is 8 to 12.
Description of drawings
Fig. 1 explanation is used to measure the method for the coefficient of friction of CMP (Chemical Mechanical Polishing) process.
Embodiment
The invention provides a kind of chemico-mechanical polishing (CMP) system, it comprises the polishing component, is enough to provide 0.1 weight % or more SiO
2Oxidant, and the water of at least a portion of water-soluble silicate compound, oxidase substrate of amount, wherein the pH value of this polishing system is 8 to 12.Water and any dissolving or be suspended in the polishing composition that wherein component forms chemical-mechanical polishing system.Unless otherwise noted, otherwise the amount of component described herein all based on the total weight of polishing composition (that is, water and any dissolving or be suspended in the weight of component wherein).
The polishing component is selected from polishing pad, grinding agent, reaches the combination of polishing pad and grinding agent.If there is grinding agent, then grinding agent can be any suitable form (for example abrasive grains).Grinding agent can be fixed on the polishing pad and/or it can be particulate form and suspends in water.Polishing pad can be any suitable polishing pad, and wherein many are as known in the art.
Grinding agent can be any suitable grinding agent, and for example grinding agent can be natural or syntheticly, and can comprise metal oxide, carbide, nitride, diamond dust etc.Grinding agent also can be polymer beads or the particle through applying.Grinding agent desirably comprises metal oxide.Preferably, this metal oxide is selected from aluminium oxide, ceria, silicon dioxide, zirconia, it forms product (coformed product) and combination thereof altogether.Abrasive grains has the particle mean size (for example average grain diameter) of 20nm to 500nm usually.Preferably, abrasive grains has the particle mean size of 30nm to 400nm (for example, 40nm to 300nm, or 50nm to 250nm, or 75nm to 200nm).
When grinding agent is suspended in water (, when grinding agent is the component of polishing composition), the grinding agent of any suitable amount can be present in the polishing composition.Usually, the grinding agent of 0.01 weight % or more (for example 0.05 weight % or more) can be present in the polishing composition.More specifically, 0.1 weight % or more grinding agent can be present in the polishing composition.The amount of grinding agent can not surpass 20 weight % usually in the polishing composition, more generally can not surpass 10 weight % (for example can not surpass 5 weight %).Preferably, the amount of grinding agent is 0.05 weight % to 2 weight % in the polishing composition, and 0.1 weight % to 1 weight % more preferably.
Polishing system can comprise any suitable polishing pad (for example polished surface).Suitable polishing pad comprises, for example, and braiding and non-woven polishing pad.Resilience when in addition, suitable polishing pad can comprise different densities, hardness, thickness, compressibility, compression and any suitable polymers of modulus of compressibility.Suitable polymers comprises, for example, polyvinyl chloride, polyvinyl fluoride, nylon, fluorocarbon, Merlon, polyester, polyacrylate, polyethers, polyethylene, polyamide, polyurethane, polystyrene, polypropylene, its form altogether product, and composition thereof.
Polishing system comprises water-soluble silicate compound.This water-soluble silicate compound can be any suitable water-soluble silicate compound.Desirably, this water-soluble silicate compound is an alkali silicate.Preferably, this water-soluble silicate compound is selected from potassium silicate, sodium metasilicate, potassium metasilicate and sodium metasilicate.More preferably, this water-soluble silicate compound is a potassium silicate.
The water-soluble silicate compound that is suitable for use among the present invention can be silicate glass.The silicate glass high temperature by silica sand and suitable alkali metal compound (for example sodium carbonate or potash) usually merges and prepares.
Water-soluble silicate has formula M
2OmSiO
2NH
2O, wherein M is the alkali metal that is selected from sodium, potassium and lithium, and the m and the n that are called coefficient are respectively every mole of M
2The SiO of O
2And H
2The molal quantity of O.Coefficient m is SiO
2With M
2The mol ratio of O.SiO
2With M
2The weight ratio of O also is generally used for describing the composition of water-soluble alkali metal silicates.Coefficient m can be any suitable positive nonzero number (for example 1 or bigger), is generally 1 to 4, be more typically 2 to 4 (for example, 2.8 to 3.9, or 3 to 3.6).
In a preferred embodiment, this water-soluble silicate compound is for having general formula K
2OmSiO
2Potassium silicate, Coefficient m (for example, SiO wherein
2With K
2The mol ratio of O) is positive nonzero number.Potassium silicate can have any suitable coefficient.Desirably, this coefficient is 1 or bigger.Preferably, this coefficient is 2.8 to 3.9.More preferably, this coefficient is 3 to 3.6.
Water-soluble silicate compound is present in the aqueous solution in the polishing composition.A kind of method that water-soluble silicate compound is provided is that the water-soluble silicate compound with solid form is dissolved in the water so that solution to be provided.Perhaps, can dilute the concentrated solution of water-soluble silicate compound to obtain the desired concn of water-soluble silicate compound in the solution.The commercially available acquisition of the potassium silicate of each grade and sodium silicate aqueous solution, wherein said solution is by the concrete coefficient of employed silicate and the SiO of solution in its preparation
2Weight percent is K when
2O or Na
2The O percentage by weight characterizes.Zaclon, Inc. (Cleveland, OH) and PQCorporation (Valley Forge PA) is two key vendors of the solid form and the solution of potassium silicate and sodium metasilicate.
Also can obtain potassium silicate aqueous solution, wherein make silicon dioxide (SiO for example by the hydrothermal solution method
2) source and potassium hydroxide aqueous solution react under temperature that raises and/or pressure condition.The example that is used to produce the suitable hydrothermal solution method of potassium silicate aqueous solution is disclosed in United States Patent (USP) 5,084, in 262 and 5,238,668.
The polishing composition of polishing system can comprise the water-soluble silicate compound of any suitable amount.Usually, the content that is present in the water-soluble silicate compound in the polishing composition be expressed as in water and be dissolved in any component wherein total weight by SiO that this water-soluble silicate compound was provided
2Percentage by weight.Should understand formula " SiO
2" represent that for a kind of form it allows to calculate the amount of employed water-soluble silicate compound in polishing composition, and no matter its source (for example, the aqueous solution of the water-soluble silicate compound of various compositions as described herein or solid form).Usually, this polishing composition comprises sufficient water-soluble silicate compound so that 0.1 weight % or more (for example, 0.25 weight % or more, 0.5 weight % or more, 1 weight % or more, 1.5 weight % or more or 2 weight % or more than 2) SiO to be provided
2Polishing composition preferably comprise sufficient water-soluble silicate compound with provide 8 weight % or still less (for example, 6 weight % still less or 4 weight % still less or even 3 weight % or still less) SiO
2Polishing composition most preferably comprises 0.25 weight % to 5 weight % (for example, 0.5 weight % to 4 weight %, or 1 weight % to 3 weight %) SiO
2
The polishing composition of polishing system comprises the oxidant of at least a portion of oxidase substrate.Any suitable oxidant all can be used for the present invention.Suitable oxidant comprises inorganic and organic compound (per-compound), bromate, nitrate, chlorate, chromate, iodate, molysite and mantoquita (for example, nitrate, sulfate, edta salt and citrate), rare-earth oxide and transition metal oxide (for example osmium tetroxide), the potassium ferricyanide, potassium bichromate, acid iodide, quinone etc. crossed.Cross compound (as defined) for containing at least one peroxy (compound O-O-) or contain the compound of the element that is in its highest oxidation state by Hawley ' s Condensed Chemical Dictionary.The examples for compounds that contains at least one peroxy includes, but is not limited to hydrogen peroxide and adduct thereof, for example, and perhydrit and percarbonate (ester); Organic peroxide, for example, benzoyl peroxide, Peracetic acid and di-t-butyl peroxide; Single persulfate (monopersulfate, SO
5 2-), two persulfates (dipersulfate) (S
2O
8 2-) and sodium peroxide.The examples for compounds that contains the element that is in its highest oxidation state includes, but is not limited to periodic acid, periodates, perbromic acid, perbromate, crosses chloric acid, perchlorate, perboric acid, perborate and permanganate.Preferably, this oxidant is selected from complex salt (hydrogen peroxymonosulfate sulfate), molybdate, ferric nitrate, nitrate, quinone and the combination thereof of hydrogen peroxide, iodate, permanganate, persulfate (persulfate), peroxidating monosulfate and sulfate.More preferably, this oxidant is Potassiumiodate or hydrogen peroxide.
When oxidant was salt, this oxidant can have any suitable cation.Suitable cationic limiting examples comprises potassium, ammonium etc.
When oxidant was quinone, this oxidant can be any suitable quinone.The limiting examples of suitable quinone comprises benzoquinones, naphthoquinones and anthraquinone.Quinone can be replaced by any suitable substituents or substituent combination in any available position.Preferred substituted is included in the group of giving quinone dissolubility or emulsibility in the water of polishing composition.Suitable substituents includes, but is not limited to hydroxyl, amino, alkyl monosubstituted amino, dialkyl amido, sulfonic acid, carboxyl, phosphonic acids, its salt and combination thereof.In execution mode, quinone is replaced by at least one hydroxyl.In other embodiments, quinone is replaced by at least one acid substituting group or its salt.Preferably, this at least one acid substituting group is selected from sulfonic acid, carboxyl and phosphonic acids.More preferably, this at least one acid substituting group is sulfonic acid (SO
3H).Should understand acid substituting group and can form salt, and have acid substituent quinone in this and can be used as acid, salt and exist, perhaps replace or can be used as part salt (for example single salt of disulfonic acid) existence when polysubstituted when two.Have acid substituent quinone can sour form or salt form provide to be used for polishing composition of the present invention.Preferred anthraquinone is selected from anthraquinone-2,6-disulfonic acid, anthraquinone-2-sulfonic acid, anthraquinone-1,8-disulfonic acid, anthraquinone-1,5-disulfonic acid, acid blue 45, its salt and combination thereof.Preferred benzoquinones comprises 1,4-benzoquinones and 2,5-dihydroxy-1,4-benzoquinones.Preferred naphthoquinones comprises 1,2-naphthoquinones-4-sulfonic acid and salt thereof.
The concentration of the oxidant in the polishing composition of polishing system desirably is 1mM or bigger (for example, 2mM or bigger, or 3mM or bigger, or 5mM or bigger).The concentration of oxidant is preferably 1M or littler (for example, 0.5M or littler, or 0.25M or littler, or 0.1M or littler) in the polishing composition.The desired concn of oxidant can obtain by any suitable method, for example by using in water and dissolving in the preparation of polishing composition or being suspended in the oxidant of 0.05 weight % to 20 weight % of the weight of any component wherein.
Polishing system have a pH value of 8 to 12.Preferably, the pH value of polishing system is 8 to 11, more preferably 9 to 11.The pH value of polishing system can and/or be kept by any suitable method acquisition.More specifically, polishing system can further comprise pH value conditioning agent, pH value buffer or its combination.The aqueous solution that obtain by dissolve silicates glass (for example alkali silicate) or the water-soluble silicate compound by the preparation of hydrothermal solution method has 11 or bigger strong basicity pH value, and its salt by highly basic and weak acid is formed.If need, then can come the M of the strong alkali solution of acidifying water-soluble silicate compound by the acid of adding capacity with the existing abundance that neutralizes
2O is obtaining required pH value, thus the pH value of regulating polishing system.PH value conditioning agent can be any suitable pH value and regulates compound.For example, pH value conditioning agent can be enough strong to produce any suitable acid of required final pH value.The embodiment of suitable acid comprises nitric acid, acetate, phosphoric acid etc.If need, then can increase the pH value by adding highly basic.The example of highly basic comprises potassium hydroxide, ammonium hydroxide and tetraalkylammonium hydroxide (for example tetramethyl ammonium hydroxide).
PH value buffer can be any suitable reducing, for example, and phosphate, acetate, borate, ammonium salt etc.When using buffer to regulate the pH value of polishing system, the buffer that should understand abundance adds in the polishing system with the sufficient M that neutralizes
2O, thus required pH value is provided.Polishing system can comprise the pH value conditioning agent and/or the pH value buffer of any suitable amount, as long as such amount is enough to obtain and/or maintain the pH value of the polishing system in the listed scope of this paper.
The pH value that can regulate polishing system in any suitable time.For example, can in the polishing composition that water-soluble silicate compound is added to polishing system as described herein, regulate the pH value in the back.Also the water-soluble silicate compound of aequum can be added in the polishing composition, wherein this polishing composition comprises the pH value conditioning agent and/or the pH value buffer of capacity, makes water-soluble silicate compound and polishing composition are being mixed fully the required pH value of back acquisition.In other embodiments, in the pH value of using point (point-of-use) surface of substrate (for example) to regulate polishing system.
Polishing system randomly comprises corrosion inhibitor (being film forming agent).Corrosion inhibitor can be any suitable corrosion inhibitor of any parts that are used for substrate.Preferably, corrosion inhibitor is a copper corrosion inhibitor.For purposes of the present invention, corrosion inhibitor is any compound of the formation that promotes passivation layer (that is, dissolving suppresses layer) at least a portion at polished surface just or the mixture of compound.Useful corrosion inhibitor comprises, for example, and nitrogen-containing heterocycle compound.Corrosion inhibitor desirably comprises one or more 5 yuan or 6 yuan of heterocycles and contains azo-cycle.Preferred corrosion inhibitor comprises 1,2,3-triazoles, 1,2,4-triazole, BTA, benzimidazole, benzothiazole and derivative thereof, for example, it is through hydroxyl, amino, imino group, carboxyl, sulfydryl, nitro, urea, thiocarbamide or alkyl-substituted derivatives.Most preferably, this corrosion inhibitor is selected from BTA, 1,2,3-triazoles, 1,2, the 4-triazole, and composition thereof.Polishing system of the present invention can comprise the corrosion inhibitor of any suitable amount.Usually, the polishing composition of polishing system comprises the corrosion inhibitor of 0.005 weight % to 1 weight % (for example, 0.01 weight % to 0.5 weight %, or 0.02 weight % to 0.2 weight %).
Polishing system randomly further comprises one or more other additive.Such additive comprises any suitable surfactant and/or rheology control agent.Suitable surfactant comprises, for example, and cationic surfactant, anion surfactant, anionic polyelectrolyte, nonionic surface active agent, amphoteric surfactant, fluorinated surfactant, its mixture etc.
Polishing system randomly further comprises defoamer.This defoamer can be any suitable defoamer.Suitable defoamer includes, but is not limited to based on silicon and based on the defoamer of acetylenic glycols.The amount of the defoamer that exists in the polishing composition of polishing system is generally 40ppm to 140ppm.
Polishing system randomly further comprises biocide.This biocide can be any suitable biocide, for example OIT biocide.The amount that is used in the biocide in the polishing system is generally 1ppm to 500ppm, and is preferably 10ppm to 200ppm.
The polishing composition of polishing system can be by the preparation of any suitable technique, and wherein many are well known by persons skilled in the art.Polishing composition can intermittence or continuation method preparation.Usually, this polishing composition can be by preparing its component with any sequential combination.Term as used herein " component " comprises any combination of independent composition (for example, grinding agent, water-soluble silicate compound etc.) and composition (for example, grinding agent, water-soluble silicate compound, oxidant etc.).
The polishing composition of polishing system also can be used as concentrate and provides, and this concentrate is intended to before use with an amount of water dilution.In such execution mode, the polishing composition concentrate can comprise grinding agent, water-soluble silicate compound, oxidant and water, its amount makes that each component of polishing composition will be present in the polishing composition the described amount in proper range of each component with above after diluting concentrate with an amount of water.For example, grinding agent, water-soluble silicate compound and oxidant can respectively think above to 2 times of the described concentration of each component (for example, 3 times, 4 times or 5 times) amount be present in the concentrate, make and (for example work as with isopyknic water, use 2 times of isopyknic water, 3 times of isopyknic water or 4 times of isopyknic water respectively) dilution is during concentrate, and each component can be present in the polishing composition with the amount in the above scope listed to each component.In addition, should understand as those of ordinary skills, this concentrate can contain the water that is present in the appropriate fraction in the final polishing composition, is dissolved in this concentrate at least in part or fully to guarantee water-soluble silicate compound, oxidant and other suitable additive.
Being used for any component of the present invention can provide at the mixture of water or the form of solution.Two or more components desirably store separately and mix subsequently to form the polishing composition of polishing system then.In this, preparation polishing composition (for example, all components being mixed), it is suitable being sent to substrate surface then.Prepare polishing composition at substrate surface, by sending the component from the polishing composition of two or more separate sources, to converge on substrate surface (for example use point) also be suitable to these components of polishing composition thus.In either case, before polishing processing or the component that in polishing processing, all can change polishing composition be sent to substrate surface flow velocity (promptly, the conveying capacity of the specific components of polishing composition), make polishing system the polishing characteristic for example polishing speed change.
Polishing composition can be used as the single packaging system that comprises water-soluble silicate compound, oxidant and water and provides.Perhaps, water-soluble silicate compound and water can be provided in first container, and oxidant can dried forms or be provided in second container as solution or dispersion in water.Can be with optional component, for example grinding agent, surfactant and/or corrosion inhibitor place first and/or second container, or in the 3rd container.In addition, the component in first or second container can be dried forms, and the component in the corresponding container can be water-borne dispersions or solution form simultaneously.In addition, the component in first or second container has different pH values, perhaps have similar or even the pH value that equates be suitable.If optional component for example grinding agent is a solid, then it can dried forms or provides as the mixture in water.Desirably, other component of oxidant and polishing composition provides respectively, and by for example final user with other component of itself and polishing composition soon before use (for example, 1 week or shorter time, 1 day before use or shorter time, 1 hour before use or shorter time, 10 minutes before use or shorter time or 1 minute before use or shorter time) before use merge.In the ken that is combined in those of ordinary skills of the component of other two containers or three or more containers, polishing composition.
Though the component of the polishing composition of polishing system can be before use or even combination well soon before use, can use point or use near the component of the merging polishing composition point.As used herein, term " use point " is meant polishing composition and the contacted point of substrate surface.When using point to merge the component of polishing composition, the component of polishing composition is stored in respectively in two or more storage facilitiess.
In order to use point or to use near the component of mixing the polishing composition that is contained in the storage facilities point, storage facilities provides one or more usually and leads to the fluid line (flow line) of the use point (for example, workbench (platen) or substrate surface) of polishing composition from each storage facilities.Term " fluid line " is meant the path of the fluid of the use point from independent reservoir vessel to the component that wherein stores.Described one or more fluid line can directly lead to the use point separately, and perhaps, under situation about using more than a fluid line, two or more fluid lines can be merged into the single fluid line that uses point that leads at any point.In addition, any described one or more fluid line (for example, the independent fluid line or the fluid line of merging) all can before the use point that arrives component, at first lead to one or more miscellaneous equipments (for example, pumping equipment, measuring equipment, mixing apparatus etc.).
The component of polishing composition can be sent to independently uses point (for example, in polishing processing, these components are sent to substrate surface, these components are mixed at substrate surface), and perhaps these components can be sent to the merging not long ago of use point.If these components arrive to use point merge in preceding 10 seconds, preferably arrive use point merge in preceding 5 seconds, more preferably arrive use point to merge in preceding 1 second or even merging is (for example when component is sent to use, these components merge in distributor), then these components " being sent to the use point not long ago " merge.If these components are within the 5m that uses point, for example, within the 1m that uses point or even using that (for example, within the 1cm that uses point) merges within the 10cm of point, then these components also are that " using point not long ago being sent to " merges.
When two or more components of the polishing composition of polishing system arrive when merging before using point, these components can merge and be sent to use and not use mixing apparatus in fluid line.Perhaps, one or more fluid line can lead in the mixing apparatus to promote the merging of two or more components.Can use any suitable mixing apparatus.For example, this mixing apparatus can be two or more components through its nozzle that flows through or spout (for example high pressure nozzle or spout).Perhaps, this mixing apparatus can be the container type mixing apparatus that comprises one or more inlets and at least one outlet, wherein two or more components of polishing composition are introduced blender via described inlet, and the component through mixing is left blender by this at least one outlet and directly or via other element (for example, via one or more fluid line) that installs is sent to the use point.In addition, mixing apparatus can comprise the chamber more than, and each chamber has at least one inlet and at least one outlet, and wherein two or more components merge in each chamber.If use the container type mixing apparatus, then this mixing apparatus preferably comprises the merging of mixing machinery device (mixing mechanism) with further promotion component.The mixing machinery device is widely known by the people in the art, and comprises blender, blender, agitator, vane-type baffle (paddled baffle), gas distributor (gas sparger) system, vibrator etc.
The present invention further provides a kind of method of using polishing system polishing substrate as herein described.The method of described polishing substrate comprises: substrate is contacted with aforementioned polishing system, and (ii) wear and tear or at least a portion of removing substrate with polishing substrate.
Particularly, the inventive method may further comprise the steps: (i) make substrate and comprise the polishing component, be enough to provide 0.1 weight % or more SiO
2Oxidant, and the chemical-mechanical polishing system contact of water of at least a portion of water-soluble silicate compound, oxidase substrate of amount, wherein the pH value of this polishing system is 8 to 12, at least a portion that reaches the substrate that (ii) weares and teares is with polishing substrate.
According to the present invention, substrate can polish with polishing system as herein described by any suitable technique.Method of the present invention especially is fit to use with chemico-mechanical polishing (CMP) device.Usually, this device comprises the polishing pad that is in the motion and moves with workbench when having by the workbench of track, linearity or the speed that circular motion caused, with the workbench contact and when being in motion in, reaches and fixedly treat by contacting with the surface of polishing pad and with respect to moving and the clamper (carrier) of the substrate that polishes on the surface of polishing pad when using.The polishing of substrate is carried out by the following method: substrate is placed to polishing system of the present invention contacts, and polishing pad is moved with respect to substrate, other component that polishing system is arranged therebetween is with wearing and tearing and remove the part of substrate, with at least a portion of polishing substrate.
This substrate can be any suitable substrate that can polish by method of the present invention.This substrate (for example can comprise metal, copper, tantalum, aluminium, titanium, molybdenum etc.), metal alloy (for example, stainless steel, cobalt-chromium etc.), semiconductor (for example, gallium nitride, GaAs etc.), the pottery (for example, carborundum), polymer (for example, Merlon), optical material (for example, sapphire, zinc sulphide, zinc selenide etc.), diamond and insulating material.
This substrate can comprise any suitable microelectronic substrate (for example, integrated circuit, metal, ILD layer, semiconductor, film, MEMS, magnetic head), and can further comprise any suitable insulation, metal or metal alloy layer (for example, metal conducting layer).Preferably, this metal level comprises tantalum.More preferably, this substrate further comprises the metal level of cupric.This insulating barrier can be metal oxide, porous metal oxide, glass, organic polymer, fluoridizes organic polymer or any other suitable high or low k insulating barrier.It is 3.5 or lower dielectric material that this insulating barrier preferably comprises dielectric constant.
The example of low-k (promptly low k dielectric) material include, but is not limited to flourine deped silicon dioxide, for example carbon doped silicon dioxide (CDO) through organically-modified silex glass, fluorocarbons, and for example fluoridize or without the organic material of Parylene of fluoridizing and polyimides.Low k dielectric can be porous or non-porous.The example of porous low dielectric material is porous silica structure, low temperature depositing silicon-carbon film, the low temperature depositing Si-O-C film of porous hydrogen silsesquioxane (hydrosilsequioxane) or porous methyl silsesquioxane, for example aeroge and the porous silica that is doped with methyl.Preferably, this insulating barrier is through organically-modified silex glass or carbon doped silicon dioxide.
Advantageously, polishing system of the present invention allows to reduce the coefficient of friction relevant with the chemico-mechanical polishing of substrate, keeps acceptable polishing speed simultaneously.
Desirably, the CMP device further comprises the original position polishing endpoint detection system, many being well known in the art wherein.Be well known in the art from the light of the surface reflection of substrate or the technology that other radiation detected and monitored polishing process by analysis.Desirably, the detection or the monitoring of the process of the polishing process of the substrate that polishing made it possible to determine polishing end point, promptly determine when particular substrate is stopped polishing process.
Littler embodiment progress explanation the present invention limits category of the present invention by any way but should not be construed as certainly.
Embodiment
This embodiment proof is using the inventive method polishing to comprise reducing of observed coefficient of friction in the substrate of tantalum.
The similar substrate that comprises the 250nm tantalum layer with different polishing composition (polishing composition A and B) polishing.Each polishing composition A and B all contain ceria that the pH value is 11 0.5 weight % in water and the Potassiumiodate of 0.20 weight %.Polishing composition B further contains the potassium silicate of 3 weight %.
This substrate uses polyurethane polishing pad to use following burnishing parameters polishing 60 seconds on Logitech Model CDP polishing machine: substrate is 13.8kPa (2psi) with respect to the downforce of polishing pad, rotating speed of table is 66rpm, the clamper rotating speed is 70rpm, the polishing composition flow velocity is 160mL/min, and uses polyurethane polishing pad.After the polishing, use resistivity measurements to measure and remove speed.
Relation between displacement by clamper axle in the polishing operation process and the power that produced by the friction between polishing pad and the substrate is determined coefficient of friction.With reference to figure 1, the clamper axle (30) that will be electrically connected to the contiguous polishing machine of non-contact capacitive displacement transducer (10) (40) of recording equipment (20) is placed, and has gap (50) therebetween.The displacement of the caused clamper axle of power F (60) that is caused by the frictional force that produces in the polishing process of substrate causes the change of the output voltage of transducer.Obtain calibration curve by the measuring transducer output voltage as the function that is applied to the known force of clamper axle in direction perpendicular to the central shaft of clamper axle.Use the average output voltage in 60 seconds polishing times to determine the polishing experiments process, to be applied to the mean force F of clamper axle from calibration curve
aFrom equation μ=F
a/ P is by power F
aAnd substrate (80) calculates coefficientoffriction with respect to the downforce (70) of polishing pad P (90).These the results are shown in the following table.
Table: potassium silicate removes the influence of speed to coefficient of friction and tantalum
Can find out that as the result from list in this table it is about 20% to exist the potassium silicate of 3 weight % to cause comprising in polishing composition of the present invention to observe in the polishing of substrate of tantalum layer coefficient of friction to reduce, tantalum removes speed and only reduces about 12% simultaneously.Therefore, the result of this embodiment proof can realize that friction reduces by polishing composition of the present invention and method.
Claims (33)
1. chemical-mechanical polishing system that is used for polishing substrate, it comprises:
(a) the polishing component that is selected from polishing pad, grinding agent and makes up,
(b) water-soluble silicate compound presents in an amount at least sufficient to provide 0.1 weight % or more SiO
2,
(c) oxidant of at least a portion of oxidase substrate, and
(d) water,
Wherein the pH value of this polishing system is 8 to 12.
2. the polishing system of claim 1, wherein this water-soluble silicate compound is selected from potassium silicate, sodium metasilicate, potassium metasilicate and sodium metasilicate.
3. the polishing system of claim 2, wherein this water-soluble silicate compound is a potassium silicate.
4. the polishing system of claim 3, wherein this potassium silicate is to be enough to provide 0.25 weight % or more SiO
2Amount exist.
5. the polishing system of claim 3, the wherein SiO of this potassium silicate
2: K
2The O mol ratio is 2.8 to 3.9.
6. the polishing system of claim 5, the wherein SiO of this potassium silicate
2: K
2The O mol ratio is 3 to 3.6.
7. the polishing system of claim 1, wherein this oxidant is selected from complex salt (hydrogenperoxymonosulfate sulfate), molybdate, ferric nitrate, nitrate, quinone and the combination thereof of hydrogen peroxide, iodate, permanganate, persulfate, peroxidating monosulfate and sulfate.
8. the polishing system of claim 1, wherein this polishing system further comprises grinding agent, and wherein this grinding agent suspends in water.
9. the polishing system of claim 8, wherein this grinding agent is selected from aluminium oxide, ceria, silicon dioxide, zirconia and combination thereof.
10. the polishing system of claim 1, wherein this polishing system comprises polishing pad and grinding agent, and wherein this grinding agent is fixed on this polishing pad.
11. the polishing system of claim 1, wherein this water-soluble silicate compound exists with 0.5 weight % or bigger amount.
12. the polishing system of claim 1, wherein this pH value is 9 to 11.
13. the method that substrate is carried out chemico-mechanical polishing, this method comprises:
(i) substrate is contacted with chemical-mechanical polishing system, this chemical-mechanical polishing system comprises:
(a) the polishing component that is selected from polishing pad, grinding agent and makes up,
(b) water-soluble silicate compound presents in an amount at least sufficient to provide 0.1 weight % or more SiO
2,
(c) oxidant of at least a portion of oxidase substrate, and
(d) water, and
(ii) wear and tear at least a portion of this substrate polishing this substrate,
Wherein the pH value of this polishing system is 8 to 12.
14. the method for claim 13, wherein this water-soluble silicate compound is selected from potassium silicate, sodium metasilicate, potassium metasilicate and sodium metasilicate.
15. the method for claim 14, wherein this water-soluble silicate compound is a potassium silicate.
16. the method for claim 15, wherein this potassium silicate is to be enough to provide 0.25 weight % or more SiO
2Amount exist.
17. the method for claim 15, the wherein SiO of this potassium silicate
2: K
2The O mol ratio is 2.8 to 3.9.
18. the method for claim 17, the wherein SiO of this potassium silicate
2: K
2The O mol ratio is 3 to 3.6.
19. the method for claim 13, wherein this oxidant is selected from complex salt, molybdate, ferric nitrate, nitrate, quinone and the combination thereof of hydrogen peroxide, iodate, permanganate, persulfate, peroxidating monosulfate and sulfate.
20. the method for claim 13, wherein this polishing system further comprises grinding agent, and wherein this grinding agent suspends in water.
21. the method for claim 20, wherein this grinding agent is selected from aluminium oxide, ceria, silicon dioxide, zirconia and combination thereof.
22. the method for claim 13, wherein this polishing system comprises polishing pad and grinding agent, and wherein this grinding agent is fixed on this polishing pad.
23. the method for claim 13, wherein this water-soluble silicate compound exists with 0.5 weight % or bigger amount.
24. the method for claim 13, wherein this pH value is 9 to 11.
25. the method for claim 13, wherein this substrate comprises metal level.
26. the method for claim 25, wherein this metal level comprises tantalum.
27. the method for claim 26, wherein this metal level further comprises copper.
28. the method for claim 13, wherein to comprise dielectric constant be 3.5 or lower dielectric layer to this substrate.
29. the method for claim 28, wherein this dielectric layer is through organically-modified silex glass.
30. the method for claim 28, wherein this dielectric layer is a carbon doped silicon dioxide.
31. the method for claim 28, wherein this substrate further comprises metal level.
32. the method for claim 31, wherein this metal level comprises tantalum.
33. the method for claim 32, wherein this metal level further comprises copper.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/287,039 US20070117497A1 (en) | 2005-11-22 | 2005-11-22 | Friction reducing aid for CMP |
US11/287,039 | 2005-11-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN101313388A true CN101313388A (en) | 2008-11-26 |
Family
ID=38054171
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNA2006800437962A Pending CN101313388A (en) | 2005-11-22 | 2006-10-24 | Friction reducing aid for cmp |
Country Status (6)
Country | Link |
---|---|
US (1) | US20070117497A1 (en) |
JP (1) | JP2009516928A (en) |
KR (1) | KR20080070675A (en) |
CN (1) | CN101313388A (en) |
TW (1) | TWI311091B (en) |
WO (1) | WO2007149113A2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110358454A (en) * | 2019-07-20 | 2019-10-22 | 大连理工大学 | A kind of general chemistry machine polishing liquor |
CN113423799A (en) * | 2019-10-03 | 2021-09-21 | 日产化学株式会社 | Polishing composition containing cation for eliminating swelling around laser mark |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8162723B2 (en) * | 2006-03-09 | 2012-04-24 | Cabot Microelectronics Corporation | Method of polishing a tungsten carbide surface |
EP2527309B1 (en) * | 2011-05-24 | 2016-08-03 | Rohm and Haas Company | Improved quality multi-spectral zinc sulfide |
SG11201403556WA (en) * | 2011-12-28 | 2014-07-30 | Advanced Tech Materials | Compositions and methods for selectively etching titanium nitride |
CN102775916B (en) * | 2012-07-16 | 2015-01-07 | 芜湖海森材料科技有限公司 | Polishing composition for improving surface quality of sapphire |
US9259818B2 (en) * | 2012-11-06 | 2016-02-16 | Sinmat, Inc. | Smooth diamond surfaces and CMP method for forming |
JP6007094B2 (en) * | 2012-12-18 | 2016-10-12 | 花王株式会社 | Polishing liquid composition for sapphire plate |
US20150360340A1 (en) * | 2013-01-04 | 2015-12-17 | Fujimi Incorporated | Method for polishing alloy material and method for manufacturing alloy material |
SG11201506102TA (en) * | 2013-02-28 | 2015-09-29 | Fujimi Inc | Polishing slurry for cobalt removal |
US9633831B2 (en) * | 2013-08-26 | 2017-04-25 | Rohm And Haas Electronic Materials Cmp Holdings, Inc. | Chemical mechanical polishing composition for polishing a sapphire surface and methods of using same |
CN103589344B (en) * | 2013-11-14 | 2015-06-10 | 上海新安纳电子科技有限公司 | Method for preparing alumina polishing solution |
JPWO2016043089A1 (en) * | 2014-09-16 | 2017-08-10 | 山口精研工業株式会社 | Abrasive composition for sapphire substrate |
KR102447178B1 (en) | 2015-09-01 | 2022-09-26 | 삼성전자주식회사 | Methods of manufacturing semiconductor devices |
WO2017142885A1 (en) * | 2016-02-16 | 2017-08-24 | Cabot Microelectronics Corporation | Method of polishing group iii-v materials |
US10253216B2 (en) | 2016-07-01 | 2019-04-09 | Versum Materials Us, Llc | Additives for barrier chemical mechanical planarization |
DE102017110198A1 (en) * | 2017-05-11 | 2018-11-15 | Walter Maschinenbau Gmbh | Grinding and / or EDM machine and method for measuring and / or referencing the machine |
JP7071495B2 (en) | 2017-11-15 | 2022-05-19 | サン-ゴバン セラミックス アンド プラスティクス,インコーポレイティド | Compositions for performing material removal operations and methods for forming them |
US11879094B2 (en) | 2022-06-03 | 2024-01-23 | Halliburton Energy Services, Inc. | Enhancing friction reduction and protection of wellbore equipment during hydraulic fracturing |
Family Cites Families (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2710997C3 (en) * | 1977-03-14 | 1980-08-14 | Dr. Karl Thomae Gmbh, 7950 Biberach | 4-Alkoxy carbonylamino-phenylethanolamines, their production and their use as pharmaceuticals |
JPH0228112A (en) * | 1988-04-21 | 1990-01-30 | Kaken Pharmaceut Co Ltd | Intraocular tension regulator for instillation |
US5352277A (en) * | 1988-12-12 | 1994-10-04 | E. I. Du Pont De Nemours & Company | Final polishing composition |
DE3902753A1 (en) * | 1989-01-31 | 1990-08-02 | Henkel Kgaa | METHOD FOR THE HYDROTHERMAL PRODUCTION OF POTASSIUM SILICATE SOLUTIONS WITH HIGH SI0 (DOWN ARROW) 2 (DOWN ARROW): K (DOWN ARROW) 2 (DOWN ARROW) 0-MOLE RATIO |
DE3938789A1 (en) * | 1989-11-23 | 1991-05-29 | Henkel Kgaa | METHOD FOR THE HYDROTHERMAL PRODUCTION OF POTASSIUM SILICATE SOLUTIONS |
DE19643592A1 (en) * | 1996-10-22 | 1998-04-23 | Bayer Ag | Process for the preparation of alpha-alkoxy-alpha-trifluoromethyl-arylacetic acid esters and -arylacetic acids |
SG54606A1 (en) * | 1996-12-05 | 1998-11-16 | Fujimi Inc | Polishing composition |
AU7147798A (en) * | 1997-04-23 | 1998-11-13 | Advanced Chemical Systems International, Inc. | Planarization compositions for cmp of interlayer dielectrics |
TW593331B (en) * | 1997-07-25 | 2004-06-21 | Inspire Pharmaceuticals Inc | Method for large-scale production of di(uridine 5')-tetraphosphate and salts thereof |
US6051605A (en) * | 1997-08-08 | 2000-04-18 | Warner-Lambert Company | Method of treating psychosis and schizophrenia |
JPH11140427A (en) * | 1997-11-13 | 1999-05-25 | Kobe Steel Ltd | Polishing liquid and polishing |
CO5070714A1 (en) * | 1998-03-06 | 2001-08-28 | Nalco Chemical Co | PROCESS FOR THE PREPARATION OF STABLE COLOIDAL SILICE |
US6217416B1 (en) * | 1998-06-26 | 2001-04-17 | Cabot Microelectronics Corporation | Chemical mechanical polishing slurry useful for copper/tantalum substrates |
US6276996B1 (en) * | 1998-11-10 | 2001-08-21 | Micron Technology, Inc. | Copper chemical-mechanical polishing process using a fixed abrasive polishing pad and a copper layer chemical-mechanical polishing solution specifically adapted for chemical-mechanical polishing with a fixed abrasive pad |
JP3941284B2 (en) * | 1999-04-13 | 2007-07-04 | 株式会社日立製作所 | Polishing method |
WO2001046195A1 (en) * | 1999-12-21 | 2001-06-28 | Gpi Nil Holdings, Inc. | Hydantoin derivative compounds, pharmaceutical compositions, and methods of using same |
US6602117B1 (en) * | 2000-08-30 | 2003-08-05 | Micron Technology, Inc. | Slurry for use with fixed-abrasive polishing pads in polishing semiconductor device conductive structures that include copper and tungsten and polishing methods |
US6551935B1 (en) * | 2000-08-31 | 2003-04-22 | Micron Technology, Inc. | Slurry for use in polishing semiconductor device conductive structures that include copper and tungsten and polishing methods |
US6709316B1 (en) * | 2000-10-27 | 2004-03-23 | Applied Materials, Inc. | Method and apparatus for two-step barrier layer polishing |
US20030032078A1 (en) * | 2001-01-23 | 2003-02-13 | Board Of Regents, The University Of Texas System | Methods and compositions for the treatment of macular and retinal degenerations |
JP3945745B2 (en) * | 2001-03-09 | 2007-07-18 | 三井金属鉱業株式会社 | Cerium-based abrasive and abrasive slurry and method for producing cerium-based abrasive |
US6656241B1 (en) * | 2001-06-14 | 2003-12-02 | Ppg Industries Ohio, Inc. | Silica-based slurry |
US6800218B2 (en) * | 2001-08-23 | 2004-10-05 | Advanced Technology Materials, Inc. | Abrasive free formulations for chemical mechanical polishing of copper and associated materials and method of using same |
JP4008219B2 (en) * | 2001-09-27 | 2007-11-14 | 触媒化成工業株式会社 | Abrasive |
JP4278020B2 (en) * | 2001-10-30 | 2009-06-10 | 日揮触媒化成株式会社 | Abrasive particles and method for producing abrasives |
PA8557501A1 (en) * | 2001-11-12 | 2003-06-30 | Pfizer Prod Inc | BENZAMIDA, HETEROARILAMIDA AND INVESTED AMIDAS |
US6685755B2 (en) * | 2001-11-21 | 2004-02-03 | Saint-Gobain Abrasives Technology Company | Porous abrasive tool and method for making the same |
US6827639B2 (en) * | 2002-03-27 | 2004-12-07 | Catalysts & Chemicals Industries Co., Ltd. | Polishing particles and a polishing agent |
US6913517B2 (en) * | 2002-05-23 | 2005-07-05 | Cabot Microelectronics Corporation | Microporous polishing pads |
JP2004128112A (en) * | 2002-10-01 | 2004-04-22 | Renesas Technology Corp | Manufacturing method of semiconductor device |
US20060281821A1 (en) * | 2003-03-14 | 2006-12-14 | Krzysztof Palczewski | Retinoid replacements and opsin agonists and methods for the use thereof |
JP2005007520A (en) * | 2003-06-19 | 2005-01-13 | Nihon Micro Coating Co Ltd | Abrasive pad, manufacturing method thereof, and grinding method thereof |
US7485241B2 (en) * | 2003-09-11 | 2009-02-03 | Cabot Microelectronics Corporation | Chemical-mechanical polishing composition and method for using the same |
US20050136670A1 (en) * | 2003-12-19 | 2005-06-23 | Ameen Joseph G. | Compositions and methods for controlled polishing of copper |
US7566808B2 (en) * | 2004-02-17 | 2009-07-28 | President And Fellows Of Harvard College | Management of ophthalmologic disorders, including macular degeneration |
US20060252107A1 (en) * | 2005-02-22 | 2006-11-09 | Acucela, Inc. | Compositions and methods for diagnosing and treating retinal diseases |
US20070039926A1 (en) * | 2005-08-17 | 2007-02-22 | Cabot Microelectronics Corporation | Abrasive-free polishing system |
-
2005
- 2005-11-22 US US11/287,039 patent/US20070117497A1/en not_active Abandoned
-
2006
- 2006-10-24 WO PCT/US2006/041420 patent/WO2007149113A2/en active Application Filing
- 2006-10-24 JP JP2008542318A patent/JP2009516928A/en active Pending
- 2006-10-24 CN CNA2006800437962A patent/CN101313388A/en active Pending
- 2006-10-24 KR KR1020087012131A patent/KR20080070675A/en not_active Application Discontinuation
- 2006-11-08 TW TW095141357A patent/TWI311091B/en not_active IP Right Cessation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110358454A (en) * | 2019-07-20 | 2019-10-22 | 大连理工大学 | A kind of general chemistry machine polishing liquor |
CN113423799A (en) * | 2019-10-03 | 2021-09-21 | 日产化学株式会社 | Polishing composition containing cation for eliminating swelling around laser mark |
Also Published As
Publication number | Publication date |
---|---|
WO2007149113A3 (en) | 2008-04-10 |
JP2009516928A (en) | 2009-04-23 |
TW200734117A (en) | 2007-09-16 |
KR20080070675A (en) | 2008-07-30 |
WO2007149113A9 (en) | 2008-02-28 |
US20070117497A1 (en) | 2007-05-24 |
WO2007149113A2 (en) | 2007-12-27 |
TWI311091B (en) | 2009-06-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101313388A (en) | Friction reducing aid for cmp | |
TWI251020B (en) | Silica and silica-based slurry | |
CN101356628B (en) | High throughput chemical mechanical polishing composition for metal film planarization | |
KR101330956B1 (en) | Polishing solution for cmp and polishing method | |
EP3049216B1 (en) | Chemical-mechanical planarization of polymer films | |
KR101378259B1 (en) | Silicon oxide polishing method utilizing colloidal silica | |
KR101325333B1 (en) | Rate-enhanced cmp compositions for dielectric films | |
JP2004502860A (en) | Ready-to-use stable chemical mechanical polishing slurry | |
TW200300442A (en) | Chemical mechanical polishing compositions | |
WO2004063301A1 (en) | Composition and method used for chemical mechanical planarization of metals | |
JP5144516B2 (en) | Polishing system without abrasives | |
TW201726883A (en) | Polishing composition and polishing method using same, and method for producing an object intended to be and has been polished using polishing composition and polishing method | |
WO2012165016A1 (en) | Cmp polishing liquid and method of polishing semiconductor substrate | |
CN103831706B (en) | A kind of CMP process | |
TWI662096B (en) | Cmp compositions selective for oxide and nitride with improved dishing and pattern selectivity | |
JP6551053B2 (en) | Polishing liquid for CMP and polishing method using the same | |
CN111378367A (en) | Chemical mechanical polishing solution | |
Kim et al. | Acid colloidal silica slurry for Cu CMP |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination |