JPH09137155A - Polishing composition and polishing method - Google Patents
Polishing composition and polishing methodInfo
- Publication number
- JPH09137155A JPH09137155A JP32223595A JP32223595A JPH09137155A JP H09137155 A JPH09137155 A JP H09137155A JP 32223595 A JP32223595 A JP 32223595A JP 32223595 A JP32223595 A JP 32223595A JP H09137155 A JPH09137155 A JP H09137155A
- Authority
- JP
- Japan
- Prior art keywords
- polishing
- reducing agent
- polishing composition
- composition according
- reducing
- 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 title claims abstract description 141
- 239000000203 mixture Substances 0.000 title claims description 63
- 238000000034 method Methods 0.000 title description 25
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 62
- 239000002245 particle Substances 0.000 claims abstract description 27
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 25
- 230000001603 reducing effect Effects 0.000 claims abstract description 25
- 239000004065 semiconductor Substances 0.000 claims abstract description 14
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 13
- 239000010703 silicon Substances 0.000 claims abstract description 13
- 229910052814 silicon oxide Inorganic materials 0.000 claims abstract description 13
- 239000000758 substrate Substances 0.000 claims abstract description 12
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims abstract description 10
- 150000001299 aldehydes Chemical class 0.000 claims abstract description 9
- 150000001412 amines Chemical class 0.000 claims abstract description 8
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000003513 alkali Substances 0.000 claims abstract description 6
- CMCWWLVWPDLCRM-UHFFFAOYSA-N phenidone Chemical compound N1C(=O)CCN1C1=CC=CC=C1 CMCWWLVWPDLCRM-UHFFFAOYSA-N 0.000 claims abstract description 4
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims abstract description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 35
- 150000001875 compounds Chemical class 0.000 claims description 25
- 239000010419 fine particle Substances 0.000 claims description 23
- 239000007864 aqueous solution Substances 0.000 claims description 17
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 16
- 229940024606 amino acid Drugs 0.000 claims description 14
- 150000001413 amino acids Chemical class 0.000 claims description 14
- -1 alkali metal salt Chemical class 0.000 claims description 8
- 229910021529 ammonia Inorganic materials 0.000 claims description 8
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 8
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 6
- 239000000243 solution Substances 0.000 claims description 6
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 5
- ZVNPWFOVUDMGRP-UHFFFAOYSA-N 4-methylaminophenol sulfate Chemical compound OS(O)(=O)=O.CNC1=CC=C(O)C=C1.CNC1=CC=C(O)C=C1 ZVNPWFOVUDMGRP-UHFFFAOYSA-N 0.000 claims description 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims description 4
- XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 claims description 4
- 150000003863 ammonium salts Chemical class 0.000 claims description 4
- WHUUTDBJXJRKMK-UHFFFAOYSA-N glutamic acid Chemical compound OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 claims description 4
- PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 claims description 3
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 claims description 3
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 claims description 3
- 239000004473 Threonine Substances 0.000 claims description 3
- 239000004471 Glycine Substances 0.000 claims description 2
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 2
- UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical compound NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 claims 2
- WRUZLCLJULHLEY-UHFFFAOYSA-N N-(p-hydroxyphenyl)glycine Chemical compound OC(=O)CNC1=CC=C(O)C=C1 WRUZLCLJULHLEY-UHFFFAOYSA-N 0.000 claims 1
- 229940000635 beta-alanine Drugs 0.000 claims 1
- 125000000687 hydroquinonyl group Chemical group C1(O)=C(C=C(O)C=C1)* 0.000 claims 1
- 238000007517 polishing process Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 16
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 13
- 239000000463 material Substances 0.000 abstract description 7
- 239000010408 film Substances 0.000 description 42
- 239000003002 pH adjusting agent Substances 0.000 description 11
- 235000001014 amino acid Nutrition 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 239000006185 dispersion Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 230000001737 promoting effect Effects 0.000 description 8
- 239000006061 abrasive grain Substances 0.000 description 7
- 239000011229 interlayer Substances 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
- AZFNGPAYDKGCRB-XCPIVNJJSA-M [(1s,2s)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1-methyl-4-propan-2-ylbenzene Chemical compound [Ru+]Cl.CC(C)C1=CC=C(C)C=C1.C1=CC(C)=CC=C1S(=O)(=O)[N-][C@@H](C=1C=CC=CC=1)[C@@H](N)C1=CC=CC=C1 AZFNGPAYDKGCRB-XCPIVNJJSA-M 0.000 description 4
- 229910000420 cerium oxide Inorganic materials 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 4
- 235000010289 potassium nitrite Nutrition 0.000 description 4
- 239000004304 potassium nitrite Substances 0.000 description 4
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 4
- 238000005229 chemical vapour deposition Methods 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000010979 pH adjustment Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 2
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 235000004279 alanine Nutrition 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229960002989 glutamic acid Drugs 0.000 description 2
- 235000013922 glutamic acid Nutrition 0.000 description 2
- 239000004220 glutamic acid Substances 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 238000009775 high-speed stirring Methods 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- 235000008521 threonine Nutrition 0.000 description 2
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- WFCQTAXSWSWIHS-UHFFFAOYSA-N 4-[bis(4-hydroxyphenyl)methyl]phenol Chemical compound C1=CC(O)=CC=C1C(C=1C=CC(O)=CC=1)C1=CC=C(O)C=C1 WFCQTAXSWSWIHS-UHFFFAOYSA-N 0.000 description 1
- JVVRCYWZTJLJSG-UHFFFAOYSA-N 4-dimethylaminophenol Chemical compound CN(C)C1=CC=C(O)C=C1 JVVRCYWZTJLJSG-UHFFFAOYSA-N 0.000 description 1
- LJCWONGJFPCTTL-UHFFFAOYSA-N 4-hydroxyphenylglycine Chemical compound OC(=O)C(N)C1=CC=C(O)C=C1 LJCWONGJFPCTTL-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 1
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- YGYBNQXFTUQBME-UHFFFAOYSA-N OC=1C(=C(C=CC1)O)N(CC)CC Chemical compound OC=1C(=C(C=CC1)O)N(CC)CC YGYBNQXFTUQBME-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 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
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229910001593 boehmite Inorganic materials 0.000 description 1
- 239000005380 borophosphosilicate glass Substances 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 150000001720 carbohydrates Chemical class 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
- 239000011248 coating agent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229960003067 cystine Drugs 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FAHBNUUHRFUEAI-UHFFFAOYSA-M hydroxidooxidoaluminium Chemical compound O[Al]=O FAHBNUUHRFUEAI-UHFFFAOYSA-M 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 238000001459 lithography Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 239000012788 optical film Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001709 polysilazane Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
- 235000019252 potassium sulphite Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003405 preventing effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 239000011863 silicon-based powder Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Landscapes
- Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)
- Mechanical Treatment Of Semiconductor (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は研磨用組成物および
研磨方法に係り、特に、半導体基板上に形成されたケイ
素またはケイ素酸化膜の研磨において、研磨表面の性状
を損うことなく効率よく研磨し得る研磨用組成物および
研磨方法に関する。TECHNICAL FIELD The present invention relates to a polishing composition and a polishing method, and particularly to polishing a silicon or silicon oxide film formed on a semiconductor substrate efficiently without damaging the properties of the polishing surface. The present invention relates to a polishing composition and a polishing method.
【0002】[0002]
【従来の技術】半導体装置の製造分野においては、通
常、金属シリコン等の半導体基板上に、不純物拡散、エ
ッチング、配線形成、該配線上への層間絶縁膜(ケイ素
膜、ケイ素酸化膜等)の形成等、多数の工程を繰り返し
て配線を積み上げていく。このためシリコン基板上に複
雑な回路(パターン)が形成され、このパターン形状に
基づき凹凸が発生する。2. Description of the Related Art In the field of manufacturing semiconductor devices, usually, on a semiconductor substrate such as metal silicon, impurity diffusion, etching, wiring formation, and interlayer insulating film (silicon film, silicon oxide film, etc.) on the wiring are formed. A number of steps such as formation are repeated to stack the wiring. Therefore, a complicated circuit (pattern) is formed on the silicon substrate, and irregularities are generated based on this pattern shape.
【0003】特に近年、LSI、超LSI等の電子部品
における高密度化、高精度化がますます進み、凹凸の程
度が次第に激しくなる傾向にある。そのため、ホトリソ
グラフィー法によるパターニングの際、これら凹凸によ
る段差が露光時の焦点深度の限界を超えてしまうという
状況が発生し、これを防ぐために、リソグラフィやエッ
チングを適用する過程におけるある段階で、例えば上述
した層間絶縁膜(下地)等をあらかじめ十分に平坦化
し、できるだけ凹凸部の段差を小さくする技術が重要と
なっている。In particular, in recent years, the density and precision of electronic parts such as LSI and VLSI have become higher and higher, and the degree of unevenness tends to become more and more severe. Therefore, when patterning by the photolithography method, a situation in which the step due to these irregularities exceeds the limit of the depth of focus during exposure occurs, and in order to prevent this, at some stage in the process of applying lithography or etching, for example, It is important to have a technique in which the above-described interlayer insulating film (base) is sufficiently flattened in advance to reduce the step of the uneven portion as much as possible.
【0004】上記の平坦化の方法としては、リフトオフ
法、エッチバック法、SOG(スピン・オン・ガラス)
法など多種提案されているが、その1つとして化学機械
研磨(CMP:chemical mechanical polishing )法が
ある。このCMP法によれば、例えばアルミ配線上へC
VD(化学蒸着法)等で層間絶縁膜(ケイ素酸化膜等)
の厚膜を形成した後、表面凸部をCMP用の研磨剤で研
磨し、全体を平坦化する。Lift-off method, etch-back method, SOG (spin-on-glass) is used as the above-mentioned planarization method.
Although various methods such as a method have been proposed, one of them is a chemical mechanical polishing (CMP) method. According to this CMP method, for example, C
Interlayer insulation film (silicon oxide film, etc.) by VD (chemical vapor deposition), etc.
After forming the thick film, the surface protrusions are polished with a polishing agent for CMP to flatten the entire surface.
【0005】そしてこのCMP用の研磨剤として、シリ
コン基板製造時における鏡面研磨に使用されてきた金属
シリコン研磨用スラリーを、上記絶縁膜の研磨にも応用
しているのが現状であるが、絶縁膜の研磨には必ずしも
適するものではなかった。As a polishing agent for this CMP, the metal silicon polishing slurry that has been used for mirror polishing during the production of silicon substrates is currently applied to the above-mentioned insulating film polishing. It was not always suitable for polishing a film.
【0006】例えば、上記金属シリコン研磨用スラリー
としては、砥粒(研磨材微粒子)をアルカリ(水酸化ナ
トリウム等)水溶液に分散したものが使用されていた
が、これを絶縁膜の研磨に適用すると、研磨効率が悪
く、スループットが低いという問題があった。研磨効率
を上げる手段としては、砥粒の粒径を大きくする、硬度
の高い砥粒を使用する、または強アルカリにも溶解しな
い砥粒を使い、pH値の高い研磨用組成物を用いる等の
方法が考えられる。しかしながら、粒径の大きい砥粒や
硬い砥粒を用いると、研磨表面にスクラッチ、オレンジ
ピール等の欠陥が生じるなどの問題があり、一方、強ア
ルカリ性の研磨用組成物では汚染対策の面から必ずしも
実用的ではなかった。For example, as the above-mentioned metal silicon polishing slurry, abrasive grains (abrasive fine particles) dispersed in an alkali (sodium hydroxide or the like) aqueous solution have been used. When this is applied to the polishing of an insulating film, However, there is a problem that polishing efficiency is poor and throughput is low. As means for increasing the polishing efficiency, such as increasing the grain size of the abrasive grains, using abrasive grains with high hardness, or using abrasive grains that do not dissolve in strong alkali and using a polishing composition with a high pH value, etc. A method can be considered. However, when using abrasive grains having a large particle diameter or hard abrasive grains, there are problems such as scratches on the polishing surface, defects such as orange peel, and the like, while in the case of a strongly alkaline polishing composition, it is not always possible to prevent contamination. It wasn't practical.
【0007】特開平2−158682号公報、特開平2
−158683号公報等には、研磨表面の性状が劣化す
ることなく、研磨効率を向上させる方法として添加剤
(研磨促進剤)を含有した研磨用組成物が報告されてい
る。これらは水にα−アルミナ砥粒を分散させた組成物
に、研磨促進剤として金属の亜硝酸塩や、ベーマイト、
無機酸または有機酸のアンモニウム塩を添加したもので
あるが、該研磨用組成物は酸性または中性にpH調整さ
れているため、アルミニウムなどの金属部分を研磨する
には適するが、ケイ素酸化膜等の絶縁膜を研磨する場合
には研磨速度が遅く実用的ではない。Japanese Unexamined Patent Publication Nos. 2-158682 and 2
JP-A-158683 reports a polishing composition containing an additive (polishing accelerator) as a method for improving polishing efficiency without deteriorating the properties of the polishing surface. These are a composition in which α-alumina abrasive grains are dispersed in water, a metal nitrite as a polishing accelerator, and boehmite,
Although an ammonium salt of an inorganic acid or an organic acid is added, the polishing composition has a pH adjusted to be acidic or neutral, and therefore is suitable for polishing a metal part such as aluminum. When polishing an insulating film such as, the polishing rate is low and not practical.
【0008】[0008]
【発明が解決しようとする課題】本発明は上記事情に鑑
みてなされたもので、その課題は、特に半導体基板上の
層間絶縁膜等の研磨表面の性状を損なうことなく、効率
よく研磨し得る研磨用組成物およびこれを用いた研磨方
法を提供することにある。SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and the problem is that polishing can be performed efficiently without damaging the properties of the polishing surface such as an interlayer insulating film on a semiconductor substrate. An object is to provide a polishing composition and a polishing method using the same.
【0009】[0009]
【課題を解決するための手段】本発明者は、上記課題を
解決するために鋭意研究を重ねた結果、特に半導体装置
の層間絶縁膜等の研磨において、アルカリ水溶液に研磨
材微粒子と還元性物質を含有させ、これを研磨剤組成物
として用いることにより、上記課題を解決し得るという
知見を得、これに基づいて本発明を完成するに至った。As a result of intensive studies to solve the above problems, the present inventor has found that in the polishing of interlayer insulating films of semiconductor devices, fine abrasive particles and reducing substances are added to an alkaline aqueous solution. The present invention was completed based on the finding that the above problems can be solved by containing the above-mentioned substance and using it as an abrasive composition.
【0010】すなわち本発明は、アルカリ側にpH調整
された水溶液に、研磨材微粒子と、研磨促進剤として還
元性を有する化合物を含有してなる研磨用組成物を提供
するものである。That is, the present invention provides a polishing composition comprising fine particles of an abrasive and a compound having a reducing property as a polishing accelerator in an aqueous solution whose pH is adjusted to the alkaline side.
【0011】また本発明は、上記研磨用組成物を用い
て、半導体基板上に形成されたケイ素またはケイ素酸化
膜を研磨する、研磨方法を提供するものである。The present invention also provides a polishing method for polishing a silicon or silicon oxide film formed on a semiconductor substrate using the above polishing composition.
【0012】[0012]
【発明の実施の形態】以下に本発明について詳細に説明
する。BEST MODE FOR CARRYING OUT THE INVENTION The present invention will be described in detail below.
【0013】本発明に用いられる研磨材微粒子は、一般
に半導体装置等の研磨剤組成物に用いられ得るものであ
れば、特に制限されることなく使用することができる。
具体的には、酸化アルミニウム(Al2 O3 )、酸化ケ
イ素(SiO2 )、酸化ジルコニウム(ZrO2 )、酸
化セリウム(CeO2 )等が挙げられる。中でも、汚染
を嫌う半導体にあって、膜厚1μm前後の薄膜を精密に
研磨するのに適するものとして、酸化ケイ素、酸化セリ
ウムが特に好ましい。The fine abrasive particles used in the present invention can be used without particular limitation as long as they can be generally used in an abrasive composition for semiconductor devices and the like.
Specific examples thereof include aluminum oxide (Al 2 O 3 ), silicon oxide (SiO 2 ), zirconium oxide (ZrO 2 ), and cerium oxide (CeO 2 ). Among them, silicon oxide and cerium oxide are particularly preferable as a material suitable for precisely polishing a thin film having a thickness of about 1 μm in a semiconductor which does not like contamination.
【0014】これら研磨材微粒子は常法により得ること
ができる。例えば、酸化ケイ素微粒子としては、焼成シ
リカゲルを粉砕分球したもの、イオン交換法で作ったケ
イ酸溶液をアルカリ条件下で成長させたいわゆるシリカ
ゾル、金属ケイ素粉末を高温酸化させたもの、四塩化ケ
イ素を高温加水分解させたもの、ケイ酸エチルを加水分
解させたもの等、種々の製法により得ることができる
が、これらいずれの方法により得られたものでも特に限
定されることなく用いることができる。These fine abrasive particles can be obtained by a conventional method. For example, as the silicon oxide fine particles, those obtained by pulverizing and calcining calcined silica gel, so-called silica sols obtained by growing a silicic acid solution prepared by an ion exchange method under alkaline conditions, those obtained by high-temperature oxidation of metal silicon powder, and silicon tetrachloride are used. It can be obtained by various production methods such as high-temperature hydrolyzed product, ethyl silicate hydrolyzed product, etc., and any of these methods can be used without particular limitation.
【0015】研磨材微粒子の粒径は、大きいと研磨速度
は速いが沈殿しやすくなり、一方、小さいと研磨速度が
遅くなり増粘あるいは凝集しやすい傾向を示すことか
ら、用いる研磨材微粒子の種類によっても異なるが、一
般に0.01〜5μmが好ましく、特には0.01〜
0.1μmが好ましい。酸化セリウム微粒子は、特に高
速度での研磨を要求する場合に向いており、粒径0.0
5〜1μm程度のものが好ましい。If the particle size of the abrasive fine particles is large, the polishing rate is high but the particles tend to precipitate. On the other hand, if the particle size is small, the polishing rate is slow and the particles tend to thicken or aggregate. Generally, 0.01 to 5 μm is preferable, but 0.01 to 5 μm is particularly preferable.
0.1 μm is preferred. The cerium oxide fine particles are suitable especially when polishing at a high speed is required, and have a particle size of 0.0
It is preferably about 5 to 1 μm.
【0016】研磨材微粒子は、ある程度まで濃度を上げ
ることにより被研磨材との接点が増加し研磨速度の向上
が望めるが、反面、小さい粒子における表面活性の増加
のため粘度の上昇などがあり、研磨速度の低下を引き起
こす。また研磨速度と研磨材微粒子濃度との関係は、研
磨に使用するパッドや研磨圧力、スピード等によっても
変化する。したがって、研磨材微粒子の含有量はこれら
の総合的条件で決めることが必要であって一義的に最適
な濃度範囲は決められないが、一般に研磨用組成物に対
して2〜50重量%程度含有させるのが好ましく、特に
は2〜20重量%である。By increasing the concentration of the abrasive fine particles to a certain degree, the number of contact points with the material to be abraded increases and the polishing rate can be expected to be improved. Causes a decrease in polishing rate. Further, the relationship between the polishing rate and the concentration of fine particles of the polishing material changes depending on the pad used for polishing, the polishing pressure, the speed, and the like. Therefore, it is necessary to determine the content of the abrasive fine particles under these comprehensive conditions, and the optimum concentration range cannot be uniquely determined. However, the content of the abrasive fine particles is generally about 2 to 50% by weight based on the polishing composition. It is preferable that the amount is 2 to 20% by weight.
【0017】本発明の研磨用組成物では、研磨材微粒子
を安定に分散させるため、また絶縁膜の化学的研磨、具
体的には研磨促進効果、研磨面の仕上り向上のため、ア
ルカリ側にpH調整されている必要がある。この目的の
ために通常、pH調整剤が使用される。pH調整剤とし
ては水酸化ナトリウム、水酸化カリウム、アンモニア、
ヒドラジン、ヒドロキシルアミン、モノメチルアミン等
が例示される。研磨効果の点からいえば水酸化カリウ
ム、アンモニアが特に好ましい。半導体の分野では配線
不良等の原因となる金属による汚染を特に嫌うため、こ
の点からいえば非金属化合物のアルカリ(例えばアンモ
ニア等)が好適に用いられる。したがってpH調整剤は
研磨の目的に合わせて選択することが望ましい。In the polishing composition of the present invention, in order to stably disperse the abrasive fine particles, and to chemically polish the insulating film, specifically, to enhance the polishing effect and improve the finish of the polished surface, the pH of the alkaline side is increased. Must be adjusted. A pH adjuster is usually used for this purpose. As pH adjusters, sodium hydroxide, potassium hydroxide, ammonia,
Examples thereof include hydrazine, hydroxylamine, monomethylamine and the like. From the viewpoint of polishing effect, potassium hydroxide and ammonia are particularly preferable. In the field of semiconductors, metal contamination that causes wiring defects is particularly disliked. From this point, a non-metal compound alkali (eg, ammonia) is preferably used. Therefore, it is desirable to select the pH adjusting agent according to the purpose of polishing.
【0018】これらpH調整剤は、研磨用組成物のpH
が8〜11、好ましくは9.5〜10.5の範囲になる
ように添加される。pHが8未満では研磨材微粒子を安
定に分散させることが難しく、一方、pHが11超では
十分な研磨効果が得られ難い。具体的には、例えば研磨
材微粒子に酸化ケイ素(シリカ)粒子を用いた場合、p
Hが7(中性)付近であるとシリカ粒子の増粘が著し
く、粒子の分散安定性が損なわれ、一方、pHが11を
超えると、シリカ粒子がケイ酸塩を作り溶液中に溶解し
てしまうため機械的研磨効果が失われるという問題があ
るpH調整剤による研磨促進効果としては、硬めの、ま
た粒径が大きめの研磨材微粒子を用いた場合には、これ
ら微粒子自体による機械的研磨の速度が大きいため、p
H調整剤を入れたことによる相対的な研磨速度の大幅な
増加はないが、研磨後の絶縁膜表面の性状に優れる。These pH adjusters are used to adjust the pH of the polishing composition.
Is added in a range of 8 to 11, preferably 9.5 to 10.5. When the pH is less than 8, it is difficult to stably disperse the abrasive fine particles, and when the pH is more than 11, it is difficult to obtain a sufficient polishing effect. Specifically, for example, when silicon oxide (silica) particles are used as abrasive fine particles, p
When H is around 7 (neutral), the silica particles are remarkably thickened and the dispersion stability of the particles is impaired. On the other hand, when the pH exceeds 11, the silica particles form a silicate and are dissolved in the solution. There is a problem that the mechanical polishing effect is lost because the polishing agent has a problem of promoting the polishing by the pH adjusting agent. In the case of using abrasive fine particles which are harder and have a larger particle size, mechanical polishing by the fine particles themselves is used. Because the speed of
Although the relative polishing rate is not significantly increased by adding the H-adjusting agent, the properties of the insulating film surface after polishing are excellent.
【0019】本発明組成物では、研磨促進剤として還元
性を有する化合物が用いられる。ここで「還元性を有す
る化合物」とは、他の物質を還元し自らは酸化される物
質を意味する。本発明では、この還元性を有する物質と
して無機系、有機系の還元剤や、グルコース等の糖類な
どが適用可能である。上記有機系の還元剤として、好ま
しくはアルデヒド類系還元剤、ヒドロキシフェニル系還
元剤およびアミン系還元剤の中から選ばれる少なくとも
1種が用いられる。In the composition of the present invention, a compound having a reducing property is used as a polishing accelerator. Here, the “compound having a reducing property” means a substance that reduces another substance and is itself oxidized. In the present invention, an inorganic or organic reducing agent, a saccharide such as glucose, or the like can be applied as the reducing substance. As the organic reducing agent, at least one selected from aldehyde reducing agents, hydroxyphenyl reducing agents and amine reducing agents is preferably used.
【0020】特に無機系還元剤は還元力が強く、研磨促
進効果に優れる点で好ましく、該無機系還元剤と、アル
デヒド類系還元剤、ヒドロキシフェニル系還元剤および
アミン系の中から選ばれる少なくとも1種との混合物が
より好適に用いられる。Particularly, the inorganic reducing agent is preferable in that it has a strong reducing power and an excellent polishing promoting effect, and at least it is selected from the inorganic reducing agent, an aldehyde type reducing agent, a hydroxyphenyl type reducing agent and an amine type. A mixture with one is more preferably used.
【0021】ここで無機系還元剤は、具体的には亜硫
酸、亜硝酸および亜リン酸またはこれらのアルカリ金属
塩若しくはアンモニウム塩のほか、塩化錫、塩化鉄等の
第一金属ハロゲン化物、その他亜塩素酸等が例示され
る。なお、上記アルカリ金属塩としては、具体的にはカ
リウム塩、ナトリウム塩、リチウム塩等が挙げられる。Here, the inorganic reducing agent is specifically sulfurous acid, nitrous acid and phosphorous acid, or their alkali metal salts or ammonium salts, as well as first metal halides such as tin chloride and iron chloride, and other submetals. Examples include chloric acid and the like. Specific examples of the alkali metal salt include potassium salt, sodium salt, lithium salt and the like.
【0022】アルデヒド類系還元剤は、具体的にはホル
ムアルデヒド、アセトアルデヒド、グルタルアルデヒ
ド、グリオキサール等が例示される。Specific examples of the aldehyde-based reducing agent include formaldehyde, acetaldehyde, glutaraldehyde, glyoxal and the like.
【0023】ヒドロキシフェニル系還元剤は、具体的に
はカテコール、p−ヒドロキシフェニルグリシン、4−
アミノフェノール、2,4−ジアミノフェノール、p−
ヒドロキシジエチルアミノフェノール、p−ジメチルア
ミノフェノール、p−メチルアミノフェノールサルフェ
ート、ヒドロキノン、トリスフェノール系化合物〔例え
ば、トリス(4−ヒドロキシフェニル)メタン等)等が
例示される。The hydroxyphenyl-based reducing agent is specifically catechol, p-hydroxyphenylglycine, 4-
Aminophenol, 2,4-diaminophenol, p-
Examples thereof include hydroxydiethylaminophenol, p-dimethylaminophenol, p-methylaminophenol sulfate, hydroquinone, and trisphenol compounds (eg, tris (4-hydroxyphenyl) methane).
【0024】アミン系還元剤は、具体的には1−フェニ
ル−3−ピラゾリジン、テトラメチルエチレンジアミ
ン、アスコルビン酸、ヒドロキシアミン、メチルアミ
ン、p−フェニレンジアミン等が例示される。Specific examples of the amine-based reducing agent include 1-phenyl-3-pyrazolidine, tetramethylethylenediamine, ascorbic acid, hydroxyamine, methylamine and p-phenylenediamine.
【0025】本発明に用いられる還元性を有する化合物
として好適なものは、用いるpH調整剤によっても異な
り、例えば、pH調整剤として水酸化カリウム、水酸化
ナトリウム等を用いた場合は、亜硝酸または亜硫酸のア
ルカリ金属塩、ヒドロキノン等が好ましく、pH調整剤
としてアンモニアを用いた場合は、亜硫酸または亜硝酸
のアンモニウム塩、p−メチルアミノフェノールサルフ
ェート等が好ましく用いられる。Suitable reducing compounds for use in the present invention differ depending on the pH adjusting agent used. For example, when potassium hydroxide, sodium hydroxide or the like is used as the pH adjusting agent, nitrous acid or Alkali metal salts of sulfurous acid, hydroquinone and the like are preferable, and when ammonia is used as a pH adjuster, ammonium salts of sulfurous acid or nitrous acid, p-methylaminophenol sulfate and the like are preferably used.
【0026】還元性を有する化合物は、単独で用いても
よく、あるいは2種以上を混合して用いてもよく、研磨
用組成物の研磨促進効果、その他の総合的効果を向上さ
せる点では混合系が好ましい。例えば、p−メチルアミ
ノフェノールサルフェート、ヒドロキノン等のヒドロキ
シフェニル系の還元剤を用いた研磨用組成物は、保存中
に変色することがあるが、亜硫酸塩等の無機系還元剤を
混合使用することにより、変色防止効果と研磨促進効果
の両者を向上せしめることができる。The reducing compounds may be used alone or as a mixture of two or more kinds, and they are mixed from the viewpoint of improving the polishing promoting effect of the polishing composition and other overall effects. Systems are preferred. For example, a polishing composition using a hydroxyphenyl-based reducing agent such as p-methylaminophenol sulfate and hydroquinone may be discolored during storage, but an inorganic reducing agent such as sulfite should be mixed and used. As a result, both the discoloration preventing effect and the polishing promoting effect can be improved.
【0027】これら還元性を有する化合物は、研磨用組
成物1kgに対し0.001〜0.5モルの割合で配合
されるのが好ましく、より好ましくは0.01〜0.1
モル、特には0.03モル程度である。0.001モル
未満では、研磨促進効果が十分に発現せず、一方、0.
5モルを超えると研磨材微粒子の凝集が起こりやすく、
粘度の上昇をきたすため分散安定性が損なわれる。さら
にパッドと被研磨体の間への研磨用組成物の供給が不十
分となり、研磨にばらつきが生じる等の問題がある。2
種以上の還元剤を混合して用いる場合、それぞれの混合
割合は特に限定されるものではなく、それらの合計量が
上記範囲内となるようにすればよいが、無機系還元剤1
モルに対してその他の還元剤が0.1〜10モル、特に
は1〜2モルとなるように混合するのが研磨促進効果の
点で特に好ましい。These reducing compounds are preferably added in a proportion of 0.001 to 0.5 mol, more preferably 0.01 to 0.1, relative to 1 kg of the polishing composition.
It is about mol, particularly about 0.03 mol. If it is less than 0.001 mol, the polishing promoting effect is not sufficiently exhibited, while on the other hand, it is less than 0.
If it exceeds 5 moles, agglomeration of abrasive fine particles easily occurs,
Since the viscosity is increased, the dispersion stability is impaired. Further, there is a problem that the polishing composition is insufficiently supplied between the pad and the object to be polished, resulting in uneven polishing. 2
When a mixture of two or more reducing agents is used, the mixing ratio of each is not particularly limited, and the total amount thereof may be set within the above range.
It is particularly preferable to mix the other reducing agent in an amount of 0.1 to 10 mol, particularly 1 to 2 mol, based on mol, from the viewpoint of the polishing promoting effect.
【0028】本発明においては、上記還元性を有する化
合物に加えて、さらにアミノ酸を添加するのが好まし
い。これらアミノ酸として、例えばアラニン、グリシ
ン、チロシン、システィン、グルタミン酸、トレオニン
等が挙げられる。In the present invention, it is preferable to add an amino acid in addition to the above-mentioned reducing compound. Examples of these amino acids include alanine, glycine, tyrosine, cystine, glutamic acid, threonine and the like.
【0029】該アミノ酸の配合量は、研磨促進効果を十
分に発揮し、さらには安定した研磨用組成物の分散性を
得るには、研磨用組成物1kgに対し0.001〜0.
5モルの割合で配合されるのが好ましく、より好ましく
は0.01〜0.1モル、特には0.02モル程度であ
る。また、研磨効率の点で、特に無機系還元剤と混合し
て用いるのが好ましく、無機系還元剤1モルに対して
0.1〜10モル、特には1〜2モルが好ましい。The amount of the amino acid blended is 0.001 to 0.10 per 1 kg of the polishing composition in order to sufficiently exert the polishing promoting effect and to obtain stable dispersibility of the polishing composition.
It is preferably blended in a ratio of 5 mol, more preferably 0.01 to 0.1 mol, and especially about 0.02 mol. Further, in terms of polishing efficiency, it is particularly preferably used by mixing with an inorganic reducing agent, and 0.1 to 10 moles, particularly 1 to 2 moles are preferable relative to 1 mole of the inorganic reducing agent.
【0030】上記還元性を有する化合物およびアミノ酸
の組み合せとしては、無機系還元剤に対して、アルデヒ
ド系還元剤、ヒドロキシフェニル系還元剤またはアミノ
酸を組み合わせることが、研磨促進効果に優れ最も好ま
しい。具体的には、pH調整剤に水酸化カリウムを用い
た場合には、亜硫酸カリウムとヒドロキノンの組み合わ
せ、または亜硝酸カリウムとアラニン、トレオニン、グ
ルタミン酸の中から選ばれる少なくとも1種との組み合
わせが好適である。pH調整剤にアンモニアを用いた場
合には、亜硫酸アンモニウムとカテコール、1−フェニ
ル−3−ピラゾリドン、4−アミノフェノールまたは
2,4−ジアミノフェノールとの組み合せが好ましい。As the combination of the compound having reducing properties and the amino acid, it is most preferable to combine an inorganic reducing agent with an aldehyde reducing agent, a hydroxyphenyl reducing agent, or an amino acid because of excellent polishing promoting effect. Specifically, when potassium hydroxide is used as the pH adjuster, a combination of potassium sulfite and hydroquinone, or a combination of potassium nitrite and at least one selected from alanine, threonine and glutamic acid is preferable. . When ammonia is used as the pH adjuster, a combination of ammonium sulfite and catechol, 1-phenyl-3-pyrazolidone, 4-aminophenol or 2,4-diaminophenol is preferable.
【0031】これら還元剤の研磨促進効果は、pH調整
剤、および研磨材微粒子との組み合せにより異なり、特
にpH調整剤の塩基強度に対して特性は変化する。The polishing-promoting effect of these reducing agents differs depending on the combination with the pH adjusting agent and the abrasive fine particles, and in particular, the characteristics change with respect to the base strength of the pH adjusting agent.
【0032】本発明の研磨用組成物には、所望に応じて
殺菌剤、活性剤、分散安定のための水溶性化合物、ある
いは高分子化合物等を本発明の効果を損なわない範囲で
添加することができる。この場合、これらの化合物は上
記還元性を有する化合物との反応性が低いことが好まし
い。If desired, a bactericide, an activator, a water-soluble compound for stabilizing dispersion, or a polymer compound may be added to the polishing composition of the present invention within a range that does not impair the effects of the present invention. You can In this case, it is preferable that these compounds have low reactivity with the compound having the above-mentioned reducing property.
【0033】本発明の研磨用組成物は、例えば以下の方
法により調製することができる。The polishing composition of the present invention can be prepared, for example, by the following method.
【0034】まず、研磨材微粒子を水中に均一に分散さ
せる。研磨材微粒子が粉体の場合には、計量した水を高
速撹拌式ホモジナイザー等で撹拌しながらこれに分別し
た粉体を加えていくことにより均一に分散させる。分散
方法としては、サンドミル、ボールミル、ロールミル、
マイクロフリューダイザー等の公知の方法により行うこ
とができる。このとき、分散効率を上げるため、最終的
に含有される研磨材微粒子の濃度より高濃度(例えば3
0重量%以上)にしておくことが好ましい。First, fine abrasive particles are uniformly dispersed in water. In the case where the abrasive fine particles are powder, the measured powder of water is stirred by a high-speed stirring homogenizer or the like, and the separated powder is added thereto to uniformly disperse the powder. As a dispersion method, a sand mill, a ball mill, a roll mill,
It can be carried out by a known method such as Microfluidizer. At this time, in order to increase the dispersion efficiency, a concentration higher than the concentration of the abrasive fine particles finally contained (for example, 3
0 wt% or more) is preferable.
【0035】また研磨材微粒子が粉体ではなく、ケイ酸
水溶液をアルカリ条件下で加熱し合成されたシリカゾル
の場合、これらは既に均一に分散された形で市販されて
いるものがあるので、これをそのまま使用することがで
きる。Further, when the abrasive fine particles are not powders but silica sol synthesized by heating an aqueous solution of silicic acid under alkaline conditions, these are already commercially available in a uniformly dispersed form. Can be used as is.
【0036】その後、上記研磨材微粒子が均一に分散さ
れた液に、pH調整用のアルカリ水溶液を加える。この
とき、研磨用組成物は中和点付近で高粘度化し、撹拌し
づらくなるため、アルカリ水溶液中に、研磨材微粒子分
散液を加えていくやり方も好ましい。After that, an alkaline aqueous solution for pH adjustment is added to the liquid in which the fine abrasive particles are uniformly dispersed. At this time, the polishing composition becomes highly viscous near the neutralization point and becomes difficult to stir. Therefore, it is also preferable to add the fine abrasive particle dispersion to an alkaline aqueous solution.
【0037】次いで、還元性を有する化合物の水あるい
はアルカリ水溶液を加えた後、必要により他の添加物を
加え、次いで上記のpH調整用のアルカリ水溶液、また
は水を加え最終的な研磨材微粒子濃度(例えば12重量
%程度)、およびpH(例えばpH=10程度)に調整
することにより、最終的な研磨用組成物を得ることがで
きる。Next, after adding water or an alkaline aqueous solution of a reducing compound, if necessary, other additives are added, and then the above-mentioned alkaline aqueous solution for pH adjustment or water is added to obtain the final concentration of fine abrasive particles. The final polishing composition can be obtained by adjusting the pH (for example, about 12% by weight) and the pH (for example, pH = about 10).
【0038】このようにして得られた本発明の研磨用組
成物を用いて、半導体基板上に形成された層間絶縁膜
や、平坦化膜、表面保護膜等を研磨することができる。
これにより、これら被研磨体の表面の性状を変えること
なく、しかも研磨効率の向上した研磨方法が得られる。The thus obtained polishing composition of the present invention can be used to polish an interlayer insulating film, a flattening film, a surface protective film and the like formed on a semiconductor substrate.
As a result, a polishing method with improved polishing efficiency can be obtained without changing the surface properties of the objects to be polished.
【0039】本発明の研磨用組成物は、種々のケイ素
膜、ケイ素酸化膜やガラスの研磨などに好適に使用で
き、例えば、CVD法、スパッタ法、塗布法、熱酸化法
等の方法により形成された種々の酸化膜、例えばSiO
2 膜、有機SOG膜、PSG膜、BPSG膜、BSG
膜、Si3 N4 膜、ポリシラザン膜等を研磨するのに適
するが、これらに限られるものでない。The polishing composition of the present invention can be suitably used for polishing various silicon films, silicon oxide films and glass. For example, it is formed by a method such as a CVD method, a sputtering method, a coating method or a thermal oxidation method. Various oxide films such as SiO
2 films, organic SOG film, PSG film, BPSG film, BSG
It is suitable for polishing a film, a Si 3 N 4 film, a polysilazane film, etc., but is not limited to these.
【0040】本発明の研磨用組成物は、研磨促進剤とし
て還元性を有する化合物を用いているので、上記の種々
の酸化膜等を還元しながら物理的に効率よく研磨をする
ことができる。Since the polishing composition of the present invention uses a compound having a reducing property as a polishing accelerator, it can be physically and efficiently polished while reducing the above various oxide films and the like.
【0041】以下に本発明を実施例によりさらに詳細に
説明するが、本発明はこれによってなんら限定されるも
のではない。Hereinafter, the present invention will be described in more detail with reference to Examples, but the present invention is not limited thereto.
【0042】[0042]
(実施例1)粒径0.005〜0.05μmのヒューム
ドシリカ(「レオロシール CP−102」;徳山曹達
(株)製)3kgを純水7kgに分散し、次いで超音波
ホモジナイザー(US−150T;日本精機製作所
(株)製)を用いて、200g/5minで照射を行
い、濃度30重量%の研磨材分散液を調製した。(Example 1) 3 kg of fumed silica ("Roleoseal CP-102"; manufactured by Tokuyama Soda Co., Ltd.) having a particle diameter of 0.005 to 0.05 µm was dispersed in 7 kg of pure water, and then an ultrasonic homogenizer (US-150T) was used. Irradiation was carried out at 200 g / 5 min using Nippon Seiki Seisakusho Co., Ltd. to prepare an abrasive dispersion having a concentration of 30% by weight.
【0043】次いで、上記分散液に濃度10重量%水酸
化カリウム水溶液を加え、pH=10に調整し、これを
シリカ分散原液とした。Then, a 10 wt% aqueous potassium hydroxide solution was added to the above dispersion to adjust the pH to 10, and this was used as a silica dispersion stock solution.
【0044】次いで、還元剤として亜硝酸カリウム8.
5gを純水2kgに溶解した溶液に、上記のシリカ分散
原液2kgをかき混ぜながら混合し、さらに、上記の水
酸化カリウム水溶液、および純水を加え、希釈とpH調
整を繰り返し、pH=10.5、研磨材微粒子濃度12
重量%の研磨用組成物5kgを調製した。Then, potassium nitrite as a reducing agent 8.
A solution prepared by dissolving 5 g in 2 kg of pure water was mixed while stirring 2 kg of the above silica dispersion stock solution, and the above potassium hydroxide aqueous solution and pure water were added, and dilution and pH adjustment were repeated until pH = 10.5. , Abrasive particle concentration 12
5 kg of a polishing composition of wt% was prepared.
【0045】調製終了後、2μmの孔径を有するカート
リッジ型ろ過器によりろ過したものを評価用とした。こ
のとき還元剤の含有量は0.02モル/kgであった。After completion of the preparation, the product filtered by a cartridge type filter having a pore size of 2 μm was used for evaluation. At this time, the content of the reducing agent was 0.02 mol / kg.
【0046】CZ−P型のシリコンウェーハを熱酸化し
て1μm膜厚のケイ素酸化膜を形成したものを被研磨体
とした。A CZ-P type silicon wafer was thermally oxidized to form a silicon oxide film having a thickness of 1 μm, which was used as an object to be polished.
【0047】研磨定盤(パッド)に硬質発泡ウレタン
(「ケモメット−I」;ビューラー社製)を用い、調製
した上記研磨用組成物を50ml/minの速度で一定
量ずつ滴下し、2分間研磨を行った。被研磨体とパッド
との相対線速度48m/min、研磨圧力150g/c
m2 の条件で研磨を行った。Hard urethane foam ("Chemomet-I"; manufactured by Buehler) was used on a polishing platen (pad), and the above polishing composition prepared was dropped at a constant rate of 50 ml / min and polished for 2 minutes. I went. Relative linear velocity between the object to be polished and the pad 48 m / min, polishing pressure 150 g / c
Polishing was performed under the condition of m 2 .
【0048】研磨終了後、基板表面を純水で洗浄した
後、研磨速度、酸化膜表面の性状を下記基準により評価
した。結果を表1に示す。After the completion of polishing, the surface of the substrate was washed with pure water, and the polishing rate and the properties of the oxide film surface were evaluated according to the following criteria. Table 1 shows the results.
【0049】[研磨速度]研磨前後の酸化膜の膜厚の差
から、1分間あたりの研磨量を研磨速度として表示し
た。なお酸化膜の膜厚の測定は、エリプソメータによる
酸化膜表面の屈折率の測定結果から光学式膜厚測定機
(ナノスペック;ナノメトリック社製)を用いて行っ
た。[Polishing rate] From the difference in the thickness of the oxide film before and after polishing, the amount of polishing per minute was expressed as the polishing rate. The film thickness of the oxide film was measured using an optical film thickness meter (Nanospec; manufactured by Nanometric Co., Ltd.) based on the measurement result of the refractive index of the oxide film surface by an ellipsometer.
【0050】[酸化膜表面の性状]微分干渉型顕微鏡を
用いて研磨後の酸化膜表面のスクラッチ、オレンジピー
ル、曇りの状態について目視観察を行い、良好だったも
のを○、曇りなどがみられたものを×とした。[Properties of oxide film surface] A scratch, orange peel and cloudiness of the oxide film surface after polishing were visually observed using a differential interference microscope. The thing was marked as x.
【0051】(実施例2〜10)還元剤、アミノ酸の種
類および含有量を表1に示したとおりに代えた以外は、
実施例1と同様にして試験を行った。結果を表1に示
す。(Examples 2 to 10) Except that the type and content of the reducing agent and amino acid were changed as shown in Table 1,
The test was conducted in the same manner as in Example 1. Table 1 shows the results.
【0052】(比較例1)還元剤を用いなかった以外
は、実施例1と同様にして試験を行った。結果を表1に
示す。Comparative Example 1 A test was conducted in the same manner as in Example 1 except that no reducing agent was used. Table 1 shows the results.
【0053】[0053]
【表1】 (実施例11〜20)pH調整剤として、上記の水酸化
カリウムの代わりにアンモニアを用い、さらに還元剤の
種類および含有量を表2に示したとおりに代えた以外
は、実施例1と同様にして試験を行った。結果を表2に
示す。[Table 1] (Examples 11 to 20) As Example 1 except that ammonia was used as the pH adjuster instead of the above potassium hydroxide, and the type and content of the reducing agent were changed as shown in Table 2. Was tested. Table 2 shows the results.
【0054】(比較例2)還元剤を用いなかった以外
は、実施例11と同様にして試験を行った。結果を表2
に示す。Comparative Example 2 A test was conducted in the same manner as in Example 11 except that no reducing agent was used. Table 2 shows the results
Shown in
【0055】[0055]
【表2】 (実施例21)粒径0.01〜0.02μm、pH=
9.0〜10.5、研磨材微粒子濃度30重量%のシリ
カゾル(「アデライトAT−30」;旭電化工業(株)
製)1.33kgを、あらかじめ還元剤として亜硝酸カ
リウム3gとD,L−グルタミン酸6.6gとを純水に
溶解し、さらに10重量%水酸化カリウム水溶液により
pH=10に調整した溶液にかき混ぜながら混合した。[Table 2] Example 21 Particle size 0.01 to 0.02 μm, pH =
Silica sol with 9.0 to 10.5 and abrasive particle concentration of 30% by weight (“Adelite AT-30”; Asahi Denka Co., Ltd.)
1.33 kg of potassium nitrite as a reducing agent and 3 g of D, L-glutamic acid were dissolved in pure water in advance, and the mixture was further stirred into a solution adjusted to pH = 10 with a 10 wt% potassium hydroxide aqueous solution. Mixed.
【0056】その後、全重量が1.9kg、pH=1
0.3になるように上記水酸化カリウム水溶液、および
純水を加え調整を行った。Thereafter, the total weight is 1.9 kg and pH = 1.
The above potassium hydroxide aqueous solution and pure water were added to adjust the concentration to 0.3.
【0057】さらに1時間撹拌を続けた後、全重量が2
kgになるまで希釈を行い、pH=10.3、研磨材微
粒子濃度20重量%の研磨用組成物を調製した。このと
き還元剤とアミノ酸の合計含有量は0.04モル/kg
であった。After stirring for another hour, the total weight was 2
The mixture was diluted to kg to prepare a polishing composition having a pH of 10.3 and an abrasive fine particle concentration of 20% by weight. At this time, the total content of the reducing agent and the amino acid is 0.04 mol / kg.
Met.
【0058】シリコンウェーハ上に絶縁膜形成用塗布液
(OCD TYPE−10;東京応化工業(株)製)を
塗布し、N2 雰囲気中、400℃で30分間焼成し、酸
化膜を形成し、これを被研磨体とした。A coating liquid for forming an insulating film (OCD TYPE-10; manufactured by Tokyo Ohka Kogyo Co., Ltd.) was applied onto a silicon wafer and baked at 400 ° C. for 30 minutes in an N 2 atmosphere to form an oxide film. This was used as the object to be polished.
【0059】その後の操作、試験は実施例1と同様にし
て行った。評価結果を表3に示す。Subsequent operations and tests were carried out in the same manner as in Example 1. Table 3 shows the evaluation results.
【0060】(実施例22〜26)還元剤、アミノ酸の
種類および含有量を表3に示したとおりに代えた以外
は、実施例1と同様にして試験を行った。結果を表3に
示す。(Examples 22 to 26) Tests were carried out in the same manner as in Example 1 except that the types and contents of reducing agents and amino acids were changed as shown in Table 3. Table 3 shows the results.
【0061】(比較例3)還元剤、アミノ酸を用いなか
った以外は、実施例21と同様にして試験を行った。結
果を表3に示す。(Comparative Example 3) A test was conducted in the same manner as in Example 21 except that the reducing agent and the amino acid were not used. Table 3 shows the results.
【0062】[0062]
【表3】 (実施例27)粒径0.7μmの酸化セリウム(「ルミ
ノックス E101」;セイミケミカル(株)製)1k
gを純水3kgに加え、次いで高速撹拌型ホモミキサー
(「TKホモミキサー 16A」;特殊機械工業(株)
製)により6000rpmで20分間分散を行った。[Table 3] (Example 27) Cerium oxide having a particle size of 0.7 μm (“Luminox E101”; manufactured by Seimi Chemical Co., Ltd.) 1k
g to 3 kg of pure water, and then a high-speed stirring homomixer (“TK homomixer 16A”; Tokushu Kikai Kogyo Co., Ltd.)
Manufactured by K.K.) for 20 minutes at 6000 rpm.
【0063】次いで、100gの純水に亜硝酸カリウム
21.3gを溶解した溶液を加え、さらに、10重量%
の水酸化カリウム水溶液、および純水を加えpH=1
0.0、研磨材微粒子濃度20重量%の研磨用組成物5
kgを調製した。この時還元剤の含有量は0.05モル
/kgであった。Then, a solution prepared by dissolving 21.3 g of potassium nitrite in 100 g of pure water was added, and further 10% by weight was added.
PH of 1 by adding aqueous potassium hydroxide solution and pure water
0.0, Abrasive fine particle concentration 20% by weight, polishing composition 5
kg was prepared. At this time, the content of the reducing agent was 0.05 mol / kg.
【0064】その後の操作、試験は実施例1と同様にし
て行った。結果を表4に示す。Subsequent operations and tests were carried out in the same manner as in Example 1. Table 4 shows the results.
【0065】(実施例28)還元剤、アミノ酸の種類お
よび含有量を表4に示したとおりに代えた以外は、実施
例27と同様にして試験を行った。結果を表4に示す。Example 28 A test was conducted in the same manner as in Example 27, except that the types and contents of reducing agent and amino acid were changed as shown in Table 4. Table 4 shows the results.
【0066】(比較例4)還元剤を用いなかった以外
は、実施例27と同様にして試験を行った。結果を表4
に示す。Comparative Example 4 A test was conducted in the same manner as in Example 27 except that no reducing agent was used. Table 4 shows the results
Shown in
【0067】[0067]
【表4】 表1〜4から明らかなように、還元剤を添加した場合は
研磨速度、表面の性状が優れ、特に無機系還元剤と他の
還元剤との混合系を用いた場合においては還元剤を添加
しなかった場合に比べて研磨速度が向上し、場合によっ
ては2倍以上の効果を奏するものもあった。[Table 4] As is clear from Tables 1 to 4, when a reducing agent is added, the polishing rate and surface properties are excellent, and especially when a mixed system of an inorganic reducing agent and another reducing agent is used, the reducing agent is added. The polishing rate was improved as compared with the case where it was not performed, and in some cases, the effect was more than doubled.
【0068】[0068]
【発明の効果】以上詳述したように本発明によれば、研
磨材微粒子が分散されたアルカリ水溶液に還元性の化合
物を添加することにより、半導体基板上に形成された層
間絶縁膜等の被研磨体の研磨表面の性状を損なうことな
く、効率的に研磨することができる。As described in detail above, according to the present invention, by adding a reducing compound to an alkaline aqueous solution in which fine abrasive particles are dispersed, a covering material such as an interlayer insulating film formed on a semiconductor substrate can be obtained. The polishing can be efficiently performed without damaging the properties of the polishing surface of the polishing body.
Claims (19)
に、研磨材微粒子と、研磨促進剤として還元性を有する
化合物を含有してなる、研磨用組成物。1. A polishing composition comprising abrasive fine particles and a reducing compound as a polishing accelerator in an aqueous solution whose pH is adjusted to the alkaline side.
剤、アルデヒド類系還元剤、ヒドロキシフェニル系還元
剤およびアミン系還元剤の中から選ばれる少なくとも1
種である、請求項1に記載の研磨用組成物。2. The reducing compound is at least one selected from an inorganic reducing agent, an aldehyde reducing agent, a hydroxyphenyl reducing agent, and an amine reducing agent.
The polishing composition according to claim 1, which is a seed.
と、アルデヒド類系還元剤、ヒドロキシフェニル系還元
剤およびアミン系還元剤の中から選ばれる少なくとも1
種との混合物である、請求項2に記載の研磨用組成物。3. The reducing compound is at least one selected from an inorganic reducing agent, an aldehyde reducing agent, a hydroxyphenyl reducing agent, and an amine reducing agent.
The polishing composition according to claim 2, which is a mixture with a seed.
類系還元剤、ヒドロキシフェニル系還元剤およびアミン
系還元剤の中から選ばれる少なくとも1種が0.1〜1
0モルの割合で配合されてなる、請求項3に記載の研磨
用組成物。4. At least one selected from an aldehyde-based reducing agent, a hydroxyphenyl-based reducing agent and an amine-based reducing agent is used in an amount of 0.1 to 1 with respect to 1 mol of an inorganic reducing agent.
The polishing composition according to claim 3, which is blended at a ratio of 0 mol.
亜リン酸またはこれらのアルカリ金属塩若しくはアンモ
ニウム塩の中から選ばれる少なくとも1種である、請求
項2〜4のいずれかに記載の研磨用組成物。5. The inorganic reducing agent according to claim 2, wherein the inorganic reducing agent is at least one selected from sulfurous acid, nitrous acid and phosphorous acid, or an alkali metal salt or ammonium salt thereof. Polishing composition.
ヒドである、請求項2〜4のいずれかに記載の研磨用組
成物。6. The polishing composition according to claim 2, wherein the aldehyde-based reducing agent is glutaraldehyde.
キノン、N−(p−ヒドロキシフェニル)グリシン、4
−アミノフェノール、2,4−ジアミノフェノール、カ
テコールおよびp−メチルアミノフェノールサルフェー
トの中から選ばれる少なくとも1種である、請求項2〜
4のいずれかに記載の研磨用組成物。7. The hydroxyphenyl reducing agent is hydroquinone, N- (p-hydroxyphenyl) glycine, or 4,
-Aminophenol, 2,4-diaminophenol, catechol and at least one selected from p-methylaminophenol sulfate.
4. The polishing composition according to any one of 4 above.
ラゾリドンである、請求項2〜4のいずれかに記載の研
磨用組成物。8. The polishing composition according to claim 2, wherein the amine-based reducing agent is 1-phenyl-3-pyrazolidone.
1kgに対して0.001〜0.5モルの割合で配合さ
れてなる、請求項1〜8のいずれかに記載の研磨用組成
物。9. The polishing composition according to claim 1, wherein the compound having a reducing property is blended in a proportion of 0.001 to 0.5 mol with respect to 1 kg of the polishing composition. Stuff.
mである、請求項1〜9のいずれかに記載の研磨用組成
物。10. The abrasive fine particles have a particle size of 0.01 to 5 μm.
The polishing composition according to any one of claims 1 to 9, which is m.
H調整された水溶液中に、還元性を有する化合物として
亜硝酸のアルカリ金属塩とヒドロキノンとの混合物を含
有してなる、請求項1〜5、7、9〜10のいずれかに
記載の研磨用組成物。11. A potassium hydroxide is used to add p to the alkali side.
The polishing solution according to any one of claims 1 to 5, 7, 9 and 10, wherein the H-adjusted aqueous solution contains a mixture of an alkali metal salt of nitrous acid and hydroquinone as a reducing compound. Composition.
整された水溶液中に、還元性を有する化合物として亜硫
酸アンモニウムと、カテコール、4−アミノフェノー
ル、2,4−ジアミノフェノール、およびN−(p−ヒ
ドロキシフェニル)グリシンの中から選ばれる少なくと
も1種とを含有してなる、請求項1〜5、7、9〜10
のいずれかに記載の研磨用組成物。12. Ammonium sulfite as a reducing compound, catechol, 4-aminophenol, 2,4-diaminophenol, and N- (p-hydroxyphenyl) in an aqueous solution whose pH is adjusted to the alkaline side with ammonia. ) Glycine and at least one selected from the group consisting of 1 to 5, 7, 9 to 10.
The polishing composition according to any one of 1.
整された水溶液中に、還元性を有する化合物として亜硫
酸アンモニウムと1−フェニル−3−ピラゾリドンとの
混合物を含有してなる、請求項1〜5、8〜10のいず
れかに記載の研磨用組成物。13. A mixture of ammonium sulfite and 1-phenyl-3-pyrazolidone as a reducing compound in an aqueous solution whose pH has been adjusted to the alkaline side with ammonia. 10. The polishing composition according to any one of 10 to 10.
項1〜13のいずれかに記載の研磨用組成物。14. The polishing composition according to claim 1, which further contains an amino acid.
ンおよびD,L−グルタミン酸の中から選ばれる少なく
とも1種である、請求項14に記載の研磨用組成物。15. The polishing composition according to claim 14, wherein the amino acid is at least one selected from β-alanine, threonine and D, L-glutamic acid.
して0.001〜0.5モルの割合で配合されてなる、
請求項14または15に記載の研磨用組成物。16. An amino acid is blended in a proportion of 0.001 to 0.5 mol with respect to 1 kg of a polishing composition,
The polishing composition according to claim 14 or 15.
アミノ酸が0.1〜10モルの割合で配合されてなる、
請求項14〜16のいずれかに記載の研磨用組成物。17. A mole of a compound having a reducing property,
Amino acids are mixed in a ratio of 0.1 to 10 mol,
The polishing composition according to any one of claims 14 to 16.
H調整された水溶液中に、還元性を有する化合物として
亜硝酸のアルカリ金属塩を含有してなる、請求項14〜
17のいずれかに記載の研磨用組成物。18. A potassium hydroxide is added to the alkali side with potassium hydroxide.
The H-adjusted aqueous solution contains an alkali metal salt of nitrous acid as a compound having a reducing property.
18. The polishing composition according to any one of 17.
磨用組成物を用いて、半導体基板上に形成されたケイ素
またはケイ素酸化膜を研磨する、研磨方法。19. A polishing method of polishing a silicon or silicon oxide film formed on a semiconductor substrate using the polishing composition according to claim 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP32223595A JPH09137155A (en) | 1995-11-16 | 1995-11-16 | Polishing composition and polishing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP32223595A JPH09137155A (en) | 1995-11-16 | 1995-11-16 | Polishing composition and polishing method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH09137155A true JPH09137155A (en) | 1997-05-27 |
Family
ID=18141439
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP32223595A Pending JPH09137155A (en) | 1995-11-16 | 1995-11-16 | Polishing composition and polishing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH09137155A (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001015463A (en) * | 1999-06-16 | 2001-01-19 | Eternal Chemical Co Ltd | Polishing composition |
| JP2001035820A (en) * | 1999-07-21 | 2001-02-09 | Hitachi Chem Co Ltd | Cmp polishing solution |
| KR100799965B1 (en) * | 2000-07-08 | 2008-02-01 | 에포크 머티리얼 컴퍼니, 리미티드 | Chemical-Mechanical Abrasive Compositions and Polishing Methods |
| JP2009297815A (en) * | 2008-06-11 | 2009-12-24 | Shin-Etsu Chemical Co Ltd | Synthetic silica glass substrate polishing agent |
| JP4773370B2 (en) * | 2004-01-07 | 2011-09-14 | キャボット マイクロエレクトロニクス コーポレイション | Chemical mechanical polishing of oxidized metals |
| US8592317B2 (en) | 2010-05-07 | 2013-11-26 | Hitachi Chemical Co., Ltd. | Polishing solution for CMP and polishing method using the polishing solution |
| US9022834B2 (en) | 2008-12-11 | 2015-05-05 | Hitachi Chemical Company, Ltd. | Polishing solution for CMP and polishing method using the polishing solution |
| WO2016186214A1 (en) * | 2015-05-20 | 2016-11-24 | Hoya株式会社 | Method for polishing glass substrate, polishing liquid, method for manufacturing glass substrate, method for manufacturing glass substrate for magnetic disc, and method for manufacturing magnetic disc |
| US9919962B2 (en) | 2008-06-11 | 2018-03-20 | Shin-Etsu Chemical Co., Ltd. | Polishing agent for synthetic quartz glass substrate |
| WO2018055985A1 (en) * | 2016-09-23 | 2018-03-29 | 株式会社フジミインコーポレーテッド | Polishing composition, polishing method in which same is used, and method for producing semiconductor substrate |
| JP2022050446A (en) * | 2017-10-03 | 2022-03-30 | 昭和電工マテリアルズ株式会社 | Polishing liquid, polishing liquid set, polishing method and defect suppression method |
| US11814547B2 (en) | 2018-09-28 | 2023-11-14 | Kao Corporation | Polishing liquid composition for silicon oxide film |
-
1995
- 1995-11-16 JP JP32223595A patent/JPH09137155A/en active Pending
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001015463A (en) * | 1999-06-16 | 2001-01-19 | Eternal Chemical Co Ltd | Polishing composition |
| JP2001035820A (en) * | 1999-07-21 | 2001-02-09 | Hitachi Chem Co Ltd | Cmp polishing solution |
| KR100799965B1 (en) * | 2000-07-08 | 2008-02-01 | 에포크 머티리얼 컴퍼니, 리미티드 | Chemical-Mechanical Abrasive Compositions and Polishing Methods |
| JP4773370B2 (en) * | 2004-01-07 | 2011-09-14 | キャボット マイクロエレクトロニクス コーポレイション | Chemical mechanical polishing of oxidized metals |
| JP2009297815A (en) * | 2008-06-11 | 2009-12-24 | Shin-Etsu Chemical Co Ltd | Synthetic silica glass substrate polishing agent |
| US9919962B2 (en) | 2008-06-11 | 2018-03-20 | Shin-Etsu Chemical Co., Ltd. | Polishing agent for synthetic quartz glass substrate |
| US9022834B2 (en) | 2008-12-11 | 2015-05-05 | Hitachi Chemical Company, Ltd. | Polishing solution for CMP and polishing method using the polishing solution |
| US8592317B2 (en) | 2010-05-07 | 2013-11-26 | Hitachi Chemical Co., Ltd. | Polishing solution for CMP and polishing method using the polishing solution |
| WO2016186214A1 (en) * | 2015-05-20 | 2016-11-24 | Hoya株式会社 | Method for polishing glass substrate, polishing liquid, method for manufacturing glass substrate, method for manufacturing glass substrate for magnetic disc, and method for manufacturing magnetic disc |
| WO2018055985A1 (en) * | 2016-09-23 | 2018-03-29 | 株式会社フジミインコーポレーテッド | Polishing composition, polishing method in which same is used, and method for producing semiconductor substrate |
| JPWO2018055985A1 (en) * | 2016-09-23 | 2019-07-11 | 株式会社フジミインコーポレーテッド | Polishing composition, and polishing method and semiconductor substrate using the same |
| JP2022050446A (en) * | 2017-10-03 | 2022-03-30 | 昭和電工マテリアルズ株式会社 | Polishing liquid, polishing liquid set, polishing method and defect suppression method |
| US12365815B2 (en) | 2017-10-03 | 2025-07-22 | Resonac Corporation | Polishing liquid, polishing liquid set, polishing method, and defect suppression method |
| US11814547B2 (en) | 2018-09-28 | 2023-11-14 | Kao Corporation | Polishing liquid composition for silicon oxide film |
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