KR20060110712A - 갈바닉 부식을 억제하는 비수성 포토레지스트 스트립퍼 - Google Patents
갈바닉 부식을 억제하는 비수성 포토레지스트 스트립퍼 Download PDFInfo
- Publication number
- KR20060110712A KR20060110712A KR1020050039700A KR20050039700A KR20060110712A KR 20060110712 A KR20060110712 A KR 20060110712A KR 1020050039700 A KR1020050039700 A KR 1020050039700A KR 20050039700 A KR20050039700 A KR 20050039700A KR 20060110712 A KR20060110712 A KR 20060110712A
- Authority
- KR
- South Korea
- Prior art keywords
- composition
- substrate
- photoresist
- residue
- cleaning
- Prior art date
Links
- 229920002120 photoresistant polymer Polymers 0.000 title claims abstract description 40
- 238000005260 corrosion Methods 0.000 title claims abstract description 39
- 230000007797 corrosion Effects 0.000 title claims abstract description 39
- 239000000203 mixture Substances 0.000 claims abstract description 87
- 238000004140 cleaning Methods 0.000 claims abstract description 39
- 229920000768 polyamine Polymers 0.000 claims abstract description 15
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000003495 polar organic solvent Substances 0.000 claims abstract description 12
- 239000005725 8-Hydroxyquinoline Substances 0.000 claims abstract description 11
- 229960003540 oxyquinoline Drugs 0.000 claims abstract description 11
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000003112 inhibitor Substances 0.000 claims abstract description 9
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims abstract description 9
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims abstract description 5
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims abstract description 5
- HEBKCHPVOIAQTA-QWWZWVQMSA-N D-arabinitol Chemical compound OC[C@@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-QWWZWVQMSA-N 0.000 claims abstract description 5
- 239000004386 Erythritol Substances 0.000 claims abstract description 5
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229930195725 Mannitol Natural products 0.000 claims abstract description 5
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 claims abstract description 5
- 235000019414 erythritol Nutrition 0.000 claims abstract description 5
- 229940009714 erythritol Drugs 0.000 claims abstract description 5
- 239000000594 mannitol Substances 0.000 claims abstract description 5
- 235000010355 mannitol Nutrition 0.000 claims abstract description 5
- 150000002772 monosaccharides Chemical class 0.000 claims abstract description 5
- 239000000600 sorbitol Substances 0.000 claims abstract description 5
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 5
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000012964 benzotriazole Substances 0.000 claims abstract description 4
- 239000000758 substrate Substances 0.000 claims description 40
- 229910052751 metal Inorganic materials 0.000 claims description 29
- 239000002184 metal Substances 0.000 claims description 29
- 238000004377 microelectronic Methods 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 21
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 20
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 19
- -1 alkane diols Chemical class 0.000 claims description 15
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 13
- HXMVNCMPQGPRLN-UHFFFAOYSA-N 2-hydroxyputrescine Chemical compound NCCC(O)CN HXMVNCMPQGPRLN-UHFFFAOYSA-N 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 230000002401 inhibitory effect Effects 0.000 claims description 9
- 150000002739 metals Chemical class 0.000 claims description 9
- 150000003141 primary amines Chemical group 0.000 claims description 8
- 150000003335 secondary amines Chemical class 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- LHENQXAPVKABON-UHFFFAOYSA-N 1-methoxypropan-1-ol Chemical compound CCC(O)OC LHENQXAPVKABON-UHFFFAOYSA-N 0.000 claims description 4
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 4
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims description 4
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims description 4
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 229960001124 trientine Drugs 0.000 claims description 4
- 239000000811 xylitol Substances 0.000 claims description 4
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims description 4
- 235000010447 xylitol Nutrition 0.000 claims description 4
- 229960002675 xylitol Drugs 0.000 claims description 4
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 3
- 240000007124 Brassica oleracea Species 0.000 claims 2
- 125000001302 tertiary amino group Chemical group 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 229910052782 aluminium Inorganic materials 0.000 description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 10
- 239000010949 copper Substances 0.000 description 9
- 230000008569 process Effects 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 230000009972 noncorrosive effect Effects 0.000 description 6
- 150000003512 tertiary amines Chemical group 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 229910052802 copper Inorganic materials 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 239000002798 polar solvent Substances 0.000 description 5
- 239000006117 anti-reflective coating Substances 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 239000006184 cosolvent Substances 0.000 description 4
- NFDRPXJGHKJRLJ-UHFFFAOYSA-N edtmp Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CCN(CP(O)(O)=O)CP(O)(O)=O NFDRPXJGHKJRLJ-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000005530 etching Methods 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 description 2
- CMJLMPKFQPJDKP-UHFFFAOYSA-N 3-methylthiolane 1,1-dioxide Chemical compound CC1CCS(=O)(=O)C1 CMJLMPKFQPJDKP-UHFFFAOYSA-N 0.000 description 2
- 229910018182 Al—Cu Inorganic materials 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 2
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
- 239000011358 absorbing material Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 238000004380 ashing Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- PFURGBBHAOXLIO-UHFFFAOYSA-N cyclohexane-1,2-diol Chemical compound OC1CCCCC1O PFURGBBHAOXLIO-UHFFFAOYSA-N 0.000 description 2
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 239000011733 molybdenum Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- BYEAHWXPCBROCE-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-ol Chemical compound FC(F)(F)C(O)C(F)(F)F BYEAHWXPCBROCE-UHFFFAOYSA-N 0.000 description 1
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 1
- RJLKIAGOYBARJG-UHFFFAOYSA-N 1,3-dimethylpiperidin-2-one Chemical compound CC1CCCN(C)C1=O RJLKIAGOYBARJG-UHFFFAOYSA-N 0.000 description 1
- WDQFELCEOPFLCZ-UHFFFAOYSA-N 1-(2-hydroxyethyl)pyrrolidin-2-one Chemical compound OCCN1CCCC1=O WDQFELCEOPFLCZ-UHFFFAOYSA-N 0.000 description 1
- AIDFJGKWTOULTC-UHFFFAOYSA-N 1-butylsulfonylbutane Chemical compound CCCCS(=O)(=O)CCCC AIDFJGKWTOULTC-UHFFFAOYSA-N 0.000 description 1
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- JEXYCADTAFPULN-UHFFFAOYSA-N 1-propylsulfonylpropane Chemical compound CCCS(=O)(=O)CCC JEXYCADTAFPULN-UHFFFAOYSA-N 0.000 description 1
- FCKYPQBAHLOOJQ-UWVGGRQHSA-N 2-[[(1s,2s)-2-[bis(carboxymethyl)amino]cyclohexyl]-(carboxymethyl)amino]acetic acid Chemical compound OC(=O)CN(CC(O)=O)[C@H]1CCCC[C@@H]1N(CC(O)=O)CC(O)=O FCKYPQBAHLOOJQ-UWVGGRQHSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- FCKYPQBAHLOOJQ-UHFFFAOYSA-N Cyclohexane-1,2-diaminetetraacetic acid Chemical compound OC(=O)CN(CC(O)=O)C1CCCCC1N(CC(O)=O)CC(O)=O FCKYPQBAHLOOJQ-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001565 benzotriazoles Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- VCVOSERVUCJNPR-UHFFFAOYSA-N cyclopentane-1,2-diol Chemical compound OC1CCCC1O VCVOSERVUCJNPR-UHFFFAOYSA-N 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000000586 desensitisation Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- DUYCTCQXNHFCSJ-UHFFFAOYSA-N dtpmp Chemical compound OP(=O)(O)CN(CP(O)(O)=O)CCN(CP(O)(=O)O)CCN(CP(O)(O)=O)CP(O)(O)=O DUYCTCQXNHFCSJ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 125000003916 ethylene diamine group Chemical group 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- SAMYCKUDTNLASP-UHFFFAOYSA-N hexane-2,2-diol Chemical compound CCCCC(C)(O)O SAMYCKUDTNLASP-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000001020 plasma etching Methods 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 230000027756 respiratory electron transport chain Effects 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229940071182 stannate Drugs 0.000 description 1
- 125000005402 stannate group Chemical group 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- HHVIBTZHLRERCL-UHFFFAOYSA-N sulfonyldimethane Chemical compound CS(C)(=O)=O HHVIBTZHLRERCL-UHFFFAOYSA-N 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/26—Processing photosensitive materials; Apparatus therefor
- G03F7/42—Stripping or agents therefor
- G03F7/422—Stripping or agents therefor using liquids only
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3723—Polyamines or polyalkyleneimines
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/26—Processing photosensitive materials; Apparatus therefor
- G03F7/42—Stripping or agents therefor
- G03F7/422—Stripping or agents therefor using liquids only
- G03F7/425—Stripping or agents therefor using liquids only containing mineral alkaline compounds; containing organic basic compounds, e.g. quaternary ammonium compounds; containing heterocyclic basic compounds containing nitrogen
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/26—Processing photosensitive materials; Apparatus therefor
- G03F7/42—Stripping or agents therefor
- G03F7/422—Stripping or agents therefor using liquids only
- G03F7/426—Stripping or agents therefor using liquids only containing organic halogen compounds; containing organic sulfonic acids or salts thereof; containing sulfoxides
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/14—Hard surfaces
- C11D2111/22—Electronic devices, e.g. PCBs or semiconductors
Landscapes
- General Physics & Mathematics (AREA)
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Cleaning Or Drying Semiconductors (AREA)
- Detergent Compositions (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Laminated Bodies (AREA)
- Pens And Brushes (AREA)
- Golf Clubs (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
Abstract
Description
조성물/중량부 | |||||
성분 | 1 | 2 | 3 | 4 | 5 |
NMP | 60 | 60 | |||
SFL | 15 | 15 | |||
DMSO | 15 | 15 | |||
CARB | 87 | 77 | 89 | ||
EG | 1 | ||||
GE | |||||
AEEA | 9 | 9 | 10 | 20 | 10 |
CAT | 1 | 3 | 3 | ||
8HQ | 1 | 1 |
조성물/중량부 | |||||
성분 | 6 | 7 | 8 | 9 | 10 |
NMP | 24 | 30 | |||
SFL | |||||
DMSO | 24 | ||||
CARB | 84 | 60 | 60 | 60 | 60 |
EG | 24 | ||||
GE | |||||
AEEA | 15 | 15 | 15 | 15 | 9 |
CAT | 1 | ||||
8HQ | 1 | 1 | 1 | 1 |
조성물/중량부 | |||
성분 | 11 | 12 | 13 |
NMP | 30 | ||
SFL | 20 | ||
DMSO | 30 | ||
CARB | 60 | ||
EG | |||
GE | 84 | 40 | |
AEEA | 9 | 15 | 9 |
CAT | |||
8HQ | 1 | 1 | 1 |
Claims (20)
- (a) 하나 이상의 극성 유기 용매;(b) 하나 이상의 1차 아민기와 하나 이상의 2차 또는 3차 아민기를 갖는, 하나 이상의 다음 화학식의 디- 또는 폴리아민; 및(c) 8-히드록시퀴놀린 및 그의 이성질체, 벤조트리아졸, 카테콜, 단당류, 및 만니톨, 소르비톨, 아라비톨, 자일리톨, 에리트리톨, 알칸 디올 및 시클로알칸 디올로부터 선택된 다가 알코올로 이루어진 군에서 선택된 하나 이상의 부식 억제제를 포함하는, 마이크로전자 기판으로부터 포토레지스트 및 잔류물을 세척하기 위한 비수성 세척 조성물.<화학식>상기 식에서 R1, R2, R4, 및 R5는 각각 독립적으로 H, OH, 히드록시알킬 및 아미노알킬기로 이루어진 군에서 선택되고; R6 및 R7은 각각 H 또는 알킬기로 이루어진 군에서 독립적으로 선택되고; m 및 n은 각각 독립적으로 1 이상의 정수이며; 단 R1, R2, R4, 및 R5는 화합물에 하나 이상의 1차 아민기 및 하나 이상의 2차 또는 3차 아민기가 있도록 선택된다.
- 제1항에 있어서, 조성물의 약 50 내지 약 90중량%의 극성 유기 용매 성분 (a); 조성물의 약 5 내지 약 20중량%의 디- 또는 폴리아민 성분 (b); 및 조성물의 약 0.1 내지 약 10 중량%의 부식 억제 성분(c)을 포함하는 세척 조성물.
- 제1항에 있어서, 조성물의 약 85 내지 약 90중량%의 극성 유기 용매 성분 (a); 조성물의 약 5 내지 약 15중량%의 디- 또는 폴리아민 성분 (b); 및 조성물의 약 0.3 내지 약 3 중량%의 부식 억제 성분(c)을 포함하는 세척 조성물.
- 제1항에 있어서, 극성 유기 용매 성분 (a)이 술폴란, 디메틸술폭사이드, N-메틸-2-피롤리돈, 카르비톨, 에틸렌 글리콜, 메톡시 프로판올 및 이들의 혼합물로 이루어진 군에서 선택되고, 디- 또는 폴리아민 성분 (b)이 2-아미노에틸-2-아미노에탄올, 디에틸렌 트리아민 및 트리에틸렌 테트라민로 이루어진 군에서 선택되며, 부식 억제 성분(c)이 8-히드록시퀴놀린 및 카테콜로부터 선택되는 세척 조성물.
- 제3항에 있어서, 극성 유기 용매 성분 (a)이 술폴란, 디메틸술폭사이드, N-메틸-2-피롤리돈, 카르비톨, 에틸렌 글리콜, 메톡시 프로판올 및 이들의 혼합물로 이루어진 군에서 선택되고, 디- 또는 폴리아민 성분 (b)이 2-아미노에틸-2-아미노에탄올, 디에틸렌 트리아민 및 트리에틸렌 테트라민로 이루어진 군에서 선택되며, 부식 억제 성분(c)이 8-히드록시퀴놀린 및 카테콜로부터 선택되는 세척 조성물.
- 제1항에 있어서, 디- 또는 폴리아민 성분 (b)이 (2-아미노에틸)-2-아미노에탄올인 세척 조성물.
- 제5항에 있어서, 디- 또는 폴리아민 성분 (b)이 (2-아미노에틸)-2-아미노에탄올인 세척 조성물.
- 제7항에 있어서, 극성 유기 용매 성분 (a)로서 카르비톨을, 부식 억제 성분 (c)으로서 8-히드록시퀴놀린을 포함하는 세척 조성물.
- 기판을, 기판으로부터 포토레지스트 또는 잔류물을 세척하기에 충분한 시간동안 제1항의 조성물을 포함하는 세척 조성물과 접촉시키는 것을 포함하는, 마이크로전자 기판으로부터 포토레지스트 또는 잔류물을 세척하는 방법.
- 기판을, 기판으로부터 포토레지스트 또는 잔류물을 세척하기에 충분한 시간동안 제2항의 조성물을 포함하는 세척 조성물과 접촉시키는 것을 포함하는, 마이크로전자 기판으로부터 포토레지스트 또는 잔류물을 세척하는 방법.
- 기판을, 기판으로부터 포토레지스트 또는 잔류물을 세척하기에 충분한 시간동안 제3항의 조성물을 포함하는 세척 조성물과 접촉시키는 것을 포함하는, 마이크 로전자 기판으로부터 포토레지스트 또는 잔류물을 세척하는 방법.
- 기판을, 기판으로부터 포토레지스트 또는 잔류물을 세척하기에 충분한 시간동안 제4항의 조성물을 포함하는 세척 조성물과 접촉시키는 것을 포함하는, 마이크로전자 기판으로부터 포토레지스트 또는 잔류물을 세척하는 방법.
- 기판을, 기판으로부터 포토레지스트 또는 잔류물을 세척하기에 충분한 시간동안 제5항의 조성물을 포함하는 세척 조성물과 접촉시키는 것을 포함하는, 마이크로전자 기판으로부터 포토레지스트 또는 잔류물을 세척하는 방법.
- 기판을, 기판으로부터 포토레지스트 또는 잔류물을 세척하기에 충분한 시간동안 제6항의 조성물을 포함하는 세척 조성물과 접촉시키는 것을 포함하는, 마이크로전자 기판으로부터 포토레지스트 또는 잔류물을 세척하는 방법.
- 기판을, 기판으로부터 포토레지스트 또는 잔류물을 세척하기에 충분한 시간동안 제7항의 조성물을 포함하는 세척 조성물과 접촉시키는 것을 포함하는, 마이크로전자 기판으로부터 포토레지스트 또는 잔류물을 세척하는 방법.
- 기판을, 기판으로부터 포토레지스트 또는 잔류물을 세척하기에 충분한 시간동안 제8항의 조성물을 포함하는 세척 조성물과 접촉시키는 것을 포함하는, 마이크 로전자 기판으로부터 포토레지스트 또는 잔류물을 세척하는 방법.
- 제9항에 있어서, 마이크로전자 기판이 상이한 금속을 가진 적층 소자인 방법.
- 제13항에 있어서, 마이크로전자 기판이 상이한 금속을 가진 적층 소자인 방법.
- 제14항에 있어서, 마이크로전자 기판이 상이한 금속을 가진 적층 소자인 방법.
- 제16항에 있어서, 마이크로전자 기판이 상이한 금속을 가진 적층 소자인 방법.
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- 2005-05-12 KR KR1020050039700A patent/KR101088568B1/ko active IP Right Grant
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- 2006-03-16 AT AT06738451T patent/ATE498859T1/de active
- 2006-03-16 WO PCT/US2006/009389 patent/WO2006112994A1/en active Application Filing
- 2006-03-16 ES ES06738451T patent/ES2361271T3/es active Active
- 2006-03-16 SG SG201002616-9A patent/SG161273A1/en unknown
- 2006-03-16 CA CA002605236A patent/CA2605236A1/en not_active Abandoned
- 2006-03-16 JP JP2008507660A patent/JP4677030B2/ja not_active Expired - Fee Related
- 2006-03-16 DE DE602006020125T patent/DE602006020125D1/de active Active
- 2006-03-16 CN CN2006800132023A patent/CN101164016B/zh active Active
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- 2006-03-16 EP EP06738451A patent/EP1877870B1/en not_active Not-in-force
- 2006-03-16 DK DK06738451.1T patent/DK1877870T3/da active
- 2006-03-16 US US11/910,281 patent/US20080280235A1/en not_active Abandoned
- 2006-03-16 BR BRPI0610852-0A patent/BRPI0610852A2/pt not_active IP Right Cessation
- 2006-03-29 MY MYPI20061377A patent/MY145299A/en unknown
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110967946A (zh) * | 2019-12-04 | 2020-04-07 | 苏州博洋化学股份有限公司 | 一种高效碱性光刻胶剥离液 |
Also Published As
Publication number | Publication date |
---|---|
PL1877870T3 (pl) | 2011-07-29 |
JP2008537182A (ja) | 2008-09-11 |
JP4677030B2 (ja) | 2011-04-27 |
TW200700549A (en) | 2007-01-01 |
ATE498859T1 (de) | 2011-03-15 |
CN101164016A (zh) | 2008-04-16 |
CN101164016B (zh) | 2010-12-01 |
EP1877870B1 (en) | 2011-02-16 |
DE602006020125D1 (de) | 2011-03-31 |
WO2006112994A1 (en) | 2006-10-26 |
EP1877870A1 (en) | 2008-01-16 |
IL186565A0 (en) | 2008-01-20 |
ZA200706296B (en) | 2008-09-25 |
DK1877870T3 (da) | 2011-05-02 |
BRPI0610852A2 (pt) | 2010-08-03 |
ES2361271T3 (es) | 2011-06-15 |
US20080280235A1 (en) | 2008-11-13 |
PT1877870E (pt) | 2011-05-24 |
MY145299A (en) | 2012-01-13 |
NO20075935L (no) | 2008-01-18 |
SG161273A1 (en) | 2010-05-27 |
CA2605236A1 (en) | 2006-10-26 |
KR101088568B1 (ko) | 2011-12-05 |
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