CN108255025A - 一种清洗液 - Google Patents
一种清洗液 Download PDFInfo
- Publication number
- CN108255025A CN108255025A CN201611231248.4A CN201611231248A CN108255025A CN 108255025 A CN108255025 A CN 108255025A CN 201611231248 A CN201611231248 A CN 201611231248A CN 108255025 A CN108255025 A CN 108255025A
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- Prior art keywords
- cleaning solution
- cleaning
- fluoride
- organic amine
- present
- Prior art date
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- 238000004140 cleaning Methods 0.000 title claims abstract description 77
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 claims abstract description 36
- 150000001412 amines Chemical class 0.000 claims abstract description 16
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims abstract description 5
- 239000003960 organic solvent Substances 0.000 claims abstract description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N dimethyl sulfoxide Natural products CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 5
- 229910052731 fluorine Inorganic materials 0.000 claims description 5
- 239000011737 fluorine Substances 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 4
- 239000003513 alkali Substances 0.000 claims description 4
- 239000000908 ammonium hydroxide Substances 0.000 claims description 4
- 230000008859 change Effects 0.000 claims description 4
- PCHPORCSPXIHLZ-UHFFFAOYSA-N diphenhydramine hydrochloride Chemical compound [Cl-].C=1C=CC=CC=1C(OCC[NH+](C)C)C1=CC=CC=C1 PCHPORCSPXIHLZ-UHFFFAOYSA-N 0.000 claims description 4
- 238000003682 fluorination reaction Methods 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- -1 4- sulfydryl phenylpropyl alcohols Chemical class 0.000 claims description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 3
- CCAFPWNGIUBUSD-UHFFFAOYSA-N diethyl sulfoxide Chemical compound CCS(=O)CC CCAFPWNGIUBUSD-UHFFFAOYSA-N 0.000 claims description 3
- 229920000768 polyamine Polymers 0.000 claims description 3
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical class CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 claims description 2
- NYCCIHSMVNRABA-UHFFFAOYSA-N 1,3-diethylimidazolidin-2-one Chemical class CCN1CCN(CC)C1=O NYCCIHSMVNRABA-UHFFFAOYSA-N 0.000 claims description 2
- QWOZZTWBWQMEPD-UHFFFAOYSA-N 1-(2-ethoxypropoxy)propan-2-ol Chemical compound CCOC(C)COCC(C)O QWOZZTWBWQMEPD-UHFFFAOYSA-N 0.000 claims description 2
- WDQFELCEOPFLCZ-UHFFFAOYSA-N 1-(2-hydroxyethyl)pyrrolidin-2-one Chemical compound OCCN1CCCC1=O WDQFELCEOPFLCZ-UHFFFAOYSA-N 0.000 claims description 2
- ZFPGARUNNKGOBB-UHFFFAOYSA-N 1-Ethyl-2-pyrrolidinone Chemical class CCN1CCCC1=O ZFPGARUNNKGOBB-UHFFFAOYSA-N 0.000 claims description 2
- RWNUSVWFHDHRCJ-UHFFFAOYSA-N 1-butoxypropan-2-ol Chemical compound CCCCOCC(C)O RWNUSVWFHDHRCJ-UHFFFAOYSA-N 0.000 claims description 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 claims description 2
- RLNZSUSARYWGKS-UHFFFAOYSA-N 2,2,2-trihydroxyethylazanium fluoride Chemical compound [F-].OC(C[NH3+])(O)O RLNZSUSARYWGKS-UHFFFAOYSA-N 0.000 claims description 2
- WMDZKDKPYCNCDZ-UHFFFAOYSA-N 2-(2-butoxypropoxy)propan-1-ol Chemical compound CCCCOC(C)COC(C)CO WMDZKDKPYCNCDZ-UHFFFAOYSA-N 0.000 claims description 2
- ORXSLDYRYTVAPC-UHFFFAOYSA-N 2-(4-sulfanylphenyl)acetic acid Chemical class OC(=O)CC1=CC=C(S)C=C1 ORXSLDYRYTVAPC-UHFFFAOYSA-N 0.000 claims description 2
- DSCJETUEDFKYGN-UHFFFAOYSA-N 2-Methoxybenzenethiol Chemical compound COC1=CC=CC=C1S DSCJETUEDFKYGN-UHFFFAOYSA-N 0.000 claims description 2
- WAEVWDZKMBQDEJ-UHFFFAOYSA-N 2-[2-(2-methoxypropoxy)propoxy]propan-1-ol Chemical compound COC(C)COC(C)COC(C)CO WAEVWDZKMBQDEJ-UHFFFAOYSA-N 0.000 claims description 2
- 150000008625 2-imidazolidinones Chemical class 0.000 claims description 2
- JPNXREVRYWWBDG-UHFFFAOYSA-N 2-propylbenzenethiol Chemical compound CCCC1=CC=CC=C1S JPNXREVRYWWBDG-UHFFFAOYSA-N 0.000 claims description 2
- RSFDFESMVAIVKO-UHFFFAOYSA-N 3-sulfanylbenzoic acid Chemical class OC(=O)C1=CC=CC(S)=C1 RSFDFESMVAIVKO-UHFFFAOYSA-N 0.000 claims description 2
- MHIJDDIBBUUVMD-UHFFFAOYSA-N 4-amino-3-sulfanylbenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1S MHIJDDIBBUUVMD-UHFFFAOYSA-N 0.000 claims description 2
- DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 claims description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical group F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 2
- 229910017665 NH4HF2 Inorganic materials 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 229910021529 ammonia Inorganic materials 0.000 claims description 2
- LDDQLRUQCUTJBB-UHFFFAOYSA-N ammonium fluoride Chemical compound [NH4+].[F-] LDDQLRUQCUTJBB-UHFFFAOYSA-N 0.000 claims description 2
- KVBCYCWRDBDGBG-UHFFFAOYSA-N azane;dihydrofluoride Chemical compound [NH4+].F.[F-] KVBCYCWRDBDGBG-UHFFFAOYSA-N 0.000 claims description 2
- 239000002585 base Substances 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- PZYDAVFRVJXFHS-UHFFFAOYSA-N n-cyclohexyl-2-pyrrolidone Chemical class O=C1CCCN1C1CCCCC1 PZYDAVFRVJXFHS-UHFFFAOYSA-N 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical group CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 claims description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- GTDKXDWWMOMSFL-UHFFFAOYSA-M tetramethylazanium;fluoride Chemical compound [F-].C[N+](C)(C)C GTDKXDWWMOMSFL-UHFFFAOYSA-M 0.000 claims description 2
- NBOMNTLFRHMDEZ-UHFFFAOYSA-N thiosalicylic acid Chemical compound OC(=O)C1=CC=CC=C1S NBOMNTLFRHMDEZ-UHFFFAOYSA-N 0.000 claims description 2
- 229940103494 thiosalicylic acid Drugs 0.000 claims description 2
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 2
- OXHNLMTVIGZXSG-UHFFFAOYSA-N 1-Methylpyrrole Chemical class CN1C=CC=C1 OXHNLMTVIGZXSG-UHFFFAOYSA-N 0.000 claims 1
- MBDUIEKYVPVZJH-UHFFFAOYSA-N 1-ethylsulfonylethane Chemical compound CCS(=O)(=O)CC MBDUIEKYVPVZJH-UHFFFAOYSA-N 0.000 claims 1
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 claims 1
- LMJXSOYPAOSIPZ-UHFFFAOYSA-N 4-sulfanylbenzoic acid Chemical class OC(=O)C1=CC=C(S)C=C1 LMJXSOYPAOSIPZ-UHFFFAOYSA-N 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 235000006408 oxalic acid Nutrition 0.000 claims 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 1
- 230000007797 corrosion Effects 0.000 abstract description 24
- 238000005260 corrosion Methods 0.000 abstract description 24
- 239000010949 copper Substances 0.000 abstract description 19
- 239000004065 semiconductor Substances 0.000 abstract description 16
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract description 13
- 229910052802 copper Inorganic materials 0.000 abstract description 13
- 238000004519 manufacturing process Methods 0.000 abstract description 8
- 239000000463 material Substances 0.000 abstract description 8
- 238000000034 method Methods 0.000 abstract description 8
- 239000003989 dielectric material Substances 0.000 abstract description 6
- 238000001020 plasma etching Methods 0.000 abstract description 6
- 229910052710 silicon Inorganic materials 0.000 abstract description 6
- 239000010703 silicon Substances 0.000 abstract description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 5
- 239000007769 metal material Substances 0.000 abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 4
- 238000007654 immersion Methods 0.000 abstract description 3
- 238000005507 spraying Methods 0.000 abstract description 3
- 230000009471 action Effects 0.000 abstract description 2
- 238000004377 microelectronic Methods 0.000 abstract description 2
- 229910052751 metal Inorganic materials 0.000 description 18
- 239000002184 metal Substances 0.000 description 18
- 230000000052 comparative effect Effects 0.000 description 7
- 239000003112 inhibitor Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 5
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 4
- 238000005530 etching Methods 0.000 description 4
- 238000001179 sorption measurement Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical class ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229920002120 photoresistant polymer Polymers 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 229910052814 silicon oxide Inorganic materials 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 150000002222 fluorine compounds Chemical class 0.000 description 2
- 238000003384 imaging method Methods 0.000 description 2
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 238000001039 wet etching Methods 0.000 description 2
- YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical compound C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- NUJILYKLNKQOOX-UHFFFAOYSA-N 1-butyl-2-methylbenzene Chemical group CCCCC1=CC=CC=C1C NUJILYKLNKQOOX-UHFFFAOYSA-N 0.000 description 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 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 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- MOFINMJRLYEONQ-UHFFFAOYSA-N [N].C=1C=CNC=1 Chemical compound [N].C=1C=CNC=1 MOFINMJRLYEONQ-UHFFFAOYSA-N 0.000 description 1
- WRLRISOTNFYPMU-UHFFFAOYSA-N [S].CC1=CC=CC=C1 Chemical compound [S].CC1=CC=CC=C1 WRLRISOTNFYPMU-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 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
- 125000003368 amide group Chemical group 0.000 description 1
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 229940043237 diethanolamine Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 229960001484 edetic acid Drugs 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 229940031098 ethanolamine Drugs 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 description 1
- 238000010849 ion bombardment Methods 0.000 description 1
- 238000005468 ion implantation Methods 0.000 description 1
- 229940102253 isopropanolamine Drugs 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- CIBMHJPPKCXONB-UHFFFAOYSA-N propane-2,2-diol Chemical compound CC(C)(O)O CIBMHJPPKCXONB-UHFFFAOYSA-N 0.000 description 1
- 230000002633 protecting effect Effects 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 229960004418 trolamine Drugs 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
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Detergent Compositions (AREA)
- Cleaning Or Drying Semiconductors (AREA)
Abstract
本发明涉及一种清洗液,其特征在于,所述清洗液按质量百分比含有以下组分:a)有机溶剂10%~80%;b)水10%~50%;c)氟化物0.01%~20%;d)有机胺2%~20%;e)硫酚及其衍生物0.01%~10%。本发明的清洗液清洗能力强,可有效去除半导体制程过程中等离子刻蚀残留物,尤其是在铜马士革工艺中灰化后的残留物,并且在高转速单片机清洗中对非金属材料(如氮氧化硅和低介质材料)和金属材料(如Cu)等有较小的腐蚀速率。本发明适用于批量浸泡式、批量旋转喷雾式清洗方式,尤其适用于高转速单片旋转式的清洗方式,具有较大操作窗口,在半导体晶片清洗等微电子领域具有良好的应用前景。
Description
技术领域
本发明涉及半导体制造工艺领域,尤其涉及一种用于半导体元件的清洗液。
背景技术
在半导体元器件制造过程中,光阻层的涂敷、曝光和成像是半导体元件图案制造的必要步骤。而在图案化的最后(即在光阻层的涂敷、成像、离子植入和蚀刻之后)进行下一工艺步骤之前,需彻底除去光阻层材料的残留物及经离子轰击硬化的光阻聚合物。在半导体制造过程中,通常,首先使用等离子干法灰化,然后使用清洗液湿法蚀刻,在湿法蚀刻过程中要求只能除去残留的聚合物光阻层和无机物,而不能攻击损害金属层。
随着半导体制造技术水平的提高以及电子器件尺寸的降低,在半导体制造领域中使用金属铜、low-k介质材料越来越多。尤其是铜双大马士革工艺越来越广泛的情况下,寻找能够有效去除刻蚀残留物的同时又能保护low-k介质材料、非金属材料和金属材料的清洗液就越来越重要。同时随着半导体制程尺寸越来越小,清洗方式也越来越广泛的使用到高速旋转单片清洗,因此对金属和非金属材料的腐蚀控制也越来越严格,开发能够适用于批量浸泡式、批量旋转喷雾式清洗方式,尤其适用于高转速单片旋转式的清洗方式的清洗液是亟待解决的问题。
现有技术中典型的清洗液有以下几种:胺类清洗液,半水性胺基(非羟胺类)清洗液以及氟化物类清洗液。其中,前两类清洗液主要应用在金属铝线的清洗工艺中,该清洗液需要在高温下清洗,一般在60℃到80℃之间,存在对金属的腐蚀速率较大的问题。而现有的氟化物类清洗液虽然能在较低的温度(室温到50℃)下进行清洗,但仍然存在着各种各样的缺点。例如,不能同时控制金属和非金属基材的腐蚀,清洗后容易造成通道特征尺寸的改变,从而改变半导体结构;采用传统苯并三氮唑(BTA)作金属铜的腐蚀抑制剂,虽然金属铜的蚀刻速率较小,但是传统唑类腐蚀抑制剂(BTA)不仅难以降解对生物体系不环保,而且在清洗结束后容易吸附在铜表面,导致集成电路的污染,会引起电路内不可预见的导电故障;有些现有技术避开传统唑类使用能够控制铜腐蚀和表面吸附的抑制剂,但是存在黏度表面张力大清洗效果不理想的问题。
US6,387,859公开了含氟同时含有羟胺的清洗液,使用BTA作为铜的腐蚀抑制剂,虽然保护效果较好,但未能解决表面吸附的问题,CN1950755B公开了含巯基化合物的清洗液,虽然控制了浸泡清洗方式下的金属腐蚀问题,但仍没有解决在高速旋转下清洗液对金属和非金属的腐蚀控制情况。CN100326231C公开了一种用于去除对铜有兼容性抗刻蚀剂组合物和方法,该清洗液不含氟并且大量使用乙二醇,尽管该清洗液对铜的保护非常优良,不存在腐蚀抑制表面吸附问题,但是其清洗液的粘度与表面张力都很大,从而影响清洗效果。
因此,为了克服现有清洗液的缺陷,适应新的清洗要求,比如保护低介电材料、环境更为友善、克服金属腐蚀抑制剂表面吸附、低缺陷水平、低刻蚀率以及适用于高转速旋转洗清方式等,亟待寻求新的清洗液。
发明内容
本发明提供一种含氟清洗液,其含有:氟化物、有机胺、有机溶剂、水和硫酚及其衍生物。本发明的清洗液不含有羟胺及氧化剂,其可有效去除半导体制程过程中等离子刻蚀残留物,尤其是在铜马士革工艺中灰化后的残留物,并且在高转速单片机清洗中对非金属材料(如氮氧化硅和低介质材料)和金属材料(如Cu)等有较小的腐蚀速率。
具体地,本发明提出一种清洗液,其按质量百分比含有以下组分:
其中,所述有机溶剂较佳的为二甲基亚砜、二乙基亚砜、甲乙基亚砜、2-咪唑烷酮、1,3-二甲基-2-咪唑烷酮、1,3-二乙基-2-咪唑烷酮、N-甲基吡咯烷酮、N-乙基吡咯烷酮、N-环己基吡咯烷酮、N-羟乙基吡咯烷酮、丙二醇单甲醚、丙二醇单乙醚、丙二醇单丁醚、二丙二醇单甲醚、二丙二醇单乙醚、二丙二醇单丁醚、三丙二醇单甲醚中的一种或多种。
其中,所述氟化物较佳的选自氟化氢类、氟化氨类或氟化氢与碱形成的盐;优选氟化氢(HF)、氟化铵(NH4F)、氟化氢铵(NH4HF2)、四甲基氟化铵(N(CH3)4F)和三羟乙基氟化铵(N(CH2OH)3HF)中的一种或多种,且,所述的碱较佳的选自氨水、季胺氢氧化物和醇胺。
其中,所述有机胺较佳的为含羟基、氨基和羧基的有机胺中的一种或多种。其中,所述含羟基的有机胺较佳的为醇胺,如乙醇胺、二乙醇胺、三乙醇胺、异丙醇胺、N,N-二甲基乙醇胺和N-甲基二乙醇胺;所述的含氨基的有机胺较佳的为有机多胺,如二乙烯三胺、五甲基二乙烯三胺和多乙烯多胺;所述含羧基的有机胺较佳的为含氨基的有机酸,如2-氨基乙酸、2-氨基苯甲酸、亚氨基二乙酸,氨三乙酸和乙二胺四乙酸。更加优选地,所述有机胺选自五甲基二乙烯三胺、亚氨基二乙酸和三乙醇胺中的一种或多种。所述有机胺的存在,有利于稳定清洗液体系地pH值,且提高清洗过程清洗液体系的稳定性和重现性。
其中,所述的硫酚及其衍生物较佳的为苯硫酚、硫代水杨酸、3-巯基苯甲酸、4-巯基苯甲酸、4-巯基苯乙酸、4-氨基-3-巯基苯甲酸、4-巯基苯丙酸、二甲基苯硫酚、甲基苯硫酚、丙基苯硫酚、甲氧基苯硫酚、叔丁基苯硫酚、叔丁基-2-甲基苯硫酚中的一种或多种。
本发明的积极进步效果在于:本发明的清洗液清洗能力强,可有效去除半导体制程过程中等离子刻蚀残留物,尤其是在铜马士革工艺中灰化后的残留物,并且在高转速单片机清洗中对非金属材料(如氮氧化硅和低介质材料)和金属材料(如Cu)等有较小的腐蚀速率。本发明适用于批量浸泡式、批量旋转喷雾式清洗方式,尤其适用于高转速单片旋转式的清洗方式,具有较大操作窗口,在半导体晶片清洗等微电子领域具有良好的应用前景。
此外,本发明中的清洗液,可以在25℃至55℃下清洗等离子刻蚀残留物。具体方法如下:将含有等离子刻蚀残留物的晶圆置于300rpm/min至500rpm/min的单片旋转清洗机下,使用本发明中的清洗液中,在25℃至55℃下旋转合适的时间后,取出漂洗后用高纯氮气吹干。
具体实施方式
以下结合具体实施例详细阐述本发明的优势,本发明所用试剂及原料均市售可得。本发明的清洗液由上述成分简单均匀混合即可制得。则,在本实施例中按照表1中各组分物质及其含量简单混合,即可得到本实施例1-15及对比例1-3的清洗液。
表1部分实施例及对比例清洗液的组分和含量
效果实施例
为了考察该类清洗液在浸泡、低转速(<=60rpmm/min)和高转速(>200rpm/min)下对金属和非金属材料的腐蚀情况,并进一步考察在单片高速旋转清洗方式下对含有等离子刻蚀残留物的金属孔道的清洗情况,本发明采用了如下技术手段:即将金属(Cu)空白硅片和非金属(SiON和BD)空白硅片分别浸入清洗液中,在40℃下以静止或不同转速浸泡30min,经去离子水漂洗后用高纯氮气吹干。将大马士革工艺中含有等离子刻蚀残留物的金属孔道晶圆置于高速旋转清洗方式下,在25℃至50℃下旋转1.5min,经去离子水漂洗后用高纯氮气吹干。残留物的清洗效果及对金属和非金属的腐蚀情况如表2所示。
表2部分实施例及对比例的腐蚀情况和清洗效果
表2中使用的介质如下所示:Cu=铜;SiON=氮化硅;BD=低介质(low-k)材料
从表2中可以看出:本发明的清洗液对半导体制成中所用的金属(如Cu)和非金属(SiON和BD)基本不会侵蚀,其腐蚀情况在浸泡、低转速(<=60rpmm/min)和高转速(>200rpm/min)均满足半导体业界通常在单片高速旋转清洗下的要求。
从对比例1与实施例8可以看出,使用半导体业界常用金属腐蚀抑制剂BTA腐蚀抑制剂,可以控制金属和非金属的蚀刻,但是出现了表面不均匀而且通道电性能测试不合格的问题,显而易见的是氮唑类腐蚀抑制剂吸附在晶圆表面不易漂洗掉造成了通道电性能测试不合格。对比例2使用了CN1950755B公开的巯基苯并咪唑,与实施例9相比,对比例2在高转速(>200rpm/min)下不能控制金属和非金属的腐蚀,并且清洗出现通道尺寸变宽的问题。
从对比例3与实施例10可以看出,未加硫酚及其羧酸衍生物在浸泡、低转速(<=60rpmm/min)和高转速(>200rpm/min)下均不能控制金属铜的腐蚀,进一步验证了硫酚及其羧酸衍生物的加入在保证清洗效果的同时可以有效的控制金属的腐蚀,同时在高速旋转单片机清洗下仍然可以控制金属和非金属的腐蚀速率。
应当注意的是,本发明的实施例有较佳的实施性,且并非对本发明作任何形式的限制,任何熟悉该领域的技术人员可能利用上述揭示的技术内容变更或修饰为等同的有效实施例,但凡未脱离本发明技术方案的内容,依据本发明的技术实质对以上实施例所作的任何修改或等同变化及修饰,均仍属于本发明技术方案的范围内。
Claims (9)
1.一种清洗液,其特征在于,所述清洗液按质量百分比含有以下组分:
2.如权利要求1所述的清洗液,其特征在于,所述有机溶剂选自二甲基亚砜、二乙基亚砜、甲乙基亚砜、2-咪唑烷酮、1,3-二甲基-2-咪唑烷酮、1,3-二乙基-2-咪唑烷酮、N-甲基吡咯烷酮、N-乙基吡咯烷酮、N-环己基吡咯烷酮、N-羟乙基吡咯烷酮、丙二醇单甲醚、丙二醇单乙醚、丙二醇单丁醚、二丙二醇单甲醚、二丙二醇单乙醚、二丙二醇单丁醚、三丙二醇单甲醚中的一种或多种。
3.如权利要求1所述的清洗液,其特征在于,所述氟化物选自氟化氢类、氟化氨类或氟化氢与碱形成的盐。
4.如权利要求3所述的清洗液,其特征在于,所述氟化物选自氟化氢(HF)、氟化铵(NH4F)、氟化氢铵(NH4HF2)、四甲基氟化铵(N(CH3)4F)和三羟乙基氟化铵(N(CH2OH)3HF)中的一种或多种,所述的碱选自氨水、季胺氢氧化物和醇胺中的一种或多种。
5.如权利要求1所述的清洗液,其特征在于,所述有机胺选自含羟基、氨基和羧基的有机胺中的一种或多种。
6.如权利要求5所述的清洗液,其特征在于,所述含羟基的有机胺为醇胺;所述含氨基的有机胺为有机多胺;所述含羧基的有机胺为含氨基的有机酸。
7.如权利要求6所述的清洗液,其特征在于,所述有机胺选自五甲基二乙烯三胺、亚氨基二乙酸和三乙醇胺中的一种或多种。
8.如权利要求1所述的清洗液,其特征在于,所述的硫酚及其衍生物选自苯硫酚、硫代水杨酸、3-巯基苯甲酸、4-巯基苯甲酸、4-巯基苯乙酸、4-氨基-3-巯基苯甲酸、4-巯基苯丙酸、二甲基苯硫酚、甲基苯硫酚、丙基苯硫酚、甲氧基苯硫酚、叔丁基苯硫酚、叔丁基-2-甲基苯硫酚中的一种或多种。
9.如权利要求1所述的清洗液,其特征在于,所述硫酚及其衍生物的质量百分比浓度为0.01-3%。
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