WO2017218147A1 - Cleaning compositions for microelectronic substrates containing aluminum - Google Patents
Cleaning compositions for microelectronic substrates containing aluminum Download PDFInfo
- Publication number
- WO2017218147A1 WO2017218147A1 PCT/US2017/034122 US2017034122W WO2017218147A1 WO 2017218147 A1 WO2017218147 A1 WO 2017218147A1 US 2017034122 W US2017034122 W US 2017034122W WO 2017218147 A1 WO2017218147 A1 WO 2017218147A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- weight
- cleaning
- water
- aluminum
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 79
- 238000004140 cleaning Methods 0.000 title claims abstract description 58
- 239000000758 substrate Substances 0.000 title claims abstract description 40
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 27
- 238000004377 microelectronic Methods 0.000 title claims abstract description 27
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 25
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims abstract description 36
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims abstract description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 20
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims abstract description 15
- 238000000034 method Methods 0.000 claims abstract description 15
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims abstract description 15
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims abstract description 14
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims abstract description 10
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229910052751 metal Inorganic materials 0.000 claims description 24
- 239000002184 metal Substances 0.000 claims description 24
- 238000005260 corrosion Methods 0.000 claims description 21
- 230000007797 corrosion Effects 0.000 claims description 21
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 7
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 claims description 7
- 239000010936 titanium Substances 0.000 claims description 7
- 229910052719 titanium Inorganic materials 0.000 claims description 7
- 230000008569 process Effects 0.000 claims description 5
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 22
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 229920002120 photoresistant polymer Polymers 0.000 description 15
- -1 methylene phosphonic acid Chemical compound 0.000 description 10
- 239000004094 surface-active agent Substances 0.000 description 10
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 9
- 239000003112 inhibitor Substances 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 150000002009 diols Chemical class 0.000 description 5
- 235000012431 wafers Nutrition 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000004065 semiconductor Substances 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 239000002280 amphoteric surfactant Substances 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 239000003093 cationic surfactant Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 3
- 229910052721 tungsten Inorganic materials 0.000 description 3
- 239000010937 tungsten Substances 0.000 description 3
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical group NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
- 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
- PGSWEKYNAOWQDF-UHFFFAOYSA-N 3-methylcatechol Chemical compound CC1=CC=CC(O)=C1O PGSWEKYNAOWQDF-UHFFFAOYSA-N 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 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
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
- 150000003973 alkyl amines Chemical class 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000002738 chelating agent Substances 0.000 description 2
- 230000000536 complexating effect Effects 0.000 description 2
- 239000008139 complexing agent Substances 0.000 description 2
- 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 2
- 238000005516 engineering process Methods 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
- 239000000383 hazardous chemical Substances 0.000 description 2
- 231100000206 health hazard Toxicity 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000000269 nucleophilic effect Effects 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 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
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 1
- RBNPOMFGQQGHHO-UHFFFAOYSA-N -2,3-Dihydroxypropanoic acid Natural products OCC(O)C(O)=O RBNPOMFGQQGHHO-UHFFFAOYSA-N 0.000 description 1
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 1
- NAOLWIGVYRIGTP-UHFFFAOYSA-N 1,3,5-trihydroxyanthracene-9,10-dione Chemical compound C1=CC(O)=C2C(=O)C3=CC(O)=CC(O)=C3C(=O)C2=C1 NAOLWIGVYRIGTP-UHFFFAOYSA-N 0.000 description 1
- LXOFYPKXCSULTL-UHFFFAOYSA-N 2,4,7,9-tetramethyldec-5-yne-4,7-diol Chemical class CC(C)CC(C)(O)C#CC(C)(O)CC(C)C LXOFYPKXCSULTL-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
- SIOXVLLVWKWKIR-UHFFFAOYSA-N 3-[2-carboxyethyl-[3-(8-methylnonoxy)propyl]amino]propanoic acid Chemical compound CC(C)CCCCCCCOCCCN(CCC(O)=O)CCC(O)=O SIOXVLLVWKWKIR-UHFFFAOYSA-N 0.000 description 1
- ZBCATMYQYDCTIZ-UHFFFAOYSA-N 4-methylcatechol Chemical compound CC1=CC=C(O)C(O)=C1 ZBCATMYQYDCTIZ-UHFFFAOYSA-N 0.000 description 1
- XESZUVZBAMCAEJ-UHFFFAOYSA-N 4-tert-butylcatechol Chemical compound CC(C)(C)C1=CC=C(O)C(O)=C1 XESZUVZBAMCAEJ-UHFFFAOYSA-N 0.000 description 1
- 206010000087 Abdominal pain upper Diseases 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-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
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- RBNPOMFGQQGHHO-UWTATZPHSA-N D-glyceric acid Chemical compound OC[C@@H](O)C(O)=O RBNPOMFGQQGHHO-UWTATZPHSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- 206010028813 Nausea Diseases 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000013504 Triton X-100 Substances 0.000 description 1
- 229920004890 Triton X-100 Polymers 0.000 description 1
- 206010047700 Vomiting Diseases 0.000 description 1
- ZYFGXMFXMCEIDI-UHFFFAOYSA-N [dodecyl(propanoyloxy)amino] propanoate Chemical compound CCCCCCCCCCCCN(OC(=O)CC)OC(=O)CC ZYFGXMFXMCEIDI-UHFFFAOYSA-N 0.000 description 1
- 230000037374 absorbed through the skin Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical group [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 238000000637 aluminium metallisation Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- MRUAUOIMASANKQ-UHFFFAOYSA-O carboxymethyl-[3-(dodecanoylamino)propyl]-dimethylazanium Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC(O)=O MRUAUOIMASANKQ-UHFFFAOYSA-O 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- SCIGVHCNNXTQDB-UHFFFAOYSA-N decyl dihydrogen phosphate Chemical compound CCCCCCCCCCOP(O)(O)=O SCIGVHCNNXTQDB-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 150000005205 dihydroxybenzenes Chemical class 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- GEGKMYLSPGGTQM-UHFFFAOYSA-L disodium;3-[2-(2-carboxylatoethoxy)ethyl-[2-(octanoylamino)ethyl]amino]propanoate Chemical compound [Na+].[Na+].CCCCCCCC(=O)NCCN(CCC([O-])=O)CCOCCC([O-])=O GEGKMYLSPGGTQM-UHFFFAOYSA-L 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 229940074391 gallic acid Drugs 0.000 description 1
- 235000004515 gallic acid Nutrition 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 229960004337 hydroquinone Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 230000036244 malformation Effects 0.000 description 1
- 210000001161 mammalian embryo Anatomy 0.000 description 1
- 229960002510 mandelic acid Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000008693 nausea Effects 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000000473 propyl gallate Substances 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- 229940075579 propyl gallate Drugs 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 229960001755 resorcinol Drugs 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 125000005402 stannate group Chemical group 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 231100000462 teratogen Toxicity 0.000 description 1
- 239000003439 teratogenic agent Substances 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000008673 vomiting Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3105—After-treatment
- H01L21/311—Etching the insulating layers by chemical or physical means
- H01L21/31127—Etching organic layers
- H01L21/31133—Etching organic layers by chemical means
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/261—Alcohols; Phenols
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/263—Ethers
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/32—Organic compounds containing nitrogen
- C11D7/3218—Alkanolamines or alkanolimines
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/34—Organic compounds containing sulfur
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5004—Organic solvents
- C11D7/5013—Organic solvents 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
- G03F7/425—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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02041—Cleaning
- H01L21/02057—Cleaning during device manufacture
- H01L21/02068—Cleaning during device manufacture during, before or after processing of conductive layers, e.g. polysilicon or amorphous silicon layers
-
- 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
Definitions
- This invention pertains to cleaning and stripping compositions for microelectronic substrates and particularly for cleaning metal-containing residues from aluminum-containing microelectronics components without causing undue aluminum corrosion.
- microelectronic devices are metallized with aluminum.
- Such microelectronic substrates may also be composed of and/or employ metals such as titanium, titanium nitride, tungsten and the like as adhesion promoters and diffusion barriers.
- alkaline microelectronic stripping and cleaning compositions have been proposed for the removal of cross-linked and hardened photoresists and other residues, such as post etch residues, from such microelectronic substrates.
- one problem with such stripping and cleaning composition is the possibility of metal corrosion occurring as a result of the use of such cleaning compositions. Such corrosion results in whiskers, pitting, notching of metal lines, due at least in part to the reaction of the metals in the device substrates with the alkaline strippers employed.
- One such alkaline microelectronic stripping and cleaning composition is that disclosed in U.S. Pat. No. 5,308,745.
- NMP N-methyl pyrrolidone
- NMP also may be a teratogen, i.e., a substance which could cause malformation of an embryo to a pregnant person. There therefore is a need for HA and NMP free cleaning compositions and methods that are effective at removing residue as well as negative and positive bulk photoresist from semiconductor devices containing Al.
- stripping and cleaning compositions for cleaning microelectronics substrates including: about 30% to about 50 % by weight ethylene glycol butyl ether, about 20% to about 30% by weight sulfolane, about 10% to about 45% by weight monoethanolamine, about 3% to about 15% by weight diethylene glycol, about 0.5% to about 10% dihydroxybenzene, and about 0.5% to about 50% water.
- the compositions may additionally comprise one or more components such as metal- complexing/corrosion resisting compounds, other corrosion inhibitors and surfactants.
- the composition of the invention is used for stripping and cleaning substrates containing aluminum.
- the substrates include an aluminum metallized substrate having vias and containing metal residue.
- the metal residue includes at least one layer selected from the group consisting of titanium and titanium nitride layers.
- the stripping and cleaning compositions include about 35% to about 45% by weight ethylene glycol butyl ether, about 24% to about 27% by weight sulfolane, about 13% to about 15% by weight monoethanolamine, about 4% to about 10% by weight diethylene glycol, about 3% to about 8% of a dihydroxybenzene, and about 9% to about 13% water.
- the composition is used for stripping and cleaning substrates containing aluminum.
- the inventive composition is substantially free of hydroxylamine.
- the inventive composition is substantially free of n- methylpyrrolidone (NMP).
- the present invention includes a method for cleaning
- the process comprising contacting the substrate with a cleaning composition for a time sufficient to clean the substrate, wherein the cleaning composition comprises about 30% to about 50 % by weight ethylene glycol butyl ether, about 20% to about 30% by weight sulfolane, about 10% to about 45% by weight monoethanolamine, about 3% to about 15% by weight diethylene glycol, about 0.5% to about 10% dihydroxybenzene, and about 0.5% to about 50% water.
- the cleaning composition comprises about 30% to about 50 % by weight ethylene glycol butyl ether, about 20% to about 30% by weight sulfolane, about 10% to about 45% by weight monoethanolamine, about 3% to about 15% by weight diethylene glycol, about 0.5% to about 10% dihydroxybenzene, and about 0.5% to about 50% water.
- the method for cleaning microelectronic substrates comprises a method for cleaning microelectronic substrates without producing any substantial metal corrosion, the substrate containing at least one photoresist polymeric material, etch residues and metal residues, the process comprising contacting the substrate with a cleaning composition for a time sufficient to clean the substrate, wherein the cleaning composition includes: about 30% to about 50 % by weight ethylene glycol butyl ether, about 20% to about 30% by weight sulfolane, about 10% to about 45% by weight monoethanolamine, about 5% to about 15% by weight diethylene glycol, about 0.5% to about 10% dihydroxybenzene, and about 0.5% to about 50% water.
- compositions may additionally comprise one or more components such as metal- complexing/corrosion resisting compounds, other corrosion inhibitors and surfactants.
- the method of cleaning microelectronic substrates in accordance with this invention is particularly useful for cleaning substrate that comprises an aluminum metallized substrate having vias and containing metal residue, and in an embodiment the metal residue is from at least one of layers of titanium and/or titanium nitride.
- the invention also relates to cleaning of vias that punch through metal layers of microelectronics components, such as titanium or titanium nitride layers, while being compatible with underlying aluminum structures, i.e., causing little or no metal corrosion in the
- microelectronics components The invention further relates to such cleaning compositions that also are able to clean post-ash residue from other vias and from metal lines as well as cleaning or stripping unashed photoresist from microelectronics substrates.
- a further aspect of this invention is a process of cleaning or stripping photoresist and residue from aluminum-containing microelectronics components without causing undue aluminum corrosion.
- Dihydroxybenzene includes catechol, also known as pyrocatechol or 1,2- dihydroxybenzene, and has molecular formula of C 6 H4(OH)2. It is the ortho isomer of the three isomeric benzenediols. About 20 million kg are now synthetically produced annually as a commodity organic chemical, mainly as a precursor to pesticides, flavors, and fragrances.
- catechol may also be used, including 3-methylcatechol, 4-methylcatechol, and 4- tertbutylcatechol.
- compositions of this invention may also optionally contain other additional components.
- additional components include metal-complexing/corrosion resisting compounds, other corrosion inhibitors and surfactants.
- Organic or inorganic chelating or metal complexing agents/corrosion inhibitors are not required, but may optionally be included in the compositions of this invention, but offer substantial benefits, such as for example, improved product stability when incorporated into the aqueous cleaning compositions of this invention.
- suitable chelating or complexing agents include but are not limited to trans- 1,2-cyclohexanediamine tetraacetic acid (CyDTA), ethylenediamine tetraacetic acid (EDTA), stannates, pyrophosphates, alkylidene-diphosphonic acid derivatives (e.g. ethane- 1 -hydroxy- 1,1-diphosphonate), phosphonates containing ethylenediamine, diethylenetriamine or triethylenetetramine functional moieties [e,g.
- ETMP ethylenediamine tetra(methylene phosphonic acid)
- the chelating agent will be present in the composition in an amount of from 0 to about 5 wt %, preferably from about 0.1 to about 2 wt % based on the weight of the composition.
- the aqueous cleaning compositions of this invention can also optionally contain other corrosion inhibitors and similar non-corrosive components employed in microelectronic cleaner compositions.
- the compounds may include resorcinol, gallic acid, propyl gallate, pyrogallol, hydroquinone, benzotriazole and derivatives of benzotriazole, and polyfunctional carboxylic acids such as citric acid, tartaric acid, gluconic acid, saccharic acid, glyceric acid, oxalic acid, phthalic acid, maleic acid, mandelic acid, malonic acid, lactic acid, and salicylic acid.
- These other corrosion inhibitors may be present in any suitable amount, generally in an amount of from about 0 to about 5 wt %, preferably from about 0.1 to about 3 wt %, and more preferably from about 0.2 to about 2 wt %.
- compositions of the present invention may also optionally contain any suitable water-soluble amphoteric, non-ionic, cationic or anionic surfactant.
- a surfactant will reduce the surface tension of the formulation and improve the wetting of the surface to be cleaned and therefore improve the cleaning action of the composition.
- the surfactant may also be added to reduce aluminum corrosion rates if further aluminum corrosion inhibition is desired.
- Amphoteric surfactants useful in the compositions of the present invention include betaines and sulfobetaines such as alkyl betaines, amidoalkyl betaines, alkyl sulfobetaines and amidoalkyl sulfobetaines; aminocarboxylic acid derivatives such as amphoglycinates, amphopropionates, amphodiglycinates, and amphodipropionates; iminodiacids such as alkoxyalkyl iminodiacids or alkoxyalkyl iminodiacids; amine oxides such as alkyl amine oxides and alkylamido alkylamine oxides; fluoroalkyl sulfonates and fluorinated alkyl amphoterics; and mixtures thereof.
- betaines and sulfobetaines such as alkyl betaines, amidoalkyl betaines, alkyl sulfobetaines and amidoalkyl sulf
- amphoteric surfactants are cocoamidopropyl betaine, cocoamidopropyl dimethyl betaine, cocoamidopropyl hydroxy sultaine, capryloamphodipropionate,
- cocoamidodipropionate cocoamphopropionate, cocoamphohydroxyethyl propionate, isodecyloxypropylimino dipropionic acid, laurylimino dipropionate, cocoamidopropylamine oxide and cocoamine oxide and fluorinated alkyl amphoterics.
- Non-ionic surfactants useful in the compositions of the present invention include acetylenic diols, ethoxylated acetylenic diols, fluorinated alkyl alkoxylates, fluorinated alkylesters, fluorinated polyoxyethylene alkanols, aliphatic acid esters of polyhydric alcohols, polyoxyethylene monoalkyl ethers, poiyoxyethylene diols, siloxane type surfactants, and alkylene glycol monoalkyl ethers.
- the non-ionic surfactants are acetylenic diols or ethoxylated acetylenic diols.
- Anionic surfactants useful in the compositions of the present invention include carboxylates, N-acylsarcosinates, sulfonates, sulfates, and mono and diesters of orthophosphoric acid such as decyl phosphate.
- the anionic surfactants are metal-free surfactants.
- Cationic surfactants useful in the compositions of the present invention include amine ethoxylates,
- the cationic surfactants are halogen-free surfactants.
- surfactants include, but are not limited to 3,5-dimethyl-l-hexyn-3-ol (Surfynol-61), ethoxylated 2,4,7, 9-tetramethyl-5- decyne-4,7-diol (Surfynol-465), polytetrafluoroethylene cetoxypropylbetaine (Zonyl FSK), Zonyl FSH, Triton X-100, namely octylphenoxypolyethoxyethanol, and the like.
- the surfactant will generally be present in an amount of from 0 to about 5 wt %, preferably 0.001 to about 3 wt % based on the weight of the composition.
- the closest prior art represented by U.S. Patent No. 5,308,745 includes a composition comprising a stripping solvent, a nucleophilic amine and a non-nitrogen containing weak acid in an amount sufficient to neutralize from about 19% to about 75% by weight of the nucleophilic amine.
- Data was collected to show adding acid (acetic acid) to the formulation of our invention does not contribute to photoresist stripping performance.
- Catechol is specifically required to contribute to photoresist and residue removal performance.
- the wafers tested included bulk photoresist on aluminum.
- the wafers were all processed in solutions at 65°C, for 20 minutes, and at 650 RPM. Cleaning was observed via SEM.
- U.S. Patent No. 8,178,482 which describes compositions consisting of: about 20% to about 80 wt % of the composition of N-methyl pyrrolidone, monoethanolamine in an amount of from about 10% to about 45% based on the weight of the composition, from about 5% to about 15% by weight of the composition of diethylene glycol as a metal removing compound, catechol in an amount sufficient to neutralize from about 3% to about 75% by weight of the monoethanolamine such that the stripping composition has an aqueous pH of from about 9.6 to about 10.9, and water.
- the data below shows by removing catechol and using a mix of EGBE and Sulfolane a cleaner can be obtained that can strip bulk photoresist just as well, shows improved cleaning for aluminum substrates, and does not have the environmental and health hazards associated with NMP.
- Wafers tested included bulk photoresist without metal exposed, bulk photoresist with Al exposed, thin organic residue on Al, thick organic residue on Al, and Al via cleans.
- the wafers were all processed in solutions at 65°C, for 20 minutes, at 650 RPM. Cleaning was observed via SEM.
- High levels of EGBE are effective at cleaning some residues in vias that NMP and Sulfolane chemistries cannot clean.
- Bulk PR removal requires the presence of either Sulfolane or NMP.
- Optimal cleaning solution for both bulk PR as w ell as most residue removal is a mix of high percentage of EGBE with some sulfolane. Catechol and MEA are required for all these cleans.
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Abstract
The present invention utilizes novel compositions and methods for stripping and cleaning microelectronics substrates. The composition includes ethylene glycol butyl ether, sulfolane, monoethanolamine, diethylene glycol, dihydroxybenzene, and water. In a preferred embodiment the composition is used for stripping and cleaning substrates containing aluminum. The composition is also preferably substantially free of composition is substantially free of n- methylpyrrolidone (NMP) and hydroxylamine.
Description
CLEANING COMPOSITIONS FOR MICROELECTRONIC SUBSTRATES
CONTAINING ALUMINUM
RELATED APPLICATIONS [0001] This application claims benefit of U.S. Provisional Application No. 62/349,333, entitled "CLEANING COMPOSITIONS FOR MICROELECTRONIC SUBSTRATES CONTAINING ALUMINUM" filed on June 13, 2016, which is herein incorporated by reference in its entirety.
FIELD OF THE INVENTION
[0002] This invention pertains to cleaning and stripping compositions for microelectronic substrates and particularly for cleaning metal-containing residues from aluminum-containing microelectronics components without causing undue aluminum corrosion.
BACKGROUND
[0003] During the manufacture of microelectronic devices photoresists are employed to transfer images to a microelectronic substrate to create the desired circuit layer. Many of the
microelectronic devices are metallized with aluminum. Such microelectronic substrates may also be composed of and/or employ metals such as titanium, titanium nitride, tungsten and the like as adhesion promoters and diffusion barriers.
[0004] Many alkaline microelectronic stripping and cleaning compositions have been proposed for the removal of cross-linked and hardened photoresists and other residues, such as post etch residues, from such microelectronic substrates. However, one problem with such stripping and cleaning composition is the possibility of metal corrosion occurring as a result of the use of such cleaning compositions. Such corrosion results in whiskers, pitting, notching of metal lines, due at least in part to the reaction of the metals in the device substrates with the alkaline strippers employed. One such alkaline microelectronic stripping and cleaning composition is that disclosed in U.S. Pat. No. 5,308,745. While the stripping and cleaning compositions of that patent have been commercially employed to strip hardened and cross-linked photoresist from substrates, it has been discovered that attempts to clean microelectronic substrates having aluminum metallization and containing residues of metals from layers such as layers of titanium, titanium nitride, tungsten and the like, with the cleaning composition of this patent has resulted
in significant aluminum corrosion or insufficient cleaning of the metal residues. Therefore, there is a limitation on the use of the cleaning compositions of that patent in the cleaning of vias that punch-through underlying layers of titanium, titanium nitride, tungsten and the like.
[0005] Currently the semiconductor cleaning market for aluminum technologies is dominated by hydroxylamine (HA) and/or n-methyl-pyrrolidone (NMP) based chemistries. For safety, health, and cost reasons, the semiconductor industry is moving away from NMP and HA chemistries. Such technology is exemplified in U.S. Patent No. 8,178,482, which discloses stripping and cleaning compositions including N-methyl pyrrolidone (NMP). NMP is on the special health hazard substance list, and can adversely affect an employee when accidentally inhaled or absorbed through the skin, causing headache, stomach pain, nausea, and vomiting. NMP also may be a teratogen, i.e., a substance which could cause malformation of an embryo to a pregnant person. There therefore is a need for HA and NMP free cleaning compositions and methods that are effective at removing residue as well as negative and positive bulk photoresist from semiconductor devices containing Al.
[0006] There is therefore a need for microelectronic stripping and cleaning compositions that can effectively remove such metal residues and do so without any significant aluminum corrosion resulting from the stripping and cleaning composition. There is also a need for stripping and cleaning compositions that, in addition to cleaning these metal residues, will also effectively clean post-ash residues from other vias and from metal lines, as well as cleaning unashed photoresist residue from the substrate. There is also a need for such compositions which are free from NMP, HA, and other environmentally harmful and/or toxic substances.
SUMMARY
[0007] In accordance with this invention, there are provided stripping and cleaning compositions for cleaning microelectronics substrates, the composition including: about 30% to about 50 % by weight ethylene glycol butyl ether, about 20% to about 30% by weight sulfolane, about 10% to about 45% by weight monoethanolamine, about 3% to about 15% by weight diethylene glycol, about 0.5% to about 10% dihydroxybenzene, and about 0.5% to about 50% water. The compositions may additionally comprise one or more components such as metal- complexing/corrosion resisting compounds, other corrosion inhibitors and surfactants.
[0008] In an embodiment, the composition of the invention is used for stripping and cleaning substrates containing aluminum. In an embodiment, the substrates include an aluminum metallized substrate having vias and containing metal residue. In another embodiment, the metal residue includes at least one layer selected from the group consisting of titanium and titanium nitride layers. In another embodiment, the stripping and cleaning compositions include about 35% to about 45% by weight ethylene glycol butyl ether, about 24% to about 27% by weight sulfolane, about 13% to about 15% by weight monoethanolamine, about 4% to about 10% by weight diethylene glycol, about 3% to about 8% of a dihydroxybenzene, and about 9% to about 13% water.
[0009] In an embodiment, the composition is used for stripping and cleaning substrates containing aluminum. In an embodiment, the inventive composition is substantially free of hydroxylamine. In yet another embodiment, the inventive composition is substantially free of n- methylpyrrolidone (NMP).
[0010] In another embodiment, the present invention includes a method for cleaning
microelectronic substrates without producing any substantial corrosion to an aluminum substrate, the process comprising contacting the substrate with a cleaning composition for a time sufficient to clean the substrate, wherein the cleaning composition comprises about 30% to about 50 % by weight ethylene glycol butyl ether, about 20% to about 30% by weight sulfolane, about 10% to about 45% by weight monoethanolamine, about 3% to about 15% by weight diethylene glycol, about 0.5% to about 10% dihydroxybenzene, and about 0.5% to about 50% water.
[0011] The method for cleaning microelectronic substrates according to this invention comprises a method for cleaning microelectronic substrates without producing any substantial metal corrosion, the substrate containing at least one photoresist polymeric material, etch residues and metal residues, the process comprising contacting the substrate with a cleaning composition for a time sufficient to clean the substrate, wherein the cleaning composition includes: about 30% to about 50 % by weight ethylene glycol butyl ether, about 20% to about 30% by weight sulfolane, about 10% to about 45% by weight monoethanolamine, about 5% to about 15% by weight diethylene glycol, about 0.5% to about 10% dihydroxybenzene, and about 0.5% to about 50% water.
[0012] The compositions may additionally comprise one or more components such as metal- complexing/corrosion resisting compounds, other corrosion inhibitors and surfactants. The method of cleaning microelectronic substrates in accordance with this invention is particularly useful for cleaning substrate that comprises an aluminum metallized substrate having vias and containing metal residue, and in an embodiment the metal residue is from at least one of layers of titanium and/or titanium nitride.
DETAILED DESCRIPTION
[0013] The invention also relates to cleaning of vias that punch through metal layers of microelectronics components, such as titanium or titanium nitride layers, while being compatible with underlying aluminum structures, i.e., causing little or no metal corrosion in the
microelectronics components. The invention further relates to such cleaning compositions that also are able to clean post-ash residue from other vias and from metal lines as well as cleaning or stripping unashed photoresist from microelectronics substrates. A further aspect of this invention is a process of cleaning or stripping photoresist and residue from aluminum-containing microelectronics components without causing undue aluminum corrosion.
[0014] Dihydroxybenzene, as used herein, includes catechol, also known as pyrocatechol or 1,2- dihydroxybenzene, and has molecular formula of C6H4(OH)2. It is the ortho isomer of the three isomeric benzenediols. About 20 million kg are now synthetically produced annually as a commodity organic chemical, mainly as a precursor to pesticides, flavors, and fragrances.
Derivatives of catechol may also be used, including 3-methylcatechol, 4-methylcatechol, and 4- tertbutylcatechol.
[0015] The compositions of this invention may also optionally contain other additional components. Such optional additional components include metal-complexing/corrosion resisting compounds, other corrosion inhibitors and surfactants.
[0016] Organic or inorganic chelating or metal complexing agents/corrosion inhibitors are not required, but may optionally be included in the compositions of this invention, but offer substantial benefits, such as for example, improved product stability when incorporated into the aqueous cleaning compositions of this invention. Examples of suitable chelating or complexing agents include but are not limited to trans- 1,2-cyclohexanediamine tetraacetic acid (CyDTA), ethylenediamine tetraacetic acid (EDTA), stannates, pyrophosphates, alkylidene-diphosphonic
acid derivatives (e.g. ethane- 1 -hydroxy- 1,1-diphosphonate), phosphonates containing ethylenediamine, diethylenetriamine or triethylenetetramine functional moieties [e,g.
ethylenediamine tetra(methylene phosphonic acid) (EDTMP), diethylenetriamine
penta(methylene phosphonic acid), triethylenetetramine hexa(methylene phosphonic acid). The chelating agent will be present in the composition in an amount of from 0 to about 5 wt %, preferably from about 0.1 to about 2 wt % based on the weight of the composition.
[0017] The aqueous cleaning compositions of this invention can also optionally contain other corrosion inhibitors and similar non-corrosive components employed in microelectronic cleaner compositions. The compounds may include resorcinol, gallic acid, propyl gallate, pyrogallol, hydroquinone, benzotriazole and derivatives of benzotriazole, and polyfunctional carboxylic acids such as citric acid, tartaric acid, gluconic acid, saccharic acid, glyceric acid, oxalic acid, phthalic acid, maleic acid, mandelic acid, malonic acid, lactic acid, and salicylic acid. These other corrosion inhibitors may be present in any suitable amount, generally in an amount of from about 0 to about 5 wt %, preferably from about 0.1 to about 3 wt %, and more preferably from about 0.2 to about 2 wt %.
[0018] The compositions of the present invention may also optionally contain any suitable water-soluble amphoteric, non-ionic, cationic or anionic surfactant. The addition of a surfactant will reduce the surface tension of the formulation and improve the wetting of the surface to be cleaned and therefore improve the cleaning action of the composition. The surfactant may also be added to reduce aluminum corrosion rates if further aluminum corrosion inhibition is desired. Amphoteric surfactants useful in the compositions of the present invention include betaines and sulfobetaines such as alkyl betaines, amidoalkyl betaines, alkyl sulfobetaines and amidoalkyl sulfobetaines; aminocarboxylic acid derivatives such as amphoglycinates, amphopropionates, amphodiglycinates, and amphodipropionates; iminodiacids such as alkoxyalkyl iminodiacids or alkoxyalkyl iminodiacids; amine oxides such as alkyl amine oxides and alkylamido alkylamine oxides; fluoroalkyl sulfonates and fluorinated alkyl amphoterics; and mixtures thereof.
[0019] Preferably, the amphoteric surfactants are cocoamidopropyl betaine, cocoamidopropyl dimethyl betaine, cocoamidopropyl hydroxy sultaine, capryloamphodipropionate,
cocoamidodipropionate, cocoamphopropionate, cocoamphohydroxyethyl propionate, isodecyloxypropylimino dipropionic acid, laurylimino dipropionate, cocoamidopropylamine
oxide and cocoamine oxide and fluorinated alkyl amphoterics. Non-ionic surfactants useful in the compositions of the present invention include acetylenic diols, ethoxylated acetylenic diols, fluorinated alkyl alkoxylates, fluorinated alkylesters, fluorinated polyoxyethylene alkanols, aliphatic acid esters of polyhydric alcohols, polyoxyethylene monoalkyl ethers, poiyoxyethylene diols, siloxane type surfactants, and alkylene glycol monoalkyl ethers. Preferably, the non-ionic surfactants are acetylenic diols or ethoxylated acetylenic diols. Anionic surfactants useful in the compositions of the present invention include carboxylates, N-acylsarcosinates, sulfonates, sulfates, and mono and diesters of orthophosphoric acid such as decyl phosphate.
[0020] Preferably, the anionic surfactants are metal-free surfactants. Cationic surfactants useful in the compositions of the present invention include amine ethoxylates,
dialkyldimethylammonium salts, dialkylmorpholinum salts, alkylbenzyldimethylammonium salts, alkyltrimethylammonium salts, and alkylpyridinium salts. Preferably, the cationic surfactants are halogen-free surfactants. Example of especially suitable surfactants include, but are not limited to 3,5-dimethyl-l-hexyn-3-ol (Surfynol-61), ethoxylated 2,4,7, 9-tetramethyl-5- decyne-4,7-diol (Surfynol-465), polytetrafluoroethylene cetoxypropylbetaine (Zonyl FSK), Zonyl FSH, Triton X-100, namely octylphenoxypolyethoxyethanol, and the like. The surfactant will generally be present in an amount of from 0 to about 5 wt %, preferably 0.001 to about 3 wt % based on the weight of the composition.
EXAMPLES
[0021] The present invention is further exemplified, but not limited, by the following representative examples, which are intended to illustrate the invention and are not to be construed as being limitations thereto.
Example 1
Formulation A of the present invention:
[0022] Important components for aluminum compatibility are MEA and water. Additionally, catechol is an important component for removal of residue and photoresist.
Example 2
[0023] The closest prior art, represented by U.S. Patent No. 5,308,745 includes a composition comprising a stripping solvent, a nucleophilic amine and a non-nitrogen containing weak acid in an amount sufficient to neutralize from about 19% to about 75% by weight of the nucleophilic amine. Data was collected to show adding acid (acetic acid) to the formulation of our invention does not contribute to photoresist stripping performance. In comparison to a composition with Catechol is specifically required to contribute to photoresist and residue removal performance.
[0024] The wafers tested included bulk photoresist on aluminum. The wafers were all processed in solutions at 65°C, for 20 minutes, and at 650 RPM. Cleaning was observed via SEM.
Solutions tested:
A: 40% EGBE, 25.4% Sulfolane, 5% DEG, 14% MEA, 10.6% Water, 5%
dihydroxybenzene (Inventive composition)
B: 51% NMP; 23% MEA; 13.28% DEG; 10% Water; 2.72% Acetic Acid (prior art comparative example)
C: 51% NMP; 23% MEA; 11.5% DEG; 10% Water; 5.5% Acetic Acid (prior art comparative example)
D. 24% DMSO; 46% MEA; 10% DEG; 10% Water; 10% Acetic Acid (prior art comparative example)
E. 24% DMSO; 46% MEA; 15% DEG; 10% Water; 5% Acetic Acid (prior art comparative example)
TABLE 1
E Poor
[0025] Results of the composition performance are seen in Table 1. Irrespective of solvent, it is apparent dihydroxybenzene is required for cleaning performance. Addition of just a neutralizing acid, such as acetic acid to the solutions containing NMP and DMSO results in poor cleaning performance.
Example 3
[0026] Similarly close prior art is represented by U.S. Patent No. 8,178,482, which describes compositions consisting of: about 20% to about 80 wt % of the composition of N-methyl pyrrolidone, monoethanolamine in an amount of from about 10% to about 45% based on the weight of the composition, from about 5% to about 15% by weight of the composition of diethylene glycol as a metal removing compound, catechol in an amount sufficient to neutralize from about 3% to about 75% by weight of the monoethanolamine such that the stripping composition has an aqueous pH of from about 9.6 to about 10.9, and water. The data below shows by removing catechol and using a mix of EGBE and Sulfolane a cleaner can be obtained that can strip bulk photoresist just as well, shows improved cleaning for aluminum substrates, and does not have the environmental and health hazards associated with NMP.
[0027] For Al cleans, the semiconductor industry typically requires a solution to be able to clean a wide variety of processes. 5 different types of wafers were used to compare cleaning of different systems. The goal here was primarily to look at impact of different solvent systems.
[0028] Wafers tested included bulk photoresist without metal exposed, bulk photoresist with Al exposed, thin organic residue on Al, thick organic residue on Al, and Al via cleans. The wafers were all processed in solutions at 65°C, for 20 minutes, at 650 RPM. Cleaning was observed via SEM.
Solutions tested:
A. 40% EGBE, 25.4% Sulfolane, 5% DEG, 14% MEA, 10.6% Water, 5%
dihydroxybenzene
F. 50% Sulfolane, 23% MEA, 12% DEG, 10% water, 5% catechol
G. 50% EGBE, 23% MEA, 12% DEG, 10% water, 5% catechol
46% NMP, 23% MEA, 10% DEG, 15% water, 5% Catechol
TABLE 2
[0029] High levels of EGBE are effective at cleaning some residues in vias that NMP and Sulfolane chemistries cannot clean. Bulk PR removal requires the presence of either Sulfolane or NMP. Optimal cleaning solution for both bulk PR as w ell as most residue removal is a mix of high percentage of EGBE with some sulfolane. Catechol and MEA are required for all these cleans.
[0030] Thus while there have been described what are presently believed to be preferred embodiments of the invention, those skilled in the art will realize that changes and modifications may be made thereto without departing from the spirit of the invention, and it is intended to claim all such changes and modifications as fall within the true scope of the invention.
Claims
1. A composition for cleaning microelectronics substrates, the composition comprising: about 30% to about 50% by weight ethylene glycol butyl ether, about 20% to about 30% by weight sulfolane, about 10% to about 45% by weight monoethanolamine, about 3% to about 15% by weight diethylene glycol, about 0.5% to about 10% of a dihydroxybenzene, and about 0.5% to about 50% water.
2. The composition according to claim 1 comprising about 35% to about 45% by weight ethylene glycol butyl ether, about 24% to about 27% by weight sulfolane, about 13% to about 15% by weight monoethanolamine, about 4% to about 10% by weight diethylene glycol, about 3% to about 8% of a dihydroxybenzene, and about 9% to about 13% water.
3. The composition according to claim 1 wherein said composition is used for stripping and cleaning substrates containing aluminum.
4. The composition according to claim 1 wherein said substrate comprises an aluminum metallized substrate having vias and containing metal residue.
5. The composition according to claim 4 wherein said metal residue comprises at least one layer selected from the group consisting of titanium and titanium nitride layers.
6. The composition according to claim 1 which is substantially free of hydroxylamine.
7. The composition according to claim 1 which is substantially free of n-methylpyrrolidone (NMP)
8. A method for cleaning microelectronic substrates without producing any substantial corrosion to an aluminum substrate, the process comprising contacting the substrate with a cleaning composition for a time sufficient to clean the substrate, wherein the cleaning composition comprises about 30% to about 50 % by weight ethylene glycol butyl ether, about
20% to about 30% by weight sulfolane, about 10% to about 45% by weight monoethanolamine, about 5% to about 15% by weight diethylene glycol, about 0.5% to about 10%
dihydroxybenzene, and about 0.5% to about 50% water.
9. The method according to claim 8 wherein said composition comprises from about 1.0% to about 8 % dihydrozybenzene by weight, and from about 2% to about 20% water by weight.
10. The method according to claim 8 wherein said composition is substantially free of hydroxylamine.
11. The method according to claim 8 wherein said composition is substantially free of n- methylpyrrolidone (NMP).
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005043250A2 (en) * | 2003-10-22 | 2005-05-12 | Ekc Technology, Inc. | Process for the use of bis-choline and tris-choline in the cleaning of quartz-coated polysilicon and other materials |
US20120028871A1 (en) * | 2009-02-25 | 2012-02-02 | Glenn Westwood | Stripping compositions for cleaning ion implanted photoresist from semiconductor device wafers |
US20120073607A1 (en) * | 2010-09-27 | 2012-03-29 | Eastman Chemical Company | Polymeric or monomeric compositions comprising at least one mono-amide and/or at least one diamide for removing substances from substrates and methods for using the same |
US20140248781A1 (en) * | 2011-06-01 | 2014-09-04 | Avantor Performance Materials, Inc. | Semi-aqueous polymer removal compositions with enhanced compatibility to copper, tungsten, and porous low-k dielectrics |
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2017
- 2017-05-24 WO PCT/US2017/034122 patent/WO2017218147A1/en active Application Filing
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005043250A2 (en) * | 2003-10-22 | 2005-05-12 | Ekc Technology, Inc. | Process for the use of bis-choline and tris-choline in the cleaning of quartz-coated polysilicon and other materials |
US20120028871A1 (en) * | 2009-02-25 | 2012-02-02 | Glenn Westwood | Stripping compositions for cleaning ion implanted photoresist from semiconductor device wafers |
US20120073607A1 (en) * | 2010-09-27 | 2012-03-29 | Eastman Chemical Company | Polymeric or monomeric compositions comprising at least one mono-amide and/or at least one diamide for removing substances from substrates and methods for using the same |
US20140248781A1 (en) * | 2011-06-01 | 2014-09-04 | Avantor Performance Materials, Inc. | Semi-aqueous polymer removal compositions with enhanced compatibility to copper, tungsten, and porous low-k dielectrics |
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