KR102407114B1 - 절연액, 절연체, 박막 트랜지스터 및 전자 소자 - Google Patents
절연액, 절연체, 박막 트랜지스터 및 전자 소자 Download PDFInfo
- Publication number
- KR102407114B1 KR102407114B1 KR1020150076082A KR20150076082A KR102407114B1 KR 102407114 B1 KR102407114 B1 KR 102407114B1 KR 1020150076082 A KR1020150076082 A KR 1020150076082A KR 20150076082 A KR20150076082 A KR 20150076082A KR 102407114 B1 KR102407114 B1 KR 102407114B1
- Authority
- KR
- South Korea
- Prior art keywords
- group
- unsubstituted
- substituted
- formula
- combination
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000010409 thin film Substances 0.000 title claims abstract description 47
- 239000012212 insulator Substances 0.000 title claims abstract description 30
- 239000000976 ink Substances 0.000 title 1
- 239000002105 nanoparticle Substances 0.000 claims abstract description 42
- 125000000524 functional group Chemical group 0.000 claims abstract description 36
- -1 organosilane compound Chemical class 0.000 claims abstract description 30
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 31
- 239000004065 semiconductor Substances 0.000 claims description 24
- 125000003700 epoxy group Chemical group 0.000 claims description 23
- 125000003342 alkenyl group Chemical group 0.000 claims description 19
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 16
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 16
- 239000007788 liquid Substances 0.000 claims description 16
- 239000000377 silicon dioxide Substances 0.000 claims description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 14
- 239000000126 substance Substances 0.000 claims description 14
- 125000001424 substituent group Chemical group 0.000 claims description 14
- 238000004132 cross linking Methods 0.000 claims description 12
- 238000009413 insulation Methods 0.000 claims description 12
- 239000003431 cross linking reagent Substances 0.000 claims description 11
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 125000000304 alkynyl group Chemical group 0.000 claims description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 6
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 6
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 4
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 4
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical group C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 4
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 claims description 4
- 229910002113 barium titanate Inorganic materials 0.000 claims description 4
- 229910000449 hafnium oxide Inorganic materials 0.000 claims description 4
- WIHZLLGSGQNAGK-UHFFFAOYSA-N hafnium(4+);oxygen(2-) Chemical compound [O-2].[O-2].[Hf+4] WIHZLLGSGQNAGK-UHFFFAOYSA-N 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 150000002902 organometallic compounds Chemical class 0.000 claims description 4
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 3
- 229910004283 SiO 4 Inorganic materials 0.000 claims description 3
- 125000000732 arylene group Chemical group 0.000 claims description 3
- 239000002270 dispersing agent Substances 0.000 claims description 3
- 229910044991 metal oxide Inorganic materials 0.000 claims description 3
- 150000004706 metal oxides Chemical class 0.000 claims description 3
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 claims description 3
- 239000012530 fluid Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 2
- 239000002904 solvent Substances 0.000 abstract description 11
- 239000000243 solution Substances 0.000 description 29
- 230000000052 comparative effect Effects 0.000 description 23
- 238000002360 preparation method Methods 0.000 description 22
- 230000015572 biosynthetic process Effects 0.000 description 17
- 238000003786 synthesis reaction Methods 0.000 description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- HNRMPXKDFBEGFZ-UHFFFAOYSA-N ethyl trimethyl methane Natural products CCC(C)(C)C HNRMPXKDFBEGFZ-UHFFFAOYSA-N 0.000 description 6
- 239000010931 gold Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000010936 titanium Substances 0.000 description 6
- 239000010408 film Substances 0.000 description 5
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000011651 chromium Substances 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 238000001723 curing Methods 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 239000004973 liquid crystal related substance Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 239000012752 auxiliary agent Substances 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 229910052737 gold Inorganic materials 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 239000011733 molybdenum Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 3
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 3
- 230000002194 synthesizing effect Effects 0.000 description 3
- 238000001029 thermal curing Methods 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- DEVXQDKRGJCZMV-UHFFFAOYSA-K Aluminum acetoacetate Chemical compound [Al+3].CC(=O)CC([O-])=O.CC(=O)CC([O-])=O.CC(=O)CC([O-])=O DEVXQDKRGJCZMV-UHFFFAOYSA-K 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000002131 composite material Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- VPUGDVKSAQVFFS-UHFFFAOYSA-N coronene Chemical compound C1=C(C2=C34)C=CC3=CC=C(C=C3)C4=C4C3=CC=C(C=C3)C4=C2C3=C1 VPUGDVKSAQVFFS-UHFFFAOYSA-N 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- ZZNQQQWFKKTOSD-UHFFFAOYSA-N diethoxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](OCC)(OCC)C1=CC=CC=C1 ZZNQQQWFKKTOSD-UHFFFAOYSA-N 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- YTVNOVQHSGMMOV-UHFFFAOYSA-N naphthalenetetracarboxylic dianhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=C2C(=O)OC(=O)C1=C32 YTVNOVQHSGMMOV-UHFFFAOYSA-N 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- CLYVDMAATCIVBF-UHFFFAOYSA-N pigment red 224 Chemical compound C=12C3=CC=C(C(OC4=O)=O)C2=C4C=CC=1C1=CC=C2C(=O)OC(=O)C4=CC=C3C1=C42 CLYVDMAATCIVBF-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000004528 spin coating Methods 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 229910052715 tantalum Inorganic materials 0.000 description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 2
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 2
- CYIGRWUIQAVBFG-UHFFFAOYSA-N 1,2-bis(2-ethenoxyethoxy)ethane Chemical compound C=COCCOCCOCCOC=C CYIGRWUIQAVBFG-UHFFFAOYSA-N 0.000 description 1
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- MWZJGRDWJVHRDV-UHFFFAOYSA-N 1,4-bis(ethenoxy)butane Chemical compound C=COCCCCOC=C MWZJGRDWJVHRDV-UHFFFAOYSA-N 0.000 description 1
- CZAVRNDQSIORTH-UHFFFAOYSA-N 1-ethenoxy-2,2-bis(ethenoxymethyl)butane Chemical compound C=COCC(CC)(COC=C)COC=C CZAVRNDQSIORTH-UHFFFAOYSA-N 0.000 description 1
- GZEFZLXJPGMRSP-UHFFFAOYSA-N 37,38,39,40-tetrazanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1(37),2,4,6,8,10,12(39),13,15,17,19,21,23,25,27,29,31,33,35-nonadecaene Chemical compound c1ccc2c3cc4[nH]c(cc5nc(cc6[nH]c(cc(n3)c2c1)c1ccccc61)c1ccccc51)c1ccccc41 GZEFZLXJPGMRSP-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- YENIOYBTCIZCBJ-UHFFFAOYSA-N acetic acid;1-methoxypropan-2-ol Chemical compound CC(O)=O.COCC(C)O YENIOYBTCIZCBJ-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000005103 alkyl silyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 229910052805 deuterium Inorganic materials 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 150000002363 hafnium compounds Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- OLLMEZGFCPWTGD-UHFFFAOYSA-N hexane;methanol Chemical compound OC.OC.CCCCCC OLLMEZGFCPWTGD-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 238000007641 inkjet printing Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- AUHZEENZYGFFBQ-UHFFFAOYSA-N mesitylene Substances CC1=CC(C)=CC(C)=C1 AUHZEENZYGFFBQ-UHFFFAOYSA-N 0.000 description 1
- 125000001827 mesitylenyl group Chemical group [H]C1=C(C(*)=C(C([H])=C1C([H])([H])[H])C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- SLIUAWYAILUBJU-UHFFFAOYSA-N pentacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C21 SLIUAWYAILUBJU-UHFFFAOYSA-N 0.000 description 1
- 150000002964 pentacenes Chemical class 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 238000001259 photo etching Methods 0.000 description 1
- 238000000016 photochemical curing Methods 0.000 description 1
- 229920000553 poly(phenylenevinylene) Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920002098 polyfluorene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000123 polythiophene Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 125000004950 trifluoroalkyl group Chemical group 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 229960000834 vinyl ether Drugs 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
- C09D183/06—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/20—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/102—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/46—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes silicones
-
- H01L51/0512—
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K10/00—Organic devices specially adapted for rectifying, amplifying, oscillating or switching; Organic capacitors or resistors having potential barriers
- H10K10/40—Organic transistors
- H10K10/46—Field-effect transistors, e.g. organic thin-film transistors [OTFT]
- H10K10/462—Insulated gate field-effect transistors [IGFETs]
- H10K10/468—Insulated gate field-effect transistors [IGFETs] characterised by the gate dielectrics
- H10K10/478—Insulated gate field-effect transistors [IGFETs] characterised by the gate dielectrics the gate dielectric comprising a layer of composite material comprising interpenetrating or embedded materials, e.g. TiO2 particles in a polymer matrix
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/10—Organic polymers or oligomers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/40—Organosilicon compounds, e.g. TIPS pentacene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/20—Polysiloxanes containing silicon bound to unsaturated aliphatic groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/80—Siloxanes having aromatic substituents, e.g. phenyl side groups
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K71/00—Manufacture or treatment specially adapted for the organic devices covered by this subclass
- H10K71/10—Deposition of organic active material
- H10K71/12—Deposition of organic active material using liquid deposition, e.g. spin coating
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Composite Materials (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Thin Film Transistor (AREA)
- Oil, Petroleum & Natural Gas (AREA)
Abstract
Description
도 2는 실시예 1 내지 4에 따른 박막 트랜지스터의 절연 강도를 보여주는 그래프이고,
도 3은 비교예 1에 따른 박막 트랜지스터의 절연 강도를 보여주는 그래프이고,
도 4는 비교예 2에 따른 박막 트랜지스터의 절연 강도를 보여주는 그래프이다.
실시예 1 | 실시예 2 | 실시예 3 | 실시예 4 | 비교예 1 | 비교예 2 | 비교예 3 | |
유전율 (@1kHz) |
4.26 | 5.13 | 5.21 | 5.21 | 3.8 | 3.9 | 3.5 |
전하이동도(㎠/Vㆍs) | 오프전류(Ioff) | 온-오프 전류비 (Ion/Ioff) | |
실시예 1 | 2.45 | 2.3 x 10-11 | 6.7 x 106 |
실시예 2 | 2.15 | 3.8 x 10-11 | 6.1 x 106 |
실시예 3 | 3.44 | 1.5 x 10-11 | 1.3 x 107 |
실시예 4 | 2.22 | 2.8 x 10-11 | 7.6 x 106 |
비교예 1 | 0.8 | 2.3 x 10-10 | 8.8 x 104 |
비교예 2 | 0.9 | 5.6 x 10-10 | 1.5 x 105 |
140: 게이트 절연체 154: 유기 반도체
173: 소스 전극 175: 드레인 전극
Claims (20)
- 중합성 작용기를 가진 치환기가 결합된 나노입자,
오가노실란 화합물 및 폴리오가노실록산 중 적어도 하나, 그리고
용매
를 포함하는 절연액.
- 제1항에서,
상기 중합성 작용기는 (메타)아크릴레이트기, 에폭시기, 스티렌기, 아크릴로니트릴기, N-비닐피롤리돈기, 비닐기, 이들의 유도체 또는 그 조합을 포함하는 절연액.
- 제1항에서,
상기 오가노실란 화합물 및 상기 폴리오가노실록산은 적어도 하나의 반응성 작용기를 가지는 절연액.
- 제4항에서,
상기 반응성 작용기는 치환 또는 비치환된 C2 내지 C30 알케닐기, 치환 또는 비치환된 C1 내지 C30 에폭시기 또는 이들의 조합을 포함하는 절연액.
- 제1항에서,
상기 오가노실란 화합물은 하기 화학식 2 내지 5 중 어느 하나로 표현되는 절연액:
[화학식 2]
R1R2R3SiZ1
[화학식 3]
R4R5SiZ2Z3
[화학식 4]
R6SiZ4Z5Z6
[화학식 5]
SiZ7Z8Z9Z10
상기 화학식 2 내지 5에서,
R1 내지 R6은 각각 독립적으로 수소, 치환 또는 비치환된 C1 내지 C30 알킬기, 치환 또는 비치환된 C3 내지 C30 사이클로알킬기, 치환 또는 비치환된 C6 내지 C30 아릴기, 치환 또는 비치환된 C7 내지 C30 아릴알킬기, 치환 또는 비치환된 C1 내지 C30 헤테로알킬기, 치환 또는 비치환된 C2 내지 C30 헤테로사이클로알킬기, 치환 또는 비치환된 C2 내지 C30 알케닐기, 치환 또는 비치환된 C2 내지 C30 알키닐기, 치환 또는 비치환된 C1 내지 C30 알콕시기, 치환 또는 비치환된 C1 내지 C30 에폭시기, 치환 또는 비치환된 C1 내지 C30 카르보닐기, 히드록시 또는 이들의 조합이고,
Z1 내지 Z10은 각각 독립적으로 치환 또는 비치환된 C1 내지 C6 알콕시기, 할로겐기, 카르복실기 또는 이들의 조합이다.
- 제6항에서,
상기 화학식 2 내지 5의 R1 내지 R6 중 적어도 하나는 치환 또는 비치환된 C2 내지 C30 알케닐기, 치환 또는 비치환된 C1 내지 C30 에폭시기 또는 이들의 조합을 포함하는 절연액.
- 제1항에서,
상기 폴리오가노실록산은 하기 화학식 6으로 표현되는 구조를 가지는 절연액:
[화학식 6]
(R1R2R3SiO1 /2)M1(R4R5SiO2 /2)D1(R6SiO3 /2)T1(SiO4 /2)Q1
상기 화학식 6에서,
R1 내지 R6은 각각 독립적으로 수소, 치환 또는 비치환된 C1 내지 C30 알킬기, 치환 또는 비치환된 C3 내지 C30 사이클로알킬기, 치환 또는 비치환된 C6 내지 C30 아릴기, 치환 또는 비치환된 C7 내지 C30 아릴알킬기, 치환 또는 비치환된 C1 내지 C30 헤테로알킬기, 치환 또는 비치환된 C2 내지 C30 헤테로사이클로알킬기, 치환 또는 비치환된 C2 내지 C30 알케닐기, 치환 또는 비치환된 C2 내지 C30 알키닐기, 치환 또는 비치환된 C1 내지 C30 알콕시기, 치환 또는 비치환된 C1 내지 C30 에폭시기, 치환 또는 비치환된 C1 내지 C30 카르보닐기, 히드록시 또는 이들의 조합이고,
0≤M1<1, 0≤D1<1, 0≤T1<1, 0≤Q1<1이고,
M+D+T+Q=1이다.
- 제8항에서,
상기 화학식 6의 R1 내지 R6 중 적어도 하나는 치환 또는 비치환된 C2 내지 C30 알케닐기, 치환 또는 비치환된 C1 내지 C30 에폭시기 또는 이들의 조합을 포함하는 절연액.
- 제8항에서,
상기 화학식 6의 R4 내지 R6 중 적어도 하나는 치환 또는 비치환된 C2 내지 C30 알케닐기, 치환 또는 비치환된 C1 내지 C30 에폭시기 또는 이들의 조합을 포함하는 절연액.
- 제1항에서,
상기 나노입자는 금속 산화물을 포함하는 절연액.
- 제11항에서,
상기 나노입자는 실리카, 티타니아, 티탄산바륨, 지르코니아, 황산바륨, 알루미나, 하프늄산화물 또는 이들의 조합을 포함하는 절연액.
- 제1항에서,
상기 중합성 작용기를 가진 치환기가 결합된 나노 입자는 상기 오가노실란 화합물 및 상기 폴리오가노실록산 중 적어도 하나 100 중량부에 대하여 2 내지 70중량부로 포함되는 절연액.
- 제1항에서,
가교제 및 가교 보조제 중 적어도 하나를 더 포함하는 절연액.
- 제14항에서,
상기 가교제는 (메타)아크릴레이트 화합물 또는 에테르 화합물이고,
상기 가교보조제는 유기금속화합물인
절연액.
- 제1항에서,
광 개시제, 광산발생제 및 분산제 중 적어도 하나를 더 포함하는 절연액.
- 제1항 내지 제16항 중 어느 한 항에 따른 절연액의 경화물을 포함하는 절연체.
- 게이트 전극,
상기 게이트 전극과 중첩하는 반도체,
상기 게이트 전극과 상기 반도체 사이에 위치하는 제17항에 따른 절연체, 그리고
상기 반도체와 전기적으로 연결되어 있는 소스 전극 및 드레인 전극
을 포함하는 박막 트랜지스터.
- 제18항에서,
상기 반도체는 유기 반도체인 박막 트랜지스터.
- 제18항에 따른 박막 트랜지스터를 포함하는 전자 소자.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020150076082A KR102407114B1 (ko) | 2015-05-29 | 2015-05-29 | 절연액, 절연체, 박막 트랜지스터 및 전자 소자 |
US14/919,116 US10358578B2 (en) | 2015-05-29 | 2015-10-21 | Insulating ink and insulator and thin film transistor and electronic device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020150076082A KR102407114B1 (ko) | 2015-05-29 | 2015-05-29 | 절연액, 절연체, 박막 트랜지스터 및 전자 소자 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20160140022A KR20160140022A (ko) | 2016-12-07 |
KR102407114B1 true KR102407114B1 (ko) | 2022-06-08 |
Family
ID=57399654
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020150076082A Active KR102407114B1 (ko) | 2015-05-29 | 2015-05-29 | 절연액, 절연체, 박막 트랜지스터 및 전자 소자 |
Country Status (2)
Country | Link |
---|---|
US (1) | US10358578B2 (ko) |
KR (1) | KR102407114B1 (ko) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6581446B2 (ja) * | 2015-09-09 | 2019-09-25 | 東芝メモリ株式会社 | 絶縁膜及び記憶装置 |
WO2019065561A1 (ja) | 2017-09-29 | 2019-04-04 | 東レ株式会社 | 電界効果型トランジスタ、その製造方法、それを用いた無線通信装置および商品タグ |
JP2021005625A (ja) | 2019-06-26 | 2021-01-14 | メルク、パテント、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツングMerck Patent GmbH | ゲート絶縁膜形成組成物 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100323570A1 (en) | 2007-12-28 | 2010-12-23 | Kumar Ramesh C | Copolymers of nanoparticles, vinyl monomers and silicone |
US20110086946A1 (en) | 2008-06-13 | 2011-04-14 | Dic Corporation | Ink composition for forming insulating film and insulating film formed from the ink composition |
Family Cites Families (53)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1195416A3 (de) | 2000-10-05 | 2005-12-28 | Degussa AG | Polymerisierbare siliciumorganische Nanokapseln |
US20040198882A1 (en) | 2003-03-31 | 2004-10-07 | Fuji Photo Film Co., Ltd. | Silica-containing coating composition for forming films and method for forming silica-containing films |
KR101012950B1 (ko) | 2003-10-15 | 2011-02-08 | 삼성전자주식회사 | 유기 절연체 형성용 조성물 및 이를 이용하여 제조된 유기절연체 |
WO2005121265A1 (ja) | 2004-06-11 | 2005-12-22 | Toray Industries, Inc. | シロキサン系塗料、光学物品およびシロキサン系塗料の製造方法 |
US7170093B2 (en) | 2004-11-05 | 2007-01-30 | Xerox Corporation | Dielectric materials for electronic devices |
JP4386361B2 (ja) | 2005-01-18 | 2009-12-16 | 信越化学工業株式会社 | 電極保護用シリコーンゴム組成物 |
US20070049659A1 (en) | 2005-08-25 | 2007-03-01 | Quay Jeffrey R | Functionalized alumina particles for polymer composites |
JP4939012B2 (ja) | 2005-08-26 | 2012-05-23 | ルネサスエレクトロニクス株式会社 | 半導体装置 |
JP5003081B2 (ja) | 2005-09-28 | 2012-08-15 | 東レ株式会社 | 感光性シロキサン組成物、それから形成された硬化膜、および硬化膜を有する素子 |
US8134144B2 (en) | 2005-12-23 | 2012-03-13 | Xerox Corporation | Thin-film transistor |
JP5063915B2 (ja) | 2006-04-04 | 2012-10-31 | アトミクス株式会社 | 紫外線硬化型コーティング用組成物およびこれを被覆してなる樹脂被覆品 |
KR101174769B1 (ko) | 2006-06-30 | 2012-08-17 | 엘지디스플레이 주식회사 | 박막트랜지스터의 제조방법 및 이를 이용한 tft 어레이기판의 제조방법 |
US8138355B2 (en) | 2006-08-28 | 2012-03-20 | Tosoh Corporation | Heteroacene derivative, tetrahaloterphenyl derivative, and processes for producing the same |
TWI462359B (zh) | 2006-10-20 | 2014-11-21 | Nippon Kayaku Kk | 場效電晶體及其製造方法 |
CN101528753B (zh) | 2006-10-25 | 2012-05-23 | 国立大学法人广岛大学 | 缩合多环芳香族化合物及其制造方法和用途 |
WO2008086402A1 (en) | 2007-01-09 | 2008-07-17 | Inframat Corporation | Coating compositions for marine applications and methods of making and using the same |
JP4840255B2 (ja) | 2007-05-29 | 2011-12-21 | Jsr株式会社 | パターン形成方法及びそれに用いる樹脂組成物 |
KR101353824B1 (ko) | 2007-06-12 | 2014-01-21 | 삼성전자주식회사 | 유기 절연체 형성용 조성물 및 이를 이용하여 제조된 유기절연체 |
WO2009009790A1 (en) | 2007-07-12 | 2009-01-15 | President And Fellows Of Harvard College | Air-stable, high hole mobility thieno-thiophene derivatives |
KR100884357B1 (ko) | 2007-09-18 | 2009-02-17 | 한국전자통신연구원 | 유기 게이트 절연막 및 이를 이용한 유기 박막 트랜지스터 |
JP5525152B2 (ja) | 2007-10-01 | 2014-06-18 | アトミクス株式会社 | 紫外線硬化型コーティング用組成物およびその製造方法、並びにこれを被覆してなる樹脂被覆品 |
CN101896537B (zh) | 2007-12-10 | 2012-10-24 | 株式会社钟化 | 具有碱显影性的固化性组合物、使用该组合物的绝缘性薄膜以及薄膜晶体管 |
KR20100126407A (ko) | 2008-03-18 | 2010-12-01 | 도레이 카부시키가이샤 | 게이트 절연 재료, 게이트 절연막 및 유기 전계 효과형 트랜지스터 |
JP5284677B2 (ja) | 2008-04-25 | 2013-09-11 | 山本化成株式会社 | 有機トランジスタ |
KR101040320B1 (ko) | 2008-08-29 | 2011-06-10 | 고려대학교 산학협력단 | 절연막 및 절연막의 제조 방법 |
JPWO2010044332A1 (ja) | 2008-10-14 | 2012-03-15 | コニカミノルタホールディングス株式会社 | 薄膜トランジスタ及びその製造方法 |
JP2010147206A (ja) | 2008-12-18 | 2010-07-01 | Konica Minolta Holdings Inc | 薄膜トランジスタ、及びその製造方法 |
KR101184448B1 (ko) | 2008-12-29 | 2012-09-20 | 제일모직주식회사 | 자외선 경화형 하드코팅용 조성물, 이를 이용한 내오염성이 우수한 편광판 및 하드코팅층 형성 방법 |
WO2010078320A2 (en) | 2008-12-31 | 2010-07-08 | Bridgestone Corporation | Core-first nanoparticle formation process, nanoparticle, and composition |
JP2010250733A (ja) * | 2009-04-20 | 2010-11-04 | Seiko Epson Corp | タッチパネルの製造方法、絶縁膜形成インク |
JP2011187558A (ja) | 2010-03-05 | 2011-09-22 | Adeka Corp | 有機薄膜トランジスタ |
JP2011186069A (ja) | 2010-03-05 | 2011-09-22 | Adeka Corp | 感光性樹脂組成物 |
EP2563827B1 (en) | 2010-04-26 | 2017-06-21 | Momentive Performance Materials Inc. | Chlorine-resistant crosslinkable polyolefin compositions and articles made therefrom |
JP2011246548A (ja) | 2010-05-25 | 2011-12-08 | Showa Denko Kk | 硬化性樹脂組成物および透明フィルム |
US8557943B2 (en) | 2011-04-29 | 2013-10-15 | International Business Machines Corporation | Nanostructured organosilicates from thermally curable block copolymers |
EP2791263B1 (en) | 2011-12-14 | 2016-08-31 | Dow Corning Corporation | Curable compositions of resin-linear organosiloxane block copolymers |
EP2815880A4 (en) | 2012-02-15 | 2015-10-21 | Konica Minolta Inc | FUNCTIONAL FILM, METHOD FOR PRODUCING THE SAME, AND ELECTRONIC DEVICE COMPRISING A FUNCTIONAL FILM |
JP2013234301A (ja) | 2012-05-11 | 2013-11-21 | Shin-Etsu Chemical Co Ltd | 光及び熱硬化性樹脂組成物、成形品及び物品 |
JP5884647B2 (ja) | 2012-06-01 | 2016-03-15 | 信越化学工業株式会社 | 硬化性組成物及びその硬化成形品、その硬化皮膜が形成されてなる物品並びに該硬化性組成物の硬化方法 |
CN104334351B (zh) | 2012-06-05 | 2016-08-17 | 爱克发印艺公司 | 平版印刷版前体 |
EP2671880B1 (en) | 2012-06-05 | 2015-09-16 | Samsung Electronics Co., Ltd | Fused polycyclic heteroaromatic compound, organic thin film including compound and electronic device including organic thin film |
KR20150042237A (ko) | 2012-08-08 | 2015-04-20 | 쓰리엠 이노베이티브 프로퍼티즈 캄파니 | 캡슐화 배리어 필름을 갖는 광기전 소자 |
KR20150041058A (ko) | 2012-08-08 | 2015-04-15 | 쓰리엠 이노베이티브 프로퍼티즈 캄파니 | 다이우레탄 (메트)아크릴레이트-실란 조성물 및 이를 포함하는 물품 |
JP2014037453A (ja) | 2012-08-10 | 2014-02-27 | Mitsubishi Chemicals Corp | 活性エネルギー線硬化性樹脂組成物およびそれを用いた積層体 |
JP6017894B2 (ja) | 2012-09-03 | 2016-11-02 | 信越化学工業株式会社 | ネガ型平版印刷版原版用感光性組成物及びそれを用いたネガ型平版印刷用原版 |
JP6288488B2 (ja) | 2012-09-27 | 2018-03-07 | Dic株式会社 | 絶縁材料、絶縁膜及びこれを用いたトランジスタ |
KR20150073981A (ko) | 2012-10-19 | 2015-07-01 | 다우 글로벌 테크놀로지스 엘엘씨 | 실란-개질된 중합체, 에폭시 수지 및 경화 촉매의 조성물, 및 상기 조성물을 포함하는 중합체 콘크리트 |
US9721697B2 (en) | 2012-11-08 | 2017-08-01 | Eastman Kodak Company | Organic polymeric bi-metallic composites |
KR101583119B1 (ko) | 2012-11-29 | 2016-01-07 | 주식회사 엘지화학 | 가스차단성 필름 |
KR102203794B1 (ko) | 2013-03-05 | 2021-01-15 | 제이엔씨 주식회사 | 칼코겐 함유 유기 화합물 및 그의 용도 |
JP2014218593A (ja) | 2013-05-09 | 2014-11-20 | 信越化学工業株式会社 | 低温硬化性コーティング剤組成物及びその硬化皮膜を有する物品 |
KR102153604B1 (ko) * | 2013-09-27 | 2020-09-08 | 삼성전자주식회사 | 절연체용 조성물, 절연체 및 박막 트랜지스터 |
US9431619B2 (en) | 2013-09-27 | 2016-08-30 | Samsung Electronics Co., Ltd. | Composition for insulator, insulator, and thin film transistor |
-
2015
- 2015-05-29 KR KR1020150076082A patent/KR102407114B1/ko active Active
- 2015-10-21 US US14/919,116 patent/US10358578B2/en active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100323570A1 (en) | 2007-12-28 | 2010-12-23 | Kumar Ramesh C | Copolymers of nanoparticles, vinyl monomers and silicone |
US20110086946A1 (en) | 2008-06-13 | 2011-04-14 | Dic Corporation | Ink composition for forming insulating film and insulating film formed from the ink composition |
Also Published As
Publication number | Publication date |
---|---|
US10358578B2 (en) | 2019-07-23 |
KR20160140022A (ko) | 2016-12-07 |
US20160347969A1 (en) | 2016-12-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP3029118B1 (en) | Composition, electronic device, and thin film transistor | |
EP2259289A1 (en) | Gate insulating material, gate insulating film, and organic field effect transistor | |
EP2975649A1 (en) | Field effect transistor | |
EP2147948B1 (en) | Polyimide precursor, polyimide, and coating solution for under layer film for image formation | |
EP3135739B1 (en) | Composition, electronic device, and thin film transistor | |
KR102407114B1 (ko) | 절연액, 절연체, 박막 트랜지스터 및 전자 소자 | |
US9431619B2 (en) | Composition for insulator, insulator, and thin film transistor | |
CN103828062A (zh) | 有机半导体绝缘膜用组合物及有机半导体绝缘膜 | |
KR102153604B1 (ko) | 절연체용 조성물, 절연체 및 박막 트랜지스터 | |
KR101258294B1 (ko) | 가교성 유기 절연체 형성용 조성물 및 이를 이용하여제조된 유기 절연체 | |
Oh et al. | Highly condensed fluorinated methacrylate hybrid material for transparent low-k passivation layer in LCD-TFT | |
KR102259939B1 (ko) | 절연체 표면 개질용 조성물, 절연체의 표면 개질 방법, 절연체, 및 박막 트랜지스터 | |
JP5728908B2 (ja) | ゲート絶縁材料、ゲート絶縁膜、および電界効果型トランジスタ。 | |
US8212030B2 (en) | Composition for producing insulator and organic insulator using the same | |
KR101386908B1 (ko) | 유기박막 트랜지스터용 게이트 절연막 조성물 및 그의 제조방법 | |
KR101330260B1 (ko) | 유기절연체 조성물 및 이를 이용한 유기절연막을 함유하는 유기박막트랜지스터 | |
JPWO2008096850A1 (ja) | 有機薄膜トランジスタ用絶縁膜材料及びこれを用いた有機薄膜トランジスタ | |
KR100779560B1 (ko) | 유기 박막 트랜지스터용 자가 패턴성 유전체 박막, 그 제조 방법, 및 이를 구비한 유기 박막 트랜지스터 | |
KR20140025749A (ko) | 트랜지스터용 자외선 경화형 하이브리드 게이트 절연막 조성물 및 이로부터 제조된 트랜지스터용 게이트 절연막 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 20150529 |
|
PG1501 | Laying open of application | ||
A201 | Request for examination | ||
PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20200429 Comment text: Request for Examination of Application Patent event code: PA02011R01I Patent event date: 20150529 Comment text: Patent Application |
|
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20211116 Patent event code: PE09021S01D |
|
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20220530 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20220603 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20220603 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration |