KR102497282B1 - 포토레지스트 조성물 및 이를 이용한 컬러 필터 - Google Patents
포토레지스트 조성물 및 이를 이용한 컬러 필터 Download PDFInfo
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- KR102497282B1 KR102497282B1 KR1020160118217A KR20160118217A KR102497282B1 KR 102497282 B1 KR102497282 B1 KR 102497282B1 KR 1020160118217 A KR1020160118217 A KR 1020160118217A KR 20160118217 A KR20160118217 A KR 20160118217A KR 102497282 B1 KR102497282 B1 KR 102497282B1
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- quantum dot
- meth
- photoresist composition
- acrylate
- nanocomposite
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- 239000000203 mixture Substances 0.000 title claims abstract description 98
- 229920002120 photoresistant polymer Polymers 0.000 title claims abstract description 88
- 239000002096 quantum dot Substances 0.000 claims description 181
- 239000002114 nanocomposite Substances 0.000 claims description 99
- 239000002105 nanoparticle Substances 0.000 claims description 78
- 239000010410 layer Substances 0.000 claims description 60
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 53
- 239000003999 initiator Substances 0.000 claims description 45
- 239000004054 semiconductor nanocrystal Substances 0.000 claims description 34
- 238000006243 chemical reaction Methods 0.000 claims description 29
- 239000011347 resin Substances 0.000 claims description 27
- 229920005989 resin Polymers 0.000 claims description 27
- 239000000178 monomer Substances 0.000 claims description 25
- 238000005424 photoluminescence Methods 0.000 claims description 25
- 150000001875 compounds Chemical class 0.000 claims description 24
- 239000011247 coating layer Substances 0.000 claims description 22
- 229910010272 inorganic material Inorganic materials 0.000 claims description 21
- 239000011147 inorganic material Substances 0.000 claims description 21
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 claims description 19
- 239000011230 binding agent Substances 0.000 claims description 18
- SBIBMFFZSBJNJF-UHFFFAOYSA-N selenium;zinc Chemical compound [Se]=[Zn] SBIBMFFZSBJNJF-UHFFFAOYSA-N 0.000 claims description 18
- 239000011258 core-shell material Substances 0.000 claims description 17
- 239000002904 solvent Substances 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 14
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims description 12
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 11
- 239000004593 Epoxy Substances 0.000 claims description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 10
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 10
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims description 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims description 9
- 229910004613 CdTe Inorganic materials 0.000 claims description 8
- 229910002601 GaN Inorganic materials 0.000 claims description 8
- 229910005540 GaP Inorganic materials 0.000 claims description 8
- 229910001218 Gallium arsenide Inorganic materials 0.000 claims description 8
- 229910000673 Indium arsenide Inorganic materials 0.000 claims description 8
- 229910007709 ZnTe Inorganic materials 0.000 claims description 8
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 8
- 239000012965 benzophenone Substances 0.000 claims description 8
- RPQDHPTXJYYUPQ-UHFFFAOYSA-N indium arsenide Chemical compound [In]#[As] RPQDHPTXJYYUPQ-UHFFFAOYSA-N 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 claims description 7
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 6
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- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 claims description 4
- 239000007983 Tris buffer Substances 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 4
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 claims description 4
- DMFAHCVITRDZQB-UHFFFAOYSA-N 1-propoxypropan-2-yl acetate Chemical compound CCCOCC(C)OC(C)=O DMFAHCVITRDZQB-UHFFFAOYSA-N 0.000 claims description 3
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 claims description 3
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 claims description 3
- SFAMKDPMPDEXGH-UHFFFAOYSA-N 2-hydroxyethyl propanoate Chemical compound CCC(=O)OCCO SFAMKDPMPDEXGH-UHFFFAOYSA-N 0.000 claims description 3
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 3
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 3
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 3
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 3
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 claims description 2
- MLKIVXXYTZKNMI-UHFFFAOYSA-N 1-(4-dodecylphenyl)-2-hydroxy-2-methylpropan-1-one Chemical compound CCCCCCCCCCCCC1=CC=C(C(=O)C(C)(C)O)C=C1 MLKIVXXYTZKNMI-UHFFFAOYSA-N 0.000 claims description 2
- JNGALPZRHWQEEZ-UHFFFAOYSA-N 1-(4-phenylsulfanylphenyl)octan-1-one Chemical compound C1=CC(C(=O)CCCCCCC)=CC=C1SC1=CC=CC=C1 JNGALPZRHWQEEZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 claims description 2
- YIKSHDNOAYSSPX-UHFFFAOYSA-N 1-propan-2-ylthioxanthen-9-one Chemical compound S1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C(C)C YIKSHDNOAYSSPX-UHFFFAOYSA-N 0.000 claims description 2
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 claims description 2
- BRKORVYTKKLNKX-UHFFFAOYSA-N 2,4-di(propan-2-yl)thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C(C)C)=CC(C(C)C)=C3SC2=C1 BRKORVYTKKLNKX-UHFFFAOYSA-N 0.000 claims description 2
- BTJPUDCSZVCXFQ-UHFFFAOYSA-N 2,4-diethylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC(CC)=C3SC2=C1 BTJPUDCSZVCXFQ-UHFFFAOYSA-N 0.000 claims description 2
- LZHUBCULTHIFNO-UHFFFAOYSA-N 2,4-dihydroxy-1,5-bis[4-(2-hydroxyethoxy)phenyl]-2,4-dimethylpentan-3-one Chemical compound C=1C=C(OCCO)C=CC=1CC(C)(O)C(=O)C(O)(C)CC1=CC=C(OCCO)C=C1 LZHUBCULTHIFNO-UHFFFAOYSA-N 0.000 claims description 2
- PUBNJSZGANKUGX-UHFFFAOYSA-N 2-(dimethylamino)-2-[(4-methylphenyl)methyl]-1-(4-morpholin-4-ylphenyl)butan-1-one Chemical compound C=1C=C(N2CCOCC2)C=CC=1C(=O)C(CC)(N(C)C)CC1=CC=C(C)C=C1 PUBNJSZGANKUGX-UHFFFAOYSA-N 0.000 claims description 2
- FGTYTUFKXYPTML-UHFFFAOYSA-N 2-benzoylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 FGTYTUFKXYPTML-UHFFFAOYSA-N 0.000 claims description 2
- ZCDADJXRUCOCJE-UHFFFAOYSA-N 2-chlorothioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3SC2=C1 ZCDADJXRUCOCJE-UHFFFAOYSA-N 0.000 claims description 2
- QPXVRLXJHPTCPW-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-(4-propan-2-ylphenyl)propan-1-one Chemical compound CC(C)C1=CC=C(C(=O)C(C)(C)O)C=C1 QPXVRLXJHPTCPW-UHFFFAOYSA-N 0.000 claims description 2
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 claims description 2
- MYISVPVWAQRUTL-UHFFFAOYSA-N 2-methylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(C)=CC=C3SC2=C1 MYISVPVWAQRUTL-UHFFFAOYSA-N 0.000 claims description 2
- MWDGNKGKLOBESZ-UHFFFAOYSA-N 2-oxooctanal Chemical compound CCCCCCC(=O)C=O MWDGNKGKLOBESZ-UHFFFAOYSA-N 0.000 claims description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 claims description 2
- NQSMEZJWJJVYOI-UHFFFAOYSA-N Methyl 2-benzoylbenzoate Chemical compound COC(=O)C1=CC=CC=C1C(=O)C1=CC=CC=C1 NQSMEZJWJJVYOI-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- 239000004793 Polystyrene Substances 0.000 claims description 2
- DBHQYYNDKZDVTN-UHFFFAOYSA-N [4-(4-methylphenyl)sulfanylphenyl]-phenylmethanone Chemical compound C1=CC(C)=CC=C1SC1=CC=C(C(=O)C=2C=CC=CC=2)C=C1 DBHQYYNDKZDVTN-UHFFFAOYSA-N 0.000 claims description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 claims description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 2
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 2
- LYXOWKPVTCPORE-UHFFFAOYSA-N phenyl-(4-phenylphenyl)methanone Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1C(=O)C1=CC=CC=C1 LYXOWKPVTCPORE-UHFFFAOYSA-N 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 2
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- 229920002223 polystyrene Polymers 0.000 claims description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims description 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc oxide Inorganic materials [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 2
- VRCACYBCECBXLM-UHFFFAOYSA-N 1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)N1CCOCC1 VRCACYBCECBXLM-UHFFFAOYSA-N 0.000 claims 1
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- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
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Abstract
Description
도 2는 본 발명의 일 구현예를 따르는 표시 장치의 구조를 개략적으로 나타낸 도면이다.
도 3은 합성예 1에서 제조된 제1양자점 나노 복합체의 투과 전자 현미경(TEM) 사진이다.
도 4는 합성예 2에서 제조된 제2양자점 나노 복합체의 투과 전자 현미경(TEM) 사진이다.
도 5 내지 10은 각각 미세 패턴이 형성된 실시예 2-1, 2-2 및 비교예 2-1 내지 2-4의 컬러 필터 1~6의 표면의 주사전자 현미경(SEM) 사진이다.
패턴성 평가 | |
실시예 2-1 | 양호 |
실시예 2-2 | 양호 |
비교예 2-1 | 불량 |
비교예 2-2 | 불량 |
비교예 2-3 | 불량 |
비교예 2-4 | 불량 |
포토레지스트 조성물 | 발광 유지율 (파장: 640nm) |
발광 유지율 (파장: 545nm) |
|
실시예 2-1 | 1 | 91 | - |
실시예 2-2 | 2 | - | 87 |
비교예 2-1 | 3 | 65 | - |
비교예 2-2 | 4 | - | 58 |
비교예 2-3 | 5 | 90 | - |
비교예 2-4 | 6 | - | 86 |
110, 1610: 투명 기판 120: 밴드 컷 필터
130, 1620: 격벽
140, 1630: 제1색변환층
150, 1640: 제2색변환층
160, 1650: 산란물질층
1001: 표시 장치
1100: 백라이트 장치 1200: 하부 기판
1210: 하부 편광판 1220: 제1기판
1230: TFT 어레이층 1240: 화소 전극
1300: 액정층 1400: 상부 기판
1410: 상부 편광판 1420: 제2기판
1430: 공통 전극
C1: 제1화소 영역
C2: 제2화소 영역
C3: 제3화소 영역
Claims (20)
- 포토루미네선스(photo-luminescence) 나노 복합체;
광중합성 단량체;
제1광중합 개시제;
제2광중합 개시제;
바인더 수지; 및
용매;를 포함하고,
상기 포토루미네선스 나노 복합체는 제1양자점 나노 복합체, 제2양자점 나노 복합체, 또는 이의 임의의 조합을 포함하고,
상기 제1양자점 나노 복합체는 제1양자점 나노 입자 및 상기 제1양자점 나노 입자를 둘러싸고 제1무기물을 포함한 제1코팅층을 포함하고, 상기 제2양자점 나노 복합체는 제2양자점 나노 입자 및 상기 제2양자점 나노 입자를 둘러싸고 제2무기물을 포함한 제2코팅층을 포함하고,
상기 제1광중합 개시제는 옥심계 화합물을 포함하고,
상기 제2광중합 개시제는 아세토페논계 화합물, 티오크산톤계 화합물, 벤조페논계 화합물, 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1항에 있어서,
상기 제1양자점 나노 입자는 제1반도체 나노 결정을 포함한 코어, 상기 코어를 둘러싸고 제2반도체 나노 결정을 포함한 제1쉘 및 제3반도체 나노 결정을 포함한 제2쉘을 포함한 코어-쉘-쉘 구조를 갖는, 포토레지스트 조성물. - 제2항에 있어서,
상기 제1반도체 나노 결정, 제2반도체 나노 결정 및 제3반도체 나노 결정은 서로 독립적으로, CdS, CdSe, CdTe, ZnS, ZnSe, ZnTe, InP, InN, InAs, GaN, GaP, GaAs, ZnCdS, ZnSeS, ZnCdSeS, CdZnSe, InZnP, InGaP, GaPZnS, GaPZnSe, GaPZnSeS, 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1항에 있어서,
상기 제2양자점 나노 입자는 제4반도체 나노 결정을 포함한 코어 및 상기 코어를 둘러싸고 제5반도체 나노 결정을 포함한 쉘을 포함한 코어-쉘 구조를 갖는, 포토레지스트 조성물. - 제4항에 있어서,
상기 제4반도체 나노 결정 및 상기 제5반도체 나노 결정은 서로 독립적으로, CdS, CdSe, CdTe, ZnS, ZnSe, ZnTe, InP, InN, InAs, GaN, GaP, GaAs, ZnCdS, ZnSeS, ZnCdSeS, CdZnSe, InZnP, InGaP, GaPZnS, GaPZnSe, GaPZnSeS, 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1항에 있어서,
상기 제1무기물 및 제2무기물은 서로 독립적으로, SiO2, TiO2, ZnO2, Al2O3, 알루미나 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1항에 있어서,
상기 제1양자점 나노 복합체는 상기 제1양자점 나노 입자와 상기 제1코팅층 사이에 개재된 제1보조층을 더 포함할 수 있고, 상기 제2양자점 나노 복합체는 상기 제2양자점 나노 입자와 상기 제2코팅층 사이에 개재된 제2보조층을 더 포함한, 포토레지스트 조성물. - 제7항에 있어서,
상기 제1보조층 및 제2보조층은 서로 독립적으로, 폴리비닐피롤리돈, 폴리스티렌, 폴리메틸메타크릴레이트, 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1항에 있어서,
상기 광중합성 단량체는 에틸렌 글리콜 디(메타)아크릴레이트, 디에틸렌 글리콜 디(메타)아크릴레이트, 트리에틸렌 글리콜 디(메타)아크릴레이트, 프로필렌 글리콜 디(메타)아크릴레이트, 네오펜틸 글리콜디(메타)아크릴레이트, 1,4-부탄디올 디(메타)아크릴레이트, 1,6-헥산디올 디(메타)아크릴레이트, 비스페놀A 디(메타)아크릴레이트, 펜타에리트리톨 디(메타)아크릴레이트, 펜타에리트리톨 트리(메타)아크릴레이트, 펜타에리트리톨 테트라(메타)아크릴레이트, 펜타에리트리톨 헥사(메타)아크릴레이트, 디펜타에리트리톨 디(메타)아크릴레이트, 디펜타에리트리톨 트리(메타)아크릴레이트, 디펜타에리트리톨 펜타(메타)아크릴레이트, 디펜타에리트리톨 헥사(메타)아크릴레이트, 비스페놀A 에폭시(메타)아크릴레이트, 에틸렌 글리콜 모노메틸에테르 (메타)아크릴레이트, 트리메틸올 프로판 트리(메타)아크릴레이트, 트리스(메타)아크릴로일옥시에틸 포스페이트, 노볼락에폭시 (메타)아크릴레이트, 디펜타에리트리톨펜타(메트)아크릴레이트 숙신산에스테르, 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1항에 있어서,
상기 옥심계 화합물은 1,2-옥탄디온, 2-디메틸아미노-2-(4-메틸벤질)-1-(4-모르폴린-4-일-페닐)-부탄-1-온, 1-(4-페닐술파닐페닐)-부탄-1,2-디온-2-옥심-0-벤조에이트, 1-(4-페닐술파닐페닐)-옥탄-1,2-디온-2-옥심-0-벤조에이트, 1-(4-페닐술파닐페닐)-옥탄-1-온옥심-0-아세테이트, 1-(4-페닐술파닐페닐)-부탄-1-온-2-옥심-0-아세테이트, 2-(0-벤조일옥심)-1-[4-(페닐티오)페닐]-1,2-옥탄디온, 1-(0-아세틸옥심)-1-[9-에틸-6-(2-메틸벤조일)-9H-카르바졸-3-일]에탄온, 0-에특시카르보닐-α-옥시아미노-1-페닐프로판-1-온, 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1항에 있어서,
상기 아세토페논계 화합물은 4-페녹시 디클로로아세토페논, 4-t-부틸 디클로로아세토페논, 4-t-부틸 트리클로로아세토페논, 2,2-디에톡시아세토페논, 2-히드록시-2-메틸-1-페닐-프로판-1-온, 1-(4-이소프로필페닐)-2-히드록시-2-메틸-프로판-1-온, 1-(4-도데실페닐)-2-히드록시-2-메틸프로판-1-온, 4-(2-히드록시에톡시)-페닐-(2-히드록시-2-프로필)케톤, 1-히드록시 시클로헥실 페닐 케톤 및 2-메틸-1- [4-(메틸티오)페닐]-2-모르폴리노-프로판-1-온, 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1항에 있어서,
상기 티오크산톤계 화합물은 티오크산톤, 2-클로로티오크산톤, 2- 메틸티오크산톤, 이소프로필 티오크산톤, 2,4-디에틸 티오크산톤 및 2,4-디이소프로필 티오크산톤, 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1항에 있어서,
상기 벤조페논계 화합물은 벤조페논, 벤조일 벤조산, 벤조일 벤조산 메틸 에스테르, 4-페닐 벤조페논, 히드록시 벤조페논, 4-벤조일-4'-메틸 디페닐 설파이드 및 3,3'-디메틸-4-메톡시 벤조페논, 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1항에 있어서,
상기 바인더 수지는 에폭시계 수지, 아크릴계 수지, 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1항에 있어서,
상기 용매는 에틸렌 글리콜 모노에틸 에테르, 에틸 셀로솔브 아세테이트, 2-히드록시에틸 프로피오네이트, 디에틸렌 글리콜 모노메틸, 프로필렌 글리콜 모노메틸에테르 아세테이트, 프로필렌 글리콜 프로필에테르 아세테이트, 또는 이의 임의의 조합을 포함한, 포토레지스트 조성물. - 제1화소 영역, 제2화소 영역 및 제3화소 영역을 포함하고,
상기 제1화소 영역은 입사광을 제1컬러의 광으로 변환하는 제1색변환층을 포함하고,
상기 제2화소 영역은 입사광을 제2컬러의 광으로 변환하는 제2색변환층을 포함하고,
상기 제3화소 영역은 산란 물질층을 포함하고,
상기 제1색변환층은 제1포토레지스트 조성물의 광경화물을 포함하고, 상기 제2색변환층은 제2포토레지스트 조성물의 광경화물을 포함하고,
상기 제1포토레지스트 조성물 및 제2포토레지스트 조성물은 서로 독립적으로, 제1항 내지 제15항 중 어느 한 항에 따른 포토레지스트 조성물 중에서 선택되되, 상기 제1포토레지스트 조성물 및 제2포토레지스트 조성물은 서로 상이한, 컬러 필터. - 제16항에 있어서,
상기 제1포토레지스트 조성물에 포함된 포토루미네선스 나노 복합체는 제1양자점 나노 복합체를 포함하고,
상기 제2포토레지스트 조성물에 포함된 포토루미네선스 나노 복합체는 제2양자점 나노 복합체를 포함한, 컬러 필터. - 제16항에 있어서,
상기 산란 물질층은 TiO2를 포함한, 컬러 필터. - 제16항에 있어서,
상기 입사광은 청색광인, 컬러 필터. - 제16항에 있어서,
상기 제1컬러는 적색광이고, 상기 제2컬러는 녹색광인, 컬러 필터.
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Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019181698A1 (ja) * | 2018-03-23 | 2019-09-26 | 東レ株式会社 | 感光性樹脂組成物、硬化膜、色変換基板、画像表示装置、および硬化膜の製造方法 |
US10851297B2 (en) * | 2018-07-10 | 2020-12-01 | Samsung Electronics Co., Ltd. | Composition, patterned film, and electronic device including the same |
KR20200012739A (ko) * | 2018-07-27 | 2020-02-05 | 닛뽄 가야쿠 가부시키가이샤 | 전자 부품용 봉지제, 전자 부품 및 액정 표시 셀 |
KR102634132B1 (ko) | 2018-08-27 | 2024-02-06 | 동우 화인켐 주식회사 | 컬러 필터 및 이를 포함하는 화상표시장치 |
KR102285669B1 (ko) | 2018-08-27 | 2021-08-04 | 동우 화인켐 주식회사 | 컬러 필터, 그 제조 방법, 및 컬러 필터를 포함하는 화상표시장치 |
CN109946924B (zh) * | 2019-02-21 | 2022-09-16 | 苏州星烁纳米科技有限公司 | 树脂组合物及显示装置 |
KR102153965B1 (ko) * | 2019-02-28 | 2020-09-09 | 동우 화인켐 주식회사 | 광변환 잉크 조성물, 컬러필터 및 화상표시장치 |
KR20210137521A (ko) * | 2019-03-12 | 2021-11-17 | 메르크 파텐트 게엠베하 | 조성물 |
KR102153629B1 (ko) * | 2019-03-14 | 2020-09-08 | 동우 화인켐 주식회사 | 광변환 잉크 조성물, 이를 이용하여 제조된 컬러필터 및 이를 포함하는 화상표시장치 |
CN112233567A (zh) * | 2019-06-27 | 2021-01-15 | 成都辰显光电有限公司 | 色彩转化组件及其制作方法、显示面板 |
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KR102713258B1 (ko) | 2019-06-28 | 2024-10-04 | 삼성디스플레이 주식회사 | 비카드뮴 양자점 및 이를 포함한 복합체와 표시소자 |
KR102746318B1 (ko) * | 2019-10-01 | 2024-12-24 | 삼성디스플레이 주식회사 | 양자점, 이를 포함하는 조성물과 복합체, 및 이를 포함하는 전자 소자 |
CN114503021B (zh) | 2019-10-04 | 2024-04-23 | 东友精细化工有限公司 | 色彩转换面板 |
KR20210052886A (ko) * | 2019-11-01 | 2021-05-11 | 한국전기연구원 | 양자점 색변환 구조체를 갖는 컬러필터, 이를 포함하는 표시장치 및 그 제조방법 |
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KR102753632B1 (ko) | 2020-01-31 | 2025-01-14 | 동우 화인켐 주식회사 | 색변환 소자, 이를 포함하는 색변환 필터 및 화상표시장치 |
KR102346577B1 (ko) | 2020-03-03 | 2022-01-03 | 동우 화인켐 주식회사 | 색변환 화소, 색변환 화소용 조성물 및 이를 포함하는 표시장치 |
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KR102597304B1 (ko) * | 2021-01-18 | 2023-11-02 | 주식회사 신아티앤씨 | 코어-쉘 구조 양자점 입자의 제조방법, 이에 의해 제조된 코어-쉘 구조 양자점 입자, 상기 코어-쉘 구조 양자점 입자 집단 및 이를 포함하는 디스플레이장치 |
KR20220152805A (ko) | 2021-05-10 | 2022-11-17 | 동우 화인켐 주식회사 | 색변환 화소용 잉크 조성물, 색변환 화소, 컬러필터 및 표시장치 |
KR20230000749A (ko) | 2021-06-25 | 2023-01-03 | 동우 화인켐 주식회사 | 감광성 수지 조성물, 이를 이용하여 제조된 색변환층, 이를 포함하는 컬러필터 및 화상표시장치 |
CN118076701A (zh) * | 2021-08-20 | 2024-05-24 | 默克专利股份有限公司 | 组合物 |
CN118795731B (zh) * | 2024-09-11 | 2024-12-03 | 南京理工大学 | 一种用于高分辨像元制造的量子点光刻胶 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20160011506A1 (en) | 2013-12-30 | 2016-01-14 | Boe Technology Group Co., Ltd. | Photosensitive resin composition and method for forming quantum dot pattern using the same |
US20160362602A1 (en) | 2014-12-19 | 2016-12-15 | Boe Technology Group Co., Ltd. | Modified Quantum Dot and Method for Preparing the Same, Colorant, Photosensitive Resin Composition, Color Filter and Display Device |
US20170075215A1 (en) | 2015-09-11 | 2017-03-16 | Samsung Display Co., Ltd. | Photosensitive resin composition and display device using the same |
US20170176811A1 (en) | 2015-06-24 | 2017-06-22 | Boe Technology Group Co., Ltd. | Color photoresist and its use, color film substrate, display panel and liquid crystal display |
US20170194530A1 (en) | 2016-01-04 | 2017-07-06 | Boe Technology Group Co., Ltd. | Quantum dot film, its preparation method, its patterning method, and its display device |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6322901B1 (en) | 1997-11-13 | 2001-11-27 | Massachusetts Institute Of Technology | Highly luminescent color-selective nano-crystalline materials |
KR101110071B1 (ko) | 2005-04-29 | 2012-02-24 | 삼성전자주식회사 | 자발광 lcd |
KR101588317B1 (ko) | 2008-11-11 | 2016-01-27 | 삼성전자주식회사 | 감광성 양자점, 이를 포함한 조성물 및 상기 조성물을 이용한 양자점-함유 패턴 형성 방법 |
KR101562424B1 (ko) | 2009-02-23 | 2015-10-21 | 이섬 리서치 디벨러프먼트 컴파니 오브 더 히브루 유니버시티 오브 예루살렘 엘티디. | 나노구조체를 사용하는 광학 디스플레이 장치 및 이의 방법 |
KR101463602B1 (ko) | 2012-07-03 | 2014-11-20 | 주식회사 엘엠에스 | 캡슐화된 양자점 및 이를 이용한 장치 |
KR101426448B1 (ko) | 2012-11-09 | 2014-08-05 | 주식회사 엘엠에스 | 나노 복합체, 이를 포함하는 광학 부재 및 백라이트 유닛 |
KR101879016B1 (ko) * | 2014-11-21 | 2018-07-16 | 동우 화인켐 주식회사 | 자발광 감광성 수지 조성물, 이로부터 제조된 컬러필터 및 상기 컬러필터를 포함하는 화상표시장치 |
KR102660293B1 (ko) * | 2015-01-09 | 2024-04-25 | 삼성디스플레이 주식회사 | 감광성 수지 조성물, 이를 이용한 색변환 패널 및 표시 장치 |
KR102153733B1 (ko) * | 2015-01-26 | 2020-09-08 | 동우 화인켐 주식회사 | 컬러필터 및 이를 이용한 화상표시장치 |
US9899575B2 (en) * | 2015-04-30 | 2018-02-20 | Nano And Advanced Materials Institute Limited | Method of continuous flow synthesis and method of correcting emission spectrum of light emitting device |
-
2016
- 2016-09-13 KR KR1020160118217A patent/KR102497282B1/ko active Active
-
2017
- 2017-09-07 US US15/697,992 patent/US10162259B2/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20160011506A1 (en) | 2013-12-30 | 2016-01-14 | Boe Technology Group Co., Ltd. | Photosensitive resin composition and method for forming quantum dot pattern using the same |
US20160362602A1 (en) | 2014-12-19 | 2016-12-15 | Boe Technology Group Co., Ltd. | Modified Quantum Dot and Method for Preparing the Same, Colorant, Photosensitive Resin Composition, Color Filter and Display Device |
US20170176811A1 (en) | 2015-06-24 | 2017-06-22 | Boe Technology Group Co., Ltd. | Color photoresist and its use, color film substrate, display panel and liquid crystal display |
US20170075215A1 (en) | 2015-09-11 | 2017-03-16 | Samsung Display Co., Ltd. | Photosensitive resin composition and display device using the same |
US20170194530A1 (en) | 2016-01-04 | 2017-07-06 | Boe Technology Group Co., Ltd. | Quantum dot film, its preparation method, its patterning method, and its display device |
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