CN103293858A - 感光性树脂组合物、硬化膜的制造方法、硬化膜、有机电致发光显示装置以及液晶显示装置 - Google Patents
感光性树脂组合物、硬化膜的制造方法、硬化膜、有机电致发光显示装置以及液晶显示装置 Download PDFInfo
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Images
Classifications
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- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
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- H10K85/151—Copolymers
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- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
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- 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
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- 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
- G03F7/004—Photosensitive materials
- G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
- G03F7/11—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers having cover layers or intermediate layers, e.g. subbing layers
-
- 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
- G03F7/20—Exposure; Apparatus therefor
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K59/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group H10K50/00
- H10K59/10—OLED displays
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- 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
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/621—Aromatic anhydride or imide compounds, e.g. perylene tetra-carboxylic dianhydride or perylene tetracarboxylic di-imide
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- 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
- H10K85/60—Organic compounds having low molecular weight
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
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JP2013004275A JP5593405B2 (ja) | 2012-02-28 | 2013-01-15 | 感光性樹脂組成物、硬化膜の製造方法、硬化膜、有機el表示装置および液晶表示装置 |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
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CN104658906A (zh) * | 2013-11-22 | 2015-05-27 | 上海和辉光电有限公司 | 一种半导体平坦化层的制作方法 |
CN105895661A (zh) * | 2015-02-17 | 2016-08-24 | 富士胶片株式会社 | 薄膜晶体管基板的制造方法及其应用 |
CN105938299A (zh) * | 2015-03-06 | 2016-09-14 | 东友精细化工有限公司 | 化学增幅型感光性树脂组合物及由其制造的绝缘膜 |
CN106687865A (zh) * | 2014-09-30 | 2017-05-17 | 富士胶片株式会社 | Tft基板的制造方法、有机el显示装置及其制造方法以及液晶显示装置及其制造方法 |
CN107207868A (zh) * | 2015-02-19 | 2017-09-26 | 日本瑞翁株式会社 | 树脂组合物、树脂膜及电子部件 |
Families Citing this family (3)
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WO2014054455A1 (ja) * | 2012-10-02 | 2014-04-10 | 日産化学工業株式会社 | ネガ型感光性樹脂組成物 |
JP6136727B2 (ja) * | 2013-08-02 | 2017-05-31 | Jsr株式会社 | 感放射線性樹脂組成物、硬化膜、その形成方法及び表示素子 |
KR102240965B1 (ko) * | 2013-11-13 | 2021-04-15 | 세키스이가가쿠 고교가부시키가이샤 | 액정 표시 소자용 시일제, 상하 도통 재료, 및 액정 표시 소자 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6279444A (ja) * | 1985-10-03 | 1987-04-11 | Kuraray Co Ltd | 架橋性レジスト |
CN1737683A (zh) * | 2004-08-16 | 2006-02-22 | 富士胶片株式会社 | 平版印刷版原版 |
TW201015222A (en) * | 2008-09-12 | 2010-04-16 | Sumitomo Chemical Co | A method for treating a resist layer and a use of positive resist composition |
CN101876789A (zh) * | 2009-05-01 | 2010-11-03 | 富士胶片株式会社 | 正型感光性树脂组合物以及使用了该组合物的固化膜形成方法 |
TW201140232A (en) * | 2010-01-15 | 2011-11-16 | Fujifilm Corp | Photosensitive resin composition, cured film and method of producing the same, organic EL display device, and liquid crystal display device |
-
2013
- 2013-02-21 KR KR1020130018564A patent/KR20130098909A/ko not_active Application Discontinuation
- 2013-02-27 CN CN2013100614028A patent/CN103293858A/zh active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6279444A (ja) * | 1985-10-03 | 1987-04-11 | Kuraray Co Ltd | 架橋性レジスト |
CN1737683A (zh) * | 2004-08-16 | 2006-02-22 | 富士胶片株式会社 | 平版印刷版原版 |
TW201015222A (en) * | 2008-09-12 | 2010-04-16 | Sumitomo Chemical Co | A method for treating a resist layer and a use of positive resist composition |
CN101876789A (zh) * | 2009-05-01 | 2010-11-03 | 富士胶片株式会社 | 正型感光性树脂组合物以及使用了该组合物的固化膜形成方法 |
TW201140232A (en) * | 2010-01-15 | 2011-11-16 | Fujifilm Corp | Photosensitive resin composition, cured film and method of producing the same, organic EL display device, and liquid crystal display device |
Cited By (11)
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CN104658906A (zh) * | 2013-11-22 | 2015-05-27 | 上海和辉光电有限公司 | 一种半导体平坦化层的制作方法 |
CN104658906B (zh) * | 2013-11-22 | 2017-09-01 | 上海和辉光电有限公司 | 一种半导体平坦化层的制作方法 |
CN106687865A (zh) * | 2014-09-30 | 2017-05-17 | 富士胶片株式会社 | Tft基板的制造方法、有机el显示装置及其制造方法以及液晶显示装置及其制造方法 |
CN106687865B (zh) * | 2014-09-30 | 2020-01-03 | 富士胶片株式会社 | Tft基板、有机el显示装置及液晶显示装置的制造方法 |
CN105895661A (zh) * | 2015-02-17 | 2016-08-24 | 富士胶片株式会社 | 薄膜晶体管基板的制造方法及其应用 |
CN105895661B (zh) * | 2015-02-17 | 2019-03-01 | 富士胶片株式会社 | 薄膜晶体管基板的制造方法及其应用 |
TWI710839B (zh) * | 2015-02-17 | 2020-11-21 | 日商富士軟片股份有限公司 | 薄膜電晶體基板的製造方法、有機電致發光顯示裝置及其製法、液晶顯示裝置及其製法 |
CN107207868A (zh) * | 2015-02-19 | 2017-09-26 | 日本瑞翁株式会社 | 树脂组合物、树脂膜及电子部件 |
CN107207868B (zh) * | 2015-02-19 | 2020-11-06 | 日本瑞翁株式会社 | 树脂组合物、树脂膜及电子部件 |
CN105938299A (zh) * | 2015-03-06 | 2016-09-14 | 东友精细化工有限公司 | 化学增幅型感光性树脂组合物及由其制造的绝缘膜 |
CN105938299B (zh) * | 2015-03-06 | 2020-10-09 | 东友精细化工有限公司 | 化学增幅型感光性树脂组合物及由其制造的绝缘膜 |
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