CN109315046B - 有机电致发光元件的制造方法和有机电致发光元件 - Google Patents
有机电致发光元件的制造方法和有机电致发光元件 Download PDFInfo
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- 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
- H10K71/15—Deposition of organic active material using liquid deposition, e.g. spin coating characterised by the solvent used
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- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
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US20190393426A1 (en) * | 2017-01-30 | 2019-12-26 | Idemitsu Kosan Co., Ltd. | Organic electroluminescent element and electronic device |
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WO2019194209A1 (ja) * | 2018-04-06 | 2019-10-10 | コニカミノルタ株式会社 | インク組成物、有機エレクトロルミネッセンス素子の製造方法及び有機エレクトロルミネッセンス素子 |
KR102288205B1 (ko) * | 2019-12-13 | 2021-08-11 | 엘티소재주식회사 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012089777A (ja) * | 2010-10-22 | 2012-05-10 | Konica Minolta Holdings Inc | 有機エレクトロルミネッセンス素子、照明装置及び表示装置 |
CN102823013A (zh) * | 2010-03-25 | 2012-12-12 | 通用显示公司 | 可溶液处理的掺杂的三芳基胺空穴注入材料 |
JP2015082537A (ja) * | 2013-10-22 | 2015-04-27 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、その製造方法及び有機エレクトロルミネッセンスデバイス |
CN104871332A (zh) * | 2012-12-21 | 2015-08-26 | 出光兴产株式会社 | 有机电致发光元件及电子设备 |
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JP2011009517A (ja) * | 2009-06-26 | 2011-01-13 | Konica Minolta Holdings Inc | 有機エレクトロルミネッセンス素子 |
JP5656765B2 (ja) | 2011-07-19 | 2015-01-21 | 株式会社日立製作所 | 有機発光素子、有機発光素子を用いた光源装置およびそれらの製造方法 |
JP2014017494A (ja) * | 2013-08-15 | 2014-01-30 | Konica Minolta Inc | 有機エレクトロルミネッセンス素子、該素子を備えた照明装置及び表示装置 |
JP6323093B2 (ja) | 2014-03-17 | 2018-05-16 | 住友化学株式会社 | 高分子化合物およびそれを用いた発光素子 |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102823013A (zh) * | 2010-03-25 | 2012-12-12 | 通用显示公司 | 可溶液处理的掺杂的三芳基胺空穴注入材料 |
JP2012089777A (ja) * | 2010-10-22 | 2012-05-10 | Konica Minolta Holdings Inc | 有機エレクトロルミネッセンス素子、照明装置及び表示装置 |
CN104871332A (zh) * | 2012-12-21 | 2015-08-26 | 出光兴产株式会社 | 有机电致发光元件及电子设备 |
JP2015082537A (ja) * | 2013-10-22 | 2015-04-27 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、その製造方法及び有機エレクトロルミネッセンスデバイス |
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