TWI727366B - 發光元件、顯示模組、照明模組、發光裝置、顯示裝置、電子裝置、及照明裝置 - Google Patents
發光元件、顯示模組、照明模組、發光裝置、顯示裝置、電子裝置、及照明裝置 Download PDFInfo
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- TWI727366B TWI727366B TW108124541A TW108124541A TWI727366B TW I727366 B TWI727366 B TW I727366B TW 108124541 A TW108124541 A TW 108124541A TW 108124541 A TW108124541 A TW 108124541A TW I727366 B TWI727366 B TW I727366B
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| JP2013166867 | 2013-08-09 | ||
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| TW110107362A TWI790559B (zh) | 2013-08-09 | 2014-07-30 | 發光元件、顯示模組、照明模組、發光裝置、顯示裝置、電子裝置、及照明裝置 |
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Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI727366B (zh) | 2013-08-09 | 2021-05-11 | 日商半導體能源研究所股份有限公司 | 發光元件、顯示模組、照明模組、發光裝置、顯示裝置、電子裝置、及照明裝置 |
| KR102244374B1 (ko) | 2013-08-09 | 2021-04-26 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 디스플레이 모듈, 조명 모듈, 발광 장치, 표시 장치, 전자 기기, 및 조명 장치 |
| WO2016020801A1 (en) | 2014-08-08 | 2016-02-11 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting device, electronic device, and lighting device |
| JP2016082239A (ja) | 2014-10-16 | 2016-05-16 | 株式会社半導体エネルギー研究所 | 発光素子、発光装置、電子機器及び照明装置 |
| CN107208251B (zh) * | 2015-02-10 | 2019-10-25 | 大日本印刷株式会社 | 蒸镀掩模的制造方法和蒸镀掩模 |
| CN116018040A (zh) | 2015-02-18 | 2023-04-25 | 株式会社半导体能源研究所 | 有机化合物、发光元件、显示模块、照明模块、发光装置、显示装置、电子设备以及照明装置 |
| KR102399574B1 (ko) * | 2015-04-03 | 2022-05-19 | 삼성디스플레이 주식회사 | 유기 발광 표시 장치 |
| KR102623039B1 (ko) | 2015-05-15 | 2024-01-08 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 발광 장치, 전자 기기 및 조명 장치 |
| CN104966789A (zh) * | 2015-06-30 | 2015-10-07 | 深圳市华星光电技术有限公司 | 一种电荷连接层及其制造方法、叠层oled器件 |
| CN105161633B (zh) * | 2015-08-12 | 2018-02-06 | 京东方科技集团股份有限公司 | 一种有机发光器件 |
| US20170062749A1 (en) * | 2015-09-01 | 2017-03-02 | Semiconductor Energy Laboratory Co., Ltd. | Light-Emitting Element, Light-Emitting Device, Electronic Device, and Lighting Device |
| KR102420453B1 (ko) * | 2015-09-09 | 2022-07-13 | 엘지디스플레이 주식회사 | 유기발광 표시장치 및 이를 적용한 차량용 조명장치 |
| KR101703174B1 (ko) * | 2015-11-30 | 2017-02-06 | 엘지디스플레이 주식회사 | 유기발광다이오드 및 그 제조 방법 |
| KR102642369B1 (ko) | 2016-03-25 | 2024-03-05 | 삼성디스플레이 주식회사 | 유기 발광 표시 장치 및 유기 발광 표시 장치의 제조 방법 |
| US9911937B2 (en) | 2016-05-12 | 2018-03-06 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, electronic device, and lighting device |
| KR102419770B1 (ko) * | 2016-05-20 | 2022-07-13 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 장치 및 전자 기기 |
| KR102586780B1 (ko) * | 2016-06-30 | 2023-10-12 | 삼성디스플레이 주식회사 | 표시 장치 및 이를 이용한 콘텐츠 표시 시스템 및 방법 |
| JP6151847B1 (ja) * | 2016-12-27 | 2017-06-21 | Ｌｕｍｉｏｔｅｃ株式会社 | 有機エレクトロルミネッセント素子および照明装置 |
| US10748497B2 (en) * | 2016-12-27 | 2020-08-18 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, electronic device, and lighting device |
| KR20180076857A (ko) * | 2016-12-28 | 2018-07-06 | 엘지디스플레이 주식회사 | 유기발광다이오드 표시장치 |
| KR20240123845A (ko) | 2017-04-07 | 2024-08-14 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 표시 장치, 전자 기기, 및 조명 장치 |
| EP3631859A4 (en) * | 2017-06-01 | 2021-01-06 | BOE Technology Group Co., Ltd. | ARRAY SUBSTRATE, DISPLAY BOARD THEREFORE AND METHOD FOR MANUFACTURING THE ARRAY SUBSTRATE |
| US10892296B2 (en) | 2017-11-27 | 2021-01-12 | Seoul Viosys Co., Ltd. | Light emitting device having commonly connected LED sub-units |
| US11282981B2 (en) | 2017-11-27 | 2022-03-22 | Seoul Viosys Co., Ltd. | Passivation covered light emitting unit stack |
| US10892297B2 (en) * | 2017-11-27 | 2021-01-12 | Seoul Viosys Co., Ltd. | Light emitting diode (LED) stack for a display |
| US12100696B2 (en) | 2017-11-27 | 2024-09-24 | Seoul Viosys Co., Ltd. | Light emitting diode for display and display apparatus having the same |
| US11527519B2 (en) | 2017-11-27 | 2022-12-13 | Seoul Viosys Co., Ltd. | LED unit for display and display apparatus having the same |
| US10748881B2 (en) | 2017-12-05 | 2020-08-18 | Seoul Viosys Co., Ltd. | Light emitting device with LED stack for display and display apparatus having the same |
| US10886327B2 (en) | 2017-12-14 | 2021-01-05 | Seoul Viosys Co., Ltd. | Light emitting stacked structure and display device having the same |
| US11552057B2 (en) | 2017-12-20 | 2023-01-10 | Seoul Viosys Co., Ltd. | LED unit for display and display apparatus having the same |
| US11522006B2 (en) | 2017-12-21 | 2022-12-06 | Seoul Viosys Co., Ltd. | Light emitting stacked structure and display device having the same |
| US11552061B2 (en) | 2017-12-22 | 2023-01-10 | Seoul Viosys Co., Ltd. | Light emitting device with LED stack for display and display apparatus having the same |
| US11114499B2 (en) | 2018-01-02 | 2021-09-07 | Seoul Viosys Co., Ltd. | Display device having light emitting stacked structure |
| US10784240B2 (en) | 2018-01-03 | 2020-09-22 | Seoul Viosys Co., Ltd. | Light emitting device with LED stack for display and display apparatus having the same |
| KR102136806B1 (ko) * | 2018-03-28 | 2020-07-23 | 엘지디스플레이 주식회사 | 신규한 유기화합물 및 상기 유기화합물을 포함하는 유기전계 발광소자 |
| KR20210018105A (ko) | 2019-08-09 | 2021-02-17 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 유기 화합물, 발광 디바이스, 발광 장치, 전자 기기, 및 조명 장치 |
| TWI744678B (zh) * | 2019-08-21 | 2021-11-01 | 友達光電股份有限公司 | 電子裝置及其製作方法 |
| JP7140924B2 (ja) * | 2019-09-06 | 2022-09-21 | 日本放送協会 | 電荷発生層及びその製造方法、有機エレクトロルミネッセンス素子、表示装置、照明装置、並びに有機薄膜太陽電池 |
| US20220285629A1 (en) * | 2021-02-26 | 2022-09-08 | Semiconductor Energy Laboratory Co., Ltd. | Mixed material |
| US12063856B2 (en) | 2021-03-31 | 2024-08-13 | Semiconductor Energy Laboratory Co., Ltd. | Mixed material for light-emitting device |
| KR20230076958A (ko) | 2021-11-23 | 2023-06-01 | 삼성디스플레이 주식회사 | 발광 소자 및 이를 포함한 전자 장치 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009107541A1 (ja) * | 2008-02-25 | 2009-09-03 | パイオニア株式会社 | 有機電界発光素子 |
| US20110198578A1 (en) * | 2008-10-07 | 2011-08-18 | Osram Opto Semiconductors Gmbh | Siloles substituted by fused ring systems and use thereof in organic electronics |
| US20110215714A1 (en) * | 2010-03-02 | 2011-09-08 | Semiconductor Energy Laboratory Co., Ltd. | Light-Emitting Element and Lighting Device |
| TW201244076A (en) * | 2011-03-04 | 2012-11-01 | Semiconductor Energy Lab | Display device |
Family Cites Families (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5393614A (en) | 1992-04-03 | 1995-02-28 | Pioneer Electronic Corporation | Organic electroluminescence device |
| JPH0782551A (ja) | 1993-09-09 | 1995-03-28 | Nisshinbo Ind Inc | 有機エレクトロルミネッセンス素子 |
| JP2824411B2 (ja) | 1995-08-25 | 1998-11-11 | 株式会社豊田中央研究所 | 有機薄膜発光素子 |
| JPH10270171A (ja) | 1997-01-27 | 1998-10-09 | Junji Kido | 有機エレクトロルミネッセント素子 |
| JP3848430B2 (ja) | 1997-04-08 | 2006-11-22 | 新日本製鐵株式会社 | 有機エレクトロルミネッセンス素子及びその製造方法 |
| JPH11307264A (ja) | 1998-04-17 | 1999-11-05 | Matsushita Electric Ind Co Ltd | 有機電界発光素子 |
| JP3370011B2 (ja) | 1998-05-19 | 2003-01-27 | 三洋電機株式会社 | 有機エレクトロルミネッセンス素子 |
| JP3924648B2 (ja) | 1999-11-02 | 2007-06-06 | ソニー株式会社 | 有機電界発光素子 |
| JP2001131174A (ja) | 1999-11-02 | 2001-05-15 | Sony Corp | バソフェナントロリン化合物及びその製造方法 |
| JP4876311B2 (ja) | 2000-01-14 | 2012-02-15 | 東レ株式会社 | 発光素子 |
| US6645645B1 (en) | 2000-05-30 | 2003-11-11 | The Trustees Of Princeton University | Phosphorescent organic light emitting devices |
| JP2002289360A (ja) | 2001-03-27 | 2002-10-04 | Univ Toyama | 有機電界発光素子 |
| KR100495407B1 (ko) | 2001-08-20 | 2005-06-14 | 티디케이가부시기가이샤 | 유기ｅｌ소자 및 그 제조방법 |
| SG142163A1 (en) | 2001-12-05 | 2008-05-28 | Semiconductor Energy Lab | Organic semiconductor element |
| JP3933591B2 (ja) | 2002-03-26 | 2007-06-20 | 淳二 城戸 | 有機エレクトロルミネッセント素子 |
| US7045955B2 (en) | 2002-08-09 | 2006-05-16 | Semiconductor Energy Laboratory Co., Ltd. | Electroluminescence element and a light emitting device using the same |
| JP4287198B2 (ja) | 2002-11-18 | 2009-07-01 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
| JP4327443B2 (ja) | 2002-11-25 | 2009-09-09 | ケミプロ化成株式会社 | フェナントロリン誘導体およびその用途 |
| JP2004303489A (ja) | 2003-03-28 | 2004-10-28 | Tdk Corp | 有機ｅｌ素子及び有機ｅｌディスプレイ |
| KR101286219B1 (ko) | 2003-09-26 | 2013-07-15 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광소자의 제조방법 |
| JP4361342B2 (ja) | 2003-09-30 | 2009-11-11 | Ｔｄｋ株式会社 | 有機ｅｌ素子用化合物および有機ｅｌ素子 |
| US7211948B2 (en) | 2004-01-13 | 2007-05-01 | Eastman Kodak Company | Using a crystallization-inhibitor in organic electroluminescent devices |
| KR100573137B1 (ko) | 2004-04-02 | 2006-04-24 | 삼성에스디아이 주식회사 | 플루오렌계 화합물 및 이를 이용한 유기 전계 발광 소자 |
| US7893352B2 (en) | 2004-11-24 | 2011-02-22 | The Trustees Of Princeton University | Organic photosensitive optoelectronic device having a phenanthroline exciton blocking layer |
| JP4653469B2 (ja) | 2004-12-01 | 2011-03-16 | 出光興産株式会社 | 有機電界発光素子 |
| US7714501B2 (en) | 2004-12-01 | 2010-05-11 | Semiconductor Energy Laboratory Co., Ltd. | Light emitting element, light emitting device and electronic equipment |
| JP4842587B2 (ja) | 2005-08-11 | 2011-12-21 | 株式会社半導体エネルギー研究所 | フェナントロリン誘導体化合物、並びにそれを利用する電子輸送性材料、発光素子、発光装置及び電子機器 |
| JP4804196B2 (ja) | 2006-03-31 | 2011-11-02 | キヤノン株式会社 | 有機電界発光素子及び発光装置 |
| US8115382B2 (en) | 2007-09-20 | 2012-02-14 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, and electronic device, comprising controlled carrier transport |
| US8222740B2 (en) | 2008-10-28 | 2012-07-17 | Jagdish Narayan | Zinc oxide based composites and methods for their fabrication |
| DE102008054219A1 (de) * | 2008-10-31 | 2010-05-06 | Osram Opto Semiconductors Gmbh | Organisches strahlungsemittierendes Bauelement und Verfahren zur Herstellung eines organischen strahlungsemittierenden Bauelements |
| JP5759669B2 (ja) | 2008-12-01 | 2015-08-05 | 株式会社半導体エネルギー研究所 | 発光素子、発光装置、電子機器、および照明装置 |
| DE112009003123B4 (de) | 2008-12-11 | 2020-02-06 | Osram Oled Gmbh | Organische leuchtdiode und beleuchtungsmittel |
| EP2393819B9 (de) * | 2009-01-07 | 2017-12-27 | UDC Ireland Limited | Silyl- und heteroatom-substituierte verbindungen ausgewählt aus carbazolen, dibenzofuranen, dibenzothiophenen und dibenzophospholen und ihre anwendung in der organischen elektronik |
| EP2401254B1 (de) * | 2009-02-26 | 2013-06-19 | Novaled AG | Chinonverbindungen als dotierstoff in der organischen elektronik |
| EP2436233B1 (en) * | 2009-05-29 | 2016-08-10 | Semiconductor Energy Laboratory Co, Ltd. | Light-emitting element, light-emitting device, electronic device, and lighting device |
| US8389979B2 (en) * | 2009-05-29 | 2013-03-05 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, electronic device, and lighting device |
| EP2463929A4 (en) | 2009-08-04 | 2013-10-02 | Mitsubishi Chem Corp | PHOTOELECTRIC CONVERTER ELEMENT AND SOLAR CELL THEREWITH |
| KR101815072B1 (ko) * | 2009-11-24 | 2018-01-30 | 유니버시티 오브 플로리다 리서치 파운데이션, 인크. | 적외선 검출 방법 및 장치 |
| EP2333859B1 (en) | 2009-12-03 | 2017-09-13 | Novaled GmbH | A method for forming an organic light emitting diode |
| EP2355199B1 (en) | 2010-01-29 | 2017-07-05 | Novaled GmbH | A method for producing an organic light emitting device |
| TWI415846B (zh) | 2010-03-01 | 2013-11-21 | Semiconductor Energy Lab | 雜環化合物、發光元件、發光裝置、電子裝置、及照明裝置 |
| JP5801579B2 (ja) * | 2010-03-31 | 2015-10-28 | 株式会社半導体エネルギー研究所 | 発光素子、発光装置、電子機器、及び照明装置 |
| CN103068950B (zh) * | 2010-06-18 | 2016-08-24 | 巴斯夫欧洲公司 | 包含含有至少一种金属有机化合物和至少一种金属氧化物的层的有机电子器件 |
| KR102098563B1 (ko) * | 2010-06-25 | 2020-04-08 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 발광 장치, 디스플레이 및 전자 기기 |
| US9067919B2 (en) | 2010-07-08 | 2015-06-30 | Basf Se | Use of dibenzofurans and dibenzothiophenes substituted by nitrogen-bonded five-membered heterocyclic rings in organic electronics |
| WO2012004765A2 (en) * | 2010-07-08 | 2012-01-12 | Basf Se | Use of dibenzofurans and dibenzothiophenes substituted by nitrogen-bonded five-membered heterocyclic rings in organic electronics |
| DE112012003073B4 (de) | 2011-07-22 | 2014-11-13 | Semiconductor Energy Laboratory Co., Ltd. | Dibenzo(c,g)Carbazol-Verbindung, lichtemittierendes Element, lichtemittierende Vorrichtung, Displayvorrichtung, Beleuchtungsvorrichtung und elektronische Vorrichtung |
| WO2013031509A1 (en) * | 2011-08-26 | 2013-03-07 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting device, electronic device, lighting device, and method for manufacturing the light-emitting device |
| JP5782394B2 (ja) | 2012-02-16 | 2015-09-24 | 大日精化工業株式会社 | 水性顔料分散液及びそれを用いたインクジェット用水性顔料インク |
| TWI502765B (zh) * | 2012-02-24 | 2015-10-01 | 華夏光股份有限公司 | 發光二極體裝置 |
| CN103367650A (zh) * | 2012-03-28 | 2013-10-23 | 索尼公司 | 发光元件及显示装置 |
| US8835948B2 (en) * | 2012-04-19 | 2014-09-16 | Phostek, Inc. | Stacked LED device with diagonal bonding pads |
| JP5456120B2 (ja) * | 2012-09-12 | 2014-03-26 | パイオニア株式会社 | 有機電界発光素子 |
| US10439156B2 (en) | 2013-05-17 | 2019-10-08 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, display device, lighting device, and electronic device |
| TWI727366B (zh) * | 2013-08-09 | 2021-05-11 | 日商半導體能源研究所股份有限公司 | 發光元件、顯示模組、照明模組、發光裝置、顯示裝置、電子裝置、及照明裝置 |
| KR102244374B1 (ko) | 2013-08-09 | 2021-04-26 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 디스플레이 모듈, 조명 모듈, 발광 장치, 표시 장치, 전자 기기, 및 조명 장치 |
-
2014
- 2014-07-30 TW TW108124541A patent/TWI727366B/zh not_active IP Right Cessation
- 2014-07-30 TW TW110107362A patent/TWI790559B/zh active
- 2014-07-30 TW TW111147902A patent/TW202339325A/zh unknown
- 2014-07-30 TW TW103126032A patent/TWI686971B/zh not_active IP Right Cessation
- 2014-08-05 KR KR1020140100387A patent/KR102176523B1/ko not_active Expired - Fee Related
- 2014-08-06 US US14/452,841 patent/US9515278B2/en active Active
- 2014-08-08 DE DE201410215799 patent/DE102014215799A1/de active Pending
- 2014-08-08 JP JP2014162092A patent/JP6486624B2/ja active Active
-
2016
- 2016-11-30 US US15/364,746 patent/US9780338B2/en active Active
-
2017
- 2017-09-28 US US15/718,498 patent/US9966574B2/en active Active
-
2019
- 2019-02-20 JP JP2019028059A patent/JP2019075592A/ja not_active Withdrawn
-
2020
- 2020-11-03 KR KR1020200145249A patent/KR102319366B1/ko active Active
-
2021
- 2021-02-05 JP JP2021017051A patent/JP2021068714A/ja not_active Withdrawn
- 2021-02-05 JP JP2021017052A patent/JP7043643B2/ja active Active
- 2021-03-10 JP JP2021037955A patent/JP2021100000A/ja not_active Withdrawn
- 2021-03-23 KR KR1020210037141A patent/KR102381111B1/ko active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009107541A1 (ja) * | 2008-02-25 | 2009-09-03 | パイオニア株式会社 | 有機電界発光素子 |
| US20110198578A1 (en) * | 2008-10-07 | 2011-08-18 | Osram Opto Semiconductors Gmbh | Siloles substituted by fused ring systems and use thereof in organic electronics |
| US20110215714A1 (en) * | 2010-03-02 | 2011-09-08 | Semiconductor Energy Laboratory Co., Ltd. | Light-Emitting Element and Lighting Device |
| TW201244076A (en) * | 2011-03-04 | 2012-11-01 | Semiconductor Energy Lab | Display device |
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| US9966574B2 (en) | 2018-05-08 |
| JP2019075592A (ja) | 2019-05-16 |
| JP2015057770A (ja) | 2015-03-26 |
| TW201508970A (zh) | 2015-03-01 |
| JP2021068714A (ja) | 2021-04-30 |
| KR20150018408A (ko) | 2015-02-23 |
| KR102176523B1 (ko) | 2020-11-09 |
| KR102319366B1 (ko) | 2021-10-29 |
| TWI686971B (zh) | 2020-03-01 |
| DE102014215799A1 (de) | 2015-02-12 |
| JP2021073734A (ja) | 2021-05-13 |
| US20180019445A1 (en) | 2018-01-18 |
| TW201941470A (zh) | 2019-10-16 |
| KR102381111B1 (ko) | 2022-03-30 |
| JP7043643B2 (ja) | 2022-03-29 |
| KR20200127952A (ko) | 2020-11-11 |
| TW202339325A (zh) | 2023-10-01 |
| US20150041792A1 (en) | 2015-02-12 |
| TW202125871A (zh) | 2021-07-01 |
| US9780338B2 (en) | 2017-10-03 |
| KR20210035142A (ko) | 2021-03-31 |
| TWI790559B (zh) | 2023-01-21 |
| JP2021100000A (ja) | 2021-07-01 |
| JP6486624B2 (ja) | 2019-03-20 |
| US9515278B2 (en) | 2016-12-06 |
| US20170084876A1 (en) | 2017-03-23 |
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