TWI634683B - 發光元件、發光裝置、電子裝置以及照明設備 - Google Patents
發光元件、發光裝置、電子裝置以及照明設備 Download PDFInfo
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- TWI634683B TWI634683B TW106117041A TW106117041A TWI634683B TW I634683 B TWI634683 B TW I634683B TW 106117041 A TW106117041 A TW 106117041A TW 106117041 A TW106117041 A TW 106117041A TW I634683 B TWI634683 B TW I634683B
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- 150000002894 organic compounds Chemical class 0.000 claims abstract description 166
- 150000001875 compounds Chemical class 0.000 claims abstract description 94
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- 238000000295 emission spectrum Methods 0.000 claims description 44
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- IYZMXHQDXZKNCY-UHFFFAOYSA-N 1-n,1-n-diphenyl-4-n,4-n-bis[4-(n-phenylanilino)phenyl]benzene-1,4-diamine Chemical compound C1=CC=CC=C1N(C=1C=CC(=CC=1)N(C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 IYZMXHQDXZKNCY-UHFFFAOYSA-N 0.000 description 2
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- MKAQNAJLIITRHR-UHFFFAOYSA-N 3-(3-dibenzothiophen-4-ylphenyl)phenanthro[9,10-b]pyrazine Chemical compound C1=CC=C2C3=NC(C=4C=CC=C(C=4)C4=C5SC=6C(C5=CC=C4)=CC=CC=6)=CN=C3C3=CC=CC=C3C2=C1 MKAQNAJLIITRHR-UHFFFAOYSA-N 0.000 description 2
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- JIIYLLUYRFRKMG-UHFFFAOYSA-N tetrathianaphthacene Chemical compound C1=CC=CC2=C3SSC(C4=CC=CC=C44)=C3C3=C4SSC3=C21 JIIYLLUYRFRKMG-UHFFFAOYSA-N 0.000 description 1
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- 125000001544 thienyl group Chemical group 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
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- 238000002834 transmittance Methods 0.000 description 1
- MJRFDVWKTFJAPF-UHFFFAOYSA-K trichloroiridium;hydrate Chemical compound O.Cl[Ir](Cl)Cl MJRFDVWKTFJAPF-UHFFFAOYSA-K 0.000 description 1
- QGJSAGBHFTXOTM-UHFFFAOYSA-K trifluoroerbium Chemical compound F[Er](F)F QGJSAGBHFTXOTM-UHFFFAOYSA-K 0.000 description 1
- SXXNJJQVBPWGTP-UHFFFAOYSA-K tris[(4-methylquinolin-8-yl)oxy]alumane Chemical compound [Al+3].C1=CC=C2C(C)=CC=NC2=C1[O-].C1=CC=C2C(C)=CC=NC2=C1[O-].C1=CC=C2C(C)=CC=NC2=C1[O-] SXXNJJQVBPWGTP-UHFFFAOYSA-K 0.000 description 1
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- 239000010937 tungsten Substances 0.000 description 1
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- OYQCBJZGELKKPM-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O-2].[Zn+2].[O-2].[In+3] OYQCBJZGELKKPM-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0033—Iridium compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
- H10K50/12—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
- H10K50/121—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants for assisting energy transfer, e.g. sensitization
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
- H10K50/125—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers specially adapted for multicolour light emission, e.g. for emitting white light
- H10K50/13—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers specially adapted for multicolour light emission, e.g. for emitting white light comprising stacked EL layers within one EL unit
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/14—Carrier transporting layers
- H10K50/16—Electron transporting layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/80—Constructional details
- H10K50/85—Arrangements for extracting light from the devices
- H10K50/852—Arrangements for extracting light from the devices comprising a resonant cavity structure, e.g. Bragg reflector pair
-
- 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
- H10K59/80—Constructional details
- H10K59/875—Arrangements for extracting light from the devices
- H10K59/876—Arrangements for extracting light from the devices comprising a resonant cavity structure, e.g. Bragg reflector pair
-
- 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
- H10K85/30—Coordination compounds
- H10K85/341—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H10K85/342—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising iridium
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
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| CN107254306B (zh) | 2012-03-14 | 2020-08-25 | 株式会社半导体能源研究所 | 发光元件、发光装置、电子设备及照明装置 |
| JP2013232629A (ja) | 2012-04-06 | 2013-11-14 | Semiconductor Energy Lab Co Ltd | 発光素子、発光装置、電子機器、および照明装置 |
| KR20210008947A (ko) | 2012-04-20 | 2021-01-25 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 발광 장치, 전자 기기, 및 조명 장치 |
| WO2013157591A1 (en) | 2012-04-20 | 2013-10-24 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, electronic appliance, and lighting device |
| DE102013208844A1 (de) | 2012-06-01 | 2013-12-05 | Semiconductor Energy Laboratory Co., Ltd. | Lichtemittierendes Element, lichtemittierende Vorrichtung, Anzeigevorrichtung, elektronisches Gerät und Beleuchtungsvorrichtung |
| TWI651878B (zh) | 2012-08-03 | 2019-02-21 | 日商半導體能源研究所股份有限公司 | 發光元件、發光裝置、顯示裝置、電子裝置及照明設備 |
| TWI650399B (zh) | 2012-08-03 | 2019-02-11 | 日商半導體能源研究所股份有限公司 | 發光元件 |
| KR102204794B1 (ko) | 2012-08-10 | 2021-01-18 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 발광 장치, 표시 장치, 전자 기기 및 조명 장치 |
| US10043982B2 (en) | 2013-04-26 | 2018-08-07 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, display device, electronic device, and lighting device |
| KR102100880B1 (ko) * | 2013-06-26 | 2020-04-14 | 엘지디스플레이 주식회사 | 유기발광 다이오드 표시장치 |
| CN104252199A (zh) * | 2013-06-28 | 2014-12-31 | 鸿富锦精密工业（深圳）有限公司 | 使用触控轨迹进行解锁的笔记本电脑 |
| KR102084170B1 (ko) * | 2013-07-25 | 2020-03-04 | 삼성디스플레이 주식회사 | 유기발광소자, 이를 포함하는 유기 발광 표시장치 및 그 제조방법 |
| WO2015029808A1 (en) | 2013-08-26 | 2015-03-05 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, display module, lighting module, light-emitting device, display device, electronic appliance, and lighting device |
| CN110071219B (zh) | 2013-12-02 | 2022-04-29 | 株式会社半导体能源研究所 | 发光元件以及发光装置 |
| JP6488082B2 (ja) * | 2013-12-02 | 2019-03-20 | 株式会社半導体エネルギー研究所 | 発光装置、電子機器、および照明装置 |
| KR102088883B1 (ko) * | 2013-12-02 | 2020-03-16 | 엘지디스플레이 주식회사 | 유기전계발광표시장치 |
| CN108598272B (zh) | 2013-12-02 | 2020-10-16 | 株式会社半导体能源研究所 | 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 |
| US20160372683A1 (en) | 2014-03-07 | 2016-12-22 | Konica Minolta, Inc. | Organic electroluminescence element, display device, illumination device, and light-emitting composition |
| JP2015187982A (ja) * | 2014-03-13 | 2015-10-29 | 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 |
| JP2015201279A (ja) * | 2014-04-04 | 2015-11-12 | セイコーエプソン株式会社 | 発光素子、発光装置、表示装置および電子機器 |
| TWI729649B (zh) | 2014-05-30 | 2021-06-01 | 日商半導體能源研究所股份有限公司 | 發光元件，發光裝置，電子裝置以及照明裝置 |
| WO2016020801A1 (en) | 2014-08-08 | 2016-02-11 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting device, electronic device, and lighting device |
| US9343691B2 (en) * | 2014-08-08 | 2016-05-17 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, electronic device, and lighting device |
| JP6367340B2 (ja) * | 2014-08-22 | 2018-08-01 | シャープ株式会社 | 有機エレクトロルミネッセンス素子およびその製造方法並びに発光方法 |
| US10741772B2 (en) | 2014-08-29 | 2020-08-11 | Samsung Electronics Co., Ltd. | Organic light-emitting device |
| KR102353647B1 (ko) | 2014-08-29 | 2022-01-20 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 표시 장치, 전자 기기, 및 조명 장치 |
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| US20160104855A1 (en) | 2014-10-10 | 2016-04-14 | Semiconductor Energy Laboratory Co., Ltd. | Light-Emitting Element, Display 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 |
| CN104282843B (zh) * | 2014-10-30 | 2017-04-19 | 中国科学院长春应用化学研究所 | 一种黄色有机电致发光器件及其制备方法 |
| KR102299838B1 (ko) * | 2014-10-31 | 2021-09-07 | 엘지디스플레이 주식회사 | 유기 발광 소자 및 그의 제조 방법 |
| KR20160067629A (ko) * | 2014-12-04 | 2016-06-14 | 서울대학교산학협력단 | 유기발광소자 |
| KR102381626B1 (ko) * | 2014-12-17 | 2022-04-01 | 엘지디스플레이 주식회사 | 유기발광 표시장치 |
| KR101706752B1 (ko) * | 2015-02-17 | 2017-02-27 | 서울대학교산학협력단 | 호스트, 인광 도펀트 및 형광 도펀트를 포함하는 유기발광소자 |
| US10062861B2 (en) * | 2015-02-24 | 2018-08-28 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, display device, electronic device, and lighting device |
| US10903440B2 (en) | 2015-02-24 | 2021-01-26 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, electronic device, and lighting device |
| TWI737594B (zh) * | 2015-03-09 | 2021-09-01 | 日商半導體能源研究所股份有限公司 | 發光元件，顯示裝置，電子裝置，與照明裝置 |
| TWI860824B (zh) * | 2015-03-09 | 2024-11-01 | 日商半導體能源研究所股份有限公司 | 發光元件、顯示裝置、電子裝置及照明設備 |
| CN104900815A (zh) * | 2015-05-26 | 2015-09-09 | 京东方科技集团股份有限公司 | 双层掺杂磷光发光器件及其制备方法 |
| KR102825355B1 (ko) * | 2015-07-08 | 2025-06-26 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 표시 장치, 전자 장치, 및 조명 장치 |
| US10797113B2 (en) * | 2016-01-25 | 2020-10-06 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting device with layered electrode structures |
| US10096658B2 (en) * | 2016-04-22 | 2018-10-09 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, display device, electronic device, and lighting device |
| CN113130808A (zh) | 2016-05-06 | 2021-07-16 | 株式会社半导体能源研究所 | 发光元件、显示装置 |
| US9911937B2 (en) | 2016-05-12 | 2018-03-06 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, electronic device, and lighting device |
| WO2018100476A1 (en) | 2016-11-30 | 2018-06-07 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, electronic device, and lighting device |
| CN108346750B (zh) * | 2017-08-08 | 2019-07-19 | 广东聚华印刷显示技术有限公司 | 电致发光器件及其发光层和应用 |
| JP6962773B2 (ja) * | 2017-10-12 | 2021-11-05 | 株式会社ジャパンディスプレイ | 表示装置 |
| TWI651660B (zh) | 2017-12-12 | 2019-02-21 | 財團法人工業技術研究院 | 指紋辨識裝置 |
| CN109994634B (zh) * | 2017-12-29 | 2020-12-11 | 昆山国显光电有限公司 | 有机电致发光器件 |
| CN108365112B (zh) * | 2018-01-19 | 2020-06-16 | 昆山国显光电有限公司 | 一种电致发光器件 |
| KR20250151571A (ko) | 2018-03-07 | 2025-10-21 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 표시 장치, 전자 기기, 유기 화합물, 및 조명 장치 |
| CN109378392B (zh) * | 2018-09-03 | 2020-12-08 | 云谷（固安）科技有限公司 | 一种有机电致发光器件及显示装置 |
| KR102727456B1 (ko) * | 2018-09-26 | 2024-11-08 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 디바이스, 발광 장치, 전자 기기, 및 조명 장치 |
| CN113412508A (zh) | 2019-02-06 | 2021-09-17 | 株式会社半导体能源研究所 | 发光器件、发光设备、显示装置、电子设备及照明装置 |
| KR20220002337A (ko) | 2019-04-25 | 2022-01-06 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 디바이스, 발광 장치, 전자 기기, 및 조명 장치 |
| KR102804493B1 (ko) * | 2019-04-30 | 2025-05-09 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
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| JP7478007B2 (ja) * | 2020-03-27 | 2024-05-02 | キヤノン株式会社 | 電子デバイスおよびその製造方法、電子装置ならびに移動体 |
| KR102776384B1 (ko) | 2020-05-06 | 2025-03-10 | 삼성디스플레이 주식회사 | 발광 소자 및 이를 포함하는 전자 장치 |
| KR20220085924A (ko) | 2020-12-15 | 2022-06-23 | 삼성디스플레이 주식회사 | 발광 소자 및 이를 포함하는 전자 장치 |
| US12166102B2 (en) | 2020-12-18 | 2024-12-10 | Innoscience (Suzhou) Technology Co., Ltd. | Semiconductor device and method for manufacturing the same |
| US12027615B2 (en) | 2020-12-18 | 2024-07-02 | Innoscience (Suzhou) Technology Co., Ltd. | Semiconductor device and method for manufacturing the same |
| US20220209155A1 (en) * | 2020-12-31 | 2022-06-30 | Lg Display Co., Ltd. | Display apparatus having a light-emitting layer |
| US11730008B2 (en) | 2021-02-16 | 2023-08-15 | Sharp Kabushiki Kaisha | Light emitting layer including quantum dots with improved charge carrier mobility |
| US12154864B2 (en) * | 2021-03-30 | 2024-11-26 | Innoscience (Suzhou) Technology Co., Ltd. | III-nitride-based semiconductor devices on patterned substrates and method of making the same |
| US12324179B2 (en) * | 2021-12-16 | 2025-06-03 | Wolfspeed, Inc. | Group III-nitride high-electron mobility transistors with a buried metallic conductive material layer and process for making the same |
| CN116018000A (zh) * | 2023-02-06 | 2023-04-25 | 固安翌光科技有限公司 | 一种显示装置 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW556446B (en) * | 2002-09-11 | 2003-10-01 | Opto Tech Corp | Organic light-emitting device and the manufacturing method thereof |
| TWI308467B (en) * | 2006-03-15 | 2009-04-01 | Univision Technology Inc | Organic electroluminescent device |
| TW200952538A (en) * | 2008-06-02 | 2009-12-16 | Ind Tech Res Inst | Organic light-emitting device |
Family Cites Families (102)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5420288A (en) | 1992-04-14 | 1995-05-30 | Ricoh Company, Ltd. | Electroluminescent device comprising oxadiazole compounds luminescent material, oxadiazole compounds for the device, and method of producing oxadiazole compounds |
| JPH0785972A (ja) | 1993-09-20 | 1995-03-31 | Toshiba Corp | 有機ｅｌ素子 |
| US5597890A (en) | 1993-11-01 | 1997-01-28 | Research Corporation Technologies, Inc. | Conjugated polymer exciplexes and applications thereof |
| JP3451680B2 (ja) | 1993-11-15 | 2003-09-29 | 三菱化学株式会社 | 有機電界発光素子 |
| US5409783A (en) | 1994-02-24 | 1995-04-25 | Eastman Kodak Company | Red-emitting organic electroluminescent device |
| US5709492A (en) | 1994-04-27 | 1998-01-20 | Sakura Color Products Corp. | Liquid applicator |
| JPH103990A (ja) | 1996-06-13 | 1998-01-06 | Idemitsu Kosan Co Ltd | 有機ｅｌ発光装置 |
| US6097147A (en) | 1998-09-14 | 2000-08-01 | The Trustees Of Princeton University | Structure for high efficiency electroluminescent device |
| EP3321954A1 (en) | 1999-05-13 | 2018-05-16 | The Trustees of Princeton University | Very high efficiency organic light emitting devices based on electrophosphorescence |
| JP4449113B2 (ja) * | 1999-09-10 | 2010-04-14 | ソニー株式会社 | ２次元表示装置 |
| KR100329571B1 (ko) * | 2000-03-27 | 2002-03-23 | 김순택 | 유기 전자 발광소자 |
| EP1202608B2 (en) | 2000-10-30 | 2012-02-08 | Kabushiki Kaisha Toyota Chuo Kenkyusho | Organic light-emitting devices |
| SG138466A1 (en) | 2000-12-28 | 2008-01-28 | Semiconductor Energy Lab | Luminescent device |
| TW519770B (en) | 2001-01-18 | 2003-02-01 | Semiconductor Energy Lab | Light emitting device and manufacturing method thereof |
| ITTO20010692A1 (it) | 2001-07-13 | 2003-01-13 | Consiglio Nazionale Ricerche | Dispositivo elettroluminescente organico basato sull'emissione di ecciplessi od elettroplessi e sua realizzazione. |
| US6863997B2 (en) | 2001-12-28 | 2005-03-08 | The Trustees Of Princeton University | White light emitting OLEDs from combined monomer and aggregate emission |
| US6869695B2 (en) | 2001-12-28 | 2005-03-22 | The Trustees Of Princeton University | White light emitting OLEDs from combined monomer and aggregate emission |
| 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 |
| ITBO20020165A1 (it) | 2002-03-29 | 2003-09-29 | Consiglio Nazionale Ricerche | Dispositivo elettroluminescente organico con droganti cromofori |
| US6951694B2 (en) | 2002-03-29 | 2005-10-04 | The University Of Southern California | Organic light emitting devices with electron blocking layers |
| TWI314947B (en) | 2002-04-24 | 2009-09-21 | Eastman Kodak Compan | Organic light emitting diode devices with improved operational stability |
| KR100902988B1 (ko) | 2002-08-26 | 2009-06-15 | 라이트온 테크놀러지 코포레이션 | 백색광 발광 다이오드의 제조 방법 |
| KR100624406B1 (ko) | 2002-12-30 | 2006-09-18 | 삼성에스디아이 주식회사 | 비페닐 유도체 및 이를 채용한 유기 전계 발광 소자 |
| TWI316827B (en) | 2003-02-27 | 2009-11-01 | Toyota Jidoshokki Kk | Organic electroluminescent device |
| JP4531342B2 (ja) | 2003-03-17 | 2010-08-25 | 株式会社半導体エネルギー研究所 | 白色有機発光素子および発光装置 |
| JP4905445B2 (ja) | 2003-05-27 | 2012-03-28 | 株式会社デンソー | ３級アミン化合物、有機ｅｌ素子用材料および有機ｅｌ素子 |
| JP4487587B2 (ja) | 2003-05-27 | 2010-06-23 | 株式会社デンソー | 有機ｅｌ素子およびその製造方法 |
| US7211823B2 (en) * | 2003-07-10 | 2007-05-01 | Universal Display Corporation | Organic light emitting device structure for obtaining chromaticity stability |
| JPWO2005022660A1 (ja) | 2003-08-29 | 2006-10-26 | 松下電器産業株式会社 | 有機半導体膜、それを用いた電子デバイス、およびそれらの製造方法 |
| US7175922B2 (en) | 2003-10-22 | 2007-02-13 | Eastman Kodak Company | Aggregate organic light emitting diode devices with improved operational stability |
| US7700366B2 (en) | 2003-12-04 | 2010-04-20 | Massachusetts Institute Of Technology | Fluorescent, semi-conductive polymers, and devices comprising them |
| TW200541401A (en) | 2004-02-13 | 2005-12-16 | Idemitsu Kosan Co | Organic electroluminescent device |
| JP4621201B2 (ja) * | 2004-03-25 | 2011-01-26 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
| DE102004038199A1 (de) | 2004-08-05 | 2006-03-16 | Patent-Treuhand-Gesellschaft für elektrische Glühlampen mbH | LED mit niedriger Farbtemperatur |
| US7597967B2 (en) | 2004-12-17 | 2009-10-06 | Eastman Kodak Company | Phosphorescent OLEDs with exciton blocking layer |
| JP2006203172A (ja) * | 2004-12-22 | 2006-08-03 | Fuji Photo Film Co Ltd | 有機電界発光素子 |
| US20060134464A1 (en) | 2004-12-22 | 2006-06-22 | Fuji Photo Film Co. Ltd | Organic electroluminescent element |
| JP2007073620A (ja) | 2005-09-05 | 2007-03-22 | Fujifilm Corp | 有機電界発光素子 |
| US20070090756A1 (en) | 2005-10-11 | 2007-04-26 | Fujifilm Corporation | Organic electroluminescent element |
| WO2007063754A1 (ja) | 2005-12-01 | 2007-06-07 | Nippon Steel Chemical Co., Ltd. | 有機電界発光素子用化合物及び有機電界発光素子 |
| EP1963346B1 (en) | 2005-12-05 | 2012-08-22 | Semiconductor Energy Laboratory Co., Ltd. | Organometallic complex and light-emitting element, light-emitting device and electronic device using the same |
| EP1873163B1 (en) | 2006-03-21 | 2010-08-25 | Semiconductor Energy Laboratory Co., Ltd. | Organometallic complex and light emitting element, light emitting device, and electronic device using the organometallic complex |
| EP2004616B1 (en) | 2006-03-21 | 2014-05-21 | Semiconductor Energy Laboratory Co., Ltd. | Quinoxaline derivative, and light-emitting element, light-emitting device, electronic device using the quinoxaline derivative |
| US20080079354A1 (en) | 2006-09-29 | 2008-04-03 | Semiconductor Energy Laboratory Co., Ltd. | Quinoxaline Derivative, And Light Emitting Element, Light Emitting Device, And Electronic Device Using the Quinoxaline Derivative |
| JP5238227B2 (ja) | 2006-12-27 | 2013-07-17 | 株式会社半導体エネルギー研究所 | 有機金属錯体および有機金属錯体を用いた発光素子、発光装置、並びに電子機器 |
| TW200908777A (en) * | 2007-03-23 | 2009-02-16 | Idemitsu Kosan Co | Organic el device |
| JP2008288344A (ja) | 2007-05-16 | 2008-11-27 | Nippon Hoso Kyokai <Nhk> | 有機ｅｌ素子 |
| CN105669765A (zh) | 2007-05-18 | 2016-06-15 | 株式会社半导体能源研究所 | 有机金属配合物，包含该有机金属配合物的组合物和发光元件 |
| KR101030007B1 (ko) | 2007-06-15 | 2011-04-20 | 삼성모바일디스플레이주식회사 | 헤테로방향환 함유 화합물, 이의 제조 방법 및 이를 이용한유기 발광 소자 |
| US8034465B2 (en) | 2007-06-20 | 2011-10-11 | Global Oled Technology Llc | Phosphorescent oled having double exciton-blocking layers |
| JP2009032987A (ja) * | 2007-07-27 | 2009-02-12 | Fujifilm Corp | 有機電界発光素子 |
| KR100933747B1 (ko) * | 2008-04-01 | 2009-12-24 | 단국대학교 산학협력단 | 유기 발광 소자 |
| JP5432487B2 (ja) | 2008-08-20 | 2014-03-05 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
| JP5325707B2 (ja) | 2008-09-01 | 2013-10-23 | 株式会社半導体エネルギー研究所 | 発光素子 |
| CN102217419A (zh) * | 2008-09-05 | 2011-10-12 | 株式会社半导体能源研究所 | 发光元件、发光器件和电子器件 |
| TWI422088B (zh) * | 2008-10-23 | 2014-01-01 | Nat Univ Tsing Hua | 具有奈米點之有機發光二極體及其製造方法 |
| JP5497284B2 (ja) | 2008-12-08 | 2014-05-21 | ユー・ディー・シー アイルランド リミテッド | 白色有機電界発光素子 |
| KR20100073417A (ko) * | 2008-12-23 | 2010-07-01 | 엘지디스플레이 주식회사 | 유기전계발광소자 |
| US9040718B2 (en) | 2009-01-22 | 2015-05-26 | The University Of Rochester | Hybrid host materials for electrophosphorescent devices |
| TWI467824B (zh) * | 2009-06-11 | 2015-01-01 | Ind Tech Res Inst | 白光有機發光元件 |
| US8766269B2 (en) | 2009-07-02 | 2014-07-01 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting device, lighting device, and electronic device |
| KR20120103571A (ko) | 2009-10-05 | 2012-09-19 | 손 라이팅 리미티드 | 다층구조의 유기 장치 |
| CN105399776A (zh) * | 2009-11-02 | 2016-03-16 | 株式会社半导体能源研究所 | 有机金属配合物、发光元件、显示器件、电子器件和照明器件 |
| KR101352116B1 (ko) | 2009-11-24 | 2014-01-14 | 엘지디스플레이 주식회사 | 백색 유기 발광 소자 |
| KR101317923B1 (ko) | 2009-12-07 | 2013-10-16 | 고쿠리쓰다이가쿠호진 규슈다이가쿠 | 유기 발광 재료 및 유기 발광 소자 |
| JP2011153269A (ja) | 2010-01-28 | 2011-08-11 | Nara Institute Of Science & Technology | 白色発光性高分子複合材料およびその製造方法 |
| 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 |
| EP2366753B1 (en) | 2010-03-02 | 2015-06-17 | Semiconductor Energy Laboratory Co., Ltd. | Light-Emitting Element and Lighting Device |
| JP5324513B2 (ja) | 2010-03-31 | 2013-10-23 | ユー・ディー・シー アイルランド リミテッド | 有機電界発光素子 |
| WO2011125090A1 (ja) * | 2010-04-02 | 2011-10-13 | 株式会社 日立製作所 | 有機発光装置およびこれを用いた光源装置 |
| JP2011222334A (ja) * | 2010-04-09 | 2011-11-04 | Dainippon Printing Co Ltd | 熱伝導性封止部材および素子 |
| JP5602555B2 (ja) * | 2010-05-17 | 2014-10-08 | 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 |
| JP2011258373A (ja) * | 2010-06-08 | 2011-12-22 | Nippon Hoso Kyokai <Nhk> | 有機ｅｌ素子及び有機ｅｌディスプレイ |
| JP5815341B2 (ja) * | 2010-09-09 | 2015-11-17 | 株式会社半導体エネルギー研究所 | 複素環化合物 |
| EP2433929B1 (en) * | 2010-09-27 | 2013-10-23 | Semiconductor Energy Laboratory Co, Ltd. | Organic Compound, Light-Emitting Element, Light-Emitting Device, Electronic Device, and Lighting Device |
| TW201220572A (en) * | 2010-10-20 | 2012-05-16 | Idemitsu Kosan Co | Tandem organic electroluminescent element |
| KR102071726B1 (ko) | 2010-10-22 | 2020-01-30 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 유기금속 착체, 발광 소자, 발광 장치, 전자 장치 및 조명 장치 |
| KR101910030B1 (ko) * | 2010-11-30 | 2018-10-19 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 벤조옥사졸 유도체, 발광 소자, 발광 장치, 전자기기 및 조명 장치 |
| US8847218B2 (en) * | 2011-01-20 | 2014-09-30 | Idemitsu Kosan Co., Ltd. | Organic electroluminescent element |
| KR101812673B1 (ko) | 2011-02-16 | 2017-12-27 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자 |
| WO2012111680A1 (en) | 2011-02-16 | 2012-08-23 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting body, light-emitting layer, and light-emitting device |
| KR20250026895A (ko) | 2011-02-16 | 2025-02-25 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 엘리먼트 |
| TWI831058B (zh) | 2011-02-28 | 2024-02-01 | 日商半導體能源研究所股份有限公司 | 發光元件 |
| JP2012195572A (ja) | 2011-02-28 | 2012-10-11 | Semiconductor Energy Lab Co Ltd | 発光層および発光素子 |
| CN105070846B (zh) | 2011-03-23 | 2018-07-06 | 株式会社半导体能源研究所 | 发光元件、发光装置、照明装置及电子设备 |
| JP5699282B2 (ja) * | 2011-03-24 | 2015-04-08 | パナソニックＩｐマネジメント株式会社 | 有機エレクトロルミネッセンス素子及び照明器具 |
| KR102128592B1 (ko) | 2011-03-30 | 2020-06-30 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자 |
| KR102159895B1 (ko) | 2011-04-07 | 2020-09-24 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자 |
| JP2012243983A (ja) * | 2011-05-20 | 2012-12-10 | Nippon Hoso Kyokai <Nhk> | 有機エレクトロルミネッセンス素子 |
| TWI727297B (zh) | 2011-08-25 | 2021-05-11 | 日商半導體能源研究所股份有限公司 | 發光元件，發光裝置，電子裝置，照明裝置以及新穎有機化合物 |
| CN103022370B (zh) * | 2011-09-20 | 2016-02-03 | 乐金显示有限公司 | 白色有机发光装置 |
| US10411212B2 (en) * | 2011-10-04 | 2019-09-10 | Idemitsu Kosan Co., Ltd. | Organic electroluminescent element |
| WO2013062075A1 (ja) * | 2011-10-26 | 2013-05-02 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子および有機エレクトロルミネッセンス素子用材料 |
| US20130164611A1 (en) * | 2011-12-23 | 2013-06-27 | Semiconductor Energy Laboratory Co., Ltd. | Power storage device |
| US10026905B2 (en) * | 2012-01-18 | 2018-07-17 | Duk San Neolux Co., Ltd. | Compound, organic electric element using the same, and an electronic device thereof |
| KR101803537B1 (ko) | 2012-02-09 | 2017-11-30 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자 |
| CN107254306B (zh) | 2012-03-14 | 2020-08-25 | 株式会社半导体能源研究所 | 发光元件、发光装置、电子设备及照明装置 |
| JP2013232629A (ja) * | 2012-04-06 | 2013-11-14 | Semiconductor Energy Lab Co Ltd | 発光素子、発光装置、電子機器、および照明装置 |
| KR101419810B1 (ko) | 2012-04-10 | 2014-07-15 | 서울대학교산학협력단 | 엑시플렉스를 형성하는 공동 호스트를 포함하는 유기 발광 소자 |
| JP6158542B2 (ja) | 2012-04-13 | 2017-07-05 | 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 |
| JP6158543B2 (ja) | 2012-04-13 | 2017-07-05 | 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 |
| WO2013157591A1 (en) | 2012-04-20 | 2013-10-24 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, light-emitting device, electronic appliance, and lighting device |
-
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- 2013-03-11 JP JP2013047479A patent/JP2013232629A/ja not_active Withdrawn
- 2013-03-12 US US13/795,712 patent/US9391289B2/en active Active
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW556446B (en) * | 2002-09-11 | 2003-10-01 | Opto Tech Corp | Organic light-emitting device and the manufacturing method thereof |
| TWI308467B (en) * | 2006-03-15 | 2009-04-01 | Univision Technology Inc | Organic electroluminescent device |
| TW200952538A (en) * | 2008-06-02 | 2009-12-16 | Ind Tech Res Inst | Organic light-emitting device |
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| US20140061604A1 (en) | 2014-03-06 |
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