DE102009018647A1 - Strahlungsemittierende Vorrichtung - Google Patents
Strahlungsemittierende Vorrichtung Download PDFInfo
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- DE102009018647A1 DE102009018647A1 DE102009018647A DE102009018647A DE102009018647A1 DE 102009018647 A1 DE102009018647 A1 DE 102009018647A1 DE 102009018647 A DE102009018647 A DE 102009018647A DE 102009018647 A DE102009018647 A DE 102009018647A DE 102009018647 A1 DE102009018647 A1 DE 102009018647A1
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- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- HRGDZIGMBDGFTC-UHFFFAOYSA-N platinum(2+) Chemical compound [Pt+2] HRGDZIGMBDGFTC-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000006862 quantum yield reaction Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000001552 radio frequency sputter deposition Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- DBDJXGIDPXHUGS-UHFFFAOYSA-N triphenyl-(6-triphenylsilyl-9h-carbazol-3-yl)silane Chemical compound C1=CC=CC=C1[Si](C=1C=C2C3=CC(=CC=C3NC2=CC=1)[Si](C=1C=CC=CC=1)(C=1C=CC=CC=1)C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 DBDJXGIDPXHUGS-UHFFFAOYSA-N 0.000 description 1
- 108010086502 tumor-derived adhesion factor Proteins 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- 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
- H10K50/125—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
-
- 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
- H10K50/15—Hole 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
- H10K50/10—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
- H10K2101/00—Properties of the organic materials covered by group H10K85/00
- H10K2101/10—Triplet emission
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009018647A DE102009018647A1 (de) | 2009-04-23 | 2009-04-23 | Strahlungsemittierende Vorrichtung |
| CN201080018169.XA CN102414856B (zh) | 2009-04-23 | 2010-04-22 | 发射辐射的装置 |
| KR1020117027641A KR101702155B1 (ko) | 2009-04-23 | 2010-04-22 | 복사 방출 장치 |
| EP10715233.2A EP2422381B1 (de) | 2009-04-23 | 2010-04-22 | Strahlungsemittierende vorrichtung |
| JP2012506506A JP2012524991A (ja) | 2009-04-23 | 2010-04-22 | ビーム放射装置 |
| US13/266,095 US8441187B2 (en) | 2009-04-23 | 2010-04-22 | Radiation-emitting device |
| PCT/EP2010/055368 WO2010122113A1 (de) | 2009-04-23 | 2010-04-22 | Strahlungsemittierende vorrichtung |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009018647A DE102009018647A1 (de) | 2009-04-23 | 2009-04-23 | Strahlungsemittierende Vorrichtung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE102009018647A1 true DE102009018647A1 (de) | 2010-10-28 |
Family
ID=42245006
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE102009018647A Withdrawn DE102009018647A1 (de) | 2009-04-23 | 2009-04-23 | Strahlungsemittierende Vorrichtung |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8441187B2 (https=) |
| EP (1) | EP2422381B1 (https=) |
| JP (1) | JP2012524991A (https=) |
| KR (1) | KR101702155B1 (https=) |
| CN (1) | CN102414856B (https=) |
| DE (1) | DE102009018647A1 (https=) |
| WO (1) | WO2010122113A1 (https=) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10700141B2 (en) | 2006-09-29 | 2020-06-30 | University Of Florida Research Foundation, Incorporated | Method and apparatus for infrared detection and display |
| KR101820772B1 (ko) | 2010-05-24 | 2018-01-22 | 유니버시티 오브 플로리다 리서치 파운데이션, 인크. | 적외선 업-컨버젼 장치 상에 전하 차단층을 제공하기 위한 방법 및 장치 |
| WO2012170456A2 (en) * | 2011-06-06 | 2012-12-13 | University Of Florida Research Foundation, Inc. | Infrared imaging device integrating an ir up-conversion device with a cmos image sensor |
| RU2013158845A (ru) * | 2011-06-06 | 2015-07-20 | Юниверсити Оф Флорида Рисеч Фаундэйшн, Инк. | Прозрачное устройство преобразования инфракрасного излучения в видимое излучение с повышением частоты |
| MX2013015214A (es) | 2011-06-30 | 2014-03-21 | Nanoholdings Llc | Metodo y aparato para detectar radiacion infrarroja con ganancia. |
| DE102011084276B4 (de) | 2011-10-11 | 2019-10-10 | Osram Oled Gmbh | Verkapselung für ein organisches elektronisches bauelement, ein organisches elektronisches bauelement mit der verkapselung und ein verfahren zur herstellung eines organischen elektronischen bauelements mit der verkapselung |
| US20150028311A1 (en) * | 2011-11-28 | 2015-01-29 | Ocean's King Lighting Science & Technology Co., Lt | Doped organic electroluminescent device and method for preparing same |
| CN104025333A (zh) * | 2011-11-28 | 2014-09-03 | 海洋王照明科技股份有限公司 | 一种聚合物电致发光器件及其制备方法 |
| WO2013094276A1 (ja) * | 2011-12-20 | 2013-06-27 | コニカミノルタ株式会社 | 有機ｅｌ素子 |
| RU2746407C1 (ru) | 2012-02-23 | 2021-04-13 | Стейдж Селл Терапеутикс Гмбх | Хроматографическое выделение клеток и других сложных биологических материалов |
| KR101419810B1 (ko) | 2012-04-10 | 2014-07-15 | 서울대학교산학협력단 | 엑시플렉스를 형성하는 공동 호스트를 포함하는 유기 발광 소자 |
| WO2013180539A1 (ko) * | 2012-05-31 | 2013-12-05 | 주식회사 엘지화학 | 유기전계발광소자 |
| EP2750215B1 (en) * | 2012-07-18 | 2016-10-26 | LG Display Co., Ltd. | Organic light-emitting device |
| US9859517B2 (en) * | 2012-09-07 | 2018-01-02 | Nitto Denko Corporation | White organic light-emitting diode |
| DE102013215342B4 (de) * | 2013-08-05 | 2023-05-04 | Novaled Gmbh | Verfahren zur Herstellung organisch phosphoreszenter Schichten unter Zusatz schwerer Hauptgruppenmetallkomplexe, damit hergestellte Schicht, deren Verwendung und organisches Halbleiterbauelement diese umfassend |
| EP2944620A1 (en) * | 2013-12-26 | 2015-11-18 | Shin-Etsu Quartz Products Co., Ltd. | Silica glass member for wavelength conversion, and production method therefor |
| CN104319353B (zh) * | 2014-11-07 | 2016-07-06 | 京东方科技集团股份有限公司 | 单色oled、制作方法及oled 显示面板 |
| DE102015100913B4 (de) * | 2015-01-22 | 2017-08-10 | Osram Oled Gmbh | Lichtemittierendes Bauelement, Verfahren zum Herstellen eines lichtemittierenden Bauelements und Verfahren zum Betreiben eines lichtemittierenden Bauelements |
| DE102015106941B4 (de) | 2015-05-05 | 2025-07-31 | Pictiva Displays International Limited | Organische Emitterschicht, organische Leuchtdiode und Verwendung von Schweratomen in einer organischen Emitterschicht einer organischen Leuchtdiode |
| WO2017039774A2 (en) | 2015-06-11 | 2017-03-09 | University Of Florida Research Foundation, Incorporated | Monodisperse, ir-absorbing nanoparticles and related methods and devices |
| JP7194020B2 (ja) | 2015-10-22 | 2022-12-21 | ジュノ セラピューティクス ゲーエムベーハー | 細胞の培養方法ならびにそのためのキットおよび装置 |
| US11248238B2 (en) | 2015-10-22 | 2022-02-15 | Juno Therapeutics Gmbh | Methods, kits, agents and apparatuses for transduction |
| JP7339160B2 (ja) | 2017-04-27 | 2023-09-05 | ジュノ セラピューティクス ゲーエムベーハー | オリゴマー粒子試薬およびその使用方法 |
| EP3874024A1 (en) | 2018-10-31 | 2021-09-08 | Juno Therapeutics GmbH | Methods for selection and stimulation of cells and apparatus for same |
| WO2021062574A1 (en) | 2019-08-07 | 2021-04-08 | Boe Technology Group Co., Ltd. | Display panel, display apparatus, light emitting element, and method of fabricating display panel |
| CN119894228A (zh) * | 2025-01-13 | 2025-04-25 | 京东方科技集团股份有限公司 | 发光器件和显示基板 |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005029606A2 (en) * | 2003-09-19 | 2005-03-31 | Fuji Photo Film Co., Ltd. | Organic electroluminescent device |
| WO2006097064A1 (de) * | 2005-03-15 | 2006-09-21 | Novaled Ag | Lichtemittierendes bauelement |
| WO2006130883A2 (en) * | 2005-06-01 | 2006-12-07 | The Trustees Of Princeton University | Fluorescent filtered electrophosphorescence |
| WO2008054578A1 (en) * | 2006-10-27 | 2008-05-08 | The University Of Southern California | Materials and architectures for efficient harvesting of singlet and triplet excitons for white light emitting oleds |
| DE102007020644A1 (de) * | 2007-04-30 | 2008-11-06 | Novaled Ag | Lichtemittierendes Bauelement |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6310360B1 (en) | 1999-07-21 | 2001-10-30 | The Trustees Of Princeton University | Intersystem crossing agents for efficient utilization of excitons in organic light emitting devices |
| JP2003151773A (ja) * | 2001-11-13 | 2003-05-23 | Toray Ind Inc | 発光素子 |
| JP2005108730A (ja) * | 2003-09-30 | 2005-04-21 | Tdk Corp | 有機ｅｌ素子及びその製造方法 |
| KR100657892B1 (ko) | 2004-02-11 | 2006-12-14 | 삼성에스디아이 주식회사 | 유기 전계 발광 소자 |
| JP2005285470A (ja) * | 2004-03-29 | 2005-10-13 | Sanyo Electric Co Ltd | 有機エレクトロルミネッセンス素子 |
| JP5076501B2 (ja) * | 2004-07-16 | 2012-11-21 | コニカミノルタホールディングス株式会社 | 白色有機エレクトロルミネッセンス素子、画像表示素子および照明装置 |
| US7268711B1 (en) * | 2006-03-24 | 2007-09-11 | Audio Precision, Inc. | Method and circuit for amplitude compensation in a digital-to-analog converter |
| WO2008102644A1 (ja) * | 2007-02-19 | 2008-08-28 | Dai Nippon Printing Co., Ltd. | 有機エレクトロルミネッセンス素子 |
| US8546816B2 (en) | 2007-04-30 | 2013-10-01 | Novaled Ag | Light-emitting component and method for the production thereof |
| JP5213405B2 (ja) * | 2007-10-04 | 2013-06-19 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
| DE102008063589A1 (de) | 2008-10-07 | 2010-04-08 | Osram Opto Semiconductors Gmbh | Strahlungsemittierende Vorrichtung |
-
2009
- 2009-04-23 DE DE102009018647A patent/DE102009018647A1/de not_active Withdrawn
-
2010
- 2010-04-22 US US13/266,095 patent/US8441187B2/en not_active Expired - Fee Related
- 2010-04-22 CN CN201080018169.XA patent/CN102414856B/zh not_active Expired - Fee Related
- 2010-04-22 JP JP2012506506A patent/JP2012524991A/ja active Pending
- 2010-04-22 EP EP10715233.2A patent/EP2422381B1/de active Active
- 2010-04-22 WO PCT/EP2010/055368 patent/WO2010122113A1/de not_active Ceased
- 2010-04-22 KR KR1020117027641A patent/KR101702155B1/ko not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005029606A2 (en) * | 2003-09-19 | 2005-03-31 | Fuji Photo Film Co., Ltd. | Organic electroluminescent device |
| WO2006097064A1 (de) * | 2005-03-15 | 2006-09-21 | Novaled Ag | Lichtemittierendes bauelement |
| WO2006130883A2 (en) * | 2005-06-01 | 2006-12-07 | The Trustees Of Princeton University | Fluorescent filtered electrophosphorescence |
| WO2008054578A1 (en) * | 2006-10-27 | 2008-05-08 | The University Of Southern California | Materials and architectures for efficient harvesting of singlet and triplet excitons for white light emitting oleds |
| DE102007020644A1 (de) * | 2007-04-30 | 2008-11-06 | Novaled Ag | Lichtemittierendes Bauelement |
Non-Patent Citations (3)
| Title |
|---|
| C. Schildknecht et al. "Organic Light Emitting Materials and Devices XI." Edited by Kafafi, Zakya H. |
| Franky. Proceedings of SPIE, Volume 6655, pp. 665502 (2007) (SPIE The International Society for Optical Engineering) |
| P. Erk et al. SID06 Digest 2006, 131-134 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2422381A1 (de) | 2012-02-29 |
| KR101702155B1 (ko) | 2017-02-03 |
| EP2422381B1 (de) | 2019-10-30 |
| JP2012524991A (ja) | 2012-10-18 |
| CN102414856B (zh) | 2015-06-10 |
| KR20120027254A (ko) | 2012-03-21 |
| US20120187827A1 (en) | 2012-07-26 |
| CN102414856A (zh) | 2012-04-11 |
| WO2010122113A1 (de) | 2010-10-28 |
| US8441187B2 (en) | 2013-05-14 |
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