JP4851461B2 - エレクトロルミネッセンス・デバイスのための有機素子 - Google Patents
エレクトロルミネッセンス・デバイスのための有機素子 Download PDFInfo
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- JP4851461B2 JP4851461B2 JP2007532381A JP2007532381A JP4851461B2 JP 4851461 B2 JP4851461 B2 JP 4851461B2 JP 2007532381 A JP2007532381 A JP 2007532381A JP 2007532381 A JP2007532381 A JP 2007532381A JP 4851461 B2 JP4851461 B2 JP 4851461B2
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- 150000001875 compounds Chemical class 0.000 claims description 50
- 230000005525 hole transport Effects 0.000 claims description 42
- 229910052741 iridium Inorganic materials 0.000 claims description 38
- 125000004432 carbon atom Chemical group C* 0.000 claims description 26
- 229910052782 aluminium Inorganic materials 0.000 claims description 25
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 23
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 22
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 239000001257 hydrogen Substances 0.000 claims description 20
- 125000001424 substituent group Chemical group 0.000 claims description 20
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 18
- 125000005259 triarylamine group Chemical group 0.000 claims description 18
- 239000007983 Tris buffer Substances 0.000 claims description 17
- 150000002504 iridium compounds Chemical class 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 239000013522 chelant Substances 0.000 claims description 4
- 150000002430 hydrocarbons Chemical class 0.000 claims description 4
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 125000003368 amide group Chemical group 0.000 claims 1
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 239000010410 layer Substances 0.000 description 138
- -1 aluminum chelate complex Chemical class 0.000 description 98
- 239000000463 material Substances 0.000 description 62
- 125000003118 aryl group Chemical group 0.000 description 42
- 239000002019 doping agent Substances 0.000 description 31
- 239000000758 substrate Substances 0.000 description 24
- 239000003446 ligand Substances 0.000 description 23
- 230000000903 blocking effect Effects 0.000 description 22
- 238000002347 injection Methods 0.000 description 18
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- 239000002184 metal Substances 0.000 description 18
- 229910052757 nitrogen Inorganic materials 0.000 description 18
- 238000000034 method Methods 0.000 description 17
- 229910052799 carbon Inorganic materials 0.000 description 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 14
- 125000000217 alkyl group Chemical group 0.000 description 13
- 239000011521 glass Substances 0.000 description 13
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical group C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 125000000732 arylene group Chemical group 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
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- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
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- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 9
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 8
- 125000004429 atom Chemical group 0.000 description 7
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- 125000000623 heterocyclic group Chemical group 0.000 description 7
- MILUBEOXRNEUHS-UHFFFAOYSA-N iridium(3+) Chemical compound [Ir+3] MILUBEOXRNEUHS-UHFFFAOYSA-N 0.000 description 7
- 239000011777 magnesium Substances 0.000 description 7
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 6
- 125000002947 alkylene group Chemical group 0.000 description 6
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 230000005281 excited state Effects 0.000 description 6
- 229910052744 lithium Inorganic materials 0.000 description 6
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- 229910052783 alkali metal Inorganic materials 0.000 description 5
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- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical compound [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 description 5
- 150000004982 aromatic amines Chemical class 0.000 description 5
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- 239000002904 solvent Substances 0.000 description 5
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 4
- FSEXLNMNADBYJU-UHFFFAOYSA-N 2-phenylquinoline Chemical class C1=CC=CC=C1C1=CC=C(C=CC=C2)C2=N1 FSEXLNMNADBYJU-UHFFFAOYSA-N 0.000 description 4
- VFUDMQLBKNMONU-UHFFFAOYSA-N 9-[4-(4-carbazol-9-ylphenyl)phenyl]carbazole Chemical group C12=CC=CC=C2C2=CC=CC=C2N1C1=CC=C(C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=C1 VFUDMQLBKNMONU-UHFFFAOYSA-N 0.000 description 4
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 4
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 125000003277 amino group Chemical group 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000004020 conductor Substances 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 4
- 230000005283 ground state Effects 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
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- 238000005215 recombination Methods 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- 238000000859 sublimation Methods 0.000 description 4
- 230000008022 sublimation Effects 0.000 description 4
- TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical compound [Al+3].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 TVIVIEFSHFOWTE-UHFFFAOYSA-K 0.000 description 4
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- HONWGFNQCPRRFM-UHFFFAOYSA-N 2-n-(3-methylphenyl)-1-n,1-n,2-n-triphenylbenzene-1,2-diamine Chemical compound CC1=CC=CC(N(C=2C=CC=CC=2)C=2C(=CC=CC=2)N(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 HONWGFNQCPRRFM-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 3
- CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 125000004104 aryloxy group Chemical group 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- 238000005229 chemical vapour deposition Methods 0.000 description 3
- 239000002274 desiccant Substances 0.000 description 3
- 238000000295 emission spectrum Methods 0.000 description 3
- 239000010408 film Substances 0.000 description 3
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- 150000002367 halogens Chemical class 0.000 description 3
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000005842 heteroatom Chemical group 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 3
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- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
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- 239000010409 thin film Substances 0.000 description 3
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- LPCWDYWZIWDTCV-UHFFFAOYSA-N 1-phenylisoquinoline Chemical class C1=CC=CC=C1C1=NC=CC2=CC=CC=C12 LPCWDYWZIWDTCV-UHFFFAOYSA-N 0.000 description 2
- VFMUXPQZKOKPOF-UHFFFAOYSA-N 2,3,7,8,12,13,17,18-octaethyl-21,23-dihydroporphyrin platinum Chemical compound [Pt].CCc1c(CC)c2cc3[nH]c(cc4nc(cc5[nH]c(cc1n2)c(CC)c5CC)c(CC)c4CC)c(CC)c3CC VFMUXPQZKOKPOF-UHFFFAOYSA-N 0.000 description 2
- STTGYIUESPWXOW-UHFFFAOYSA-N 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline Chemical compound C=12C=CC3=C(C=4C=CC=CC=4)C=C(C)N=C3C2=NC(C)=CC=1C1=CC=CC=C1 STTGYIUESPWXOW-UHFFFAOYSA-N 0.000 description 2
- YPUFOHGCKCFWAW-UHFFFAOYSA-N 2-n,6-n-dinaphthalen-1-yl-2-n,6-n-dinaphthalen-2-ylnaphthalene-2,6-diamine;2-n,2-n,6-n,6-n-tetrakis(4-methylphenyl)naphthalene-2,6-diamine;2-n,2-n,6-n,6-n-tetranaphthalen-1-ylnaphthalene-2,6-diamine Chemical compound C1=CC(C)=CC=C1N(C=1C=C2C=CC(=CC2=CC=1)N(C=1C=CC(C)=CC=1)C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1.C1=CC=C2C(N(C=3C=C4C=CC(=CC4=CC=3)N(C=3C=C4C=CC=CC4=CC=3)C=3C4=CC=CC=C4C=CC=3)C3=CC4=CC=CC=C4C=C3)=CC=CC2=C1.C1=CC=C2C(N(C=3C=C4C=CC(=CC4=CC=3)N(C=3C4=CC=CC=C4C=CC=3)C=3C4=CC=CC=C4C=CC=3)C=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 YPUFOHGCKCFWAW-UHFFFAOYSA-N 0.000 description 2
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Images
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- 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
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
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- C—CHEMISTRY; METALLURGY
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- 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
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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
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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
- H10K50/80—Constructional details
- H10K50/85—Arrangements for extracting light from the devices
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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
- H10K85/30—Coordination compounds
- H10K85/321—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3]
- H10K85/324—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3] comprising aluminium, e.g. Alq3
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- 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
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- C—CHEMISTRY; METALLURGY
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- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/18—Metal complexes
- C09K2211/185—Metal complexes of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/18—Metal complexes
- C09K2211/186—Metal complexes of the light metals other than alkali metals and alkaline earth metals, i.e. Be, Al or Mg
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/917—Electroluminescent
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- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
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- Inorganic Chemistry (AREA)
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- Electroluminescent Light Sources (AREA)
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| US11/015,929 | 2004-12-17 | ||
| US11/015,929 US7767316B2 (en) | 2004-09-20 | 2004-12-17 | Organic electroluminescent devices and composition |
| PCT/US2005/032146 WO2006033857A1 (en) | 2004-09-20 | 2005-09-07 | Organic electroluminescent devices and composition |
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| JP4145280B2 (ja) * | 2004-02-27 | 2008-09-03 | 富士フイルム株式会社 | 発光素子 |
| JP4362461B2 (ja) * | 2004-11-05 | 2009-11-11 | 三星モバイルディスプレイ株式會社 | 有機電界発光素子 |
| DE602006020911D1 (de) * | 2005-10-31 | 2011-05-05 | Nippon Steel Chemical Co | Organisches elektrolumineszenzbauelement |
| TWI297353B (en) * | 2005-11-10 | 2008-06-01 | Au Optronics Corp | Phosphorescent organic light-emitting diodes |
| KR101372847B1 (ko) * | 2006-02-04 | 2014-03-11 | 삼성디스플레이 주식회사 | 폴리비닐피롤계 호스트, 이를 포함한 발광층, 및 상기발광층을 구비한 유기 전계 발광 소자 |
| US20070275265A1 (en) * | 2006-05-25 | 2007-11-29 | Au Optronics Corporation | Organic light emitting layer with a reduced phosphorescent dopant concentration and applications of same |
| JP2009032989A (ja) * | 2007-07-27 | 2009-02-12 | Fujifilm Corp | 有機電界発光素子 |
| JP5130001B2 (ja) * | 2007-07-27 | 2013-01-30 | 富士フイルム株式会社 | 有機電界発光素子 |
| JP5255794B2 (ja) * | 2007-07-27 | 2013-08-07 | 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 |
| KR100882911B1 (ko) * | 2007-08-16 | 2009-02-10 | 삼성모바일디스플레이주식회사 | 유기전계발광소자 및 그의 제조방법 |
| US8129039B2 (en) | 2007-10-26 | 2012-03-06 | Global Oled Technology, Llc | Phosphorescent OLED device with certain fluoranthene host |
| US8076009B2 (en) * | 2007-10-26 | 2011-12-13 | Global Oled Technology, Llc. | OLED device with fluoranthene electron transport materials |
| US8431242B2 (en) * | 2007-10-26 | 2013-04-30 | Global Oled Technology, Llc. | OLED device with certain fluoranthene host |
| US8420229B2 (en) * | 2007-10-26 | 2013-04-16 | Global OLED Technologies LLC | OLED device with certain fluoranthene light-emitting dopants |
| CN103996798B (zh) * | 2007-11-30 | 2017-09-08 | 株式会社半导体能源研究所 | 发光元件、发光装置以及电子装置 |
| KR101055530B1 (ko) * | 2008-03-28 | 2011-08-08 | 삼성메디슨 주식회사 | 터치스크린 일체형 디스플레이부를 포함하는 초음파 시스템 |
| EP2851383A1 (en) * | 2008-04-11 | 2015-03-25 | Solvay USA Inc. | Doped conjugated polymers, devices, and methods of making devices |
| JP5448680B2 (ja) * | 2008-10-10 | 2014-03-19 | キヤノン株式会社 | 表示装置 |
| US8088500B2 (en) * | 2008-11-12 | 2012-01-03 | Global Oled Technology Llc | OLED device with fluoranthene electron injection materials |
| JP2011139044A (ja) | 2009-12-01 | 2011-07-14 | Semiconductor Energy Lab Co Ltd | 発光素子、発光装置、電子機器、および照明装置 |
| JP2011151116A (ja) * | 2010-01-20 | 2011-08-04 | Canon Inc | 有機発光素子 |
| KR102345510B1 (ko) | 2011-02-16 | 2021-12-31 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자 |
| KR102136426B1 (ko) | 2011-02-16 | 2020-07-21 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 엘리먼트 |
| KR102112967B1 (ko) | 2011-03-23 | 2020-05-19 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자 |
| KR101803537B1 (ko) | 2012-02-09 | 2017-11-30 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자 |
| JP6076153B2 (ja) | 2012-04-20 | 2017-02-08 | 株式会社半導体エネルギー研究所 | 発光素子、発光装置、表示装置、電子機器及び照明装置 |
| KR20230048452A (ko) | 2012-08-03 | 2023-04-11 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 발광 장치, 전자 장치 및 조명 장치 |
| TWI638472B (zh) | 2012-08-03 | 2018-10-11 | 日商半導體能源研究所股份有限公司 | 發光元件 |
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| CN106164033B (zh) | 2014-01-10 | 2019-04-19 | 国立研究开发法人产业技术综合研究所 | 环金属化铱配合物的原料及制造方法 |
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2004
- 2004-12-17 US US11/015,929 patent/US7767316B2/en active Active
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2005
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- 2005-09-07 KR KR1020077006286A patent/KR101200861B1/ko active IP Right Grant
- 2005-09-07 WO PCT/US2005/032146 patent/WO2006033857A1/en active Application Filing
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| JP2000164362A (ja) * | 1998-05-19 | 2000-06-16 | Sanyo Electric Co Ltd | 有機エレクトロルミネッセンス素子 |
| JP2003055652A (ja) * | 2001-06-06 | 2003-02-26 | Sanyo Electric Co Ltd | 有機エレクトロルミネッセンス素子および発光材料 |
| JP2003142264A (ja) * | 2001-10-31 | 2003-05-16 | Pioneer Electronic Corp | 有機エレクトロルミネッセンス素子 |
| WO2003083009A1 (fr) * | 2002-03-29 | 2003-10-09 | Pioneer Corporation | Element electroluminescent organique |
| JP2004179142A (ja) * | 2002-09-30 | 2004-06-24 | Sanyo Electric Co Ltd | 発光素子 |
| WO2004077886A1 (ja) * | 2003-02-27 | 2004-09-10 | Kabushiki Kaisha Toyota Jidoshokki | 有機電界発光素子 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20060063030A1 (en) | 2006-03-23 |
| TWI370166B (en) | 2012-08-11 |
| EP1791925B1 (en) | 2008-03-26 |
| DE602005005699D1 (de) | 2008-05-08 |
| EP1791925A1 (en) | 2007-06-06 |
| KR101200861B1 (ko) | 2012-11-13 |
| WO2006033857A1 (en) | 2006-03-30 |
| DE602005005699T2 (de) | 2009-04-16 |
| JP2008514005A (ja) | 2008-05-01 |
| US7767316B2 (en) | 2010-08-03 |
| TW200628584A (en) | 2006-08-16 |
| KR20070061822A (ko) | 2007-06-14 |
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