TW201004468A - Electronic device - Google Patents
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- TW201004468A TW201004468A TW098116998A TW98116998A TW201004468A TW 201004468 A TW201004468 A TW 201004468A TW 098116998 A TW098116998 A TW 098116998A TW 98116998 A TW98116998 A TW 98116998A TW 201004468 A TW201004468 A TW 201004468A
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- 239000011159 matrix material Substances 0.000 claims abstract description 143
- 239000002346 layers by function Substances 0.000 claims abstract description 29
- 239000000758 substrate Substances 0.000 claims abstract description 17
- 239000010410 layer Substances 0.000 claims description 99
- 239000000463 material Substances 0.000 claims description 89
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 claims description 40
- 239000002800 charge carrier Substances 0.000 claims description 32
- 238000004770 highest occupied molecular orbital Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 9
- 230000004888 barrier function Effects 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 230000000903 blocking effect Effects 0.000 claims description 3
- 230000027756 respiratory electron transport chain Effects 0.000 claims 1
- 238000010025 steaming Methods 0.000 claims 1
- 230000005525 hole transport Effects 0.000 description 13
- -1 12-tetraphenyl Chemical group 0.000 description 8
- 238000001704 evaporation Methods 0.000 description 8
- 230000008020 evaporation Effects 0.000 description 8
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 8
- 238000002347 injection Methods 0.000 description 7
- 239000007924 injection Substances 0.000 description 7
- AWXGSYPUMWKTBR-UHFFFAOYSA-N 4-carbazol-9-yl-n,n-bis(4-carbazol-9-ylphenyl)aniline Chemical compound C12=CC=CC=C2C2=CC=CC=C2N1C1=CC=C(N(C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=C1 AWXGSYPUMWKTBR-UHFFFAOYSA-N 0.000 description 6
- 230000005540 biological transmission Effects 0.000 description 6
- 239000004305 biphenyl Substances 0.000 description 6
- 101000837344 Homo sapiens T-cell leukemia translocation-altered gene protein Proteins 0.000 description 5
- 102100028692 T-cell leukemia translocation-altered gene protein Human genes 0.000 description 5
- 235000010290 biphenyl Nutrition 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 4
- 239000007983 Tris buffer Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 4
- UEEXRMUCXBPYOV-UHFFFAOYSA-N iridium;2-phenylpyridine Chemical compound [Ir].C1=CC=CC=C1C1=CC=CC=N1.C1=CC=CC=C1C1=CC=CC=N1.C1=CC=CC=C1C1=CC=CC=N1 UEEXRMUCXBPYOV-UHFFFAOYSA-N 0.000 description 4
- VIJYEGDOKCKUOL-UHFFFAOYSA-N 9-phenylcarbazole Chemical compound C1=CC=CC=C1N1C2=CC=CC=C2C2=CC=CC=C21 VIJYEGDOKCKUOL-UHFFFAOYSA-N 0.000 description 3
- 239000012044 organic layer Substances 0.000 description 3
- 230000006798 recombination Effects 0.000 description 3
- 238000005215 recombination Methods 0.000 description 3
- 238000004611 spectroscopical analysis Methods 0.000 description 3
- XSVXWCZFSFKRDO-UHFFFAOYSA-N triphenyl-(3-triphenylsilylphenyl)silane Chemical compound C1=CC=CC=C1[Si](C=1C=C(C=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 XSVXWCZFSFKRDO-UHFFFAOYSA-N 0.000 description 3
- DETFWTCLAIIJRZ-UHFFFAOYSA-N triphenyl-(4-triphenylsilylphenyl)silane Chemical compound C1=CC=CC=C1[Si](C=1C=CC(=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 DETFWTCLAIIJRZ-UHFFFAOYSA-N 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- 241000208340 Araliaceae Species 0.000 description 2
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 2
- 235000003140 Panax quinquefolius Nutrition 0.000 description 2
- CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 238000002484 cyclic voltammetry Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 235000008434 ginseng Nutrition 0.000 description 2
- 229910052741 iridium Inorganic materials 0.000 description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 2
- MILUBEOXRNEUHS-UHFFFAOYSA-N iridium(3+) Chemical compound [Ir+3] MILUBEOXRNEUHS-UHFFFAOYSA-N 0.000 description 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000004776 molecular orbital Methods 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 238000001420 photoelectron spectroscopy Methods 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- IWZZBBJTIUYDPZ-DVACKJPTSA-N (z)-4-hydroxypent-3-en-2-one;iridium;2-phenylpyridine Chemical compound [Ir].C\C(O)=C\C(C)=O.[C-]1=CC=CC=C1C1=CC=CC=N1.[C-]1=CC=CC=C1C1=CC=CC=N1 IWZZBBJTIUYDPZ-DVACKJPTSA-N 0.000 description 1
- 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 1
- LPCWDYWZIWDTCV-UHFFFAOYSA-N 1-phenylisoquinoline Chemical compound C1=CC=CC=C1C1=NC=CC2=CC=CC=C12 LPCWDYWZIWDTCV-UHFFFAOYSA-N 0.000 description 1
- OBAJPWYDYFEBTF-UHFFFAOYSA-N 2-tert-butyl-9,10-dinaphthalen-2-ylanthracene Chemical compound C1=CC=CC2=CC(C3=C4C=CC=CC4=C(C=4C=C5C=CC=CC5=CC=4)C4=CC=C(C=C43)C(C)(C)C)=CC=C21 OBAJPWYDYFEBTF-UHFFFAOYSA-N 0.000 description 1
- DCPGBPKLXYETTA-UHFFFAOYSA-N 3-methylphenanthro[9,10-b]pyrazine Chemical compound C1=CC=C2C3=NC(C)=CN=C3C3=CC=CC=C3C2=C1 DCPGBPKLXYETTA-UHFFFAOYSA-N 0.000 description 1
- OSQXTXTYKAEHQV-WXUKJITCSA-N 4-methyl-n-[4-[(e)-2-[4-[4-[(e)-2-[4-(4-methyl-n-(4-methylphenyl)anilino)phenyl]ethenyl]phenyl]phenyl]ethenyl]phenyl]-n-(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1N(C=1C=CC(\C=C\C=2C=CC(=CC=2)C=2C=CC(\C=C\C=3C=CC(=CC=3)N(C=3C=CC(C)=CC=3)C=3C=CC(C)=CC=3)=CC=2)=CC=1)C1=CC=C(C)C=C1 OSQXTXTYKAEHQV-WXUKJITCSA-N 0.000 description 1
- ZOKIJILZFXPFTO-UHFFFAOYSA-N 4-methyl-n-[4-[1-[4-(4-methyl-n-(4-methylphenyl)anilino)phenyl]cyclohexyl]phenyl]-n-(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1N(C=1C=CC(=CC=1)C1(CCCCC1)C=1C=CC(=CC=1)N(C=1C=CC(C)=CC=1)C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 ZOKIJILZFXPFTO-UHFFFAOYSA-N 0.000 description 1
- CRHRWHRNQKPUPO-UHFFFAOYSA-N 4-n-naphthalen-1-yl-1-n,1-n-bis[4-(n-naphthalen-1-ylanilino)phenyl]-4-n-phenylbenzene-1,4-diamine Chemical compound C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(N(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 CRHRWHRNQKPUPO-UHFFFAOYSA-N 0.000 description 1
- SNFCXVRWFNAHQX-UHFFFAOYSA-N 9,9'-spirobi[fluorene] Chemical compound C12=CC=CC=C2C2=CC=CC=C2C21C1=CC=CC=C1C1=CC=CC=C21 SNFCXVRWFNAHQX-UHFFFAOYSA-N 0.000 description 1
- MZYDBGLUVPLRKR-UHFFFAOYSA-N 9-(3-carbazol-9-ylphenyl)carbazole Chemical compound C12=CC=CC=C2C2=CC=CC=C2N1C1=CC(N2C3=CC=CC=C3C3=CC=CC=C32)=CC=C1 MZYDBGLUVPLRKR-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- XBZVWDQZBOIKQV-UHFFFAOYSA-N C(C)(C)(C)C=1C=CC2=C(C3=CC=CC=C3C(=C2C1)C1=CC2=CC=CC=C2C=C1)C1=CC2=CC=CC=C2C=C1.C(C)(C)(C)C=1C=CC2=C(C3=CC=CC=C3C(=C2C1)C1=CC2=CC=CC=C2C=C1)C1=CC2=CC=CC=C2C=C1 Chemical compound C(C)(C)(C)C=1C=CC2=C(C3=CC=CC=C3C(=C2C1)C1=CC2=CC=CC=C2C=C1)C1=CC2=CC=CC=C2C=C1.C(C)(C)(C)C=1C=CC2=C(C3=CC=CC=C3C(=C2C1)C1=CC2=CC=CC=C2C=C1)C1=CC2=CC=CC=C2C=C1 XBZVWDQZBOIKQV-UHFFFAOYSA-N 0.000 description 1
- CBGAFGVPMZQYJP-UHFFFAOYSA-N C1CCC(CC1)(C2=CC=C(C=C2)N(C3=CC=C(C=C3)S)C4=CC=C(C=C4)S)C5=CC=C(C=C5)N(C6=CC=C(C=C6)S)C7=CC=C(C=C7)S Chemical compound C1CCC(CC1)(C2=CC=C(C=C2)N(C3=CC=C(C=C3)S)C4=CC=C(C=C4)S)C5=CC=C(C=C5)N(C6=CC=C(C=C6)S)C7=CC=C(C=C7)S CBGAFGVPMZQYJP-UHFFFAOYSA-N 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- 241000237536 Mytilus edulis Species 0.000 description 1
- 101100062121 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) cyc-1 gene Proteins 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000000862 absorption spectrum Methods 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- VQGHOUODWALEFC-UHFFFAOYSA-N alpha-Phenylpyridine Natural products C1=CC=CC=C1C1=CC=CC=N1 VQGHOUODWALEFC-UHFFFAOYSA-N 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 206010008129 cerebral palsy Diseases 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000004699 copper complex Chemical class 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005281 excited state Effects 0.000 description 1
- 238000002189 fluorescence spectrum Methods 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- CECAIMUJVYQLKA-UHFFFAOYSA-N iridium 1-phenylisoquinoline Chemical compound [Ir].C1=CC=CC=C1C1=NC=CC2=CC=CC=C12.C1=CC=CC=C1C1=NC=CC2=CC=CC=C12.C1=CC=CC=C1C1=NC=CC2=CC=CC=C12 CECAIMUJVYQLKA-UHFFFAOYSA-N 0.000 description 1
- 229960005181 morphine Drugs 0.000 description 1
- 235000020638 mussel Nutrition 0.000 description 1
- YKZHNHRLNBPFBZ-UHFFFAOYSA-N n-[4-(4-aminophenyl)phenyl]benzo[a]anthracen-1-amine Chemical compound C1=CC(N)=CC=C1C(C=C1)=CC=C1NC1=CC=CC2=CC=C(C=C3C(C=CC=C3)=C3)C3=C12 YKZHNHRLNBPFBZ-UHFFFAOYSA-N 0.000 description 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 238000004838 photoelectron emission spectroscopy Methods 0.000 description 1
- 230000002035 prolonged effect Effects 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
- YYMBJDOZVAITBP-UHFFFAOYSA-N rubrene Chemical compound C1=CC=CC=C1C(C1=C(C=2C=CC=CC=2)C2=CC=CC=C2C(C=2C=CC=CC=2)=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 YYMBJDOZVAITBP-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000005428 wave function Effects 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]
- H10K50/14—Carrier 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
- H10K2101/30—Highest occupied molecular orbital [HOMO], lowest unoccupied molecular orbital [LUMO] or Fermi energy values
-
- 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
- H10K2101/90—Multiple hosts in the emissive layer
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
- Photovoltaic Devices (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008025920 | 2008-05-30 | ||
| DE102008039361.4A DE102008039361B4 (de) | 2008-05-30 | 2008-08-22 | Elektronische Vorrichtung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW201004468A true TW201004468A (en) | 2010-01-16 |
Family
ID=41254075
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW098116998A TW201004468A (en) | 2008-05-30 | 2009-05-22 | Electronic device |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8723164B2 (enExample) |
| EP (1) | EP2281318B1 (enExample) |
| JP (1) | JP5222397B2 (enExample) |
| KR (2) | KR101559607B1 (enExample) |
| CN (2) | CN102047463B (enExample) |
| DE (1) | DE102008039361B4 (enExample) |
| TW (1) | TW201004468A (enExample) |
| WO (1) | WO2009143807A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11248008B2 (en) | 2016-11-25 | 2022-02-15 | Lt Materials Co., Ltd. | Heterocyclic compound and organic light emitting element using same |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102008039361B4 (de) * | 2008-05-30 | 2025-02-06 | Pictiva Displays International Limited | Elektronische Vorrichtung |
| CN103563117B (zh) * | 2011-05-27 | 2016-06-15 | 环球展览公司 | 具有多组分发光层的有机发光装置 |
| EP2779263B1 (en) | 2011-11-11 | 2020-12-09 | Mitsubishi Chemical Corporation | Organic electroluminescent element and organic electroluminescent device |
| KR102250019B1 (ko) * | 2012-03-14 | 2021-05-11 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자 |
| TW201535818A (zh) * | 2013-10-25 | 2015-09-16 | Univ Michigan | 在有機光伏打多供體能量串聯中之激子管理 |
| US10674573B2 (en) * | 2014-12-02 | 2020-06-02 | Universiteit Gent | Light emission device with anisotropic properties |
| GB2538325A (en) * | 2015-05-15 | 2016-11-16 | Cambridge Display Tech Ltd | Organic light-emitting device |
| KR102500272B1 (ko) | 2015-09-16 | 2023-02-16 | 삼성디스플레이 주식회사 | 화합물 및 이를 포함하는 유기 발광 소자 |
| CN105280829B (zh) * | 2015-09-17 | 2018-01-12 | Tcl集团股份有限公司 | Qled及其制备方法 |
| KR102782275B1 (ko) | 2016-12-30 | 2025-03-17 | 엘지디스플레이 주식회사 | 유기 발광 표시 장치 |
| JP7299020B2 (ja) * | 2018-12-28 | 2023-06-27 | 三星電子株式会社 | 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 |
| KR102797538B1 (ko) * | 2020-05-19 | 2025-04-21 | 삼성디스플레이 주식회사 | 유기 발광 소자 및 이를 포함한 전자 장치 |
| KR102739126B1 (ko) | 2020-06-10 | 2024-12-05 | 삼성전자주식회사 | 조성물 및 이를 포함한 유기 발광 소자 |
| CN111697146B (zh) * | 2020-06-11 | 2022-04-19 | 云谷（固安）科技有限公司 | 发光器件及显示面板 |
| KR20230030716A (ko) * | 2021-08-25 | 2023-03-07 | 삼성디스플레이 주식회사 | 발광 소자 및 이를 포함하는 표시 장치 |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4076769B2 (ja) | 2000-12-28 | 2008-04-16 | 株式会社半導体エネルギー研究所 | 発光装置及び電気器具 |
| SG115435A1 (en) * | 2000-12-28 | 2005-10-28 | Semiconductor Energy Lab | Luminescent device |
| US6720090B2 (en) * | 2001-01-02 | 2004-04-13 | Eastman Kodak Company | Organic light emitting diode devices with improved luminance efficiency |
| JP4076773B2 (ja) * | 2001-02-01 | 2008-04-16 | 株式会社半導体エネルギー研究所 | 発光素子およびそれを用いた表示装置、電気器具 |
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| KR101100570B1 (ko) * | 2006-11-17 | 2011-12-29 | 콸콤 인코포레이티드 | 내용 주소화 메모리 |
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| DE102008039361B4 (de) * | 2008-05-30 | 2025-02-06 | Pictiva Displays International Limited | Elektronische Vorrichtung |
-
2008
- 2008-08-22 DE DE102008039361.4A patent/DE102008039361B4/de active Active
-
2009
- 2009-05-18 KR KR1020107025270A patent/KR101559607B1/ko not_active Expired - Fee Related
- 2009-05-18 CN CN2009801199541A patent/CN102047463B/zh active Active
- 2009-05-18 JP JP2011510821A patent/JP5222397B2/ja active Active
- 2009-05-18 KR KR1020157017565A patent/KR101661437B1/ko active Active
- 2009-05-18 CN CN201310118010.0A patent/CN103268920B/zh active Active
- 2009-05-18 EP EP09753523.1A patent/EP2281318B1/de active Active
- 2009-05-18 WO PCT/DE2009/000701 patent/WO2009143807A1/de not_active Ceased
- 2009-05-18 US US12/995,457 patent/US8723164B2/en active Active
- 2009-05-22 TW TW098116998A patent/TW201004468A/zh unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11248008B2 (en) | 2016-11-25 | 2022-02-15 | Lt Materials Co., Ltd. | Heterocyclic compound and organic light emitting element using same |
| TWI756308B (zh) * | 2016-11-25 | 2022-03-01 | 南韓商Ｌｔ素材股份有限公司 | 雜環化合物以及使用此雜環化合物的有機發光裝置 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102047463A (zh) | 2011-05-04 |
| KR101661437B1 (ko) | 2016-09-29 |
| US20110291080A1 (en) | 2011-12-01 |
| CN102047463B (zh) | 2013-05-08 |
| KR20150083141A (ko) | 2015-07-16 |
| WO2009143807A1 (de) | 2009-12-03 |
| KR20110021765A (ko) | 2011-03-04 |
| CN103268920B (zh) | 2016-06-01 |
| US8723164B2 (en) | 2014-05-13 |
| EP2281318A1 (de) | 2011-02-09 |
| JP5222397B2 (ja) | 2013-06-26 |
| CN103268920A (zh) | 2013-08-28 |
| DE102008039361B4 (de) | 2025-02-06 |
| EP2281318B1 (de) | 2013-07-10 |
| KR101559607B1 (ko) | 2015-10-12 |
| DE102008039361A1 (de) | 2009-12-03 |
| JP2011522406A (ja) | 2011-07-28 |
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