JP2012151033A5 - - Google Patents
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- Publication number
- JP2012151033A5 JP2012151033A5 JP2011009853A JP2011009853A JP2012151033A5 JP 2012151033 A5 JP2012151033 A5 JP 2012151033A5 JP 2011009853 A JP2011009853 A JP 2011009853A JP 2011009853 A JP2011009853 A JP 2011009853A JP 2012151033 A5 JP2012151033 A5 JP 2012151033A5
- Authority
- JP
- Japan
- Prior art keywords
- organic
- layer
- transport
- display device
- electron
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 239000010410 layer Substances 0.000 claims description 131
- 238000002347 injection Methods 0.000 claims description 38
- 239000007924 injection Substances 0.000 claims description 38
- 238000000034 method Methods 0.000 claims description 25
- -1 nitrogen-containing heterocyclic compound Chemical class 0.000 claims description 21
- 230000005525 hole transport Effects 0.000 claims description 20
- 239000012044 organic layer Substances 0.000 claims description 20
- 238000000576 coating method Methods 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 10
- 238000007740 vapor deposition Methods 0.000 claims description 9
- 239000000758 substrate Substances 0.000 claims description 8
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000004528 spin coating Methods 0.000 claims description 3
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 2
- 239000003086 colorant Substances 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims 8
- 125000005843 halogen group Chemical group 0.000 claims 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 6
- 125000004432 carbon atom Chemical group C* 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- 229920003026 Acene Polymers 0.000 claims 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 238000001704 evaporation Methods 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 claims 1
- 239000000463 material Substances 0.000 description 27
- 230000003287 optical effect Effects 0.000 description 7
- 238000001035 drying Methods 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 239000002861 polymer material Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000178 monomer Substances 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 230000005281 excited state Effects 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000004696 coordination complex Chemical class 0.000 description 2
- VPUGDVKSAQVFFS-UHFFFAOYSA-N coronene Chemical compound C1=C(C2=C34)C=CC3=CC=C(C=C3)C4=C4C3=CC=C(C=C3)C4=C2C3=C1 VPUGDVKSAQVFFS-UHFFFAOYSA-N 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 0 *c1nc(C=C*(B[Al])C=C2)c2[n]1* Chemical compound *c1nc(C=C*(B[Al])C=C2)c2[n]1* 0.000 description 1
- KLCLIOISYBHYDZ-UHFFFAOYSA-N 1,4,4-triphenylbuta-1,3-dienylbenzene Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)=CC=C(C=1C=CC=CC=1)C1=CC=CC=C1 KLCLIOISYBHYDZ-UHFFFAOYSA-N 0.000 description 1
- UVHXEHGUEKARKZ-UHFFFAOYSA-N 1-ethenylanthracene Chemical compound C1=CC=C2C=C3C(C=C)=CC=CC3=CC2=C1 UVHXEHGUEKARKZ-UHFFFAOYSA-N 0.000 description 1
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
- GUPMCMZMDAGSPF-UHFFFAOYSA-N 1-phenylbuta-1,3-dienylbenzene Chemical compound C=1C=CC=CC=1[C](C=C[CH2])C1=CC=CC=C1 GUPMCMZMDAGSPF-UHFFFAOYSA-N 0.000 description 1
- NIDFGXDXQKPZMA-UHFFFAOYSA-N 14h-benz[4,5]isoquino[2,1-a]perimidin-14-one Chemical compound C1=CC(N2C(=O)C=3C4=C(C2=N2)C=CC=C4C=CC=3)=C3C2=CC=CC3=C1 NIDFGXDXQKPZMA-UHFFFAOYSA-N 0.000 description 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 1
- MGADZUXDNSDTHW-UHFFFAOYSA-N 2H-pyran Chemical compound C1OC=CC=C1 MGADZUXDNSDTHW-UHFFFAOYSA-N 0.000 description 1
- LGZLRERYRQQCFM-UHFFFAOYSA-N 4-butyl-n-[4-[4-(4-butylanilino)phenyl]phenyl]aniline Chemical compound C1=CC(CCCC)=CC=C1NC1=CC=C(C=2C=CC(NC=3C=CC(CCCC)=CC=3)=CC=2)C=C1 LGZLRERYRQQCFM-UHFFFAOYSA-N 0.000 description 1
- 125000004860 4-ethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- VESMRDNBVZOIEN-UHFFFAOYSA-N 9h-carbazole-1,2-diamine Chemical compound C1=CC=C2C3=CC=C(N)C(N)=C3NC2=C1 VESMRDNBVZOIEN-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- XBDYBAVJXHJMNQ-UHFFFAOYSA-N Tetrahydroanthracene Natural products C1=CC=C2C=C(CCCC3)C3=CC2=C1 XBDYBAVJXHJMNQ-UHFFFAOYSA-N 0.000 description 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N anhydrous quinoline Natural products N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- WZJYKHNJTSNBHV-UHFFFAOYSA-N benzoquinoline Natural products C1=CN=C2C3=CC=CC=C3C=CC2=C1 WZJYKHNJTSNBHV-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000009920 chelation Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- HHNHBFLGXIUXCM-GFCCVEGCSA-N cyclohexylbenzene Chemical compound [CH]1CCCC[C@@H]1C1=CC=CC=C1 HHNHBFLGXIUXCM-GFCCVEGCSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000000295 emission spectrum Methods 0.000 description 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
- GVVPGTZRZFNKDS-JXMROGBWSA-N geranyl diphosphate Chemical compound CC(C)=CCC\C(C)=C\CO[P@](O)(=O)OP(O)(O)=O GVVPGTZRZFNKDS-JXMROGBWSA-N 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000008707 rearrangement 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
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical group C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 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
- IBBLKSWSCDAPIF-UHFFFAOYSA-N thiopyran Chemical compound S1C=CC=C=C1 IBBLKSWSCDAPIF-UHFFFAOYSA-N 0.000 description 1
- NZFNXWQNBYZDAQ-UHFFFAOYSA-N thioridazine hydrochloride Chemical compound Cl.C12=CC(SC)=CC=C2SC2=CC=CC=C2N1CCC1CCCCN1C NZFNXWQNBYZDAQ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011009853A JP5819069B2 (ja) | 2011-01-20 | 2011-01-20 | 有機ｅｌ表示装置 |
| US13/348,762 US20120187386A1 (en) | 2011-01-20 | 2012-01-12 | Organic electro luminescence display device and method for manufacturing same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011009853A JP5819069B2 (ja) | 2011-01-20 | 2011-01-20 | 有機ｅｌ表示装置 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2012151033A JP2012151033A (ja) | 2012-08-09 |
| JP2012151033A5 true JP2012151033A5 (enExample) | 2014-02-27 |
| JP5819069B2 JP5819069B2 (ja) | 2015-11-18 |
Family
ID=46543515
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011009853A Active JP5819069B2 (ja) | 2011-01-20 | 2011-01-20 | 有機ｅｌ表示装置 |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US20120187386A1 (enExample) |
| JP (1) | JP5819069B2 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101960387B1 (ko) * | 2012-12-21 | 2019-03-20 | 엘지디스플레이 주식회사 | 플렉서블 표시장치 및 그의 제조방법 |
| KR102046157B1 (ko) * | 2012-12-21 | 2019-12-03 | 삼성디스플레이 주식회사 | 유기 발광 표시 장치 및 그 제조 방법 |
| CN117608145A (zh) * | 2013-05-21 | 2024-02-27 | 株式会社半导体能源研究所 | 显示装置和电子装置 |
| TWI567972B (zh) * | 2013-06-12 | 2017-01-21 | Joled Inc | Organic EL display device |
| CN104851980B (zh) * | 2014-02-13 | 2017-02-08 | 上海和辉光电有限公司 | 全彩有机发光二极管结构 |
| KR102332591B1 (ko) * | 2014-06-09 | 2021-11-30 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| US10444559B2 (en) * | 2014-10-01 | 2019-10-15 | Sony Corporation | Display unit and electronic apparatus |
| CN105609534A (zh) * | 2016-01-06 | 2016-05-25 | 京东方科技集团股份有限公司 | 一种oled显示基板及显示装置 |
| US10873050B2 (en) * | 2016-03-29 | 2020-12-22 | Sharp Kabushiki Kaisha | Organic EL display device and organic EL display device manufacturing method |
| US10777103B2 (en) | 2016-09-28 | 2020-09-15 | Sharp Kabushiki Kaisha | Display apparatus and method for manufacturing same |
| US10461132B2 (en) | 2016-09-30 | 2019-10-29 | Sharp Kabushiki Kaisha | Display apparatus and method for manufacturing same |
| WO2018070348A1 (ja) | 2016-10-13 | 2018-04-19 | シャープ株式会社 | 表示装置およびその製造方法 |
| KR102878528B1 (ko) * | 2017-02-28 | 2025-10-29 | 엘지디스플레이 주식회사 | 전계발광 표시장치 |
| JP2018181492A (ja) * | 2017-04-06 | 2018-11-15 | 株式会社ジャパンディスプレイ | 表示装置及びその製造方法 |
| KR102577233B1 (ko) * | 2017-12-28 | 2023-09-08 | 엘지디스플레이 주식회사 | 전계발광 표시 장치 |
| JP7419821B2 (ja) | 2020-01-06 | 2024-01-23 | セイコーエプソン株式会社 | 有機エレクトロルミネッセンス装置および電子機器 |
| JP7415561B2 (ja) * | 2020-01-06 | 2024-01-17 | セイコーエプソン株式会社 | 有機エレクトロルミネッセンス装置および電子機器 |
| US20230292541A1 (en) * | 2020-06-22 | 2023-09-14 | Sharp Kabushiki Kaisha | Display device |
| CN112635694A (zh) * | 2021-01-18 | 2021-04-09 | 深圳市华星光电半导体显示技术有限公司 | Oled显示面板 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3899566B2 (ja) * | 1996-11-25 | 2007-03-28 | セイコーエプソン株式会社 | 有機ｅｌ表示装置の製造方法 |
| JP3900724B2 (ja) * | 1999-01-11 | 2007-04-04 | セイコーエプソン株式会社 | 有機ｅｌ素子の製造方法および有機ｅｌ表示装置 |
| JP2006344869A (ja) * | 2005-06-10 | 2006-12-21 | Toyo Ink Mfg Co Ltd | フルカラー有機電界発光素子の作製方法 |
| TW200738636A (en) * | 2006-01-30 | 2007-10-16 | Chisso Corp | Novel chemical compound and organic electroluminescent device using the same |
| JP2008300503A (ja) * | 2007-05-30 | 2008-12-11 | Sony Corp | 有機電界発光素子および表示装置 |
| JP5353233B2 (ja) * | 2007-12-27 | 2013-11-27 | Ｊｎｃ株式会社 | ピリジルフェニル基を有するアントラセン誘導体化合物及び有機電界発光素子 |
| JP2010027885A (ja) * | 2008-07-22 | 2010-02-04 | Sony Corp | 有機電界発光素子 |
| CN104292152A (zh) * | 2009-05-29 | 2015-01-21 | Jnc株式会社 | 电子传输材料及使用其的有机电致发光元件 |
| KR101058109B1 (ko) * | 2009-09-15 | 2011-08-24 | 삼성모바일디스플레이주식회사 | 유기 발광 디스플레이 장치 |
-
2011
- 2011-01-20 JP JP2011009853A patent/JP5819069B2/ja active Active
-
2012
- 2012-01-12 US US13/348,762 patent/US20120187386A1/en not_active Abandoned
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