journal article·2010-10-27

Managing Charge Balance and Triplet Excitons to Achieve High-Power-Efficiency Phosphorescent Organic Light-Emitting Diodes

Youtian Tao, Qiang Wang, Chuluo Yang, Jingui Qin, Dongge Ma

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Abstract

High-efficiency phosphorescent organic light-emitting diodes (PhOLEDs) have been achieved by using an ortho-linked triphenylamine/oxadiazole hybrid, namely p -TPA- o -OXD, as host material. The high HOMO level of the compound (5.25 eV) can facilitate efficient hole injection from 1, 4-bis[(1-naphthylphenyl)amino]biphenyl (NPB) layer to the emissive layer. As a result, low driving voltages and high power efficiencies have been attained as compared to the carbazole-based hosts with lower HOMO levels and higher injection barriers under similar device structures. By introducing 1,3,5-tris( N -phenylbenzimidazol-2-yl)benzene (TPBI) to replace 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP)/tris(8-hydroxyquinoline)aluminum (Alq3) as hole blocking/electron transporting layer, followed by tuning the thicknesses of hole-transport NPB layer to manipulate the charge balance, high-efficiency PhOLEDs have been achieved, with maximum current efficiency/power efficiency/external quantum efficiency of 85.7 cd/A/99.7 lm/W/22.2% for green (ppy) 2 Ir(acac)-based devices, 55.2 cd/A/64.2 lm/W/19.0% for yellow (fbi) 2 Ir(acac)-based devices, and 11.4 cd/A/11.8 lm/W/14.8% for deep red (piq) 2 Ir(acac)-based devices. By inserting 10 nm of p -TPA- o -OXD as self-triplet exciton blocking layer between hole transporting and emissive layer to confine triplet excitons, device performances have been further improved in green PhOLED, with peak current efficiency/power efficiency/external quantum efficiency of 90.0 cd/A/97.7 lm/W/23.5%.
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Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Luminescence and Fluorescent Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, Hubei Key Lab on Organic and Polymeric Optoelectronic Materials, Wuhan University, Wuhan 430072, People’s Republic of China, and State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, People’s Republic of China

References (35)

Show source-provided references
1. Baldo M. A. · Nature · 1998 · 395 · 15110.1038/25954 ↗
2. Baldo M. A. · Appl. Phys. Lett. · 1999 · 75 · 410.1063/1.124258 ↗
3. Adachi C. · J. Appl. Phys. · 2001 · 90 · 504810.1063/1.1409582 ↗
4. Tao Y. · J. Phys. Chem. C · 2009 · 114 · 60110.1021/jp908886d ↗
5. Lamansky S. · J. Am. Chem. Soc. · 2001 · 123 · 430410.1021/ja003693s ↗
6. Watanabe S. · Jpn. J. Appl. Phys. · 2007 · 46 · 118610.1143/JJAP.46.1186 ↗
7. Tanaka D. · Jpn. J. Appl. Phys. · 2007 · 46 · L1010.1143/JJAP.46.L10 ↗
8. Ikai M. · Appl. Phys. Lett. · 2001 · 79 · 15610.1063/1.1385182 ↗
9. Chien C. H. · Org. Electron. · 2009 · 10 · 87110.1016/j.orgel.2009.04.013 ↗
10. Gao Z. Q. · Adv. Mater. · 2009 · 21 · 68810.1002/adma.200702877 ↗
11. Tsai M.-H. · Adv. Mater. · 2006 · 18 · 121610.1002/adma.200502283 ↗
12. Tsai M.-H. · Adv. Mater. · 2007 · 19 · 86210.1002/adma.200600822 ↗
13. Tao Y. · Angew. Chem., Int. Ed. · 2008 · 47 · 810410.1002/anie.200803396 ↗
14. Tao Y. · Adv. Funct. Mater. · 2010 · 20 · 30410.1002/adfm.200901615 ↗
15. Hsu F. M. · Chem. Mater. · 2009 · 21 · 101710.1021/cm802199d ↗
16. Li C.-L. · Adv. Funct. Mater. · 2005 · 15 · 38710.1002/adfm.200305100 ↗
17. Yang C. · Adv. Funct. Mater. · 2007 · 17 · 65110.1002/adfm.200600663 ↗
18. Tsuboyama A. · J. Am. Chem. Soc. · 2003 · 125 · 1297110.1021/ja034732d ↗
19. Huang W. S. · Chem. Mater. · 2004 · 16 · 248010.1021/cm0498943 ↗
20. Jeon S. O. · Org. Electron. · 2009 · 10 · 99810.1016/j.orgel.2009.03.013 ↗
21. Kanno H. · Appl. Phys. Lett. · 2007 · 90 · 12350910.1063/1.2643908 ↗
22. Tao L. · Chem. Mater. · 2009 · 21 · 128410.1021/cm803087c ↗
23. Shih P.-I. · Adv. Funt. Mater. · 2007 · 17 · 351410.1002/adfm.200700191 ↗
24. Tao Y. · Chem. Commun. · 2009 · 7710.1039/B816264F ↗
25. You H. · J. Appl. Phys. · 2007 · 101 · 02610510.1063/1.2430511 ↗
26. He G. · Appl. Phys. Lett. · 2004 · 85 · 391110.1063/1.1812378 ↗
27. Tong Q.-X. · Chem. Mater. · 2007 · 19 · 585110.1021/cm0712624 ↗
28. Aziz H. · Appl. Phys. Lett. · 2002 · 80 · 218010.1063/1.1455697 ↗
29. Vanslyke S. A. · Appl. Phys. Lett. · 1996 · 69 · 216010.1063/1.117151 ↗
30. Li Y. Q. · Adv. Mater. · 2002 · 14 · 131710.1002/1521-4095(20020916)14:18<1317::AID-ADMA1317>3.0.CO;2-S ↗
31. Adamovich V. I. · Org. Electron. · 2003 · 4 · 7710.1016/j.orgel.2003.08.003 ↗
32. Kondakova M. E. · J. Appl. Phys. · 2008 · 104 · 09450110.1063/1.3000046 ↗
33. Tao Y. T. · Appl. Phys. Lett. · 2000 · 77 · 93310.1063/1.1288811 ↗
34. Chen Y.-C. · J. Am. Chem. Soc. · 2006 · 128 · 854910.1021/ja060936t ↗
35. Li Y. Z. · Appl. Phys. Lett. · 2009 · 95 · 03330710.1063/1.3186040 ↗