journal article·2005-06-01

Highly Efficient Electrophosphorescent Devices with Saturated Red Emission from a Neutral Osmium Complex

Yu-Hua Niu, Yung-Liang Tung, Yun Chi, Ching-Fong Shu, Joo Hyun Kim, Baoquan Chen, Jingdong Luo, Arthur J. Carty, Alex K.-Y. Jen

Chemistry of Materials· Volume 17· Issue 13
Publisher page

Abstract

Highly efficient electrophosphorescent polymer light-emitting diodes (LEDs) with saturated red emission (Commission Internationale de L'Eclairage chromaticity coordinates exactly at x = 0.67, y = 0.33) are achieved by blending a novel neutral Osmium complex into a single-component bipolar polymer host that possesses balanced hole- and electron-transporting ability. By using a tetraphenylenebiphenyldiamine (TPD)-based cross-linkable hole-transport layer as well as a layer of 1,3,5-tris( N -phenylbenzimidazol-2-yl)benzene (TPBI) as an electron-transport layer, a device structure with both effective hole/electron injection and efficient carriers/excitons blocking or confinement at both electrode sides is constituted. In this way, external quantum efficiency 12.8% is reached the first time with an organometallic complex with heavy metal core other than iridium.
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Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Conducting polymers and applications · Organic Electronics and Photovoltaics

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

Affiliations

Department of Materials Science and Engineering, Box 352120, University of Washington, Seattle, Washington 98195, Department of Chemistry, National Tsing Hua University, Hsinchu 300, Taiwan, Department of Applied Chemistry, National Chiao Tung University, Hsinchu 30035, Taiwan, and Steacie Institute for Molecular Sciences, National Research Council Canada, Ontario K1A 0R6, Canada

References (33)

Show source-provided references
1. Burroughes J. H. · Nature · 1990 · 347 · 53910.1038/347539a0 ↗
2. Gustafsson G. · J. Nature · 1992 · 357 · 47710.1038/357477a0 ↗
3. Niu Y.-H. · Adv. Mater. · 2003 · 15 · 80710.1002/adma.200304619 ↗
4. Cao Y. · J. Nature · 1999 · 397 · 41410.1038/17087 ↗
5. Wohlgenannt M. · Nature · 2001 · 409 · 49410.1038/35054025 ↗
6. Adachi C. · J. Appl. Phys. · 2001 · 90 · 504810.1063/1.1409582 ↗
7. Ikai M. · Appl. Phys. Lett. · 2001 · 79 · 15610.1063/1.1385182 ↗
8. Adachi C. · Appl. Phys. Lett. · 2001 · 78 · 162210.1063/1.1355007 ↗
9. Su Y.-J. · Adv. Mater. · 2003 · 15 · 88410.1002/adma.200304630 ↗
10. Tsuboyama A. · J. Am. Chem. Soc. · 2003 · 125 · 1297110.1021/ja034732d ↗
11. Jiang C. · Adv. Mater. · 2004 · 16 · 53710.1002/adma.200306331 ↗
12. Baldo M. A. · Phys. Rev. B · 2000 · 62 · 1096710.1103/PhysRevB.62.10967 ↗
13. Lamansky S. · J. Am. Chem. Soc. · 2001 · 123 · 430410.1021/ja003693s ↗
14. Carlson B. · J. Am. Chem. Soc. · 2002 · 124 · 1416210.1021/ja0176705 ↗
15. Ma Y. G. · Synth. Met. · 1998 · 94 · 24510.1016/S0379-6779(97)04166-0 ↗
16. Jiang X. · Appl. Phys. Lett. · 2002 · 81 · 312510.1063/1.1514401 ↗
17. Jiang X. · Appl. Phys. Lett. · 2002 · 80 · 71310.1063/1.1445272 ↗
18. Wu P.-C. · Organometallics · 2003 · 22 · 493810.1021/om034037e ↗
19. Jiang X. · Adv. Funct. Mater. · 2002 · 12 · 74510.1002/adfm.200290002 ↗
20. Brown T. M. · Appl. Phys. Lett. · 2001 · 79 · 17410.1063/1.1383800 ↗
21. Greenham N. C. · Adv. Mater. · 1994 · 6 · 49110.1002/adma.19940060612 ↗
22. Tung Y.-L. · Organometallics · 2004 · 23 · 374510.1021/om0498246 ↗
23. Föster T. · Discuss. Faraday Soc. · 1959 · 27 · 710.1039/DF9592700007 ↗
24. Dexter D. L. · J. Chem. Phys. · 1953 · 21 · 83610.1063/1.1699044 ↗
25. Gong X. · J. Adv. Funct. Mater. · 2003 · 13 · 43910.1002/adfm.200304334 ↗
26. Shu C.-F. · Macromolecules · 2003 · 36 · 669810.1021/ma030123e ↗
27. Song, Y.H.; Yeh, S.J.; Chen, C.T.; Chi, Y.; Liu, C.S.; Yu, J.K.; Hu, Y.H.; Chou, P.T.; Peng, S.M.; Lee, G.H.Adv. Funct. Mater.2004, in press.
28. Kan S. · Adv. Funct. Mater. · 2003 · 13 · 60310.1002/adfm.200304304 ↗
29. Gong X. · J. Adv. Mater. · 2002 · 14 · 58110.1002/1521-4095(20020418)14:8<581::AID-ADMA581>3.0.CO;2-B ↗
30. Li Y. · Adv. Mater. · 2002 · 14 · 131710.1002/1521-4095(20020916)14:18<1317::AID-ADMA1317>3.0.CO;2-S ↗
31. Connick W. B. · Inorg. Chem. · 1999 · 38 · 326410.1021/ic981387y ↗
32. Kalinowski J. · Phys. Rev. B · 2002 · 66 · 23532110.1103/PhysRevB.66.235321 ↗
33. Niu Y.-H. · Appl. Phys. Lett. · 2004 · 85 · 161910.1063/1.1786369 ↗