New Bipolar Host Materials for Realizing Blue Phosphorescent Organic Light-Emitting Diodes with High Efficiency at 1000 cd/m2
Source abstract
Abstract
New host molecules such as 9-(6-(9H-carbazol-9-yl)pyridin-3-yl)-6-(9H-carbazol-9-yl)-9H-pyrido[2,3-b]indole (pPCB2CZ) and 9-(6-(9H-carbazol-9-yl)pyridin-2-yl)-6-(9H-carbazol-9-yl)-9H-pyrido[2,3-b]indole (mPCB2CZ) were designed and synthesized for blue phosphorescent organic light-emitting diodes (PhOLEDs). The glass transition temperatures of two host molecules were measured higher than 120 °C, and the identical triplet energies were determined to be 2.92 eV for both molecules. The bis(3,5-difluoro-2-(2-pyridyl)phenyl-(2-carboxypyridyl)iridium(III) (FIrpic)-doped mPCB2CZ-based PhOLED exhibited practically useful driving voltage of 4.8 V in a simple organic three layer device configuration which has a smaller number of interfaces in conventional multilayer PhOLEDs. Also, the high quantum efficiency of 23.7% is reported at the practically useful brightness value of 1000 cd/m2.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Research Institute for Natural Sciences, Korea University, 5 Anam-dong, Sungbuk-Gu, Seoul 136-701, Republic of Korea
Department of Information Display, Kyung Hee University, Dongdaemoon-gu, Seoul 130-701, Republic of Korea
LG Display, Co., LTD., 1007 Deogeon-ri, Wollong-myeon, Paju-si, Gyeonggi-do 413-811, Republic of Korea
Funding
LG Display · National Research Foundation of Korea
References (25)
Show source-provided references
1. Ulbricht C. · Adv. Mater. · 2009 · 21 · 441810.1002/adma.200803537 ↗
2. Duan L. · Adv. Mater. · 2011 · 23 · 113710.1002/adma.201003816 ↗
3. Chaskar A. · Adv. Mater. · 2011 · 23 · 387610.1002/adma.201101848 ↗
4. Tao Y. · Chem. Soc. Rev. · 2011 · 40 · 294310.1039/c0cs00160k ↗
5. Adachi C. · Appl. Phys. Lett. · 2001 · 79 · 208210.1063/1.1400076 ↗
6. Holmes R. J. · Appl. Phys. Lett. · 2003 · 82 · 242210.1063/1.1568146 ↗
7. Yook K. S. · Adv. Mater. · 2012 · 24 · 316910.1002/adma.201200627 ↗
8. Duan L. · Adv. Mater. · 2011 · 23 · 113710.1002/adma.201003816 ↗
9. Tsai M.-H. · Adv. Mater. · 2006 · 18 · 121610.1002/adma.200502283 ↗
10. Li J. · Chem. Mater. · 2005 · 17 · 120810.1021/cm034731k ↗
11. Lin M.-S. · J. Mater. Chem. · 2012 · 22 · 1611410.1039/c2jm32717a ↗
12. Williams E. L. · Adv. Mater. · 2007 · 19 · 19710.1002/adma.200602174 ↗
13. Su S.-J. · Chem. Mater. · 2008 · 20 · 169110.1021/cm703682q ↗
14. Chien C.-H. · J. Mater. Chem. · 2008 · 18 · 346110.1039/b804192j ↗
15. Zeng L. · J. Mater. Chem. · 2009 · 19 · 877210.1039/b909787b ↗
16. Li W. · Adv. Funct. Mater. · 2012 · 22 · 279710.1002/adfm.201200116 ↗
17. Wang Q. · J. Mater. Chem. C · 2013 · 1 · 222410.1039/c3tc00588g ↗
18. Chang C.-H. · J. Mater. Chem. · 2012 · 22 · 383210.1039/c2jm14686j ↗
19. Liu H. · Adv. Funct. Mater. · 2012 · 22 · 283010.1002/adfm.201103126 ↗
20. Jeon S. O. · Adv. Mater. · 2011 · 23 · 143610.1002/adma.201004372 ↗
21. Chou H. · Adv. Mater. · 2010 · 22 · 246810.1002/adma.201000061 ↗
22. Motoyama T. · Chem. Lett. · 2011 · 40 · 30610.1246/cl.2011.306 ↗
23. Lee C. W. · Chem. Mater. · 2014 · 26 · 161610.1021/cm403750p ↗
24. Lee C. W. · Adv. Mater. · 2013 · 25 · 545010.1002/adma.201301091 ↗
25. Kim S. J. · Chem. Commun. · 2013 · 49 · 678810.1039/c3cc42569j ↗