Simple Bipolar Host Materials for High-Efficiency Blue, Green, and White Phosphorescence OLEDs
Source abstract
Abstract
3-(1H-Pyrazol-1-yl)pyridine is used as electron-transporting unit to construct bipolar host materials o-CzPyPz, m-CzPyPz, and p-CzPyPz for application in phosphorescent organic light-emitting diodes (PhOLEDs). By varying the ortho-, meta-, or para-linking mode between the n-type 3-(1H-pyrazol-1-yl)pyridine and the p-type carbazole on phenylene bridge, the optoelectronic parameters are tuned to large extent. The highly twisted o-CzPyPz has high triplet energy of 2.95 eV, while the isomer p-CzPyPz with more coplanar conformation has smaller triplet energy of 2.67 eV. The m-CzPyPz-hosted blue PhOLED exhibits a peak current efficiency of 49.1 cd A(-1) (corresponding to an external quantum efficiency of 24.5%) and low-efficiency roll-off, while the p-CzPyPz-hosted green PhOLEDs turns on at 2.8 V and exhibits high efficiencies of 91.8 cd A(-1) (96.1 lm W(-1) and 27.3%). Furthermore, two-emitting-layer white OLEDs are fabricated with m-CzPyPz or p-CzPyPz as common hosts for both blue and orange phosphors, which realize high efficiencies of 57.8 cd A(-1) (45.4 lm W(-1) and 23.6%) and 60.7 cd A(-1) (38.1 lm W(-1) and 23.1%). The optimization of host structure for good matching of host and dopant and finally for the ideal performance is discussed.
Source: openalex_inverted_index · Quality: baseline
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
State Key Laboratory of Fine Chemicals, College of Chemical Engineering, Dalian University of Technology, 2 Linggong Road, Dalian 116024, China
Funding
Ministry of Education of the People's Republic of China · National Natural Science Foundation of China
References (43)
Show source-provided references
1. 10.1038/2595410.1038/25954 ↗
2. 10.1016/S0379-6779(97)04166-010.1016/S0379-6779(97)04166-0 ↗
3. 10.1103/PhysRevB.62.1096710.1103/PhysRevB.62.10967 ↗
4. 10.1002/adfm.20100206610.1002/adfm.201002066 ↗
5. 10.1002/adma.20130109110.1002/adma.201301091 ↗
6. 10.1002/ange.20130804610.1002/ange.201308046 ↗
7. 10.1021/acsami.5b0829110.1021/acsami.5b08291 ↗
8. 10.1039/b908139a10.1039/b908139a ↗
9. 10.1039/c3tc31893a10.1039/c3tc31893a ↗
10. 10.1039/c0cs00160k10.1039/c0cs00160k ↗
11. 10.1016/j.dyepig.2013.11.00710.1016/j.dyepig.2013.11.007 ↗
12. 10.1002/adma.20090424910.1002/adma.200904249 ↗
13. 10.1002/adma.20100312810.1002/adma.201003128 ↗
14. 10.1021/cm703682q10.1021/cm703682q ↗
15. 10.1021/cm102975d10.1021/cm102975d ↗
16. 10.1002/adma.20120092710.1002/adma.201200927 ↗
17. 10.1039/b507375h10.1039/b507375h ↗
18. 10.1021/am507592s10.1021/am507592s ↗
19. 10.1021/acsami.5b0411210.1021/acsami.5b04112 ↗
20. 10.1039/C4TC01467G10.1039/C4TC01467G ↗
21. 10.1039/C5TC02997J10.1039/C5TC02997J ↗
22. 10.1002/adom.20140015410.1002/adom.201400154 ↗
23. 10.1002/adfm.20150510610.1002/adfm.201505106 ↗
24. 10.1063/1.140007610.1063/1.1400076 ↗
25. 10.1063/1.156814610.1063/1.1568146 ↗
26. 10.1149/1.241092910.1149/1.2410929 ↗
27. 10.1149/1.213436510.1149/1.2134365 ↗
28. 10.1016/j.polymer.2011.06.01910.1016/j.polymer.2011.06.019 ↗
29. 10.1039/c6sc01797e10.1039/c6sc01797e ↗
30. Frisch M. J. · 2004
31. 10.1039/C2TC00305H10.1039/C2TC00305H ↗
32. 10.1039/c2jm31765f10.1039/c2jm31765f ↗
33. 10.1039/b920227g10.1039/b920227g ↗
34. 10.1002/ange.20120270210.1002/ange.201202702 ↗
35. 10.1002/adma.20110421410.1002/adma.201104214 ↗
36. 10.1021/ja308273y10.1021/ja308273y ↗
37. 10.1002/adma.20110030210.1002/adma.201100302 ↗
38. 10.1002/adfm.20150382610.1002/adfm.201503826 ↗
39. 10.1002/adma.20150596310.1002/adma.201505963 ↗
40. 10.1021/acsami.6b0086110.1021/acsami.6b00861 ↗
41. 10.1038/nature0464510.1038/nature04645 ↗
42. 10.1002/adma.20150596310.1002/adma.201505963 ↗
43. 10.1016/j.mser.2016.06.00110.1016/j.mser.2016.06.001 ↗