journal article·2016-04-20

Highly Efficient Sky-Blue Fluorescent Organic Light Emitting Diode Based on Mixed Cohost System for Thermally Activated Delayed Fluorescence Emitter (2CzPN)

Jin Won Sun, Kwon-Hyeon Kim, Chang-Ki Moon, Jeong-Hwan Lee, Jang-Joo Kim

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Abstract

The mixed cohosts of 1,3-bis(N-carbazolyl)benzene and 2,8-bis(diphenylphosphoryl)dibenzothiophene have been developed for a highly efficient blue fluorescent oragnic light emitting diode (OLED) doped with a thermally activated delayed fluorescence (TADF) emitter [4,5-di (9H-carbazol-9-yl) phthalonitrile (2CzPN)]. We have demonstrated one of the highest external quantum efficiency of 21.8% in blue fluorescent OLEDs, which is identical to the theoretically achievable maximum electroluminescence efficiency using the emitter. Interestingly, the efficiency roll-off is large even under the excellent charge balance in the device and almost the same as the single host based devices, indicating that the efficiency roll-off in 2CzPN based TADF host is related to the material characteristics, such as low reverse intesystem crossing rate rather than charge imbalance.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Thin-Film Transistor Technologies

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

Affiliations

Department of Materials Science and Engineering, Research Institute of Advanced Materials, Seoul National University, 151-744 Seoul, South Korea

Funding

Korea Evaluation Institute of Industrial Technology

References (29)

Show source-provided references
1. 10.1038/nature1168710.1038/nature11687 ↗
2. 10.1016/j.orgel.2013.07.01010.1016/j.orgel.2013.07.010 ↗
3. 10.1039/C3TC31936A10.1039/C3TC31936A ↗
4. 10.1038/nphoton.2014.1210.1038/nphoton.2014.12 ↗
5. 10.1038/nmat415410.1038/nmat4154 ↗
6. 10.1002/adma.20140547410.1002/adma.201405474 ↗
7. 10.1002/adma.20150026710.1002/adma.201500267 ↗
8. 10.1021/acs.chemmater.5b0251510.1021/acs.chemmater.5b02515 ↗
9. 10.1002/adma.20150205310.1002/adma.201502053 ↗
10. 10.1039/C5TC04057D10.1039/C5TC04057D ↗
11. 10.1143/JJAP.33.L177210.1143/JJAP.33.L1772 ↗
12. 10.1063/1.274522410.1063/1.2745224 ↗
13. 10.1063/1.346496910.1063/1.3464969 ↗
14. 10.1002/adma.20110184810.1002/adma.201101848 ↗
15. 10.1002/adfm.20130054710.1002/adfm.201300547 ↗
16. 10.1002/adma.20140140710.1002/adma.201401407 ↗
17. 10.1063/1.288511710.1063/1.2885117 ↗
18. 10.1002/adma.20140095510.1002/adma.201400955 ↗
19. 10.1016/j.chemphys.2008.10.03510.1016/j.chemphys.2008.10.035 ↗
20. 10.1063/1.330970510.1063/1.3309705 ↗
21. 10.1063/1.477318810.1063/1.4773188 ↗
22. 10.1016/j.orgel.2012.09.01410.1016/j.orgel.2012.09.014 ↗
23. 10.1002/adfm.20130010410.1002/adfm.201300104 ↗
24. 10.1063/1.275463510.1063/1.2754635 ↗
25. 10.1063/1.310726710.1063/1.3107267 ↗
26. 10.1149/1.300723910.1149/1.3007239 ↗
27. 10.1063/1.314371810.1063/1.3143718 ↗
28. 10.1016/j.orgel.2009.12.00210.1016/j.orgel.2009.12.002 ↗
29. 10.1016/j.orgel.2011.07.01510.1016/j.orgel.2011.07.015 ↗