journal article·2022-03Open access

Extremely High Power Efficiency Solution‐Processed Orange‐Red TADF OLEDs via a Synergistic Strategy of Molecular and Device Engineering

Dehao Jiang, Hisahiro Sasabe, Hiroki Arai, Kohei Nakao, Kengo Kumada, Junji Kido

Advanced Optical Materials· Volume 10· Issue 6

Abstract

Abstract The development of high‐performance, solution‐processed, orange‐red organic light‐emitting diodes (OLEDs) based on thermally activated delayed fluorescence (TADF) emitters is a challenging endeavor. In this study, two orange‐red TADF emitters, namely 2DMAC‐DBP‐2tBuCz and 2SPAC‐DBP‐2tBuCz, are developed by a novel donor–acceptor–functional‐group (D‐A‐R) molecular design strategy. This design makes the molecules highly soluble and inhibits concentration quenching of excitons, rendering the emitter suitable for use in devices with high concentration to boost their performance. The solution‐processed, orange‐red OLEDs manufactured in this study achieve a state‐of‐the‐art maximum external quantum efficiency (EQEmax) value of 23.7% and an extremely high maximum power efficiency (PEmax) of 48.8 lm W−1, which is nearly twice higher than the previously reported best value (27.1 lm W−1). Therefore, the collaboration of molecular engineering and sophisticated device design provides a novel method for extremely low power consumption solution‐processed OLEDs.
Source: crossref · 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

Department of Organic Materials Science Yamagata University 4‐3‐16 Jonan Yonezawa Yamagata 992–8510 Japan

Frontier Center for Organic Materials (FROM) Research Center for Organic Electronics (ROEL) Yamagata University 4‐3‐16 Jonan Yonezawa Yamagata 992–8510 Japan

Funding

Japan Science and Technology Agency · Japan Society for the Promotion of Science

References (25)

Show source-provided references
1. 10.1039/C8TC01139G10.1039/C8TC01139G ↗
2. 10.1038/ncomms675610.1038/ncomms6756 ↗
3. 10.1016/j.synthmet.2015.02.00910.1016/j.synthmet.2015.02.009 ↗
4. 10.1021/acs.chemmater.7b0296410.1021/acs.chemmater.7b02964 ↗
5. 10.1002/adma.20150449010.1002/adma.201504490 ↗
6. 10.1002/adma.20170564110.1002/adma.201705641 ↗
7. 10.1002/adma.20140218810.1002/adma.201402188 ↗
8. 10.1038/nature1168710.1038/nature11687 ↗
9. 10.1002/adma.20160544410.1002/adma.201605444 ↗
10. 10.1021/acs.chemmater.6b0532410.1021/acs.chemmater.6b05324 ↗
11. 10.1038/natrevmats.2018.2010.1038/natrevmats.2018.20 ↗
12. 10.1002/adom.20180025510.1002/adom.201800255 ↗
13. 10.1002/adfm.20190102510.1002/adfm.201901025 ↗
14. 10.1039/C8TC02179A10.1039/C8TC02179A ↗
15. 10.1002/adma.20190140410.1002/adma.201901404 ↗
16. 10.1002/adma.20200772410.1002/adma.202007724 ↗
17. 10.1021/acsami.9b0872910.1021/acsami.9b08729 ↗
18. 10.1021/acsami.0c0790610.1021/acsami.0c07906 ↗
19. 10.1039/c2jm32717a10.1039/c2jm32717a ↗
20. 10.1021/cm703682q10.1021/cm703682q ↗
21. 10.1002/adma.20140391410.1002/adma.201403914 ↗
22. 10.1002/adma.20150186610.1002/adma.201501866 ↗
23. 10.1021/acsami.7b1469510.1021/acsami.7b14695 ↗
24. 10.1021/acsami.9b2282610.1021/acsami.9b22826 ↗
25. 10.1002/aelm.20190084310.1002/aelm.201900843 ↗