The Design of Fused Amine/Carbonyl System for Efficient Thermally Activated Delayed Fluorescence: Novel Multiple Resonance Core and Electron Acceptor
Source abstract
Abstract
Abstract Multiple resonances induced thermally activated delayed fluorescence (MR‐TADF) has great advantages in high color purity display. Up to now, current MR‐TADF emitters are only based on the boron‐nitrogen‐containing fragment. Reported herein is a novel class of MR‐TADF emitter, quinolino[3,2,1‐de]acridine‐5,9‐dione (QAO), realized by the opposite resonance effect of the carbonyl and the nitrogen atoms, which is also the smallest TADF emitter reported so far. The QAO‐based pure blue organic light‐emitting diode achieves a maximum external quantum efficiency (EQEmax) of 19.4% with a small full width at half maximum of 39 nm. Moreover, tert‐butyl modified QAO can be employed as an efficient electron acceptor to construct an efficient yellow‐green evaporation and solution process feasible TADF emitter, 7‐(tert‐butyl)‐3,11‐bis(9,9‐dimethylacridin‐10(9H)‐yl)quinolino[3,2,1‐de]acridine‐5,9‐dione (QAO‐DAd), with significantly improved performance as compared to the previous flexible diketone‐based emitters.
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Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Thin-Film Transistor Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of Functional Nano & Soft Materials (FUNSOM) Jiangsu Key Laboratory for Carbon‐Based Functional Materials & Devices Soochow University 199 Ren'ai Road Suzhou Jiangsu 215123 P. R. China
School of Optoelectronic Science and Engineering University of Electronic Science and Technology of China (UESTC) Chengdu Sichuan 610054 China
Institute of Organic Optoelectronics Jiangsu Industrial Technology Research Institute (JITRI) Wujiang, Suzhou Jiangsu 215211 China
Funding
National Natural Science Foundation of China
References (31)
Show source-provided references
1. 10.1002/adma.20090098310.1002/adma.200900983 ↗
2. 10.1038/nature1168710.1038/nature11687 ↗
3. 10.1038/nmat415410.1038/nmat4154 ↗
4. 10.1038/nphoton.2014.1210.1038/nphoton.2014.12 ↗
5. 10.1002/adma.20160167510.1002/adma.201601675 ↗
6. 10.1002/adfm.20160250110.1002/adfm.201602501 ↗
7. 10.1002/adma.20130057510.1002/adma.201300575 ↗
8. 10.1021/jacs.5b1095010.1021/jacs.5b10950 ↗
9. 10.1002/adma.20170496110.1002/adma.201704961 ↗
10. 10.1021/jacs.7b0384810.1021/jacs.7b03848 ↗
11. 10.1002/anie.20120628910.1002/anie.201206289 ↗
12. 10.1038/nphoton.2012.3110.1038/nphoton.2012.31 ↗
13. 10.1002/adma.20170540610.1002/adma.201705406 ↗
14. 10.1021/acs.chemmater.6b0532410.1021/acs.chemmater.6b05324 ↗
15. 10.1002/adfm.20180255810.1002/adfm.201802558 ↗
16. 10.1002/adfm.20170098610.1002/adfm.201700986 ↗
17. 10.1002/anie.20180448310.1002/anie.201804483 ↗
18. 10.1039/C6CS00368K10.1039/C6CS00368K ↗
19. 10.1002/adma.20150549110.1002/adma.201505491 ↗
20. 10.1002/anie.20180632310.1002/anie.201806323 ↗
21. 10.1002/anie.20150633510.1002/anie.201506335 ↗
22. 10.1039/C4DT03608E10.1039/C4DT03608E ↗
23. 10.1038/s41566-018-0112-910.1038/s41566-018-0112-9 ↗
24. 10.1021/jo026883p10.1021/jo026883p ↗
25. 10.1002/anie.20140299210.1002/anie.201402992 ↗
26. 10.1039/C6SC00542J10.1039/C6SC00542J ↗
27. 10.1021/ja510144h10.1021/ja510144h ↗
28. 10.1002/adma.20150322510.1002/adma.201503225 ↗
29. 10.1002/adma.20140218810.1002/adma.201402188 ↗
30. 10.1002/adfm.20150299510.1002/adfm.201502995 ↗
31. 10.1002/adom.20150063410.1002/adom.201500634 ↗