A Series of Imidazo[1,2‐f]phenanthridine‐Based Sky‐Blue TADF Emitters Realizing EQE of over 20%
Source abstract
Abstract
Abstract Although imidazole derivatives are promising as blue fluorescent emitters in organic light‐emitting devices (OLEDs), the corresponding blue thermally activated delayed fluorescence (TADF) emitter is rarely explored. In this study, a series of imidazo[1,2‐f]phenanthridine‐based TADF materials in the blue to sky‐blue region is developed. The resultant benzimidazole (BIP)‐based TADF materials, with π‐expanded acceptor and electron‐donor phenoxazine (PXZ), namely PXZ‐BIP, shows a high maximum external quantum efficiency (ηext,max) of 21% with CIE coordinates of (0.21, 0.37). These results have clearly demonstrated that PXZ‐BIP exhibits the highest ηext,max among imidazole‐based fluorescent sky‐blue OLEDs. The corresponding imidazophenanthridine derivative, with a less π‐expanded acceptor, shows inferior OLED performances, with a ηext,max of 5.9% and CIE of (0.19, 0.30). This study provides a critical molecular design to realize high‐efficiency TADF materials based on imidazole derivatives.
Source: crossref · 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 Organic Materials Science Graduate School of Organic Materials Science Yamagata University 4‐3‐16 Jonan Yonezawa Yamagata 992‐8510 Japan
Frontier Center for Organic Materials (FROM) Yamagata University 4‐3‐16 Jonan Yonezawa Yamagata 992‐8510 Japan
Research Center for Organic Electronics (ROEL) Yamagata University 4‐3‐16 Jonan Yonezawa Yamagata 992‐8510 Japan
Funding
Japan Society for the Promotion of Science
References (39)
Show source-provided references
1. 10.7567/JJAP.53.06010110.7567/JJAP.53.060101 ↗
2. 10.1039/C6CS00368K10.1039/C6CS00368K ↗
3. 10.1021/acs.chemmater.6b0532410.1021/acs.chemmater.6b05324 ↗
4. 10.1002/adma.20160544410.1002/adma.201605444 ↗
5. 10.1117/1.JPE.8.03210810.1117/1.JPE.8.032108 ↗
6. 10.1002/adma.20170560010.1002/adma.201705600 ↗
7. 10.1038/nature1168710.1038/nature11687 ↗
8. 10.1038/nphoton.2014.1210.1038/nphoton.2014.12 ↗
9. 10.1038/ncomms947610.1038/ncomms9476 ↗
10. 10.1002/adma.20160167510.1002/adma.201601675 ↗
11. 10.1002/adma.20160644810.1002/adma.201606448 ↗
12. 10.1021/jacs.7b0384810.1021/jacs.7b03848 ↗
13. 10.1002/advs.20170098910.1002/advs.201700989 ↗
14. 10.1002/adma.20170560010.1002/adma.201705600 ↗
15. 10.1002/adma.20150378210.1002/adma.201503782 ↗
16. 10.1039/C5TC04057D10.1039/C5TC04057D ↗
17. 10.1002/chem.20160430310.1002/chem.201604303 ↗
18. 10.1002/adom.20160084310.1002/adom.201600843 ↗
19. 10.1002/asia.20160164110.1002/asia.201601641 ↗
20. 10.1021/acsami.6b1348210.1021/acsami.6b13482 ↗
21. 10.1021/acs.chemmater.7b0240310.1021/acs.chemmater.7b02403 ↗
22. 10.1002/chem.20170526210.1002/chem.201705262 ↗
23. 10.1002/adom.20180037610.1002/adom.201800376 ↗
24. 10.1002/adom.20180025810.1002/adom.201800258 ↗
25. 10.1039/C6SC05619A10.1039/C6SC05619A ↗
26. 10.1002/adma.20120222210.1002/adma.201202222 ↗
27. 10.1021/acsami.6b1463810.1021/acsami.6b14638 ↗
28. 10.1039/C7TC05576E10.1039/C7TC05576E ↗
29. 10.1021/ol500248h10.1021/ol500248h ↗
30. 10.1021/jo502632b10.1021/jo502632b ↗
31. 10.1021/ic901834v10.1021/ic901834v ↗
32. 10.1021/ic400950u10.1021/ic400950u ↗
33. 10.1016/j.orgel.2013.06.02910.1016/j.orgel.2013.06.029 ↗
34. 10.1002/adma.20140162110.1002/adma.201401621 ↗
35. 10.1038/ncomms600810.1038/ncomms6008 ↗
36. 10.1016/j.orgel.2014.08.03810.1016/j.orgel.2014.08.038 ↗
37. 10.1038/nmat415410.1038/nmat4154 ↗
38. 10.1021/cm801727d10.1021/cm801727d ↗
39. 10.1021/bk-1997-0672.ch02510.1021/bk-1997-0672.ch025 ↗