journal article·2019-05-15

Isomeric Quinoxalinedicarbonitrile as Color-Managing Acceptors of Thermally Activated Delayed Fluorescent Emitters

Shantaram Kothavale, Kyung Hyung Lee, Jun Yeob Lee

ACS Applied Materials & Interfaces· Volume 11· Issue 19
Publisher page

Abstract

Highly efficient yellow and red thermally activated delayed fluorescent (TADF) organic light-emitting diodes were developed using two quinoxalinedicarbonitrile units, quinoxaline-6,7-dicarbonitrile (6,7-DCQx) and quinoxaline-5,8-dicarbonitrile (5,8-DCQx) as electron acceptors, and t-butylcarbazole or 9,9-dimethylacridan as electron donors. The strong electron-withdrawing capability of the 5,8-DCQx and 6,7-DCQx acceptors enabled from yellow to red emission in the TADF emitters. Comparing 5,8-DCQx and 6,7-DCQx, a red-shifted emission by about 40 nm was observed in the 5,8-DCQx acceptor-based emitters, but the external quantum efficiency of the TADF devices was over 20% irrespective of the acceptor, proving the usefulness of the two acceptor moieties as the building blocks of the TADF emitters. Therefore, the quinoxalinedicarbonitrile acceptors are promising as the acceptor moiety for designing yellow or red TADF emitters.
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

School of Chemical Engineering, Sungkyunkwan University, 2066, Seobu-ro, Jangan-gu, Suwon, Gyeonggi 440-746, Korea

Funding

National Research Foundation of Korea

References (40)

Show source-provided references
1. 10.1038/nature1168710.1038/nature11687 ↗
2. 10.1002/adma.20140253210.1002/adma.201402532 ↗
3. 10.7567/JJAP.53.06010110.7567/JJAP.53.060101 ↗
4. 10.1002/adfm.20150299510.1002/adfm.201502995 ↗
5. 10.1002/anie.20141210710.1002/anie.201412107 ↗
6. 10.1002/anie.20150668710.1002/anie.201506687 ↗
7. 10.1002/adfm.20130010410.1002/adfm.201300104 ↗
8. 10.1002/adma.20130109110.1002/adma.201301091 ↗
9. 10.1002/adma.20140140710.1002/adma.201401407 ↗
10. 10.1002/adma.20140139310.1002/adma.201401393 ↗
11. 10.1021/acsami.5b0122010.1021/acsami.5b01220 ↗
12. 10.1002/adma.20150026710.1002/adma.201500267 ↗
13. 10.1002/adma.20150205310.1002/adma.201502053 ↗
14. 10.1002/anie.20100382610.1002/anie.201003826 ↗
15. 10.1002/adma.20130075310.1002/adma.201300753 ↗
16. 10.1002/anie.20150020310.1002/anie.201500203 ↗
17. 10.1021/jacs.5b0793210.1021/jacs.5b07932 ↗
18. 10.1021/ja00366a05110.1021/ja00366a051 ↗
19. 10.1021/ja951345y10.1021/ja951345y ↗
20. 10.1002/adma.20120493810.1002/adma.201204938 ↗
21. 10.1002/adma.20090331210.1002/adma.200903312 ↗
22. 10.1063/1.233527510.1063/1.2335275 ↗
23. 10.1002/anie.20150703110.1002/anie.201507031 ↗
24. 10.1002/adfm.20110219110.1002/adfm.201102191 ↗
25. 10.1021/cr000013v10.1021/cr000013v ↗
26. 10.1002/asia.20090059610.1002/asia.200900596 ↗
27. 10.1002/adom.20180025510.1002/adom.201800255 ↗
28. 10.1002/anie.20160011310.1002/anie.201600113 ↗
29. 10.1021/cm402428a10.1021/cm402428a ↗
30. 10.1016/j.dyepig.2017.02.03510.1016/j.dyepig.2017.02.035 ↗
31. 10.1002/adma.20130057510.1002/adma.201300575 ↗
32. 10.1021/acsami.6b1479610.1021/acsami.6b14796 ↗
33. 10.1002/adom.20170114710.1002/adom.201701147 ↗
34. 10.1002/anie.20140299210.1002/anie.201402992 ↗
35. 10.1021/ja510144h10.1021/ja510144h ↗
36. 10.1039/C7TC00025A10.1039/C7TC00025A ↗
37. 10.1002/adma.20170496110.1002/adma.201704961 ↗
38. 10.1002/advs.20180043610.1002/advs.201800436 ↗
39. 10.1039/C8TC01746H10.1039/C8TC01746H ↗
40. 10.1002/anie.20170646410.1002/anie.201706464 ↗