journal article·2017-03

Significant Enhancement of Blue OLED Performances through Molecular Engineering of Pyrimidine‐Based Emitter

Kohei Nakao, Hisahiro Sasabe, Ryutaro Komatsu, Yuya Hayasaka, Tatsuya Ohsawa, Junji Kido

Advanced Optical Materials· Volume 5· Issue 6
Publisher page

Abstract

Although pyrimidine‐based emitters are one of the most promising classes of compounds, a structure–property relationship for an effective molecular design strategy has not yet been elucidated. In this study, the authors develop three types of blue pyrimidine emitters for high‐performance thermally activated delayed fluorescence (TADF) organic light‐emitting devices (OLEDs). 2,4,6‐triphenylpyrimidine is used as an acceptor, and tri‐ or penta‐substituted acridine as a donor unit for the blue TADF emitters. The authors investigate the effects of the nitrogen position on the photophysical properties and OLED performances, and develop a blue device with a high external quantum efficiency close to 25%. The device performances are among the best so far for blue TADF OLEDs.
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Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Luminescence and Fluorescent Materials

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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 Science and Technology Corporation

References (27)

Show source-provided references
1. 10.1126/science.267.5202.133210.1126/science.267.5202.1332 ↗
2. 10.1038/nature0464510.1038/nature04645 ↗
3. 10.1117/12.79375810.1117/12.793758 ↗
4. 10.1038/nature0800310.1038/nature08003 ↗
5. 10.1126/science.120299210.1126/science.1202992 ↗
6. 10.1038/nphoton.2011.31810.1038/nphoton.2011.318 ↗
7. 10.1039/c2tc00584k10.1039/c2tc00584k ↗
8. 10.1002/ejoc.20130054410.1002/ejoc.201300544 ↗
9. 10.1038/nature1168710.1038/nature11687 ↗
10. 10.1002/adfm.20160250110.1002/adfm.201602501 ↗
11. 10.1038/nmat415410.1038/nmat4154 ↗
12. 10.1002/adma.20160167510.1002/adma.201601675 ↗
13. 10.1038/nphoton.2014.1210.1038/nphoton.2014.12 ↗
14. Lee S. Y. · Angew. Chem. Int. Ed. · 2014 · 53 · 110.1002/anie.201310509 ↗
15. 10.1039/C5CC00307E10.1039/C5CC00307E ↗
16. 10.1002/ange.20150827010.1002/ange.201508270 ↗
17. 10.1039/C5TC04057D10.1039/C5TC04057D ↗
18. 10.1039/C6TC02027E10.1039/C6TC02027E ↗
19. 10.1002/chem.20160270510.1002/chem.201602705 ↗
20. 10.1021/acsami.5b0564810.1021/acsami.5b05648 ↗
21. 10.1002/adma.20150205310.1002/adma.201502053 ↗
22. 10.1021/acs.chemmater.5b0251510.1021/acs.chemmater.5b02515 ↗
23. 10.1016/j.tetlet.2006.10.09010.1016/j.tetlet.2006.10.090 ↗
24. 10.1039/c003526b10.1039/c003526b ↗
25. 10.1021/acsami.5b1012910.1021/acsami.5b10129 ↗
26. 10.1039/b812270a10.1039/b812270a ↗
27. 10.1021/bk-1997-0672.ch02510.1021/bk-1997-0672.ch025 ↗