Molecular asymmetry and rigidification as strategies to activate and enhance thermally activated delayed fluorescence in deep-blue MR-TADF emitters

被引:1
作者
Weerasinghe, Rangani Wathsala [1 ]
dos Santos, John Marques [2 ]
Chitose, Youhei [1 ,3 ]
Matulaitis, Tomas [2 ]
Warriner, Stuart L. [6 ]
Barman, Debasish [1 ]
Chan, Chin-Yiu [4 ,5 ]
Tsuchiya, Youichi [1 ]
Zysman-Colman, Eli [2 ]
Adachi, Chihaya [1 ,3 ]
机构
[1] Kyushu Univ, Ctr Organ Photon & Elect Res OPERA, Fukuoka 8190395, Japan
[2] Univ St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Scotland
[3] Kyushu Univ, Ctr Mol Syst CMS, Grad Sch Engn, Dept Appl Chem, 744 Motooka, Fukuoka 8190395, Japan
[4] City Univ Hong Kong, Dept Mat Sci & Engn, Kowloon, Tat Chee Ave, Hong Kong, Peoples R China
[5] City Univ Hong Kong, Dept Chem, Kowloon, Tat Chee Ave, Hong Kong, Peoples R China
[6] Univ Leeds, Sch Chem, Leeds LS2 9JT, England
关键词
EMISSION;
D O I
10.1039/d4cp02664k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two novel deep-blue multi-resonance thermally activated delayed fluorescence (MR-TADF) emitters, 1B-CzCrs and 2B-CzCrs, containing a fused carbazole unit were synthesized. The carbazole contributed to the emergence of TADF in these small molecules. Particularly, organic light-emitting diodes with 1B-CzCrs doped in the mCP host achieve a maximum external quantum efficiency of 12.8% at CIE coordinates of (0.146, 0.062). Two novel deep-blue multi-resonance thermally activated delayed fluorescence (MR-TADF) emitters, 1B-CzCrs and 2B-CzCrs, containing a fused carbazole unit were synthesized.
引用
收藏
页码:21337 / 21341
页数:5
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