Deep-blue thermally activated delayed fluorescence materials with high glass transition temperature

被引:13
作者
Zhu, Xiang-Dong [1 ]
Tian, Qi-Sheng [1 ]
Zheng, Qi [1 ]
Wang, Ya-Kun [1 ]
Yuan, Yi [1 ]
Li, Yun [1 ]
Jiang, Zuo-Quan [1 ]
Liao, Liang-Sheng [1 ]
机构
[1] Soochow Univ, Inst Funct Nano & Soft Mat FUNSOM, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Joint Int Res Lab Carbon Based Funct Mat & Device, Suzhou, Jiangsu, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Deep-blue emission; Thermally activated delayed fluorescence; Spiro-type material; High thermal stability; Organic light-emitting diodes; Small singlet-triplet splitting; LIGHT-EMITTING-DIODES; HIGH-EFFICIENCY; MOLECULAR DESIGN; HOST MATERIALS; PHOSPHORESCENT; EMITTERS; DERIVATIVES; DONOR; TADF; SUBSTITUTION;
D O I
10.1016/j.jlumin.2018.10.017
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Two thermally activated delayed fluorescence (TADF) deep-blue emitters (4-SCZ, 4-SCZ-F) were developed by combining a novel spiro-type donor moiety with different triazine-based unit. By modifying the interplay between the donors and acceptor through tuning the phenylene linker using a fluorine substituent, singlet-triplet splitting (Delta E-ST) can be regulated. In addition, the rigid geometry of these emitters also ensures their high photoluminance quantum yield (PLQY). As a result, when applied 4-SCZ-F as the emitter, good performance with current efficiency (CE)/power efficiency (PE)/external quantum efficiency (EQE) of 11.16 cd/A/9.74 lm/W/7.21% and Commission Internationale de l'Eclairage (CIE) coordinate at (0.16, 0.17) was achieved.
引用
收藏
页码:146 / 153
页数:8
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