Molecular Design Tactics for Highly Efficient Thermally Activated Delayed Fluorescence Emitters for Organic Light Emitting Diodes

被引:40
|
作者
Konidena, Rajendra Kumar [1 ]
Lee, Jun Yeob [1 ]
机构
[1] Sungkyunkwan Univ, Sch Chem Engn, 2066 Seobu Ro, Suwon, Gyeonggi, South Korea
来源
CHEMICAL RECORD | 2019年 / 19卷 / 08期
基金
新加坡国家研究基金会;
关键词
organic light emitting diodes; thermally activated delayed fluorescence; quantum efficiency; donor and acceptor; life time; AGGREGATION-INDUCED EMISSION; EXTERNAL QUANTUM EFFICIENCY; NARROW EMISSION; HOST MATERIALS; ROLL-OFF; BLUE; ACCEPTOR; DONOR; STRATEGY; PHOSPHORESCENCE;
D O I
10.1002/tcr.201800136
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently, pure organic thermally activated delayed fluorescence (TADF) emitters have attracted considerable interest from the scientific community in the field of organic light emitting diodes (OLEDs) as they can theoretically realize 100 % of the internal quantum efficiency by exploiting both the singlet and triplet excitons via the reverse intersystem crossing enabled by small singlet-triplet energy splitting. Currently, the external quantum efficiency of the TADF emitters is reaching the level of phosphorescent emitters. Therefore, the TADF approach is considered as a potential alternative to the low efficiency conventional fluorescent and expensive phosphorescent emitters. In this account, we summarized our recent development of blue and green TADF molecular designs to improve the device performances of the TADF devices.
引用
收藏
页码:1499 / 1517
页数:19
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