Purely Organic Thermally Activated Delayed Fluorescence Materials for Organic Light-Emitting Diodes

被引:1722
作者
Wong, Michael Y. [1 ]
Zysman-Colman, Eli [1 ]
机构
[1] Univ St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, Scotland
基金
英国工程与自然科学研究理事会;
关键词
EXTERNAL QUANTUM EFFICIENCY; AGGREGATION-INDUCED EMISSION; BIPOLAR HOST MATERIALS; HIGH-POWER-EFFICIENCY; PHOSPHINE-OXIDE HOST; HIGH TRIPLET ENERGY; LOW ROLL-OFF; HIGHLY EFFICIENT; DEEP-BLUE; MOLECULAR DESIGN;
D O I
10.1002/adma.201605444
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The design of thermally activated delayed fluorescence (TADF) materials both as emitters and as hosts is an exploding area of research. The replacement of phosphorescent metal complexes with inexpensive organic compounds in electroluminescent (EL) devices that demonstrate comparable performance metrics is paradigm shifting, as these new materials offer the possibility of developing low-cost lighting and displays. Here, a comprehensive review of TADF materials is presented, with a focus on linking their optoelectronic behavior with the performance of the organic light-emitting diode (OLED) and related EL devices. TADF emitters are cross-compared within specific color ranges, with a focus on blue, green-yellow, orange-red, and white OLEDs. Organic small-molecule, dendrimer, polymer, and exciplex emitters are all discussed within this review, as is their use as host materials. Correlations are provided between the structure of the TADF materials and their optoelectronic properties. The success of TADF materials has ushered in the next generation of OLEDs.
引用
收藏
页数:54
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