All-organic thermally activated delayed fluorescence materials for organic light-emitting diodes

被引:983
作者
Liu, Yuchao [1 ]
Li, Chensen [1 ]
Ren, Zhongjie [1 ]
Yan, Shouke [1 ]
Bryce, Martin R. [2 ]
机构
[1] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Chem Resource Engn, Beijing, Peoples R China
[2] Univ Durham, Dept Chem, Durham, England
来源
NATURE REVIEWS MATERIALS | 2018年 / 3卷 / 04期
基金
英国工程与自然科学研究理事会;
关键词
EXTERNAL QUANTUM EFFICIENCY; GREEN IRIDIUM DENDRIMERS; BIPOLAR HOST MATERIAL; HIGHLY EFFICIENT; CHARGE-TRANSFER; MOLECULAR DESIGN; TRIPLET ENERGY; CONJUGATED POLYMERS; DEEP-BLUE; ROLL-OFF;
D O I
10.1038/natrevmats.2018.20
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Thermally activated delayed fluorescence (TADF) emitters, which produce light by harvesting both singlet and triplet excitons without noble metals, are emerging as next-generation organic electroluminescent materials. In the past few years, there have been rapid advances in molecular design criteria, our understanding of the photophysics underlying TADF and the applications of TADF materials as emitters in organic light-emitting diodes (OLEDs). This topic is set to remain at the forefront of research in optoelectronic organic materials for the foreseeable future. In this Review, we focus on state-of-the-art materials design and understanding of the photophysical processes, which are being leveraged to optimize the performance of OLED devices. Notably, we also appraise dendritic and polymeric TADF emitters-macromolecular materials that offer the potential advantages of low cost, solution processable and large-area OLED fabrication.
引用
收藏
页数:20
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