Deep-Blue Thermally Activated Delayed Fluorescence Emitters Containing Diphenyl Sulfone Group for Organic Light Emitting Diodes

被引:0
|
作者
Lee, In Hye [1 ]
Kim, Ki Ju [1 ]
Kim, Young Kwan [2 ]
Kim, Young Sik [2 ]
Shin, Deng Myung [1 ]
机构
[1] Hongik Univ, Dept Chem Engn, Seoul 04066, South Korea
[2] Hongik Univ, Dept Informat Display, Seoul 04066, South Korea
基金
新加坡国家研究基金会;
关键词
Organic Light Emitting Diodes; Thermally Activated Delayed Fluorescence; Deep-Blue Emitter; Diphenyl Sulfone Derivative; ELECTROLUMINESCENCE; EFFICIENCY;
D O I
10.1166/jnn.2019.16702
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Novel blue thermally activated delayed fluorescence (TADF) emitters, D1-DPS and D2-DPS, were designed and synthesized. Diphenyl sulfone (DPS) group functioned as a common acceptor, and it combined with each of two different spiro-acridine groups, D1 and D2. The calculated energy differences (Delta E-ST) of the singlet and triplet excited states of D1-DPS (0.062 eV) and D2-DPS (0.128 eV) had sufficiently small Delta E-ST values, which is favorable in the thermally activated reverse intersystem crossing (RISC) process from the T-1 state to the S-1 state. A device doped 10 wt% of D2-DPS with ADN host material, obtained 5.05% of external quantum efficiency with deep-blue emission having CIExy coordinates of (0.152, 0.065). The results showed that these molecules are promising host-free TADF deep-blue emitters by inhibiting concentration quenching.
引用
收藏
页码:4583 / 4589
页数:7
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