Dipole-Dipole Interaction Management for Efficient Blue Thermally Activated Delayed Fluorescence Diodes

被引:114
作者
Han, Chunmiao [1 ,2 ]
Zhang, Zhen [1 ,2 ]
Ding, Dongxue [1 ,2 ]
Xu, Hui [1 ,2 ]
机构
[1] Heilongjiang Univ, Key Lab Funct Inorgan Mat Chem, Minist Educ, 74 Xuefu Rd, Harbin 150080, Heilongjiang, Peoples R China
[2] Heilongjiang Univ, Sch Chem & Mat Sci, 74 Xuefu Rd, Harbin 150080, Heilongjiang, Peoples R China
来源
CHEM | 2018年 / 4卷 / 09期
基金
中国国家自然科学基金;
关键词
EXTERNAL QUANTUM EFFICIENCY; LIGHT-EMITTING-DIODES; PHOSPHINE-OXIDE HOST; HIGH TRIPLET ENERGY; BIPOLAR HOST; HIGH-PERFORMANCE; ELECTRICAL-PROPERTIES; UNIVERSAL HOST; PHOSPHORESCENT; DEVICES;
D O I
10.1016/j.chempr.2018.06.005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Thermally activated delayed fluorescence (TADF) diodes have emerged in recent years. However, blue devices still suffer from low luminance and serious efficiency roll-off, partially because of the utilization of unipolar host materials, which can suppress interaction-induced quenching at the cost of carrier flux unbalance. Herein, we demonstrate that the strong host excited-state dipole field can significantly worsen exciton quenching of blue TADF dopants through hostdopant dipole-dipole interactions. To integrate low excited-state polarity and ambipolar characteristics, we developed a donor-s-acceptor host with dramatically reduced excited-state dipole moments by one order of magnitude to only similar to 2 Debye, which gave rise to state-of-the-art external quantum efficiency beyond 20% from its devices, as well as record-low roll-off. Comparison between the device efficiencies of the hosts and various excited-state polarities revealed that the suppression of dipole-dipole interaction-induced quenching is the primary determinant of device performance for ambipolar blue TADF hosts.
引用
收藏
页码:2154 / 2167
页数:14
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