系统间交叉
接受者
分子内力
光化学
量子产额
芴
单重态
材料科学
荧光
光致发光
激发态
化学
化学物理
光电子学
原子物理学
聚合物
物理
光学
立体化学
复合材料
凝聚态物理
作者
Feng‐Ming Xie,Hao‐Ze Li,Kai Zhang,Yang Shen,Xin Zhao,Yanqing Li,Jian‐Xin Tang
标识
DOI:10.1002/anie.202213823
摘要
Organic materials featuring intramolecular through-space charge transfer (TSCT) excited states are advantageous for efficient thermally activated delayed fluorescence (TADF), although the realization of multiple TSCT systems remains challenging. Herein, a rigid molecule with a three-dimensional dislocated sandwich acceptor-donor-acceptor configuration has been developed by a linking biphenazine (2PXZ) donor and 2,4,6-triphenyl-1,3,5-triazine (TRZ) acceptor through the twin-locking of two spiro-fluorene bridges. The twin-locking construction with multiple TSCT effects suppresses the intramolecular rotations of various segments in 2PXZ-2TRZ, leading to a small singlet-triplet energy difference, a fast reverse intersystem crossing process, and high photoluminescence quantum yield. This material simultaneously possesses the capabilities of TADF and aggregation-induced emission. The device employing 2PXZ-2TRZ as a dopant displays an optimal external quantum efficiency of 27.1 % and a low efficiency roll-off.
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