三苯胺
量子产额
有机发光二极管
系统间交叉
光化学
电致发光
材料科学
双层
猝灭(荧光)
光致发光
光电子学
接受者
荧光
激子
量子效率
化学
图层(电子)
纳米技术
激发态
光学
物理
膜
原子物理学
量子力学
生物化学
单重态
凝聚态物理
作者
Bingjie Zhao,Huiqin Wang,Chunmiao Han,Peng Ma,Zhe Li,Peng Chang,Hui Xu
标识
DOI:10.1002/anie.202008885
摘要
Device simplification is of practical significance for organic light emitting diodes (OLEDs), and remains the great challenge for deep-red emitters. Herein, a deep-red thermally activated delayed fluorescence molecule (pTPA-DPPZ) is reported which features a T shaped structure containing two triphenylamine (TPA) donors, one either side of a planar dipyridophenazine (DPPZ) acceptor. The rational spatial arrangement of the functional groups leads to limited but sufficient molecular packing for effective carrier transport. The neat pTPA-DPPZ film achieves an around 90-fold improved radiation rate constant of 107 s-1 and the nearly unitary reverse intersystem crossing (RISC) efficiency, as well as accelerated emission decays for quenching suppression. The high radiation and RISC result in a photoluminescence quantum yield of 87 %. The bilayer OLED based on the pTPA-DPPZ emissive layer achieved the record external quantum efficiencies of 12.3 % for maximum and 10.4 % at 1000 nits, accompanied by the deep-red electroluminescence with the excellent color purity.
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