量子效率
有机发光二极管
材料科学
光电子学
共发射极
偶极子
光致发光
接受者
电致发光
化学
纳米技术
物理
凝聚态物理
有机化学
图层(电子)
作者
Jiaoyun Wang,Nengquan Li,Qiaodeng Chen,Yepeng Xiang,Xuan Zeng,Shaolong Gong,Yang Zou,Yuan Liu
标识
DOI:10.1016/j.cej.2022.137805
摘要
The combination of acridine/phenoxazine donors and triarylboron acceptor has afforded two thermally activated delayed fluorescence (TADF) emitters with D3-A typed architectures, namely 3DMAC-TB and 3PXZ-TB. Attributing to the highly steric hindrance between D/A groups as well as intense intramolecular charge transfer state, both emitters exhibit well-separated frontier molecular orbitals (FMOs) distributions and distinct TADF characteristics. The high rigidity molecular structures of 3DMAC-TB and 3PXZ-TB contribute to high photoluminescence quantum yields (PLQYs) up to 0.94 and 0.89, respectively. The “star-shaped” configuration endows both emitters with high ratios of horizontal dipole orientation of 86% and 80%, respectively. The organic light emitting diodes (OLEDs) involving 3DMAC-TB and 3PXZ-TB as emitting dopants achieve maximum external quantum efficiencies of 38.8% and 29.4%, respectively. The efficiency of 3DMAC-TB based device is among the state-of-the-art efficiency for green TADF OLEDs. This work unveils great potential with triarylboron-cored multi-donors molecular design strategy in the development of excellent TADF molecules simultaneously possessing high quantum yields and preferentially horizontal emitting dipole orientations.
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