系统间交叉
深铬移
有机发光二极管
发光
荧光
聚集诱导发射
喹啉
光化学
光电子学
材料科学
量子效率
共发射极
化学
纳米技术
物理
光学
有机化学
核物理学
激发态
单重态
图层(电子)
作者
Fengping Hu,Wei Yang,Lili Li,Jingsheng Miao,Shaolong Gong,Changqing Ye,Xiang Gao,Chuluo Yang
标识
DOI:10.1016/j.cej.2023.142678
摘要
Organic multifunctional luminescent materials have drawn growing attention due to their diverse emissive mechanism and potential application in luminescent field. Herein, a series of cyanobenzene-decorated dimethylacridine-quinoline conjugates is designed and synthesized, which exhibit thermally activated delayed fluorescence (TADF), aggregation-induced emission (AIE), polymorphism and multicolor mechanochromic luminescence (MCL) with high contrast beyond 75 nm. Significantly, structure-property investigations via the in-depth analysis of molecular conformations and three-dimensional supramolecular framework of the polymorphic crystals demonstrate that the diverse conformations and abundant noncovalent interactions have a predominant impact on aggregation-dependent TADF property and emission wavelength. The quasi-equatorial conformational electron-donating unit and quasi-planar structural electron-withdrawing segment in aggregation states of the emitter are beneficial for accelerating the rate of the reverse intersystem crossing, enhancing TADF character, and promoting the emission with a bathochromic shift. The organic light-emitting diodes (OLEDs) employing these emitters achieve good device performance with an external quantum efficiency (EQE) of 14.6%.
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