系统间交叉
材料科学
有机发光二极管
量子产额
量子效率
光致发光
光电子学
色度
接受者
电致发光
荧光
光化学
纳米技术
单重态
光学
化学
原子物理学
物理
图层(电子)
凝聚态物理
激发态
作者
Zhengqi Xiao,Yang Zou,Zhanxiang Chen,Jingsheng Miao,Yuntao Qiu,Zhongyan Huang,Xiaosong Cao,Xiaojun Peng,Chuluo Yang
标识
DOI:10.1002/adma.202419601
摘要
The hyperfluorescence (HF) technology holds great promise for the development of high-quality organic light-emitting diodes (OLEDs) for their excellent color purity, high efficiency, and low-efficiency roll-off. Sensitizer plays a crucial role in the performance of HF devices. However, designing sensitizers with simultaneous high photoluminescence quantum yield (PLQY), rapid radiative decay (kr), and fast reverse intersystem crossing rate (kRISC) poses a great challenge, particularly for the thermally activated delayed fluorescence (TADF) sensitizers targeting deep-blue HF device. Herein, by introducing a boron-containing multi-resonance-type acceptor into the multi-tert-butyl-carbazole encapsulated benzene molecular skeleton, two TADF emitters featuring hybridized multi-channel charge-transfer pathways, including short-range multi-resonance, weakened through-bond, and compact face-to-face through-space charge-transfer. Benefiting from the rational molecular design, the proof-of-concept sensitizers exhibit simultaneous rapid kr of 5.3 × 107 s-1, fast kRISC up to 5.9 × 105 s-1, a PQLY of near-unity, as well as ideal deep-blue emission in both solution and film. Consequently, the corresponding deep-blue HF devices not only achieve chromaticity coordinates that fully comply with the latest BT. 2020 standards, but also showcase record-high maximum external quantum efficiencies nearing 40%, along with suppressed efficiency roll-off.
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