半最大全宽
有机发光二极管
量子效率
材料科学
光致发光
光电子学
系统间交叉
量子产额
咔唑
偶极子
二极管
激发态
单重态
荧光
光学
光化学
化学
物理
纳米技术
原子物理学
有机化学
图层(电子)
作者
Jihoon Kang,Soon Ok Jeon,Ha Lim Lee,Junseop Lim,Unhyeok Jo,Jun Yeob Lee
标识
DOI:10.1016/j.mattod.2023.09.002
摘要
Excellent color purity and high external quantum efficiency (EQE) are major requirements in the development of deep-blue organic light-emitting diodes (OLEDs). To achieve this, multiple-resonance (MR)–thermally activated delayed fluorescence (TADF) emitters have been considered as promising options. Herein, we suggest a novel expanded MR design strategy to fabricate deep-blue MR–TADF emitters derived from a fused indolo[3,2,1-jk]carbazole framework. The expanded MR structure managed a triplet excited state for the accelerated spin–vibronic coupling-assisted reverse intersystem crossing and increased the emission dipole orientation while maintaining the high efficiency and deep-blue emission color. The rigid and planar structure of the MR core yielded a small full-width at half-maximum (FWHM; less than 16 nm), high photoluminescence quantum yield (over 97%), and high horizontal emitting dipole orientation (over 90%), and facilitated a second-order spin–vibronic coupling-assisted triplet-to-singlet spin crossover. The fabricated MR–TADF OLEDs recorded a high EQE of 24.3% and FWHM of 21 nm at a CIEy of 0.044, thereby satisfying the BT.2020 blue standard. Additionally, further optimized device architecture provided an EQE of 26.8%.
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