半最大全宽
基态
激发态
粘结长度
发射光谱
谱线
有机发光二极管
材料科学
窄带
分子物理学
计算物理学
原子物理学
化学
光学
光电子学
物理
纳米技术
分子
量子力学
图层(电子)
作者
Xubin Wang,Changwei Wang,Shiwei Yin
标识
DOI:10.1021/acs.jctc.4c00766
摘要
Color purity is crucial for achieving a high-quality organic light-emitting diode. An essential property for evaluating color purity is the full width at half-maximum (fwhm) of emission spectra. Theoretically estimating fwhm requires the detailed knowledge of vibronic coupling constants for all vibrational modes, which is time-consuming to obtain via quantum mechanical calculations, particularly for optimizing the geometry of the lowest singlet excited state. These calculations pose a bottleneck for high-throughput screening of narrowband emitters. To address this challenge, we propose a simple model to assess the reorganization energy based on the relationship between bond-length alteration (ΔBL) and vertical bond-order alteration (ΔBO) in optimized ground-state structures. Additionally, a one-mode model is employed to rapidly and effectively estimate fwhm. Our new model yields results comparable to experimental data and more accurate theoretical approaches based on vibronic coupling constants of all vibrational modes but with significantly lower computational costs. This model holds promise for the virtual screening of narrowband emitter candidates.
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