系统间交叉
有机发光二极管
紫外线
激子
光电子学
简并能级
材料科学
光化学
物理
原子物理学
化学
激发态
纳米技术
凝聚态物理
量子力学
单重态
图层(电子)
作者
Haoyuan Qi,Hao Huang,Shuyao He,Shengnan Wang,Ling Peng,Yuchao Liu,Shanfeng Xue,Dongge Ma,Shian Ying,Shouke Yan
标识
DOI:10.1021/acsmaterialslett.4c02336
摘要
Ultraviolet (UV) organic light-emitting diodes (OLEDs) utilizing hybridized local and charge transfer (HLCT) emitters exhibit significant potential, where a favorable high-lying reverse intersystem crossing process is pivotal for attaining both triplet exciton utilization and low efficiency roll-off. Herein, a degenerate strategy induced by multiple donor moieties is proposed to design and synthesize a highly efficient UV HLCT fluorophore, namely 3,6-mCPCNC3. Comparatively, it not only demonstrates exceptional morphological stability and a rapid radiative decay rate but also enriches the reverse intersystem crossing channels from high-lying triplet to singlet states. Consequently, the 3,6-mCPCNC3-based device exhibits an astonishing external quantum efficiency (EQE) of 8.73% coupled with an impressive exciton utilization efficiency of 86.3%. Even at a luminance of 1000 cd m–2, the EQE still maintains a remarkable value of 8.29%, showcasing an exceptionally low efficiency roll-off. Remarkably, the device emits stable UV light with a peak wavelength at 389 nm and a narrow full-width half-maximum of 41 nm, corresponding to the color coordinates (0.161, 0.021). The record-high EQE achieved at 1000 cd m–2 represents the state-of-the-art efficiency among the currently reported UV-OLEDs operating at high luminance levels.
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