磷光
单独一对
激子
离域电子
激发态
杂原子
化学
化学物理
材料科学
原子物理学
物理
分子
凝聚态物理
量子力学
戒指(化学)
有机化学
荧光
作者
Fulong Ma,Bo Wu,Siwei Zhang,Jinhui Jiang,Jinghong Shi,Zeyang Ding,Yue Zhang,Haozhe Tan,Parvej Alam,Jacky W. Y. Lam,Yujiu Xiong,Zhen Li,Ben Zhong Tang,Zhaoke Zheng
标识
DOI:10.26434/chemrxiv-2024-z9sfs
摘要
The generation and stabilization of triplet excitons is the key to realize efficient organic room temperature phosphorescence (RTP), which is challenging owing to the obscure mechanism and structure-property relationships. Herein, a strategy of lone pairs-mediated multiple through-space interactions is proposed to availably induce RTP. By introducing through-space nn and n interactions by dint of heteroatoms, the lone pairs are delocalized within the structure, causing dense excited-state energy level splitting. Thus, more matched energy levels with small energy gap between singlet and triplet states appear, resulting in multiple ISC transition channels which assist triplet excitons generation. The strong TSIs also effectively rigidify the molecular structures and thus stabilize generated triplet excitons for radiation. Furthermore, the manipulation of TSIs intensity allows efficiency enhancement, lifetime prolongation, and tolerance to high temperature of RTP. This work not only explores the fundamental principle of RTP mechanism from a new view, but also provides a universal strategy for ISC promotion and triple excitons stabilization.
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