余辉
磷光
掺杂剂
系统间交叉
分子间力
发光
激发态
材料科学
光化学
化学物理
荧光
化学
兴奋剂
原子物理学
光电子学
单重态
分子
有机化学
物理
光学
伽马射线暴
天文
作者
Zhe Mo,Xiaogang Wang,Jiuyang Li,Qianqian Yan,Kaka Zhang
标识
DOI:10.1021/acs.jpclett.3c03060
摘要
Dopant-matrix organic afterglow materials exhibit ease of fabrication and intriguing functions in diverse fields. However, a deep and comprehensive understanding of their photophysical behaviors remains elusive. Here we report manipulation of a room-temperature phosphorescence/thermally activated delayed fluorescence (RTP/TADF) afterglow mechanism via the mismatch/match of intermolecular charge transfer between dopants and matrices. When dispersed in inert crystalline matrices, the luminescent dopants show RTP lifetimes up to 2 s. Interestingly, when suitable organic matrices are selected, the resultant dopant-matrix materials display a TADF-type afterglow under ambient conditions due to the formation of dopant-matrix intermolecular charge transfer complexes. Detailed studies reveal that reverse intersystem crossing from dopants' T1 states to charge transfer complexes' S1 states, which features a moderate kRISC of 101-102 s-1, is responsible for the emergence of a TADF-type organic afterglow in rigid crystalline matrices. Such less reported delicate photophysics reveals a new aspect of the excited state property in dopant-matrix afterglow systems.
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