磷光
系统间交叉
激发态
量子产额
荧光
发光
光致发光
材料科学
光化学
单重态
辐射传输
基态
持续发光
光电子学
量子效率
自发辐射
三重态
原子物理学
紫外线
分子物理学
有机发光二极管
原子电子跃迁
波长
作者
Dehai Dou,wenlan Liu,Xin Zhou,Qiqi Yang,Xiao Tan,Naz Ugur,Chongyao Li,Charusheela Ramanan,X. Liu,Gert‐Jan A. H. Wetzelaer,Denis Andrienko,Martin Baumgarten,Paul W. M. Blom,Yungui Li
标识
DOI:10.1038/s41377-025-02063-x
摘要
Abstract Triplet dynamics play a key role in room temperature phosphorescence (RTP) and thermally activated delayed fluorescence (TADF). In this work, we report a model emitter with three emission components: prompt fluorescence (PF) in nanoseconds, delayed fluorescence in microseconds, and RTP in milliseconds, with the emission spectrum ranging from ultraviolet to deep blue. We experimentally and theoretically verify that a second triplet excited state, T 2 , below the singlet state S 1 is involved in facilitating simultaneous PF, TADF, and RTP in the model emitter. The reverse intersystem crossing (rISC) from T 2 to S 1 contributes to the TADF, while the radiative transition from T 1 to the ground state is the origin of the long-lived RTP. By transferring the energy of multiple excited states to a series of conventional fluorescence emitters, a multi-color emissive system covering the entire visible wavelength range has been realized, with the photoluminescence decay ranging from 10 −9 s to 10 −1 s. By slightly tuning the energy difference between these excited states in the model molecule, a highly efficient organic luminescent material with only PF and RTP emission has been obtained with an RTP quantum yield above 30%. This work provides insights into the key role of higher-lying triplet states in the development of efficient TADF and RTP materials.
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