Max Planck Institute for Polymer Research, Mainz, Germany
Martin Baumgarten (martin.baumgarten@mpip-mainz.mpg.de)
Paul W. M. Blom (blom@mpip-mainz.mpg.de)
Yungui Li (yungui.li@mpip-mainz.mpg.de)
收稿:2025-05-14,
修回:2025-09-12,
录用:2025-09-17,
网络出版:2026-01-01,
纸质出版:2026-01-31
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Dehai Dou, Wenlan Liu, Xin Zhou, 等. Simultaneous delayed fluorescence and phosphorescence in organic luminescent material employing multiple excited states[J]. Light: Science & Applications, 2026,15(1):151-166.
Dou, D. H. et al. Simultaneous delayed fluorescence and phosphorescence in organic luminescent material employing multiple excited states. Light: Science & Applications, 15, 151-166 (2026).
Dehai Dou, Wenlan Liu, Xin Zhou, 等. Simultaneous delayed fluorescence and phosphorescence in organic luminescent material employing multiple excited states[J]. Light: Science & Applications, 2026,15(1):151-166. DOI: 10.1038/s41377-025-02063-x.
Dou, D. H. et al. Simultaneous delayed fluorescence and phosphorescence in organic luminescent material employing multiple excited states. Light: Science & Applications, 15, 151-166 (2026). DOI: 10.1038/s41377-025-02063-x.
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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