Revealing the excited-state mechanisms of the polymorphs of a hot exciton material

被引:0
|
作者
Deng, Ziqi [1 ]
Huang, Chao [1 ]
Luo, Yunfeng [1 ]
He, Jiaxing [1 ]
Li, Lan [1 ]
Pang, Xinyu [2 ]
Huang, Guanheng [1 ]
Phillips, David Lee [1 ]
机构
[1] Univ Hong Kong, Dept Chem, Pokfulam Rd, Hong Kong 999077, Peoples R China
[2] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Peoples R China
关键词
ACTIVATED DELAYED FLUORESCENCE; CHARGE-TRANSFER; MOLECULAR DESIGN; EMITTERS;
D O I
10.1038/s41467-024-55569-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
As the investigation of high efficiency thermally activated delayed fluorescence (TADF) materials become more mature, regulating the emission properties for single organic luminescence molecules has gained increasing interest recently. Herein, the donor-acceptor compounds F-AQ comprised of fluorene and anthraquinone is reported, and it exhibits a polymorphism with muti-color emission and TADF from high-level intersystem crossing (hRISC). The photodynamics and excited-state transient species were studied by femtosecond transient absorption (fs-TA) spectroscopy. As a result, an unambiguous signal of through space charge transfer (TSCT) was observed in the fs-TA spectra of the crystal with the pi-pi interaction between the fluorene and anthraquinone groups, whereas the other amorphous solids and crystal only show a conventional deactivation pathway of hRISC-TADF. In this study, we successfully realize the direct observation of the morphism-dependent TSCT in a crystal, which provides the observations in solid-state ultrafast excited-state dynamics and deepens the insight into the design of potential mechanochromic materials and thermochromic utilization of the polymorphism of organic luminescence molecules.
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页数:11
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