Deng Ziqi, Huang Chao, Luo Yunfeng, He Jiaxing, Li Lan, Pang Xinyu, Huang Guanheng, Phillips David Lee
Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, 999077, China.
Department of Chemistry, Southern University of Science and Technology, Shenzhen, 518055, China.
Nat Commun. 2025 Jan 2;16(1):258. doi: 10.1038/s41467-024-55569-0.
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 π-π 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.
随着高效热激活延迟荧光(TADF)材料的研究日益成熟,调控单个有机发光分子的发射特性近来受到越来越多的关注。在此,报道了由芴和蒽醌组成的供体-受体化合物F-AQ,它表现出多态性,具有多色发射以及来自高能级系间窜越(hRISC)的TADF。通过飞秒瞬态吸收(fs-TA)光谱研究了光动力学和激发态瞬态物种。结果,在芴和蒽醌基团之间存在π-π相互作用的晶体的fs-TA光谱中观察到了明确的空间电荷转移(TSCT)信号,而其他非晶态固体和晶体仅显示出hRISC-TADF的传统失活途径。在本研究中,我们成功地在晶体中实现了对形态依赖的TSCT的直接观测,这为固态超快激发态动力学提供了观测结果,并加深了对潜在机械变色材料设计以及有机发光分子多态性的热致变色利用的理解。