j聚集增强热激活延迟荧光放大自发发射

Jinlong Zhu, Qing Liao, Han Huang, Liyuan Fu, Meihui Liu, Chunling Gu, H. Fu
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引用次数: 4

摘要

通过控制分子堆叠排列来调制激发态能级结构是调节荧光和热激活延迟荧光(TADF)放大自发发射(ASE)的有效策略,但仍然是一个关键的挑战。本文中,我们通过聚集体效应控制激发态动力学,证明了荧光和TADF ASE在有机晶体多晶中的调控作用。实验和理论研究表明,绿色晶体发射的是绿色荧光ASE,而红色晶体发射的是红色TADF ASE,这是因为红色晶体中较高的j聚集度显著导致单线态和三重态之间的能隙大幅减小至0.24 eV,从而实现了系统间的反向交叉过程。我们的研究结果表明,分子填充提供了一种强大的方法来定制辐射通道,并且对调谐纯有机晶体中的荧光和TADF ASE至关重要。
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J-Aggregation Enhanced Thermally Activated Delayed Fluorescence for Amplified Spontaneous Emission
Modulation of excited-state energy-level structures through controlled molecular-stacking arrangement provides an effective strategy to tuning fluorescence and thermally activated delayed fluorescence (TADF) amplified spontaneous emission (ASE), but remains a critical challenge. Herein, we demonstrated the regulation of fluorescence and TADF ASE in organic crystalline polymorphs by controlling the excited-state dynamics through aggregate effects. Experimental and theoretical studies show that green crystals emit green fluorescence ASE while red crystals emit red TADF ASE, because higher degree of J-aggregation in red crystals significantly results in a substantial decrease of energy gaps between singlet and triplet to 0.24 eV for the realization of reverse intersystem crossing process. Our results suggest that molecular packing presents a powerful approach to tailor the radiative channels and fundamentally important to tuning fluorescence and TADF ASE in pure organic crystals.
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