Targeting Compact and Ordered Emitters by Supramolecular Dynamic Interactions for High‐performance Organic Ambient Phosphorescence

磷光 材料科学 系统间交叉 超分子化学 纳米技术 激子 光电子学 荧光 有机化学 分子 单重态 量子力学 物理 激发态 核物理学 化学
作者
Guang‐Qiang Yin,Jiayin Zhou,Wei Lü,Longqiang Li,Depeng Liu,Min Qi,Ben Zhong Tang,Patrick Théato,Tao Chen
出处
期刊:Advanced Materials [Wiley]
被引量:9
标识
DOI:10.1002/adma.202311347
摘要

Abstract Purely organic room‐temperature phosphorescence (RTP) materials have received intense attention due to their fascinating optical properties and advanced optoelectronic applications. The promotion of intersystem crossing (ISC) and minimalization of nonradiative dissipation under ambient conditions are key prerequisites for realizing high‐performance organic RTP; However, the ISC process is generally inefficient for organic fluorogens and the populated triplet excitons are always too susceptible to be well stabilized by conventional means. Particularly, organizing organic fluorophores into compact and ordered entities by supramolecular dynamic interactions has proven to be a newly‐emerged strategy to boost the ISC process greatly and suppress the non‐radiative relaxations immensely, facilitating the population and stabilization of triplet excitons to access high‐performance organic RTP. Consequently, well‐defined organic emitters enable robust RTP emission even in the solution state, thus greatly extending the applications. Here, this review is focused on a timely and brief introduction to recent progress in tailoring ordered high‐performance RTP emitters by supramolecular dynamic interactions. Their typical preparation strategies, optoelectronic properties, and applications are thoroughly summarized. In the summary section, key challenges and perspectives of this field are highlighted to suggest potential directions for future study.
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