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
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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