磷光
系统间交叉
三重态
分子内力
光化学
咔唑
二苯并呋喃
发光
材料科学
化学
光电子学
分子
单重态
原子物理学
荧光
激发态
物理
有机化学
光学
作者
Weijun Zhao,Tsz Shing Cheung,Nan Jiang,Wenbin Huang,Jacky W. Y. Lam,Xuepeng Zhang,Zikai He,Ben Zhong Tang
标识
DOI:10.1038/s41467-019-09561-8
摘要
Abstract Persistent luminescence is a fascinating phenomenon with exceptional applications. However, the development of organic materials capable of persistent luminescence, such as organic persistent room-temperature phosphorescence, lags behind for their normally low efficiency. Moreover, enhancing the phosphorescence efficiency of organic luminophores often results in short lifetime, which sets an irreconcilable obstacle. Here we report a strategy to boost the efficiency of phosphorescence by intramolecular triplet-triplet energy transfer. Incorpotation of (bromo)dibenzofuran or (bromo)dibenzothiophene to carbazole has boosted the intersystem crossing and provided an intramolecular triplet-state bridge to offer a near quantitative exothermic triplet–triplet energy transfer to repopulate the lowest triplet-state of carbazole. All these factors work together to contribute the efficient phosphorescence. The generation and transfer of triplet excitons within a single molecule is revealed by low-temperature spectra, energy level and lifetime investigations. The strategy developed here will enable the development of efficient phosphorescent materials for potential high-tech applications.
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