余辉
青色
材料科学
发光
纳米技术
化学
光化学
化学物理
光电子学
光学
物理
天文
伽马射线暴
作者
Siqian Cui,Bowei Wang,Yuxuan Zan,Zhuoyao Shen,Shuai Liu,Wangwang Fang,Xilong Yan,Li Yang,Ligong Chen
标识
DOI:10.1016/j.cej.2021.133373
摘要
Metal-free afterglow materials have brought about widespread attention due to application advantages. Nevertheless, it is an attractive but formidable challenge to achieve long-persistent afterglow materials with high quantum yield (QY) at ambient conditions. Particularly, those with tunable afterglow are very rare. Herein, an economical strategy is proposed to construct a series of multi-color (cyan, green and orange) afterglow materials via one-step melting (within 5–10 min) of boric acid (BA) with unconventional precursors. The highly rigid framework, B − C bond and hydrogen bond interactions can efficiently inhibit non-radiative deactivation by locking the triplet excitons in carbon dots (CDs) clusters. 66.13% high QY and 1.74 s long lifetime have been achieved simultaneously, as well as the afterglow can be observed by naked eyes for ∼ 26 s. According to the adjustment of the precursor structure, dynamic afterglow color-changing (from orange, yellow, white to cyan) material was successfully realized. These excellent features allow them to be more applicable in time-resolved information security. In brief, this work provides a simple, flexible and effective strategy to construct highly efficient afterglow materials, and further facilitates their optical regulation and various potential applications.
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