磷光
系统间交叉
余辉
材料科学
光化学
兴奋剂
羧甲基纤维素
纳米技术
化学工程
化学
单重态
激发态
光电子学
荧光
光学
原子物理学
物理
伽马射线暴
工程类
钠
天文
冶金
作者
Zhengdong Zhao,Yuan Shen,Yang Liu,Jiaqi Wang,Mingjian Ma,Jiangbo Pan,Di Wang,Chengyu Wang,Jian Li
标识
DOI:10.1016/j.jcis.2024.05.227
摘要
The remarkable optical properties of carbon dots, particularly their tunable room-temperature phosphorescence, have garnered significant interest. However, challenges such as aggregation propensity and complex phosphorescence control via energy level manipulation during synthesis persist. Addressing these issues, we present a facile gel platform for tunable afterglow materials. This involves chemically cross-linking biomass-derived silicon-doped carbon dots with carboxymethylcellulose and incorporating non-precious metal salts (BaCl2, CaCl2, MgCl2, ZnCl2, ZnBr2, ZnSO4) to enhance phosphorescence. Metal salts boost intersystem crossing via spin–orbit coupling, elevating triplet state transitions and activating phosphorescence. Chemical bonding and salt-induced coordination/electrostatic interactions establish confinement effects, suppressing non-radiative transitions. Diverse salt-gel interactions yield gels with tunable phosphorescence lifetimes (9.48 ms to 32.13–492.39 ms), corresponding to afterglow durations ranging from 3.20 to 11.86 s. With its broad tunability and high recognition, this gel material exhibits promising potential for dynamic multilevel anti-counterfeiting applications.
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