磷光
材料科学
系统间交叉
电离
光化学
光电子学
化学
荧光
激发态
原子物理学
光学
单重态
物理
离子
有机化学
作者
Qijun Li,Shuai Meng,Yuchen Li,Dengke Cheng,Hailing Gu,Zhenxiao Zhao,Zikang Tang,Jing Tan,Songnan Qu
出处
期刊:Carbon
[Elsevier]
日期:2022-08-01
卷期号:195: 191-198
被引量:56
标识
DOI:10.1016/j.carbon.2022.03.063
摘要
Stimuli-responsive phosphorescence materials with dynamic color-changing properties are highly promising for advanced information security. Herein, we demonstrate a novel strategy that effectively induces tunable dynamic phosphorescence color from carbon dots (CDs) on papers via surface ionization engineering for multimode encryption and information storage. Alkali-induced phenolic hydroxyl ionization on CDs can boost intersystem crossing rates, while surface-ionized groups with negative charges significantly passivate the surface defects and reduce non-radiative transitions, which can activate surface state-related blue phosphorescence emission. Combined with the carbon core state-related yellow-green phosphorescence, excitation/time-dependent phosphorescence color-changing from yellow-green to blue are realized from alkali (Na2CO3) treated CDs on paper. Furthermore, benefiting from the transition from NaHCO3 to Na2CO3 under thermal treatment, dynamic color-changing phosphorescence can also be activated by thermally stimulating NaHCO3-treated CDs on paper. Finally, multi-stimuli (alkali or thermal) and multi-modal dynamic phosphorescent colors from a single CDs system are realized for the first time. Based on these unique features, multimode encryption and smart 3D codes with anti-counterfeiting and monitoring functions for medicine during transport or storage are demonstrated by combining an inkjet printing technique using CD inks.
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