材料科学
磷光
激发
余辉
发光
碳纤维
光电子学
光致发光
航程(航空)
大气温度范围
煅烧
光化学
波长
可见光谱
纳米晶
发射光谱
光子上转换
荧光粉
工作(物理)
作者
Ziting Zhong,Jinkun Liu,Jueran Cao,Zhun Ran,Yong Li,Xuejie Zhang,Jianle Zhuang,Chaofan Hu
标识
DOI:10.1002/adom.202503439
摘要
ABSTRACT Developing single‐component carbon dot (CD)‐based composites with long‐lived emission, tunable colors, and broad excitation range remains scientifically challenging. Herein, CDs and alumina composites (CDs@Al 2 O 3 ) with broad excitation range were synthesized through a one‐step calcination method using benzamide as the carbon source. The room temperature phosphorescence (RTP) emission color shifts from blue to green to yellow as excitation wavelength increases. CDs@Al 2 O 3 synthesized at an optimized calcination temperature of 500°C exhibits lifetimes of up to 1.36 s under 258 nm excitation and 0.63 s at 520 nm. Photophysical analysis reveals that the multicolor afterglow originates from multiple emission centers within the CDs. N, O co‐doping creates novel surface states, while the rigid matrix confines emission centers, suppressing non‐radiative decay and enabling phosphorescence tuning. CDs@Al 2 O 3 demonstrates potential in anti‐counterfeiting and information encryption due to its unique optical properties. This work provides a novel strategy for designing single‐component optical materials with color‐tunable emission and broad excitation range.
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