石墨氮化碳
光催化
光化学
光致发光
氮化碳
材料科学
光降解
吸收边
化学
催化作用
可见光谱
荧光
量子产额
带隙
光电子学
有机化学
物理
量子力学
作者
Yongli Li,Peipei Li,Jinshu Wang,Yilong Yang,Wenqing Yao,Zhen Wei,Junshu Wu,Xiaoxiao Yan,Xiangfeng Xu,Yuhan Liu,Yongfa Zhu
标识
DOI:10.1016/j.apcatb.2017.12.017
摘要
A one-step salt melt assisted thermal polymerization for the synthesis of nitrogen-rich water soluble graphitic carbon nitride (WS-GCN) is presented. The as-prepared WS-GCN shows strong tunable excitation-emission pathways that have multi-colored photoluminescence from blue to green with extremely high absolute quantum yields (AQY) of 22%, which is almost 6 fold of pristine graphitic carbon nitride (GCN) nanosheets. It also shows significant red-shift of response edge benefiting from the narrowed band energy, due to the feature of N-defected surface and N-rich inner of WS-GCN. After being decorated onto TiO2, the WS-GCN endows a great enhancement of NO-photodegradation under visible light irradiation, 5.5-fold increase to comparison with what the pristine GCN does. Further, the starting edge of photocatalysis is enlarged to about 650 nm for TiO2/WS-GCN from about 450 nm for TiO2/GCN. This is ascribed to both enhanced light-response range and efficiently restraining the radiative transition probability of WS-GCN owing to the migration of photoinduced electrons from the CB of WS-GCN to TiO2. This multi-functional material may provide a way for the development of bio-imaging, file secrecy and broad absorption photocatalysts.
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