Improving the photocatalytic activity of benzyl alcohol oxidation by Z-scheme SnS/g-C3N4

被引:29
|
作者
Li, Yan [1 ]
Pan, Chengsi [1 ]
Wang, Guangli [1 ]
Leng, Yan [1 ]
Jiang, Pingping [1 ]
Dong, Yuming [1 ]
Zhu, Yongfa [2 ]
机构
[1] Jiangnan Univ, Int Joint Res Ctr Photorespons Mol & Mat, Sch Chem & Mat Engn, Wuxi 214122, Jiangsu, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
FACILE SYNTHESIS; SELECTIVE OXIDATION; NANOCOMPOSITES; HETEROJUNCTION; CONSTRUCTION; BENZALDEHYDE; PERFORMANCE; EFFICIENCY; MECHANISM; DESIGN;
D O I
10.1039/d1nj00923k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Until now, the effective photocatalytic oxidation of benzyl alcohol to benzaldehyde with high selectivity is still a great challenge. It is reported that the carrier separation rate is the key factor affecting the photocatalytic activity, and the formation of heterojunction is an effective solution to hinder electron-hole recombination. SnS with a narrow band gap has excellent light absorption performance, which covers the whole visible light region. After compounding with g-C3N4, the light utilization of the SnS/g-C3N4 photocatalyst is effectively improved. In addition, a Z-scheme heterojunction is formed between SnS and g-C3N4 due to the matched energy levels, which accelerates the separation of electrons and holes and improves the conversion of benzyl alcohol effectively. In this paper, the charge separation is accelerated to promote the reaction by the in situ construction of Z-scheme heterojunctions; the preparation method, reaction mechanism and energy level structure of the photocatalyst can play a certain guiding role in the organic conversion reaction.
引用
收藏
页码:6611 / 6617
页数:7
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