Construction of Direct Z-Scheme Heterojunction NiFe-Layered Double Hydroxide (LDH)/Zn0.5Cd0.5S for Photocatalytic H2 Evolution

被引:44
|
作者
Sun, Yidong [1 ,2 ]
Wang, Xingpu [3 ]
Fu, Qiang [1 ,2 ,4 ]
Pan, Chunxu [1 ,2 ,4 ]
机构
[1] Wuhan Univ, Sch Phys & Technol, Wuhan 430072, Peoples R China
[2] Wuhan Univ, MOE Key Lab Artificial Micro & Nanostruct, Wuhan 430072, Peoples R China
[3] Beihang Univ, Sch Chem, Key Lab Bioinspired Smart Interfacial Sci & Techn, Minist Educ, Beijing 100191, Peoples R China
[4] Wuhan Univ, Ctr Electron Microscopy, Wuhan 430072, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
photocatalytic H-2 evolution; NiFe-LDH/Zn0.5Cd0.5S; energy conversion; direct Z-scheme photocatalyst; LDH; PERFORMANCE; REDUCTION; NANORODS; CAGES; CDS; CO2;
D O I
10.1021/acsami.1c09650
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
It is of great significance to construct heterojunctions using industrially produced co-catalysts. The direct Z-scheme composite photocatalyst provides an effective separation of photogenerated carriers. Herein, a kind of novel 2D/3D direct Z-scheme NiFe-LDH/Zn0.5Cd0.5S is prepared. Compared with fresh catalysts, the NiFe-layered double hydroxide (LDH)/Zn0.5Cd0.5S composite exhibits advantages including excellent visible light response ability and photoelectric performance and improved H-2 evolution rate by 11.6 times. Combining with theoretical calculations, ESR, XPS, and experimental results, the direct Z-scheme mechanism of the photocatalytic reaction is proposed. There is a channel for electron transfer between Zn0.5Cd0.5S and NiFe-LDH, and the electrons of Zn0.5Cd0.5S directly combine with the valence band holes of NiFe-LDH. Finally, the electrons remaining on NiFe-LDH can reduce H+ to generate H-2. This process effectively achieves separation of photogenerated carriers and increases photocatalytic H-2 evolution.
引用
收藏
页码:39331 / 39340
页数:10
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