Compound SnS2 sensitizer in the S-scheme of Ag2Mo2O7/CoMoO4 heterojunction to improve the hydrogen evolution of semiconductor powder

被引:15
|
作者
Liu, Zhenlu [1 ]
Xu, Jing [1 ,2 ,3 ]
Li, Zezhong [1 ]
Xu, Shengming [1 ]
Liu, Xinyu [1 ]
机构
[1] North Minzu Univ, Sch Chem & Chem Engn, Yinchuan 750021, Peoples R China
[2] North Minzu Univ, Ningxia Key Lab Solar Chem Convers Technol, Yinchuan 750021, Peoples R China
[3] North Minzu Univ, Key Lab Chem Engn & Technol, State Ethn Affairs Commiss, Yinchuan 750021, Peoples R China
关键词
Photocatalysis; S-scheme heterojunction; Ag2Mo2O7; PHOTOCATALYTIC H-2 PRODUCTION; REDUCED GRAPHENE OXIDE; ELECTROCHEMICAL PROPERTIES; STORAGE MECHANISM; ANODE MATERIAL; ENERGY; PERFORMANCE; RODS; SUPERCAPACITORS; NANOPARTICLES;
D O I
10.1016/j.ijhydene.2022.11.311
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The heterojunction construction can effectively regulate the carrier transport pathway. Ag2Mo2O7/CoMoO4 composite molybdate material was successfully synthesized by one step hydrothermal calcination method. The preparation method makes the contact of the two molybdate salts closer, forming a stable S-scheme heterojunction. Then SnS2 was added under physical agitation to improve the mobility of photogenerated carriers. The excellent structure of the ternary composite catalyst was proved by morphology and element analysis. The electron transfer mechanism of the S-scheme heterojunction was studied by photoelectric chemical test and spectral analysis. Because of the successful construction of S-scheme heterojunction and the introduction of sensitizer SnS2, the composite catalyst showed excellent hydrogen evolution performance (1599 mmol & BULL;g-1 & BULL;h-1). This is because the S-scheme heterojunction and the sensitizer cooperatively promote the electron accumulation at the conduction band of CoMoO4. This work will provide a new strategy for molybdate in a heterojunction construction scheme.& COPY; 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:20303 / 20313
页数:11
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