Co3O4/CdS p-n heterojunction for enhancing photocatalytic hydrogen production: Co-S bond as a bridge for electron transfer

被引:109
作者
Chen, Liuyun [1 ]
Xie, Xinling [1 ]
Su, Tongming [1 ]
Ji, Hongbing [1 ,2 ]
Qin, Zuzeng [1 ]
机构
[1] Guangxi Univ, Sch Chem & Chem Engn, Guangxi Key Lab Electrochem Energy Mat, Nanning 530004, Peoples R China
[2] Sun Yat Sen Univ, Sch Chem, Fine Chem Ind Res Inst, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalytic water splitting; Hydrogen production; P-n heterojunction; Co-S bond; GRAPHENE OXIDE; WATER; CDS; PERFORMANCE; REDUCTION; TIO2; NANOPARTICLES; EVOLUTION; SHELL; ENHANCEMENT;
D O I
10.1016/j.apsusc.2021.150849
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
Photocatalytic hydrogen production from water splitting production is a promising strategy to solve the energy crisis and environmental pollution. In the present work, Co3O4/CdS composites were prepared by ultrasonication and stirring, and used for photocatalytic water splitting. The results showed a Co-S chemical bonds were formed at the interfaces between the Co3O4 and the CdS, which promoted the charge transfer rate between the CdS and Co3O4. Meanwhile, the recombination of the electron-hole pairs was further restrained by the Co3O4/CdS p-n heterojunction. The 10%-Co3O4/CdS composites exhibited an excellent photocatalytic hydrogen production rate of 142.62 mu mol.h(-1), which was 20 times higher than that of CdS (6.85 mu mol.h(-1)), and the Co3O4/CdS showed excellent stability in the photocatalytic water splitting reaction. Moreover, a formation process of Co3O4/CdS p-n heterojunction and a mechanism of Co3O4/CdS p-n heterojunction avoiding the recombination of photocatalytic electrons and holes to enhance photocatalytic activity was proposed.
引用
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页数:13
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