A cathodic photocorrosion-assisted strategy to construct a CdS/Pt heterojunction photocatalyst for enhanced photocatalytic hydrogen evolution

被引:12
|
作者
Fan, Jianming [1 ]
Xiong, Jinhua [1 ,2 ]
Liu, Dayue [1 ]
Tang, Yuanping [1 ]
He, Song [1 ]
Hu, Zhibiao [1 ]
机构
[1] Longyan Univ, Fujian Prov Key Lab Clean Energy Mat, Longyan 364000, Peoples R China
[2] Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350002, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORK; H-2; EVOLUTION; PHOTOCHEMICAL DEPOSITION; NANOPARTICLES; NANORODS; MOS2; SEPARATION; NANOSHEETS; MECHANISM; DEFECTS;
D O I
10.1039/d1nj01711j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel strategy was developed to fabricate a CdS/Pt photocatalyst (defined as CdS/w%Pt-PAR) via the cathodic photocorrosion effect of CdS. A tentative mechanism for Pt deposition on CdS via the cathodic photocorrosion effect was proposed, based on a series of electrochemical characterization methods, such as cyclic voltammetry and Mott-Schottky tests. Transmission electron microscopy verified that Pt was grafted on the CdS surface via a heterojunction. Moreover, a strong interaction between Pt and CdS was further confirmed by X-ray photoelectron spectroscopy. The optimal photocatalytic H-2 evolution rate of CdS/2%Pt-PAR was 1086.1 mu mol h(-1), 6.4 and 2.6 fold higher than that of the reference samples synthesized by traditional photodeposition (CdS/2%Pt-PD) and chemical reduction (CdS/2%Pt-CR) methods, respectively. Linear sweep voltammetry and fluorescence experiments verified that CdS/2%Pt-PAR has a lower H-2 evolution overpotential and faster separation of photogenerated carriers, respectively, compared with CdS/2%Pt-PD and CdS/2%Pt-CR. This work paves a new route for fabricating CdS/metal photocatalysts with highly efficient and stable photocatalytic H-2 evolution activity.
引用
收藏
页码:10315 / 10324
页数:10
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