Photoelectron directional transfer over a g-C3N4/CdS heterojunction modulated with WP for efficient photocatalytic hydrogen evolution

被引:60
作者
Jian, Qiyan [1 ,2 ,3 ]
Jin, Zhiliang [1 ,2 ,3 ]
Wang, Haiyu [1 ,2 ,3 ]
Zhang, Yongke [1 ,2 ,3 ]
Wang, Guorong [1 ,2 ,3 ]
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, State Ethn Affairs Commiss, Key Lab Chem Engn & Technol, Yinchuan 750021, Peoples R China
关键词
CHARGE SEPARATION; GENERATION; TIO2; PHOTOSTABILITY; NANOPARTICLES; CONSTRUCTION; COCATALYSTS; PERFORMANCE; FACETS;
D O I
10.1039/c8dt05110k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The separation and transfer of photoelectrons is a crucial factor in the process of photocatalysis. Herein, we successfully designed and prepared WP as a cocatalyst, modified the g-C3N4(CN)/CdS heterojunction structure, achieved the effective separation and directional transfer of photoelectrons, and also efficient photocatalytic hydrogen evolution. In addition, the as-prepared WP-CN/CdS composite photocatalyst not only prominently improved the separation and pre-assigned transfer of photogenerated electrons, but also had abundant surface active sites, which greatly improved the photocatalytic performance of the catalyst; namely, the highest photocatalytic activity of WP-CN/CdS was achieved at 5% WP content and the highest hydrogen production rate could reach 18238.89 mol h(-1) g(-1), which is about 12.49 times that of pure CdS. The detailed characterization studies with SEM, TEM, XRD, XPS, DRS, UV-vis, BET, transient photocurrent, FT-IR etc. effectively supported the abovementioned results, and all the characterization results were in good agreement with each other. Moreover, a possible mechanism of the photocatalytic reaction in the WP-CN/CdS system is proposed.
引用
收藏
页码:4341 / 4352
页数:12
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