2D ultrathin CoP modified MnxCd1-xS with controllable band structure and robust photocatalytic performance for hydrogen generation

被引:32
作者
Chen, Ran [1 ]
Ao, Yanhui [1 ]
Wang, Chao [1 ]
Wang, Peifang [1 ]
机构
[1] Hohai Univ, Key Lab Integrated Regulat & Resource Dev Shallow, Coll Environm, 1 Xikang Rd, Nanjing 210098, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
LIGHT-DRIVEN PHOTOCATALYST; IN-SITU SYNTHESIS; MN-CD-S; H-2; EVOLUTION; HYDROTHERMAL SYNTHESIS; SOLID-SOLUTION; MOS2; NANOSHEETS; WATER; NANOPARTICLES; COCATALYST;
D O I
10.1039/c9dt02849h
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Considerable efforts have been directed towards constructing high-efficiency, earth-abundant and low-cost photocatalysts for hydrogen evolution under visible light irradiation. In this work, 2D ultrathin CoP-decorated bimetallic MnxCd1-xS photocatalysts were developed based on the combined strategies of controllable band structure and co-catalyst modification. An optimal H-2 production rate of 65 324 mu mol g(-1) h(-1) was obtained for the Mn0.5Cd0.5S/CoP-4% sample under visible light irradiation, which was 4.26 times higher than that of pure Mn0.5Cd0.5S as well as 38.7 times that of pure CdS. UV-vis and MS characterization results showed that the introduction of Mn into CdS could change the band potential towards a more negative direction, which would be beneficial for water reduction. Moreover, the added CoP could act as a co-catalyst to facilitate the electron transfer and restrain the recombination of photogenerated electron-hole pairs, which was testified by photocurrent, PL and EIS analyses. This work paves the way to offer a new direction towards designing efficient photocatalysts for hydrogen evolution.
引用
收藏
页码:14783 / 14791
页数:9
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