1D metallic MoO2-C as co-catalyst on 2D g-C3N4 semiconductor to promote photocatlaytic hydrogen production

被引:76
作者
Chen, Zhigang [1 ]
Xia, Kaixiang [1 ]
She, Xiaojie [1 ]
Mo, Zhao [1 ]
Zhao, Shuowei [2 ]
Yi, Jianjian [1 ]
Xu, Yuanguo [1 ]
Chen, Hanxiang [3 ]
Xu, Hui [1 ]
Li, Huaming [1 ]
机构
[1] Jiangsu Univ, Inst Energy Res, Sch Environm & Safety Engn, Zhenjiang 212013, Peoples R China
[2] Jiangsu Univ, Environm Sci Res Inst Zhenjiang, Zhenjiang 212000, Peoples R China
[3] Nanjing Univ Informat Sci & Technol, Sch Environm & Chem Engn, Nanjing 210044, Jiangsu, Peoples R China
关键词
Metallic MoO2-C; g-C3N4; Noble-metal-free co-catalyst; Hydrogen production; CARBON NITRIDE NANOSHEETS; PHOTOCATALYTIC PERFORMANCE; SUPPORTING COCATALYST; GRAPHENE; ADSORPTION; CATALYSTS; STORAGE; OXIDE; MOS2; C3N4;
D O I
10.1016/j.apsusc.2018.03.226
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 surface carrier density and hydrogen activation ability are crucial in photocatalytic hydrogen evolution reaction (HER), which can be improved by introducing noble-metal co-catalyst such as Pt into the system. However, the noble-metals suffer from high cost in terms of upscaling, thereby the exploration of low-cost HER co-catalysts is highly demanded. In this work, we report that one-dimensional (1D) metallic MoO2-C nanowire clusters can serve as a co-catalyst in assisting the photocatalytic hydrogen production over 2D g-C3N4. The multiple merits of MoO2-C are demonstrated: (i) noble-metal-free; (ii) highly effective transfer ability of the photogenerated electrons; (iii) high-density adsorption and active sites for hydrogen evolution. As demonstrated in photocatalytic hydrogen production, MoO2-C/2D g-C3N4 exhibits significant enhancement in comparison with pure 2D g-C3N4 semiconductor. The optimal hydrogen evolution rate achieving 1071.0 mu mol g(-1) h(-1), almost 157.5 times higher than that of pure 2D g-C3N4. (C) 2018 Published by Elsevier B.V.
引用
收藏
页码:732 / 739
页数:8
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