Noble-metal-free metallic MoC combined with CdS for enhanced visible-light-driven photocatalytic hydrogen evolution

被引:56
作者
Lei, Yonggang [1 ]
Wu, Xingwang [1 ]
Li, Shuhui [1 ]
Huang, Jianying [1 ,2 ]
Ng, Kim Hoong [3 ]
Lai, Yuekun [1 ,2 ]
机构
[1] Fuzhou Univ, Coll Chem Engn, Natl Engn Res Ctr Chem Fertilizer Catalyst NERC C, Fuzhou 350116, Peoples R China
[2] Qingyuan Innovat Lab, Quanzhou 362801, Peoples R China
[3] Ming Chi Univ Technol, Dept Chem Engn, New Taipei 24301, Taiwan
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
MoC; CdS; Visible light; Cocatalyst; Photocatalytic hydrogen production; H-2; EVOLUTION; QUANTUM DOTS; NANOSHEETS; COCATALYST; CATALYSTS; GRAPHENE; NANOPARTICLES; PERFORMANCE; WATER;
D O I
10.1016/j.jclepro.2021.129018
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Exploration of efficient and stable transition metal-based co-catalyst is of great importance for large-scale hydrogen production in the mean of photocatalytic water splitting. Herein, we propose an effective CdS/MoC photocatalyst for enhanced photocatalytic H-2 evolution under visible light irradiation (>= 420 nm). Upon coupling to CdS through a facile solution-mixing method, MoC was functionalized as an effective co-catalyst that accepts interface electron from CdS while promoting charges separation. Furthermore, DFT also confirmed a facilitated H* adsorption on CdS/MoC through its lowered Gibbs free energy (Delta G(H)*) of 0.37 eV, which is beneficial for H-2 production too. As a result, the optimum photocatalyst, with 5 wt% MoC coupled to CdS, induces the best hydrogen production rate of 224.5 mu mol h(-1), which is 7.5 times higher than that of pristine CdS. Meanwhile, an apparent quantum efficiency (AQE) of 7.6% was also recorded at 420 nm. In terms of H-2 generation, the synthesized CdS/MoC (5 wt%) is more superior to CdS/Pt (5 wt%) in an extent of 44.5%. This work confirms the competency of MoC as an effective cocatalyst and promising alternative to benchmarked Pt for photocatalytic hydrogen production from water.
引用
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页数:11
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