石墨氮化碳
制氢
光催化
氢
材料科学
分解水
催化作用
碳纤维
钒
氮化物
化学工程
氮化碳
电子转移
纳米技术
光化学
化学
复合数
冶金
有机化学
复合材料
工程类
图层(电子)
作者
Mengmeng Shao,Yangfan Shao,Shengjie Ding,Jingwei Wang,Jinchen Xu,Yuanju Qu,Xiongwei Zhong,Xinman Chen,Weng Fai Ip,Ning Wang,Baomin Xu,Xingqiang Shi,X.‐S. Wang,Hui Pan
标识
DOI:10.1016/j.apcatb.2018.05.084
摘要
Highly efficient, earth-abundant, and low-cost photocatalysts are widely pursued for solar-driven hydrogen generation from water. Herein, we first report vanadium disulfide (VS2) with high hydrogen evolution reaction (HER) activity both in basal and edges to be the co-catalyst of graphitic carbon nitride (g-C3N4) for ultrahigh solar-driven hydrogen production. VS2-decorated g-C3N4 shows an impressing photocatalytic hydrogen evolution with a rate of 87.4 μmol/h, 26 times higher than pristine g-C3N4. Our combined experimental and computational studies reveal that the excellent efficiency of the composite is attributed to: (1) effective electron-hole separation and electron transfer from g-C3N4 to VS2, resulting from the optimal band alignment between VS2 and g-C3N4 and metallic characteristic of VS2; (2) fast hydrogen generation on the surface due to the high surface area and excellent HER activity of VS2. Our findings demonstrate that VS2/g-C3N4 may be applicable in solar-driven water splitting, and the design principle can be applied to search for novel photocatalysts.
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