Band Engineering and Morphology Control of Oxygen-Incorporated Graphitic Carbon Nitride Porous Nanosheets for Highly Efficient Photocatalytic Hydrogen Evolution

被引:6
作者
Yunyan Wu [1 ,2 ]
Pan Xiong [1 ]
Jianchun Wu [2 ,3 ]
Zengliang Huang [2 ]
Jingwen Sun [1 ]
Qinqin Liu [2 ]
Xiaonong Cheng [2 ]
Juan Yang [1 ,2 ]
Junwu Zhu [1 ]
Yazhou Zhou [2 ]
机构
[1] Key Laboratory for Soft Chemistry and Functional Materials, Ministry of Education, Nanjing University of Science and Technology
[2] School of Materials Science and Engineering, Jiangsu University
[3] Institute of Nuclear Science and Technology, Sichuan University
基金
美国国家科学基金会;
关键词
D O I
暂无
中图分类号
TQ116.2 [氢气]; TQ426 [催化剂(触媒)]; TB383.1 [];
学科分类号
070205 ; 080501 ; 080502 ; 0817 ; 081705 ; 1406 ;
摘要
Graphitic carbon nitride(g-C3N4)-based photocatalysts have shown great potential in the splitting of water. However, the intrinsic drawbacks of g-C3N4, such as low surface area, poor diffusion, and charge separation efficiency, remain as the bottleneck to achieve highly efficient hydrogen evolution. Here, a hollow oxygen-incorporated g-C3N4nanosheet(OCN) with an improved surface area of 148.5 m~2g-1is fabricated by the multiple thermal treatments under the N2/O2atmosphere, wherein the C–O bonds are formed through two ways of physical adsorption and doping. The physical characterization and theoretical calculation indicate that the O-adsorption can promote the generation of defects, leading to the formation of hollow morphology, while the O-doping results in reduced band gap of g-C3N4. The optimized OCN shows an excellent photocatalytic hydrogen evolution activity of 3519.6 μmol g-1h-1for ~ 20 h, which is over four times higher than that of g-C3N4(850.1 μmol g-1h-1) and outperforms most of the reported g-C3N4catalysts.
引用
收藏
页码:101 / 112
页数:12
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