Regulating the Electronic Structure and Water Adsorption Capability by Constructing Carbon-Doped CuO Hollow Spheres for Efficient Photocatalytic Hydrogen Evolution

被引:27
作者
Wang, Fengliang [1 ]
Xiao, Linghan [1 ]
Chen, Jianmin [1 ]
Chen, Liyu [1 ]
Fang, Ruiqi [1 ]
Li, Yingwei [1 ]
机构
[1] South China Univ Technol, State Key Lab Pulp & Paper Engn, Sch Chem & Chem Engn, Guangzhou 510640, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon doping; copper oxide; hollow structure; metal-organic frameworks; photocatalytic H(2)production; HIGHLY EFFICIENT; DODECAHEDRAL CAGES; H-2; EVOLUTION; EOSIN-Y; CO2; FABRICATION; NANOFIBERS; REDUCTION; SHEETS;
D O I
10.1002/cssc.202001884
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Copper(II) oxide featuring a narrow bandgap and low toxicity has been frequently applied in the visible-light-driven photocatalytic hydrogen evolution, but it suffers from large intrinsic overpotential and low water adsorption capacity. Herein, we report a self-templated strategy for the preparation of carbon-doped CuO hollow spheres (C-CuO HSs) through thermal transformation of a hierarchical MOF. The hierarchical Cu-MOFs not only act as a template to form interior voids during the thermal transformation, but also serve as precursors to dope C atoms into the CuO lattice. The as-synthesized C-CuO HSs exhibits remarkable photocatalytic performance with a H(2)evolution rate of 67.3 mmol/g/h and the apparent quantum efficiency of 25.3 % at 520 nm in the present of eosin-Y photosensitizer. The high performance of C-CuO HSs is attributed to the hierarchical porous structure and modulated electronic structure of CuO by C-doping with well exposed reactive sites, high water adsorption capability, and low water reduction reaction barrier. The results presented in this work might shed light on the design of high-performance photocatalysts for various energy-related applications.
引用
收藏
页码:5711 / 5721
页数:11
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