Photocatalytic CO2 reduction over B4C/C3N4 with internal electric field under visible light irradiation

被引:64
作者
Zhang, Xiaojie [1 ,2 ,3 ]
Wang, Lei [1 ,2 ]
Du, Quanchao [4 ]
Wang, Zhiyong [1 ,2 ]
Ma, Shuguo [1 ,2 ]
Yu, Miao [1 ,2 ]
机构
[1] Univ S Carolina, Dept Chem Engn, Columbia, SC 29208 USA
[2] Univ S Carolina, Catalysis Renewable Fuels CReF Ctr, Columbia, SC 29208 USA
[3] Jiyuan Vocat & Tech Coll, Dept Met & Chem Engn, Jiyuan 459000, Peoples R China
[4] Shanxi Univ Technol, Coll Chem & Environm Sci, Hanzhong 723001, Peoples R China
基金
中国国家自然科学基金;
关键词
B4C; g-C3N4; p-n heterojunction; Visible light; CO2; reduction; GRAPHITIC CARBON NITRIDE; METAL-FREE; HYDROGEN EVOLUTION; ROOM-TEMPERATURE; WATER; DIOXIDE; EFFICIENT; JUNCTION; NANOPARTICLES; ADSORPTION;
D O I
10.1016/j.jcis.2015.11.022
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
Boron carbide/graphitic carbon nitride (B4C/g-C3N4) p-n hetero-junction photocatalyst with an internal electric field was synthesized by a facile solvent evaporation method and characterized by field emission scanning electron microscope (FESEM), UV-Vis diffuse reflectance spectra (UV-Vis DRS), photoluminescence spectra (PL), etc. Photocatalytic activity of the composite B4C/g-C3N4 loaded with Pt co-catalyst was evaluated using CO2 conversion to CH4 with H-2 as the hydrogen source and reductant under visible light irradiation. The coupling of p-type B4C with n-type g-C3N4 significantly improved the performance of photocatalytic CO2 reduction; with the optimum B4C mass fraction of 116, the composite photocatalyst showed approximately 6 and 8 times higher CH4 generation rate than g-C3N4 and B4C, respectively. The enhancement was attributed to efficient photo-excited electron/hole separation due to the formation of internal electric field at the p-B4C/n-C3N4 interface. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:89 / 95
页数:7
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