Enhanced photocatalytic mechanism of the Nd-Er co-doped tetragonal BiVO4 photocatalysts

被引:117
作者
Liu, Ting [1 ]
Tan, Guoqiang [1 ]
Zhao, Chengcheng [1 ]
Xu, Chi [1 ]
Su, Yuning [1 ]
Wang, Ying [1 ]
Ren, Huijun [2 ]
Xia, Ao [1 ]
Shao, Dan [1 ]
Yan, Shemin [3 ]
机构
[1] Shaanxi Univ Sci & Technol, Sch Mat Sci & Engn, Xian 710021, Peoples R China
[2] Shaanxi Univ Sci & Technol, Sch Arts & Sci, Xian 710021, Peoples R China
[3] Xianyang Res & Design Inst Ceram, Xian Yang 712000, Peoples R China
基金
中国国家自然科学基金;
关键词
Nd-Er/BiVO4; Impurity energy level; Up-conversion; Synergetic effect; HIGH-PERFORMANCE PHOTOCATALYSTS; VISIBLE-LIGHT; METHYL-ORANGE; SPECTROSCOPIC PROPERTIES; HYDROTHERMAL SYNTHESIS; CRYSTAL-STRUCTURE; UP-CONVERSION; SUN-LIGHT; DEGRADATION; DRIVEN;
D O I
10.1016/j.apcatb.2017.05.018
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
The Nd/Er co-doped tetragonal BiVO4 photocatalysts are synthesized by a microwave hydrothermal method, and the crystal structures, morphologies and optical properties are characterized. The substitution of Nd3+ and Er3+ for Bi3+ sites leads to distortion of the [VO4] tetrahedron chains and induces the monoclinic structure transforming into the tetragonal structure, with the morphology evolving from nano particle agglomerations to disorganized regular rods agglomerations. The impurity energy levels induced by Nd3+ and Era' in the energy band of BiVO4 act as electron traps and have further energy transfer in the up-conversion processes to facilitate the photocarriers' separation. The more positive VB positions in the co-doped BiVO4 band structures can also effectively enhance oxidation capacity. Based on the above synergetic effect, the degradation rate the degradation rate of co-doped tetragonal BiVO4 photocatalyst can reach the highest 96% within 150 min under simulated sunlight and 20 min under the NIR irradiation. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 96
页数:10
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