Preparation and visible-light activity of silver vanadate for the degradation of pollutants
被引:62
作者:
Hu, Xuexiang
论文数: 0引用数: 0
h-index: 0
机构:
Chinese Acad Sci, Ecoenvironm Sci Res Ctr, State Key Lab Environm Aquat Chem, Beijing 100085, Peoples R ChinaChinese Acad Sci, Ecoenvironm Sci Res Ctr, State Key Lab Environm Aquat Chem, Beijing 100085, Peoples R China
Hu, Xuexiang
[1
]
论文数: 引用数:
h-index:
机构:
Hu, Chun
[1
]
Qu, Jiuhui
论文数: 0引用数: 0
h-index: 0
机构:
Chinese Acad Sci, Ecoenvironm Sci Res Ctr, State Key Lab Environm Aquat Chem, Beijing 100085, Peoples R ChinaChinese Acad Sci, Ecoenvironm Sci Res Ctr, State Key Lab Environm Aquat Chem, Beijing 100085, Peoples R China
Qu, Jiuhui
[1
]
机构:
[1] Chinese Acad Sci, Ecoenvironm Sci Res Ctr, State Key Lab Environm Aquat Chem, Beijing 100085, Peoples R China
Semiconductors;
Chemical synthesis;
Catalytic properties;
Crystal structure;
D O I:
10.1016/j.materresbull.2007.11.022
中图分类号:
T [工业技术];
学科分类号:
08 [工学];
摘要:
Monoclinic structure silver vanadate Ag3VO4 Was prepared by hydrothermal process. The effects of the ratio of silver to vanadium in starting material, hydrothermal temperature on surface morphologies, structure and photoactivity of Ag3VO4 for the decolorization azodye acid red B under visible irradiation were investigated. The Ag3VO4 prepared in the excess vanadium at 160 degrees C for 48 h exhibited highest visible-light-driven activity. Excess vanadium in the preparation increased the crystallinity and suppressed the formation of grain boundaries, while the formation of Ag-0 on the surface of the catalyst promoting the electron-hole separation and interfacial charge transfer, resulting in an increase in the photocatalytic activity. Furthermore, the activity of the Ag3VO4 was increased by 11 times when NiO was loaded, which also shows high activities for the decomposition of phenol and aniline. It is possible due to the formation of a short-circuited microphotoelectrochemical cell enhancing the separation of photogenerated electron-hole pairs. (C) 2007 Elsevier Ltd. All rights reserved.