光催化
X射线光电子能谱
热重分析
傅里叶变换红外光谱
漫反射红外傅里叶变换
光化学
光谱学
核化学
化学
甲基橙
材料科学
可见光谱
透射电子显微镜
猝灭(荧光)
催化作用
分析化学(期刊)
化学工程
荧光
纳米技术
光学
光电子学
环境化学
有机化学
工程类
物理
量子力学
作者
Yunjin Yao,Lu Fang,Yanping Zhu,Fengyu Wei,Xueting Liu,Chao Lian,Shaobin Wang
标识
DOI:10.1016/j.jhazmat.2015.04.046
摘要
Novel CuFe2O4@C3N4 core-shell photocatalysts were fabricated through a self-assembly method and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, transmission electron microscopy and Uv-vis diffuse reflection spectroscopy. The photocatalytic performances of the CuFe2O4@C3N4 catalysts were evaluated in photo Fenton-like discoloration of Orange II dye using H2O2 as an oxidant under visible-light irradiation (λ>420 nm). It was found the CuFe2O4@C3N4 hybrid (mass ratio of CuFe2O4/g-C3N4 at 2:1) exhibits a superior activity as compared with single component of CuFe2O4 or g-C3N4 and the mixture of g-C3N4 and CuFe2O4, due to the elevation of the separation efficiency of photoinduced electron-hole pairs, resulted from the heterojunction between the interfaces of g-C3N4 and CuFe2O4. The quenching tests of different scavengers displayed that O2(•-), OH and h(+) are responsible for the Orange II decolorization. In addition, the effects of initial concentration of the dye contaminant (0.014-0.140 mM), different anions (Cl(-), SO4(2-), NO3(-), CH3COO(-) and HCO3(-)) and temperature (15-65 °C) in photoreaction were also investigated. The CuFe2O4@C3N4 sample exhibited stable performance without obvious loss of catalytic activity after five successive runs, showing a promising application for the photo-oxidative degradation of environmental contaminants.
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