Application of nanostructured mesoporous silica/ bismuth vanadate composite catalysts for the degradation of methylene blue and brilliant green

光催化 材料科学 钒酸铋 介孔材料 化学工程 介孔二氧化硅 纳米复合材料 纳米颗粒 亚甲蓝 可见光谱 微晶 扫描电子显微镜 核化学 催化作用 纳米技术 复合材料 有机化学 化学 冶金 工程类 光电子学
作者
S.A. El-Hakam,Fares T. Alshorifi,Reda S. Salama,Soliman Gamal,Wafaa S. Abo El‐Yazeed,Amr Awad Ibrahim,Awad I. Ahmed
出处
期刊:Journal of materials research and technology [Elsevier BV]
卷期号:18: 1963-1976 被引量:97
标识
DOI:10.1016/j.jmrt.2022.03.067
摘要

Ultrasonication method was used in the incorporation of mesoporous silica (mSiO2) on BiVO4 nanoparticles. The average crystallite size of the BiVO4 nanoparticles was controlled at around 2.4–5.1 nm on mesoporous silica surface. The composites were systematically evaluated as photocatalysts for the degradation of methylene blue (MB) and brilliant green (BG) dyes as a function of mesoporous SiO2 content. A marked compositional dependence of the photocatalytic activity was evidenced for MB and BG degradation under visible light. Compared with the corresponding bare bismuth vanadate nano species, the mSiO2-involved nanocomposites display enhanced photocatalytic activities. The enhancement of photocatalytic activity of BiVO4 nanoparticles with mesoporous silica was attributed to the synergistic effect between mesoporous silica and BiVO4 which improved the separation of photogenerated electrons and holes. Structures and morphologies of the samples were examined by TEM, SEM, XRD, EDS, FT-IR and UV–visible spectroscopy. The effects of operational parameters like dye concentration, mSiO2 content, calcination temperature and reaction time have been analyzed. The results showed that the photocatalytic activity of mSiO2/BiVO4 nanocomposites increases with the modification of BiVO4 by changing the content from 1.0 to 15.0 wt % mesoporous SiO2, the sample of 10.0 wt. % mesoporous SiO2 loaded on BiVO4 showed the higher photocatalytic activity. As the silica in the composites has a very good contact with the BiVO4 nanoparticles it enhances the photo-electron conversion of BiVO4 by reducing the recombination of photo-generated electron–hole pairs based on the band structures of BiVO4. The catalyst is found to be reusable.
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