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  • 标题:Morphology-Controlled Synthesis of ZnxCd1-xS Solid Solutions: An Efficient Solar Light Active Photocatalyst for the Degradation of 2,4,6-Trichlorophenol
  • 本地全文:下载
  • 作者:Rengaraj Selvaraj ; Kezhen Qi ; Sathish Babu Soundra Pandian
  • 期刊名称:Journal of Environmental Protection
  • 印刷版ISSN:2152-2197
  • 电子版ISSN:2152-2219
  • 出版年度:1605
  • 卷号:07
  • 期号:11
  • 页码:1605-1617
  • DOI:10.4236/jep.2016.711132
  • 语种:English
  • 出版社:Scientific Research Publishing
  • 摘要:ZnxCd1-xS solid solutions with controlled morphology have been successfully synthe-sized by a facile solution-phase method. The prepared samples were characterized by X-ray powder diffraction (XRD), UV-vis diffuse reflectance spectra, X-ray photoelec-tron spectroscopy (XPS), scanning electron microscopy (SEM) and transmission elec-tron microscopy (TEM). The photocatalytic activity of ZnxCd1-xS was evaluated in the 2,4,6-trichlorophenol (TCP) degradation and mineralization in aqueous solution under direct solar light illumination. The experiment demonstrated that TCP was effectively degraded by more than 95% with 120 min. The results show that ZnS with Cd doping (ZnxCd1-xS) exhibits the much stronger visible light adsorption than that of pure ZnS, the light adsorption increasing as the Cd2+ doping amount. These results indicate that Cd doping into a ZnS crystal lattice can result in the shift of the valence band of ZnS to a positive direction. It may lead to its higher oxidative ability than pure ZnS, which is important for organic pollutant degradation under solar light irradiation. Further-more, the photocatalytic activity studies reveal that the prepared ZnxCd1-xS nanostructures exhibit an excellent photocatalytic performance, degrading rapidly the aqueous 2,4,6-trichlorophenol solution under solar light irradiation. These results sug-gest that ZnxCd1-xS nanostructure will be a promising candidate of photocatalyst working in solar light range.
  • 关键词:Photocatalyst;Nanostructures;Solution Phase;2;4;6-Trichlorophenol;Solar Light;Photocatalytic Activity
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