4.8 Article

Coupled systems for selective oxidation of aromatic alcohols to aldehydes and reduction of nitrobenzene into aniline using CdS/g-C3N4 photocatalyst under visible light irradiation

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 158, Issue -, Pages 382-390

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2014.04.035

Keywords

CdS/g-C3N4; Selective oxidation; Reduction; Coupled system; Photocatalysis

Funding

  1. National Natural Science Foundation of China (NSFC) [51172086, 21103060, 51272081]

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A coupled system of selective oxidation of aromatic alcohols to aromatic aldehydes and reduction of nitrobenzene into aniline was realized using CdS/g-C3N4 composite as a photocatalyst under visible light illumination. The CdS/g-C3N4 composite photocatalyst was prepared by hydrothermal method. The photocatalyst was characterized by x-ray powder diffraction (XRD), UV-vis diffuse reflection spectroscopy (DRS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) specific surface area. Compared with single g-C3N4 and CdS, the CdS/g-C3N4 photocatalyst exhibits enhanced photocatalytic activity and excellent photostability under visible light illumination. It demonstrates that the selective oxidation of aromatic alcohol into aromatic aldehyde is achieved by direct holes oxidation, and the reduction of nitrobenzene into aniline is reached by direct electrons reduction. The optimum percentage of CdS is 10 wt.%. Under illumination for 4 h, the conversion of benzyl alcohol and the yield of benzaldehyde are about 48.0% and 44.6%, and the conversion of nitrobenzene and the yield of aniline are about 49.2% and 26.0%, respectively. The synergic effect of g-C3N4 and CdS, which can effectively separate and transfer photoexcited carriers, was proposed to be responsible for the enhancement of the photocatalytic activity. This study has a guiding significance for the design of a coupled system which realizes selective oxidation and reduction of organics. (C) 2014 Elsevier B.V. All rights reserved.

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