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Title: Synthesis and characterization of novel WO{sub 3} loaded Ag–ZnO and its photocatalytic activity

Journal Article · · Materials Research Bulletin
;  [1];  [2];  [1]
  1. Photocatalysis Laboratory, Department of Chemistry, Annamalai University, Annamalainagar 608002, Tamil Nadu (India)
  2. Department of Physics, Nehru Memorial College (Autonomous), Puthanampatti 621007, Tamil Nadu (India)

Graphical abstract: Display Omitted Highlights: ► A novel WO{sub 3} loaded Ag–ZnO was prepared by a simple solvothermal method. ► ‘Ag’ traps the electron from both ZnO and WO{sub 3} reducing electro–hole recombination. ► WO{sub 3}–Ag–ZnO is more efficient than Ag–ZnO, WO{sub 3}–ZnO, Ag–WO{sub 3} and undoped catalysts. ► WO{sub 3}–Ag–ZnO material will be much useful for the treatment of dye effluents. -- Abstract: A novel WO{sub 3} loaded Ag–ZnO photocatalyst was successfully synthesized by a simple solvothermal method and characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM) images, energy dispersive spectrum (EDS), diffuse reflectance spectra (DRS), photoluminescence spectra (PL), cyclic voltammetry (CV) and Brunauer–Emmett–Teller (BET) surface area measurements. The photocatalytic activity of WO{sub 3}–Ag–ZnO was investigated for the degradation of RR 120 and RO 4 dyes in aqueous solution using UV-A light. WO{sub 3}–Ag–ZnO is found to be more efficient than Ag–ZnO, WO{sub 3}–ZnO, Ag–WO{sub 3}, commercial ZnO, prepared ZnO, TiO{sub 2}-P25 and TiO{sub 2} (Merck) at neutral pH for the mineralization of dyes. First time we have reported that novel WO{sub 3} loaded Ag–ZnO has been found to be very efficient for two azo dyes removal when compared to commercially available catalyst (Degussa P25, ZnO (Merck) and TiO{sub 2} (Merck)). The mineralization of dyes has been confirmed by chemical oxygen demand (COD) measurements. A mechanism of degradation has been proposed for the higher efficiency of WO{sub 3}–Ag–ZnO.

OSTI ID:
22215772
Journal Information:
Materials Research Bulletin, Vol. 48, Issue 1; Other Information: Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0025-5408
Country of Publication:
United States
Language:
English