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Visible light degradation of textile effluent using nanostructured TiO2/Ag/CuO photocatalysts

https://doi.org/10.17586/2220-8054-2016-7-4-695-698

Abstract

TiO2, Ag and CuO nanomaterials, and nanostructured TiO2/Ag/CuO photocatalytic materials coupled in different weight percentages were synthesized. The prepared materials were characterized by XRD, SEM, EDX and UV-Vis diffuse reflectance spectroscopy. Photocatalytic degrading capabilities of the pure, as well as the nanostructured TiO2/Ag/CuO photocatalytic materials were tested on the dye effluent collected from the textile industries. The samples collected during the photocatalytic degradation of textile dye effluent were studied with UV-Vis spectroscopy. The nanostructured TiO2/Ag/CuO photocatalyst with the composition of 80:10:10 weight percentage exhibited remarkable per- formance. Coupling of Ag metal nanoparticles and narrow bandgap CuO semiconductor nanomaterial to the wide bandgap TiO2 semiconductor nanomaterial was found to modify the operative bandgap of the system and generate electron-hole pairs under visible light irradiation. The coupled TiO2/Ag/CuO system facilitates improved electron transfer to the adsorbed molecules, and thus the system improves the photocatalytic degradation of dyes by enhanced redox mechanism.

About the Authors

N. Karthikeyan
University of Madras; The Open University of Sri Lanka
India

Department of Nuclear Physics, University of Madras; Department of Physics, The Open University of Sri Lanka

Guindy Campus, Chennai, India;
Nawala, Nugegoda, Sri Lanka 



V. Narayanan
University of Madras
India

 

Guindy Campus, Chennai



A. Stephen
University of Madras
India

Department of Nuclear Physics

Guindy  Campus, Chennai



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For citations:


Karthikeyan N., Narayanan V., Stephen A. Visible light degradation of textile effluent using nanostructured TiO2/Ag/CuO photocatalysts. Nanosystems: Physics, Chemistry, Mathematics. 2016;7(4):695-698. https://doi.org/10.17586/2220-8054-2016-7-4-695-698

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ISSN 2220-8054 (Print)
ISSN 2305-7971 (Online)