Sol–gel preparation and characterization of Ag and Mg co-doped nano TiO2: efficient photocatalytic degradation of C.I. Acid Red 27

Sol–gel preparation and characterization of Ag and Mg co-doped nano TiO2: efficient... In this study, we successfully prepared pure, mono-doped, and Ag, Mg co-doped TiO2 nanoparticles using the sol–gel method, with titanium tetraisopropoxide as the Ti source. The prepared samples were characterized by X-ray powder diffraction (XRD), specific surface area and porosity (BET and BJH) measurement, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, photoluminescence, and energy dispersive X-ray spectroscopy techniques. The XRD data showed that the prepared nanoparticles had the same crystals structures as the pure TiO2. Also, DRS results indicated that the band gap of co-doped photocatalyst was smaller than that of the monometallic and undoped TiO2 and that there was a shift in the absorption band towards the visible light region. Furthermore, the photocatalytic activity of the prepared catalysts was evaluated by the degradation of C.I. Acid Red 27 in aqueous solution under visible light irradiation. The results showed that Ag (0.08 mol%), Mg (0.2 mol%) co-doped TiO2 had the highest photoactivity among all samples under visible light. It was concluded that co-doping of the Ag and Mg can significantly improve the photocatalytic activity of the prepared photocatalysts, due to the efficient inhibition of the recombination of photogenerated electron–hole pairs. The optimum calcination temperature and time were 450 °C and 3 h, respectively. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Research on Chemical Intermediates Springer Journals

Sol–gel preparation and characterization of Ag and Mg co-doped nano TiO2: efficient photocatalytic degradation of C.I. Acid Red 27

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Publisher
Springer Netherlands
Copyright
Copyright © 2015 by Springer Science+Business Media Dordrecht
Subject
Chemistry; Catalysis; Physical Chemistry; Inorganic Chemistry
ISSN
0922-6168
eISSN
1568-5675
D.O.I.
10.1007/s11164-015-2044-z
Publisher site
See Article on Publisher Site

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