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Photocatalytic activity of SnO2-α-Fe2O3 composite mixtures: exploration of number of active sites, Turnover number and Turnover frequency.

Abstract

SnO2 and α-Fe2O3 were prepared by sol-gel method and their composite (SnO2-α-Fe2O3) systems were synthesized by combining SnO2 with α-Fe2O3 in various weight percent ratios. Sn:Fe (0.25:0.75), Sn:Fe (0.5:0.5) and Sn:Fe (0.75:0.25) samples were prepared using simple grinding process and they were characterized by various analytical techniques. Photocatalytic activity was studied under UV/solar light using phenol as a model pollutant. The better performance of Sn:Fe (0.75:0.25) composite under UV/solar light irradiation was due to the efficient charge carrier separation and also due to the synergistic effects between photocatalysis and photo-Fenton reactions. Sn:Fe (0.25:075) composite shows better photocatalytic activity under solar light illumination. The photocatalytic activity of the composite systems further increases in the presence of H2O2. Extremely small amount of the catalyst (10 mg/250 ml) was capable of bringing considerable increase in the rate of the degradation reaction. Effectiveness of the catalyst at very low concentration is implicated by the calculation of number of active sites, turnover number (TON) and turnover frequency (TOF) for all the systems under both UV/solar light illumination. The photocatalytic oxidation process dominates the degradation reaction rather than the photocatalytic reduction. The staggered positions of conduction band edges of SnO2 and α-Fe2O3 with respect to one another facilitates smooth charge transfer process.

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Publication details

The article was received on 20 Nov 2017, accepted on 27 Jan 2018 and first published on 29 Jan 2018


Article type: Research Article
DOI: 10.1039/C7QM00536A
Citation: Mater. Chem. Front., 2017, Accepted Manuscript
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    Photocatalytic activity of SnO2-α-Fe2O3 composite mixtures: exploration of number of active sites, Turnover number and Turnover frequency.

    L. Gomathi Devi and S. R, Mater. Chem. Front., 2017, Accepted Manuscript , DOI: 10.1039/C7QM00536A

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