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Erschienen in: Journal of Materials Science 11/2019

08.03.2019 | Chemical routes to materials

Synergetic effect of Fe2O3 and BiVO4 as photocatalyst nanocomposites for improved photo-Fenton catalytic activity

verfasst von: Yun Wen, Yue Zhao, Mingzhen Guo, Yan Xu

Erschienen in: Journal of Materials Science | Ausgabe 11/2019

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Abstract

Photo-Fenton reactions and the related functional nanomaterials have been widely studied for applications in wastewater treatment industry. Herein, visible-light-responsive Fe2O3 nanoparticle-decorated BiVO4 nanoplates were designed and successfully prepared through a one-pot hydrothermal route. The as-prepared Fe2O3/BiVO4 nanocomposites exhibit excellent photo-Fenton catalytic activity toward the discoloration of methylene blue (MB) and Rhodamine B (RhB) dye molecules in the presence of H2O2. The experimental results indicate that nearly 100% of MB (100 mL, 10 mg L−1) and RhB (100 mL, 5 mg L−1) dye molecules are degraded in the presence of 1 g L−1 Fe2O3/BiVO4-1 (FB-1) photo-Fenton catalyst and 0.5 mL of H2O2 within 20 min. The Fe2O3/BiVO4 Fenton photocatalyst also demonstrates high reusability under visible light irradiation with λ ≥ 420 nm. The photoinduced electrons on the conduction band of BiVO4 nanoplates can move toward the surface of Fe2O3/BiVO4 to accelerate the reduction of Fe3+; then, the as-formed Fe2+ ions on the surface of the catalyst greatly enhance the decomposition of H2O2 to form reactive ·OH species for the use in photodegradation of MB and RhB dye molecules. The synergetic effect of Fe2O3 and BiVO4 reported in this work might provide more opportunity to fabricate other novel semiconductor-based Fenton nanocomposites for contamination treatments in wastewater.

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Metadaten
Titel
Synergetic effect of Fe2O3 and BiVO4 as photocatalyst nanocomposites for improved photo-Fenton catalytic activity
verfasst von
Yun Wen
Yue Zhao
Mingzhen Guo
Yan Xu
Publikationsdatum
08.03.2019
Verlag
Springer US
Erschienen in
Journal of Materials Science / Ausgabe 11/2019
Print ISSN: 0022-2461
Elektronische ISSN: 1573-4803
DOI
https://doi.org/10.1007/s10853-019-03511-x

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