Journal
JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 525, Issue -, Pages 97-106Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2018.04.057
Keywords
Bi2WO6; Porous two-dimensional nanosheet; Cr(Vl) reduction; Photocatalytic
Categories
Funding
- National Natural Science Foundation of China [61204078, 21671059]
- Program for Innovative Research Team (in Science and Technology) in University of Henan Province [131RTSTHN026]
- Innovation Scientists and Technicians Troop Construction Projects of Henan Province [154200510009]
- Key Project of Science and Technology of Henan Province [17A150033]
- Henan Science and Technology Program [162300410174, 162300410204]
- Science and technology key project of Xinxiang [CXGG17001]
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Bi2WO6 porous nanosheets (PNS) with different thickness were synthesized via one-pot hydrothermal method. The thickness of Bi2WO6 nanosheets could be well controlled from similar to 27 nm to similar to 16 nm by adjusting the precursor concentration. In addition, the PNS exhibited porous structures, high surface area and high lattice coherence, which increased the number of catalytic sites and facilitated the charge migration within the sheet structure. The Cr(VI) reduction experiments showed that the photocatalytic activity was greatly affected by the thickness of the product and the optimal photocatalytic activity under visible light irradiation was achieved by BWO-3 with thickness of similar to 18 nm. The photocatalytic ratio of Cr(VI) reduction for BWO-3 reached to similar to 99.5% after 100 min visible light irradiation, which was higher than that of BWO (similar to 78%). Based on the optical and electrochemical measurements, BWO-3 had upshifted conduction band of 0.05 V, prolonged carriers' lifetime of 2.03 ns and decreased carriers' recombination efficiency compared to BWO. These results endowed BWO-3 with high photoreduction ability, increased transfer and separation efficiency of carriers, and thus enhanced the photoreduction activity. (C) 2018 Elsevier Inc. All rights reserved.
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