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Synthesis and optimization of BiVO4 and co-catalyzed BiVO4 nanofibers for visible light-activated photocatalytic degradation of aquatic micropollutants

Authors
Nalbandian, Michael J.Zhang, MiluoSanchez, JoelChoa, Yong-HoCwiertny, David M.Myung, Nosang V.
Issue Date
Aug-2015
Publisher
ELSEVIER SCIENCE BV
Keywords
Advanced oxidation processes (AOPs); Electrospinning; Photocatalysis; Water and wastewater treatment; Nanotechnology; Nanoparticle synthesis
Citation
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, v.404, pp.18 - 26
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
Volume
404
Start Page
18
End Page
26
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/17461
DOI
10.1016/j.molcata.2015.04.003
ISSN
1381-1169
Abstract
Due to the limited photoefficeincy of TiO2 under solar irradiation, non-titania semiconductors, such as bismuth vanadate (BiVO4), have been gaining attention for use as visible light (VL) photocatalysts. In this work, electrospun BiVO4 nanofibers were synthesized as photocatalysts for VL-induced photo-oxidation of organic pollutants. BiVO4 nanofibers with varied average diameters (33-71 nm) were characterized to observe morphological, dimensional and optical properties and tested in aqueous solutions containing a model pollutant to analyze their photocatalytic activity under solar and VL irradiation conditions. Based on phenol degradation studies at pH 7, k(obs), of the BiVO4 nanofibers increased with decreasing diameter, with the 33 nm sized nanofibers slightly outperforming TiO2 nanomaterials under VL irradiation. Additionally, Ag and Au co-catalyzed BiVO4 nanofibers were developed, showing greater photocatalytic performance. Ag-BiVO4 showed enhancement due to increased carrier traps, where as Au-BiVO4 showed enhancement due to both carrier traps and surface plasmon resonance. Both co-catalyzed BiVO4 nanofibers strongly outperformed TiO2 nanomaterials under VL irradiation, with the greatest enhancement coming from 2 at.% Au-BiVO4. Electrospun BiVO4 nanofibers have the potential to become efficient VL-activated photocatalysts as a low-energy alternative to TiO2 for the removal of emerging organic contaminants. (C) 2015 Elsevier B.V. All rights reserved.
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ERICA 공학대학 (DEPARTMENT OF MATERIALS SCIENCE AND CHEMICAL ENGINEERING)
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