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dc.contributor.authorSukon Phanichphanten_US
dc.contributor.authorAuppatham Nakaruken_US
dc.contributor.authorKantapat Chansaenpaken_US
dc.contributor.authorDuangdao Channeien_US
dc.date.accessioned2020-04-02T15:21:02Z-
dc.date.available2020-04-02T15:21:02Z-
dc.date.issued2019-12-01en_US
dc.identifier.issn20452322en_US
dc.identifier.other2-s2.0-85074703650en_US
dc.identifier.other10.1038/s41598-019-52589-5en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85074703650&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/68120-
dc.description.abstract© 2019, The Author(s). The present study reported the preparation of BiVO4 by co-precipitation method. The as-prepared BiVO4 photocatalyst were deposited on rGO sheets to form BiVO4/rGO via the hydrothermal method. The crystalline structure, morphological, optical properties, and surface properties of the synthesized pure BiVO4 compared to BiVO4/rGO composite were studied using X-ray diffraction (XRD), scanning electronmicroscopy (SEM), photoluminescence (PL) spectrophotoscopy, UV–vis spectrophotometer with an integrating sphere, and N2 adsorption-desorption isotherm based on BET theory. The photocatalytic activity of the prepared samples were evaluated by the degradation of MB dye in aqueous medium under visible light irradiation. The result showed that the BiVO4/rGO composite exhibited greater photocatalytic efficiency compared to pure BiVO4 with the photocatalytic degradation efficiency remains stable up to fifth cycle. The improved activity of the BiVO4/rGO composite might be attributed to the high surface area available to adsorb more MB molecules, and efficient charge separation of BiVO4 through π electron on the rGO structure. According to experimental results, the possible photocatalytic mechanism of the BiVO4/rGO composite were determined and the active species hydroxyl radical were reported. Based on photocatalytic activity inhibition in the presence of both h+ (VB) and O2•− (CB) scavengers over the BiVO4 photocatalyst, it can be proposed that the hydroxyl radical generated during the photocatalytic degradation mechanism is mainly responsible by the main active species of h+ and O2•− at VB and CB positions, respectively.en_US
dc.subjectMultidisciplinaryen_US
dc.titleEvaluating the photocatalytic efficiency of the BiVO<inf>4</inf>/rGO photocatalysten_US
dc.typeJournalen_US
article.title.sourcetitleScientific Reportsen_US
article.volume9en_US
article.stream.affiliationsNaresuan Universityen_US
article.stream.affiliationsThailand National Science and Technology Development Agencyen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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