Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/53577
Title: Highly efficient visible-light-induced photocatalytic activity of Bi<inf>2</inf>WO<inf>6</inf>/BiVO<inf>4</inf>heterojunction photocatalysts
Authors: Saranyoo Chaiwichian
Burapat Inceesungvorn
Khatcharin Wetchakun
Sukon Phanichphant
Wiyong Kangwansupamonkon
Natda Wetchakun
Authors: Saranyoo Chaiwichian
Burapat Inceesungvorn
Khatcharin Wetchakun
Sukon Phanichphant
Wiyong Kangwansupamonkon
Natda Wetchakun
Keywords: Engineering;Materials Science;Physics and Astronomy
Issue Date: 1-Jan-2014
Abstract: The Bi2WO6/BiVO4heterojunction photocatalysts were synthesized by hydrothermal method. Physical properties of the heterojunction photocatalyst samples were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques. The XRD results indicated that BiVO4retain monoclinic and tetragonal structures, while Bi2WO6presented as orthorhombic structure. The Brunauer, Emmett and Teller (BET) adsorption-desorption of nitrogen gas for specific surface area determination at the temperature of liquid nitrogen was performed on all samples. UV-vis diffuse reflectance spectra (UV-vis DRS) were used to identify the absorption range and band gap energy of the heterojunction photocatalysts. The photocatalytic performance of Bi2WO6/BiVO4heterojunction photocatalysts was studied via the photodegradation of methylene blue (MB) under visible light irradiation. The results indicated that the heterojunction photocatalyst at 0.5:0.5 mole ratio of Bi2WO6:BiVO4shows the highest photocatalytic activity. © 2014 Elsevier Ltd. All rights reserved.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84897446321&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/53577
ISSN: 00255408
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.