Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/65670
Title: Synthesis and Characterization Ag Nanoparticles Supported on Bi<inf>2</inf>WO<inf>6</inf> Nanoplates for Enhanced Visible-Light-Driven Photocatalytic Degradation of Rhodamine B
Authors: Anukorn Phuruangrat
Paveen On Keereesaensuk
K. Karthik
Phattranit Dumrongrojthanath
Nuengruethai Ekthammathat
Somchai Thongtem
Titipun Thongtem
Authors: Anukorn Phuruangrat
Paveen On Keereesaensuk
K. Karthik
Phattranit Dumrongrojthanath
Nuengruethai Ekthammathat
Somchai Thongtem
Titipun Thongtem
Keywords: Materials Science
Issue Date: 1-Jan-2019
Abstract: © 2019, Springer Science+Business Media, LLC, part of Springer Nature. Heterostructure Ag/Bi2WO6 nanocomposites with different weight contents of Ag nanoparticles for photodegradation of rhodamine B (RhB) were successfully synthesized by solution precipitate-deposition method using sodium borohydride (NaBH4) as a reducing agent. The results of X-ray diffraction (XRD) and transmission electron microscopy (TEM) certify the successful synthesis of cubic Ag nanoparticles supported on the surface of orthorhombic Bi2WO6 nanoplates. X-ray photoelectron spectroscopy (XPS) revealed the presence of metallic Ag species supported on Bi2WO6 nanoplates. The photocatalytic performance of heterostructure Ag/Bi2WO6 nanocomposites were investigated through the degradation of RhB under visible light irradiation. In this research, Ag/Bi2WO6 nanocomposites exhibited excellent chemical stability and recyclability under visible light irradiation. The 5 wt% Ag/Bi2WO6 showed the highest photodegradation of RhB due to the Ag nanoparticles acting as an electron trapper, to restrain the recombination of photo-induced electrons and holes, to improve the charge separation, and to enhance the photocatalytic performance of Bi2WO6.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85068844013&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/65670
ISSN: 15741451
15741443
Appears in Collections:CMUL: Journal Articles

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