Please use this identifier to cite or link to this item:
Title: Photoelectrocatalytic degradation of organic pollutants in aqueous solution using a Pt-TiO?film
Authors: He, C
Abou Asi, M
Xiong, Y
Shu, D
Li, XZ
Issue Date: 2009
Publisher: Hindawi Publishing
Source: International journal of photoenergy, 2009, v. 2009, 634369, p. [1-7] How to cite?
Journal: International journal of photoenergy 
Abstract: A series of Pt-TiO? films with nanocrystaline structure was prepared by a procedure of photodeposition and subsequent dip-coating. The Pt-TiO? films were characterized by X-ray diffraction, scanning electronic microscope, electrochemical characterization to examine the surface structure, chemical composition, and the photoelectrochemical properties. The photocatalytic activity of the Pt-TiO? films was evaluated in the photocatalytic (PC) and photoelectrocatalytic (PEC) degradation of formic acid in aqueous solution. Compared with a TiO? film, the efficiency of formic acid degradation using the Pt-TiO? films was significantly higher in both the PC and PEC processes. The enhancement is attributed to the action of Pt deposits on the TiO? surface, which play a key role by attracting conduction band photoelectrons. In the PEC process, the anodic bias externally applied on the illuminated Pt-TiO? films can further drive away the accumulated photoelectrons from the metal deposits and promote a process of interfacial charge transfer.
ISSN: 1110-662X
DOI: 10.1155/2009/634369
Rights: ? 2009 Chun He et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Appears in Collections:Journal/Magazine Article

Files in This Item:
File Description SizeFormat 
634369.pdf2.21 MBAdobe PDFView/Open
View full-text via PolyU eLinks SFX Query
Show full item record


Last Week
Last month
Citations as of Feb 7, 2016


Citations as of Feb 13, 2016

Page view(s)

Checked on Feb 7, 2016

Google ScholarTM



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