Visible-induced photocatalytic reactivity of polymer-sensitized titania nanotube films

被引:184
作者
Liang, Hai-chao [1 ]
Li, Xiang-zhong [1 ]
机构
[1] Hong Kong Polytech Univ, Dept Civil & Struct Engn, Kowloon, Hong Kong, Peoples R China
关键词
Polymer; Photosensitizer; Titania nanotubes; Visible photocatalysis; SOLAR-ENERGY CONVERSION; NANOCRYSTALLINE TIO2; ELECTRON-TRANSFER; POLYTHIOPHENE; LIGHT; CELLS; DEGRADATION; SEMICONDUCTORS; POLYPYRROLE; IRRADIATION;
D O I
10.1016/j.apcatb.2008.07.015
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
In this study, polythiophene-TiO2 nanotube films (PTh/TNT) were successfully prepared by a two-step electrochemical process of anodization and electropolymerization, in which a highly ordered TiO2 nanotube (TNT) film was anodized at a low-voltage with post calcination first and then the prepared TNT film was deposited with a polythiophene layer by electropolymerization in the BFEE electrolyte. The morphology and structures of PTh/TNT composites were examined by FESEM, EDX, XRD and XPS methods. XPS spectra of PTh/TNT composites indicate the strong interaction between S sites of polymer backbone and TiO2 nanotubes, in which electron transfer from polythiophene to titania takes place. UV vis DRS analysis shows that these composites have a strong photoresponse in the visible region at 500 nm. The prepared PTh/TNT films revealed significant activity for 2,3-dichlorophenols (2,3-DCP) degradation under visible light irradiation and also sunlight irradiation, in which the PTh3/TNT film achieved the best performance. On the other hand, this study also confirmed that the side-chains of polythiophene could influence its photocatalytic activity significantly in an order from high to low as poly3-methylthiophene approximate to polythiophene > polythiophenecarboxylic acid > poly3-hexylthiophene. The results may provide useful information to further develop some effective polymer-semiconductor catalysts for pollutant degradation under sunlight irradiation for water and wastewater treatment. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:8 / 17
页数:10
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