Issue 10, 2016

Preparation of anatase TiO2 nanotube arrays dominated by highly reactive facets via anodization for high photocatalytic performances

Abstract

Well-defined uniform anatase TiO2 nanotube (TNT) arrays with predominant exposure of the highly energetic {001} facets have been prepared via a two-step anodic oxidation process of Ti foil. In order to enhance the exposure degree of the {001} facets, NH4F has been used as a capping agent during anodization and the evolution of TNT arrays has been varied by changing the duration of anodization and the concentration of NH4F. With the increase of the first-anodization time (up to 11 h) and/or the NH4F concentration, the crystallite sizes, crystallinity, and exposed {001} facets of prepared TNT arrays have been found to increase. The photocatalytic activity of the as-prepared TNT arrays, evaluated by monitoring the photodegradation of rhodamine B, has been found to increase in accordance with an increase in the exposure degree of the {001} facets, indicating that the highly energetic {001} facets enhance the photocatalytic activity of TNT arrays on a large scale. The {001} facets of TNT arrays have been considered to provide oxidation sites extensively, which produce active oxygen species such as ˙OH, ˙O2, and H2O2 upon UV irradiation. Our results have shown that ˙OH is the predominant highly active species for the photocatalytic degradation of organic dye pollutants via TNT arrays. We consider that this study may provide a new insight into the preparation and development of advanced photocatalytic anatase TiO2 materials.

Graphical abstract: Preparation of anatase TiO2 nanotube arrays dominated by highly reactive facets via anodization for high photocatalytic performances

Supplementary files

Article information

Article type
Paper
Submitted
23 May 2016
Accepted
31 Aug 2016
First published
08 Sep 2016

New J. Chem., 2016,40, 8737-8744

Preparation of anatase TiO2 nanotube arrays dominated by highly reactive facets via anodization for high photocatalytic performances

H. Lee, T. Park and D. Jang, New J. Chem., 2016, 40, 8737 DOI: 10.1039/C6NJ01625A

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