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High-temperature stable anatase-type TiO2 nanotube arrays: A study of the structure–activity relationship.

Authors :
Eskandarloo, Hamed
Hashempour, Mazdak
Vicenzo, Antonello
Franz, Silvia
Badiei, Alireza
Behnajady, Mohammad A.
Bestetti, Massimiliano
Source :
Applied Catalysis B: Environmental. May2016, Vol. 185, p119-132. 14p.
Publication Year :
2016

Abstract

Anatase-type TiO 2 nanotube arrays (TiO 2 -NTAs) were grown on Ti foil by anodic oxidation in CH 3 COOH/NH 4 F solutions followed by thermal treatment. The surface of TiO 2 -NTAs was further decorated by palladium and silver metal clusters through a chemical-reduction method and its photocatalytic activity was tested by investigating the degradation of p-nitrophenol (PNP) in aqueous solution under visible-light irradiation and electrical polarization. The effects of preparation variables both on microstructural properties of samples and photocatalytic activity were examined by using the 3D response surface and the 2D contour plots. The experimental investigations carried out by using XRD, SEM, HRTEM, EDS, XRF, ICP-AES, XPS, DRS, and PL, demonstrated a strong relation between the phase structure and the photocatalytic activity of TiO 2 -NTAs. Titania nanotubes grown in acetic acid solution and thermally post-treated have stable anatase crystal structure, to a point that by performing annealing at 800 °C for 3 h, only the 35% of anatase transforms into rutile. Finally, it was shown that the TiO 2 -NTAs decorated with Pd(0.72 wt%) and Ag(1.26 wt%) particles show higher photocatalytic activity compared with nanotubes modified with single metal particles. It is believed that the high photoactivity of TiO 2 nanotubes decorated with Pd–Ag heterostructures is due to the prolonged lifetimes of photogenerated electron–hole pairs. The possible mechanism for the enhanced photocatalytic activity is discussed in detail. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09263373
Volume :
185
Database :
Academic Search Index
Journal :
Applied Catalysis B: Environmental
Publication Type :
Academic Journal
Accession number :
112366776
Full Text :
https://doi.org/10.1016/j.apcatb.2015.11.048