Published August 15, 2008 | Version v1
Journal article

Preparation and visible-light-driven photoelectrocatalytic properties of boron-doped TiO2 nanotubes

  • 1. Institute of Environmental Pollution Control Technologies, Xixi Campus, Zhejiang University, Hangzhou 310028 (China)

Description

In the present study, chemical vapour deposition (CVD) was applied to dope boron into TiO2 nanotubes anodized Ti in C2H2O4.2H2O + NH4F electrolyte with the goal of improving the photocatalytic (PC) activity under visible light. The undoped TiO2 nanotubes had a highly self-organized structure. However, after doping through CVD, TiO2 nanotubes suffered from an observable disintegration of morphological integrity. X-ray diffraction (XRD) results confirmed that annealing temperature had an influence on the phase structure and boron impurities could retard anatase-rutile phase transition. Diffuse reflectance absorption spectra (DRS) analysis indicated that B-doped samples displayed stronger absorption in both UV and visible range. B-doped TiO2 nanotubes electrode annealed at 700 deg. C through CVD showed higher photoelectrocatalytic (PEC) efficiency in methyl orange (MO) degradation than that annealed at 400 deg. C and 550 deg. C. MO degradation was substantially enhanced with the increasing applied bias potential. Moreover, there was a synergetic effect between the electrochemical and photocatalytic processes, and the synergetic factor R reached 1.45. B-doped TiO2 nanotubes electrode showed good stability after 10 times by repeating photoelectrocatalysis of MO

Availability note (English)

Available from http://dx.doi.org/10.1016/j.matchemphys.2008.01.036

Additional details

Identifiers

DOI
10.1016/j.matchemphys.2008.01.036;
PII
S0254-0584(08)00048-5;

Publishing Information

Journal Title
Materials Chemistry and Physics
Journal Volume
110
Journal Issue
2-3
Journal Page Range
p. 239-246
ISSN
0254-0584
CODEN
MCHPDR

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.