Bismuth doping effect on TiO2 nanofibres for morphological change and photocatalytic performance

Ming Chung Wu*, Jyun Sian Chih, Wei Kang Huang

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

67 Scopus citations

Abstract

Doping bismuth ions into photocatalytic materials is one of the most effective methods for preparing highly visible-light-active photocatalysts. In order to develop high-performance photocatalytic materials that are easy to produce, even in industrial quantities, we developed a facile method to prepare bismuth-doped titanium dioxide (Bi-doped TiO2) by hydrothermal synthesis followed by thermal annealing treatment. Bi-doped TiO2 can be applied in the field of photodecolorization of organic dye and photocatalytic hydrogen generation. High concentration doping (>5.00 mol%) resulted in the morphological change of Bi-doped TiO2 from nanofibre to nanorod observed by transmission electron microscopy. The crystal structure evolution and elemental composition were analysed by combining Raman spectroscopy, X-ray crystallography and X-ray photoelectron spectroscopy. For the photodegradation of organic dye methyl orange, all Bi-doped TiO2 showed less activity than pristine TiO2 nanofibres under UV irradiation. 5.00 mol% and 10.00 mol% Bi-doped TiO2 showed higher activities than pristine TiO2 nanofibres under visible light irradiation. For the photocatalytic hydrogen generation measurement, none of the Bi-doped TiO2 showed a detectable value under visible light irradiation. However, under UV irradiation, various Bi-doped TiO2 catalysts exhibited a detectable photocatalytic hydrogen production rate. 0.50 mol% Bi-doped TiO2 exhibited the highest performance. The result could be due to the relatively lower overpotential for hydrogen production. Our study developed a series of visible-light-active Bi-doped TiO2 catalysts, and it could replace the traditional TiO2 catalysts decorated with a high-cost noble metal.

Original languageEnglish
Pages (from-to)10692-10699
Number of pages8
JournalCrystEngComm
Volume16
Issue number46
DOIs
StatePublished - 14 12 2014

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