Use este identificador para citar ou linkar para este item:
Título: TiO2-Cu photocatalysts: a study on the long- and short-range chemical environment of the dopant
Palavras-chave: TiO2
Methylene blue
Photocatalytic activity
Coordination shell
TiO2 Lattice
Data do documento: Fev-2013
Editor: Springer
Citação: CARVALHO, H. W. P. et al. TiO2-Cu photocatalysts: a study on the long- and short-range chemical environment of the dopant. Journal of Materials Science, [S.l.], v. 48, p. 3904-3912, 2013. DOI: 10.1007/s10853-013-7192-1.
Resumo: In this study, the short- and long-range chemical environments of Cu dopant in TiO2 photocatalyst have been investigated. The Cu-doped and undoped TiO2 specimens were prepared by the sol–gel approach employing CuSO4·5H2O and Ti(O-iPr)4 precursors and subjecting the dried gels to thermal treatment at 400 and 500 °C. The photocatalytic activity, investigated by methylene blue degradation under sunlight irradiation, showed a significantly higher efficiency of Cu-doped samples than that of pure TiO2. The X-ray diffraction results showed the presence of anatase phase for samples prepared at 400 and 500 °C. No crystalline CuSO4 phase was detected below 500 °C. It was also found that doping decreases the crystallite size in the (004) and (101) directions. Infrared spectroscopy results indicated that the chemical environment of sulfate changes as a function of thermal treatment, and UV–vis spectra showed that the band gap decreases with thermal treatment and Cu doping, showing the lowest value for the 400 °C sample. X-ray absorption fine structure measurements and analysis refinements revealed that even after thermal treatment and photocatalytic assays, the Cu2+ local order is similar to that of CuSO4, containing, however, oxygen vacancies. X-ray photoelectron spectroscopy data, limited to the near surface region of the catalyst, evidenced, besides CuSO4, the presence of Cu1+ and CuO phases, indicating the active role of Cu in the TiO2 lattice.
Aparece nas coleções:DQI - Artigos publicados em periódicos

Arquivos associados a este item:
Não existem arquivos associados a este item.

Os itens no repositório estão protegidos por copyright, com todos os direitos reservados, salvo quando é indicado o contrário.