SnIV-containing layered double hydroxides as precursors for nano-sized ZnO/SnO2 photocatalysts

Sn4+-containing LDH was prepared using the co-precipitation method at constant pH, and characterized using X-ray diffraction, UV–vis diffuse reflectance spectroscopy and TG/DTG methods. The obtained product was further exposed to different thermal treatments in order to obtain nano-sized coupled ZnO...

Full description

Saved in:
Bibliographic Details
Published inApplied catalysis. B, Environmental Vol. 84; no. 3-4; pp. 699 - 705
Main Authors Seftel, E.M., Popovici, E., Mertens, M., Stefaniak, E.A., Van Grieken, R., Cool, P., Vansant, E.F.
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier B.V 01.12.2008
Elsevier
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Sn4+-containing LDH was prepared using the co-precipitation method at constant pH, and characterized using X-ray diffraction, UV–vis diffuse reflectance spectroscopy and TG/DTG methods. The obtained product was further exposed to different thermal treatments in order to obtain nano-sized coupled ZnO/SnO2 systems with enhanced photocatalytic performances than the ones obtained by mixing the two semiconductor oxides. The formation of a well-defined ZnO/SnO2 system and the crystallite size, fully investigated using XRD, micro-Raman scattering and UV–vis DR techniques, were found to be influenced by the nature of the precursors and the calcination temperature. The photocatalytic activity of the ZnO/SnO2 systems, evaluated for the photodegradation of methyl orange (MO) dye, was studied as a function of the initial pH, catalyst loading and the calcination temperature. The metal dispersion supplied by layered structures proved to be an advantage when preparing coupled ZnO/SnO2 systems, the photocatalytic activity being ∼2.3 times higher comparing with the physical mixtures performances. The maximum photocatalytic activity of the coupled ZnO/SnO2 system having a layered precursor was observed when using neutral pH, at a catalyst loading of 1g/L calcined at 600°C for 4h.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2008.06.006