Keywords
(Fe3+
57Fe Mössbauer spectra
charge balance mechanism
decolorization of methyl orange
oxygen vacancies
photocatalytic activity
Sb5+)-codoped anatase TiO2
Abstract
The presence of antimony in (x at% Fe3+ + x at% Sb5+):TiO2 powder samples containing equimolar amounts (0.15 ≤ x ≤ 1) of the dopant cations was accompanied by an increase in the reaction rate constant k of the decolorization of methyl orange. Nevertheless, the increase in the rate of this test reaction, consistent with a decrease in the number of charge balance oxygen vacancies VO imputable to the codoping with Sb5+, rapidly weakened with increasing x. This effect is accounted for by the increased number of Fe3+–VO associates slowing down the outward diffusion of VO vacancies and, consequently, their rate of annealing in the studied catalyst.
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