The controlled decomposition of crystalline Ce 1− x La x (OH)CO 3 samples to give nanocrystalline Ce 1− x La x O 2−δ solid solutions is studied as a function of temperature and La(III) content. The hexagonal basic carbonates, related to the mineral bastnaesite, are shown to be suitable precursors for the obtainment of Ce(IV-III), La(III) oxides when exposed to O 2 at mild temperatures (250 °C). The oxidation of Ce(III) centers triggers the massive decomposition of the whole precursor, acting as a chemical shortcut to achieve the domain of ceria phases, at temperatures 200 °C lower than the traditional procedures. The mixed oxides exhibit higher surface areas than those obtained for traditional coprecipitation−thermal decomposition procedures, achieving values in the range of those oxides prepared by costly surfactant-assisted methods.
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Jobbágy et al. (2009) studied this question.
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