Crystalline Ce(III)−La(III) Double Basic Carbonates: A Chemical Shortcut To Obtain Nanometric La(III)-Doped Ceria
The controlled decomposition of crystalline Ce1−x La x (OH)CO3 samples to give nanocrystalline Ce1−x La x O2−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...
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Veröffentlicht in: | Journal of physical chemistry. C 2009-06, Vol.113 (25), p.10853-10857 |
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creator | Jobbágy, Matías Sorbello, Cecilia Sileo, Elsa E |
description | The controlled decomposition of crystalline Ce1−x La x (OH)CO3 samples to give nanocrystalline Ce1−x La x O2−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 O2 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. |
doi_str_mv | 10.1021/jp810321y |
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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 O2 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.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/jp810321y</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>C: Nanops and Nanostructures</subject><ispartof>Journal of physical chemistry. 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C</title><addtitle>J. Phys. Chem. C</addtitle><description>The controlled decomposition of crystalline Ce1−x La x (OH)CO3 samples to give nanocrystalline Ce1−x La x O2−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 O2 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. 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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 O2 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.</abstract><pub>American Chemical Society</pub><doi>10.1021/jp810321y</doi><tpages>5</tpages></addata></record> |
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title | Crystalline Ce(III)−La(III) Double Basic Carbonates: A Chemical Shortcut To Obtain Nanometric La(III)-Doped Ceria |
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