A set of nine samples with nominal composition Ce0.5RE0.5O1.75 (RE ≡ Dy-Lu, Sm, Gd and Y) has been used to develop a novel method based on Raman spectroscopy, useful to evaluate the RE coordination number within the fluorite-type structure (F) of the CeO2-based solid solution. The RE coordination number is a crucial indicator of defects aggregation in doped ceria, and thus of the drop in ionic conductivity observed even well below the compositional limit of the F structure. The method has been tested on several Ce1 − xRExO2 − x/2 compositions (RE ≡ Sm, Gd and Lu, 0.1 ≤ x ≤ 0.4); the obtained results are compared to literature data deriving from EXAFS spectroscopy, and advantages and criticisms of the method are thoroughly discussed. Samples were prepared by a coprecipitation method, their cationic composition was checked by SEM-EDS and their structural features were analyzed by room temperature synchrotron powder x-ray diffraction.

A novel method for the evaluation of the Rare Earth (RE) coordination number in RE-doped ceria through Raman spectroscopy

Artini, Cristina;Carnasciali, Maria Maddalena;Pani, Marcella
2017

Abstract

A set of nine samples with nominal composition Ce0.5RE0.5O1.75 (RE ≡ Dy-Lu, Sm, Gd and Y) has been used to develop a novel method based on Raman spectroscopy, useful to evaluate the RE coordination number within the fluorite-type structure (F) of the CeO2-based solid solution. The RE coordination number is a crucial indicator of defects aggregation in doped ceria, and thus of the drop in ionic conductivity observed even well below the compositional limit of the F structure. The method has been tested on several Ce1 − xRExO2 − x/2 compositions (RE ≡ Sm, Gd and Lu, 0.1 ≤ x ≤ 0.4); the obtained results are compared to literature data deriving from EXAFS spectroscopy, and advantages and criticisms of the method are thoroughly discussed. Samples were prepared by a coprecipitation method, their cationic composition was checked by SEM-EDS and their structural features were analyzed by room temperature synchrotron powder x-ray diffraction.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11567/882957
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