Structural Manipulation of Pyrochlores: Thermal Evolution of Metastable Gd2(Ti1-yZry)2O7 Powders Prepared by Mechanical Milling
K.J. Moreno; A.F. Fuentes; J. Hanuza; M. Maczka; U. Amador. Structural Manipulation of Pyrochlores: Thermal Evolution of Metastable Gd2(Ti1-yZry)2O7 Powders Prepared by Mechanical Milling. Journal of Solid State Chemistry (ISSN: 0022-4596). 2006, Vol. 179, p. 3805-2006.
The structural and microstructural characteristics of metastable Gd2(Ti1-yZry)2O7 powders prepared by mechanical milling have been studied by a combination of XRD and Raman spectroscopy. Irrespective of their Zr content, as prepared powder phases present an anion deficient fluorite-type of structure as opposed to the pyrochlore equilibrium configuration obtained for the same solid solution by other synthetic routes. These fluorites are stable versus thermal activation, at least up to temperatures of 800°C. For the Ti-rich compositions, thermal treatments at higher temperatures facilitate the rearrangement of the cation and anion substructures and the relaxation of mechanochemically induced defects whereas for compositions with high Zr content, the fluorite crystal structure is retained even at temperatures as high as 1200°C. Interestingly enough, transient pyrochlores showing a very unusual cation distribution were observed during the thermally induced defect-recovery process.
The structural and microstructural characteristics of metastable Gd2(Ti1-yZry)2O7 powders prepared by mechanical milling have been studied by a combination of XRD and Raman spectroscopy. Irrespective of their Zr content, as prepared powder phases present an anion deficient fluorite-type of structure as opposed to the pyrochlore equilibrium configuration obtained for the same solid solution by other synthetic routes. These fluorites are stable versus thermal activation, at least up to temperatures of 800°C. For the Ti-rich compositions, thermal treatments at higher temperatures facilitate the rearrangement of the cation and anion substructures and the relaxation of mechanochemically induced defects whereas for compositions with high Zr content, the fluorite crystal structure is retained even at temperatures as high as 1200°C. Interestingly enough, transient pyrochlores showing a very unusual cation distribution were observed during the thermally induced defect-recovery process.