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Title: The fluorite-pyrochlore transformation of Ho{sub 2-y}Nd{sub y}Zr{sub 2}O{sub 7}

Journal Article · · Journal of Solid State Chemistry
 [1];  [1];  [1];  [2]
  1. School of Chemistry, University of Sydney, Sydney, NSW 2006 (Australia)
  2. School of Chemistry, niversity of Sydney, Sydney, NSW 2006 (Australia)

Twelve members of the Ho{sub 2-y}Nd{sub y}Zr{sub 2}O{sub 7} series, prepared using conventional solid state methods, have been characterised by neutron powder diffraction. Ho{sub 2}Zr{sub 2}O{sub 7} has a defect fluorite structure whereas Nd{sub 2}Zr{sub 2}O{sub 7} is found to adopt the ordered pyrochlore structure with the composition induced fluorite-pyrochlore transformation occurring near y=1. Rietveld analysis on the neutron data for all the compositions reveals an increase in lattice parameter as a function of y across the entire series, with a small discontinuity associated with the transformation. The neutron profile results suggest that domains of pyrochlore-type initially begin to form before crystallising into a separate phase, and therefore that anion and cation ordering processes are distinct. There is a strong correlation between the extent of disorder in the anion sublattice and the x-parameter of 48f oxygen. These results point the way to a better understanding of the stability observed in pyrochlore structures. - Graphical abstract: Neutron diffraction profiles for Nd{sub 2-y}Ho{sub y}Zr{sub 2}O{sub 7} type oxides reveal details of the transformation from the ordered pyrochlore structure (y=0) to the disordered fluorite structure (y=2). Highlights: > Structures of twelve members of the Ho{sub 2-y}Nd{sub y}Zr{sub 2}O{sub 7} series studied using neutron powder diffraction. > Domains of pyrochlore-type materials form at low doping levels. > Higher doping stabilises the pyrochlore. > Anion and cation ordering processes are distinct.

OSTI ID:
21580186
Journal Information:
Journal of Solid State Chemistry, Vol. 184, Issue 8; Other Information: DOI: 10.1016/j.jssc.2011.05.054; PII: S0022-4596(11)00303-3; Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; ISSN 0022-4596
Country of Publication:
United States
Language:
English