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The cation distribution of the compounds (Fe0,5Ta0,5)O2 and (Fe0,45Nb0,53)O2 has been redetermined by the combined use of neutron and X-ray powder diffraction. Analysis of the powder patterns showed that the compounds are isostructural, their structure being of the rutile-type AO2. The cations are statistically distributed. There exists no partial ordering, neither of Fe and Ta nor of Fe and Nb. Neutron diffraction patterns taken at 4.2 K showed only one magnetic reflection, which is strongly broadened. The magnetic structure of (Fe0.5Ta0.5)O2 is of MnF2-type, whereas (Fe0.45Nb0.53)O2 orders in the BEY-structure. Profile analysis of these broadened reflections was carried out with the convolution integral of a Gaussian with a Lorentzian function, from which correlation lengths could be derived.
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