Crystal and magnetic structure of (1−x)BiFeO3–xSrTiO3 (x=0.2, 0.3, 0.4 and 0.8)

The effect of doping SrTiO3 into BiFeO3 on the magnetic and crystal structure has been explored using powder neutron diffraction for (1−x)BiFeO3–xSrTiO3 where x=0.2, 0.3, 0.4, 0.6 and 0.8. While the data are not sensitive to the cycloidal component of the magnetic ordering, the evolution of the coll...

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Published inJournal of solid state chemistry Vol. 207; pp. 111 - 116
Main Authors Goossens, D.J., Weekes, C.J., Avdeev, Maxim, Hutchison, W.D.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Inc 01.11.2013
Elsevier
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ISSN0022-4596
1095-726X
DOI10.1016/j.jssc.2013.09.024

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Summary:The effect of doping SrTiO3 into BiFeO3 on the magnetic and crystal structure has been explored using powder neutron diffraction for (1−x)BiFeO3–xSrTiO3 where x=0.2, 0.3, 0.4, 0.6 and 0.8. While the data are not sensitive to the cycloidal component of the magnetic ordering, the evolution of the collinear antiferromagnetic moment of the G-type antiferromagnetic component with T and x has been explored, as have structural parameters. It is found that for x≤0.4 pure phase samples form in the R3c cell, and for x=0.8 a non-magnetic Pm3¯m phase is obtained. The x=0.6 sample gives a mixed phase. Through the R3c phase the magnetic structure does not change appreciably apart from the reduction of magnetic moment magnitude with the increasing T and/or x. A simple phase diagram for (1−x)BiFeO3–xSrTiO3 , where hexagons indicate the rhombohedral R3c phase and boxes the cubic phase. Filled symbols indicate magnetic ordering. The black arrow indicates TN for BiFeO3. [Display omitted] •We have established part of the phase diagram for doping SrTiO3 into BiFeO3.•(1−x)BiFeO3–xSrTiO3 is isostructural with BiFeO3 up to x<0.4, and cubic for x>0.85.•We have examined the evolution of ordered magnetic moment with T and x.
ISSN:0022-4596
1095-726X
DOI:10.1016/j.jssc.2013.09.024