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 in | Journal of solid state chemistry Vol. 207; pp. 111 - 116 | 
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| Main Authors | , , , | 
| Format | Journal Article | 
| Language | English | 
| Published | 
        Amsterdam
          Elsevier Inc
    
        01.11.2013
     Elsevier  | 
| Subjects | |
| Online Access | Get full text | 
| ISSN | 0022-4596 1095-726X  | 
| DOI | 10.1016/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. | 
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| ISSN: | 0022-4596 1095-726X  | 
| DOI: | 10.1016/j.jssc.2013.09.024 |