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Structural and magnetic properties of the perovskites A2LaFe2SbO9 (A = Ca, Sr, Ba)
Polycrystalline samples of A2LaFe2SbO9 (A = Ca, Sr, Ba) perovskites appeared monophasic to X-ray or neutron powder diffraction but a single-crystal study utilising transmission electron microscopy revealed a greater level of complexity. Although local charge balance is maintained, compositional an...
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Published in: | Journal of solid state chemistry 2021-03, Vol.295, p.121914, Article 121914 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Polycrystalline samples of A2LaFe2SbO9 (A = Ca, Sr, Ba) perovskites appeared monophasic to X-ray or neutron powder diffraction but a single-crystal study utilising transmission electron microscopy revealed a greater level of complexity. Although local charge balance is maintained, compositional and structural variations are present among and within the submicron-sized crystals. Despite the inhomogeneity, A = Ca is monophasic with a partially-ordered distribution of Fe3+ and Sb5+ cations across two crystallographically-distinct octahedral sites, i.e. Ca2La(Fe1.25Sb0.25)2d (Fe0.75Sb0.75)2cO9. For A = Sr or Ba, the inhomogeneities result in differences in the tilting patterns of the octahedra and the ordering of the B cations. Particles of A = Sr contain a phase (Fe:Sb ~2:1) without B cation ordering and one (Fe:Sb ~1:1) with B cation ordering. Monophasic A = Ba lacks long-range cation order although ordered nanodomains are present within the disordered phase. The temperature dependence of the magnetic properties of each sample is discussed.
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•Increasing size of the substituted A cation decreases the octahedral tilts•TEM revealed local variations in the composition that maintained the charge balance•Ordered and disordered domains coexist in Ba2LaFe2SbO9 and Sr2LaFe2SbO9•Ca2LaFe2SbO9 is ferrimagnetic, whereas Ba2LaFe2SbO9 is antiferromagnetic |
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ISSN: | 0022-4596 1095-726X |
DOI: | 10.1016/j.jssc.2020.121914 |