Ferromagnetic ordering, magnetic and magnetotransport properties of R1−xSrx(Mn1−x/2Sbx/2)O3 (R = La, Pr, Nd, Sm, Eu) manganites
Neutron diffraction, magnetic and magnetotransport studies of perovskites R 1 − x 3 + Sr x 2 + ( Mn 1 − x 2 3 + Sb x 2 5 + )O3 (R = La, Pr) were carried out. It is shown that for x ∼ 0.2 systems undergo a transition from an antiferromagnetic state (x = 0) to a ferromagnetic state. In the case of the...
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Veröffentlicht in: | Materials research express 2018-06, Vol.5 (6) |
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Sprache: | eng |
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Zusammenfassung: | Neutron diffraction, magnetic and magnetotransport studies of perovskites R 1 − x 3 + Sr x 2 + ( Mn 1 − x 2 3 + Sb x 2 5 + )O3 (R = La, Pr) were carried out. It is shown that for x ∼ 0.2 systems undergo a transition from an antiferromagnetic state (x = 0) to a ferromagnetic state. In the case of the R = La series a structural transformation from the O′-orthorhombic phase (x = 0) to the O-orthorhombic one occurs, which is due to orbital disordering. At x ≥ 0.6 cluster spin glass like phases arise due to the competition between antiferromagnetic and ferromagnetic interactions, as well as due to the strong diamagnetic dilution. In case of the R = Pr series the structural transition into the O-orthorhombic phase was not observed under (Sr, Sb) codoping. As the ionic radius of the rare-earth ion decreases in the series R0.7Sr0.3Mn0.85Sb0.15O3 the crystal structure distortion increases and the ferromagnetic state (R = La, Pr, Nd) is gradually transformed into a spin glass like state (R = Sm, Eu). The ferromagnetic compounds are insulators and exhibit a large magnitude of the magnetoresistance apparently associated with very small amount of Mn4+ ions. The covalent component of the chemical bond and e.g.-orbitals disordering/mixing are assumed to be responsible for ferromagnetism in the compounds under study. |
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ISSN: | 2053-1591 |
DOI: | 10.1088/2053-1591/aac7b8 |