Role of superexchange interactions in the ferromagnetism of manganites
Igor O. Troyanchuk, Maxim V. Bushinsky, Nikita V. Volkov, В. Сиколенко, Е. А. Ефимова, C. Ritter
Abstract
Igor O. Troyanchuk, Maxim V. Bushinsky, Nikita V. Volkov, В. Сиколенко, Е. А. Ефимова, C. Ritter
Abstract
Compound La0.7Sr0.3Mn0.85Nb0.15O3, in which manganese ions are in an oxidation state close to 3+, are studied by neutron diffraction and magnetic measurements. This compound is shown to be a ferromagnet with T C = 145 K and a magnetic moment of 3.1 μB/Mn at T = 10 K. No signs of cooperative orbital ordering are detected. When Mg2+ ions substitute for some Nb5+ ions, Mn4+ ions appear but ferromagnetism is not enhanced. An increase in the structural distortions leads to a decrease in the ferromagnetic component. The ferromagnetic state is assumed to be caused by substantial hybridization of the e g orbitals of manganese and oxygen, which increases the positive part of the superexchange interactions.
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Compound La0.7Sr0.3Mn0.85Nb0.15O3, in which manganese ions are in an oxidation state close to 3+, are studied by neutron diffraction and magnetic measurements. This compound is shown to be a ferromagnet with T C = 145 K and a magnetic moment of 3.1 μB/Mn at T = 10 K. No signs of cooperative orbital ordering are detected. When Mg2+ ions substitute for some Nb5+ ions, Mn4+ ions appear but ferromagnetism is not enhanced. An increase in the structural distortions leads to a decrease in the ferromagnetic component. The ferromagnetic state is assumed to be caused by substantial hybridization of the e g orbitals of manganese and oxygen, which increases the positive part of the superexchange interactions.
Key concepts: Superexchange, Ferromagnetism, Condensed matter physics, Manganese, Ion, Neutron diffraction, Materials science, Magnetic moment