First-principles investigations of the electronic structure and magnetocrystalline anisotropy in strained magnetite Fe 3 O 4

2002; American Physical Society; Volume: 65; Issue: 9 Linguagem: Inglês

10.1103/physrevb.65.094429

ISSN

1095-3795

Autores

Horng‐Tay Jeng, Guang‐Yu Guo,

Tópico(s)

Magnetic Properties and Applications

Resumo

The electronic structure and magnetocrystalline anisotropy energy of strained fcc ${\mathrm{Fe}}_{3}{\mathrm{O}}_{4}$ have been studied by using the linear muffin-tin orbital method within density functional theory. A uniaxial strain applied along the [001] direction of the magnetite is considered. It is found that the applied strain would initially reduce the calculated band gap of the majority spin and then turn the half-metallic behavior in the cubic limit into the normal metallic state at high in-plane strains of -1.3% and 2.1%. The calculated fourth-order anisotropy constant ${K}_{1}$ of cubic ${\mathrm{Fe}}_{3}{\mathrm{O}}_{4}$ is in fair agreement with the experimental value. The magnitude of ${K}_{1}$ appears to be suppressed under large extensive lateral strains. The second order uniaxial anisotropy constant ${K}_{\mathrm{out}}$ is positive for extensive in-plane strains and is negative for compressive in-plane strains. The positive value of ${K}_{\mathrm{out}}$ minus the shape anisotropy indicates that an ${\mathrm{Fe}}_{3}{\mathrm{O}}_{4}$ film under an extensive in-plane strain larger than 0.2% would show the perpendicular magnetization, in good agreement with recent experiments on ${\mathrm{Fe}}_{3}{\mathrm{O}}_{4}$ films on MgO(100) and CoO(100). Interestingly, site decomposition shows that the A- and B-site Fe atoms in the strained magnetite have comparable anisotropy energies but with the opposite signs, while the oxygen's contribution is negligible. This implies that under an extensive lateral strain, the B-site irons would favor perpendicular magnetization while the A-site irons would prefer an in-plane magnetization. The total ${K}_{\mathrm{out}}$ is dictated by that of the B-site irons due to their number being twice that of the A-site irons.

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