Enhancement of the spin polarization of an Fe3 O4 (100) surface by nitric oxide adsorption

Physical Chemistry Chemical Physics : PCCP
Z Y LiZ J Ding

Abstract

The geometric, electronic and magnetic properties of a nitric oxide (NO) adsorbed Fe3O4(100) surface have been investigated using density functional theory (DFT) calculations. NO molecules preferentially bond with surface Fe(B) atoms via their N atoms. The generalized gradient approximation (GGA) is not recommended to be used in such a strongly correlated system since it provides not only an overestimation of the adsorption energy and an underestimation of the Fe(B)-N bond length, but also magnetic quenching of the adsorbate and the bonded Fe(B) atoms. In contrast, a tilted geometry and magnetization of the adsorbate and the bonded Fe(B) atom are obtained after including the strong on-site Coulomb interactions through a Hubbard term (GGA+U). The spin-down 2π* states of the NO molecule are filled and broadened due to the adsorbate-substrate interaction and the molecule-molecule interaction. The surface spin polarization close to the Fermi level is expected to be greatly enhanced by the NO adsorption which has significance for interface design in spintronic devices.

References

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May 27, 2015·Physical Chemistry Chemical Physics : PCCP·X SunY Yamauchi

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Citations

Oct 23, 2019·Frontiers in Chemistry·Beata LesiakP Borowicz

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Methods Mentioned

BETA
electron diffraction
X-ray
electron spectroscopy

Software Mentioned

Vienna ab initio simulation package ( VASP )
SPMDS
SPPES

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