Spatial decomposition of magnetic anisotropy in magnets: application for doped Fe16N2

Abstract

We propose a scheme of decomposition of the total relativistic energy in solids to intra- and interatomic contributions. The method is based on a variation of the speed of light from its value in relativistic theory to infinity (a non-relativistic limit). As an illustration of the method, we tested such decomposition in the case of a spin-orbit interaction variation for decomposition of the magnetic anisotropy energy (MAE) in CoPt. We further studied the α''-Fe16N2 magnet doped by Bi, Sb, Co and Pt atoms. It has been found that the addition of Pt atoms can enhance the MAE by as large as five times while Bi and Sb substitutions double the total MAE. Using the proposed technique we demonstrate the spatial distribution of these enhancements. Our studies also suggest that Sb, Pt and Co substitutions could be synthesized by experiments.

References in corpus (6)

• Constituents of magnetic anisotropy and a screening of spin-orbit coupling in solids
• Effects of alloying and strain on the magnetic properties of Fe${}_{16}$N${}_2$
• Large magnetic anisotropy predicted for rare-earth free Fe16-xCoxN2 alloys
• Magnetocrystalline anisotropy in YCo5 and LaCo5: A choice of correlation parameters and the relativistic effects
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Cited by in corpus (1)

• Giant magnetic and optical anisotropy in cerium-substituted M-type strontium hexaferrite driven by 4$f$ electrons