Effect of Chemical Disorder on the Magnetic Anisotropy in L10 FeNi from First-Principles Calculations

We use first-principles calculations to investigate how deviations from perfect chemical order affect the magnetocrystalline anisotropy energy (MAE) in L1(0) FeNi. We first analyze the local chemical environment of the Fe atoms in various partially ordered configurations, using the orbital magnetic moment anisotropy (OMA) as proxy for a local contribution to the MAE. We are able to identify a specific nearest neighbor configuration and use this "favorable environment" to successfully design various structures with MAE higher than the perfectly ordered system. However, a systematic analysis of the correlation between local environment and OMA using smooth overlap of atomic positions indicates only a partial correlation, which exists only if the deviation from full chemical order is not too large, whereas in general no such correlation can be identified even using up to third nearest neighbors. Guided by the observation that the identified favorable environment implies an Fe-rich composition, we investigate the effect of randomly inserting additional Fe into the nominal Ni planes of the perfectly ordered structure. We find that the MAE increases with Fe content, at least up to 62.5% Fe. Thus, our paper shows that the perfectly ordered case is not the one with highest MAE and that an increased MAE can be obtained for slightly Fe-rich compositions.