Our ab initio studies show clear evidence that magnetic anisotropy (MA) and the direction of magnetization in metallic magnetic multilayers can be tailored at once by surface charging. By taking Fe-Pt multilayers as a representative example, we demonstrate that surface charging has a deep effect on the magnitude of the MA, which is composition dependent, achieving remarkably large values for systems featuring a single Fe layer capped with Pt. More intriguing is the behavior of the multilayers capped with iron bilayers, for which surface charging not only affects the value of the anisotropy but an easy-axis switching is also revealed. By analyzing the electronic structure of the magnetic layers and relating the MA to the orbital moment anisotropy, some insights about the origin of the MA from a local perspective can be inferred.
We review the state of the art of surface magnetic property control with non-magnetic means, concentrating on metallic surfaces and techniques such as charge-doping or external electric field (EEF) application. Magneto-electric coupling via EEF-based charge manipulation is discussed as a way to tailor single adatom spins, exchange interaction between adsorbates or anisotropies of layered systems. The mechanisms of paramagnetic and spin-dependent electric field screening and the effect thereof on surface magnetism are discussed in the framework of theoretical and experimental studies. The possibility to enhance the effect of EEF by immersing the target system into an electrolyte or ionic liquid is discussed by the example of substitutional impurities and metallic alloy multilayers. A similar physics is pointed out for the case of charge traps, metallic systems decoupled from a bulk electron bath. In that case the charging provides the charge carrier density changes necessary to affect the magnetic moments and anisotropies in the system. Finally, the option of using quasi-free electrons rather than localized atomic spins for surface magnetism control is discussed with the example of Shockley-type metallic surface states confined to magnetic nanoislands.
Performing state-of-the-art ab initio calculations we study the effect of the electric field on magnetic properties of Co and Co-Pt chains on Pt(111). Our studies give clear evidence that an externally applied electric field could permit one to tailor magnetic anisotropy in chains. It is demonstrated that the physics behind this effect is related to the spin-dependent screening of an external electric field at the chains. A strong enhancement of magnetic anisotropy energy in mixed Co-Pt chains, compared to pure Co chains, is found. The interplay between atomic structure and the magnetic anisotropy energy is discussed.
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