RESUMO
Driven by the expected contribution of two-dimensional multiferroic systems with strong magnetoelectric coupling to the development of multifunctional nanodevices, here we propose, by means of first-principles calculations, vanadium-halide monolayers as a new class of spin-chirality-driven van der Waals multiferroics. The frustrated 120-deg magnetic structure in the triangular lattice induces a ferroelectric polarization perpendicular to the spin-spiral plane, whose sign is switched by a spin-chirality change. It follows that, in the presence of an applied electric field perpendicular to the monolayers, one magnetic chirality can be stabilized over the other, thereby allowing the long-sought electrical control of spin textures. Moreover, we demonstrate the remarkable role of spin-lattice coupling on magnetoelectricity, which adds to the expected contribution of spin-orbit interaction determined by an anion. Indeed, such compounds exhibit sizeable spin-driven structural distortions, thereby promoting the investigation of multifunctional spin-electric-lattice couplings.
RESUMO
By analysing the results of ab initio simulations performed for Mn3Si2X6 (X = Se, Te), we first discuss the analogies and the differences in electronic and magnetic properties arising from the anion substitution, in terms of size, electronegativity, band widths of p electrons and spin-orbit coupling strengths. For example, through mean-field theory and simulations based on density functional theory, we demonstrate that magnetic frustration, known to be present in Mn3Si2Te6, also exists in Mn3Si2Se6 and leading to a ferrimagnetic ground state. Building on these results, we propose a strategy, electronic doping, to reduce the frustration and thus to increase the Curie temperature (TC). To this end, we first study the effect of electronic doping on the electronic structure and magnetic properties and discuss the differences in the two compounds, along with their causes. Secondly, we perform Monte-Carlo simulations, considering from the first to the fifth nearest-neighbor magnetic interactions and single-ion anisotropy, and show that electron doping efficiently raises the TC.