Short period magnetization texture of B20-MnGe explained by thermally fluctuating local moments
Eduardo Mendive-Tapia, Manuel dos Santos Dias, Sergii Grytsiuk, Julie, B. Staunton, Stefan Bl\"ugel, Samir Lounis

TL;DR
This paper investigates the unique short-range magnetic textures in MnGe, revealing that isotropic exchange interactions, rather than chiral Dzyaloshinskii-Moriya interactions, primarily govern its magnetic properties, contrasting with other B20 compounds.
Contribution
It demonstrates that MnGe's magnetic behavior is driven by isotropic exchange interactions, and introduces a model showing how higher-order interactions stabilize complex magnetic states.
Findings
MnGe's magnetic properties are explained by isotropic exchange interactions.
Comparison with FeGe validates the theoretical approach.
Higher-order interactions stabilize triple-q magnetic states.
Abstract
B20-type compounds, such as MnSi and FeGe, host helimagnetic and skyrmion phases at the mesoscale, which are canonically explained by the combination of ferromagnetic isotropic interactions with weaker chiral Dzyaloshinskii-Moriya ones. Mysteriously, MnGe evades this paradigm as it displays a noncollinear magnetic state at a much shorter nanometer scale. Here we show that the length scale and volume-dependent magnetic properties of MnGe stem from purely isotropic exchange interactions, generally obtained in the paramagnetic state. Our approach is validated by comparing MnGe with the canonical B20-helimagnet FeGe. The free energy of MnGe is calculated, from which we show how triple-q magnetic states can stabilize by adding higher-order interactions.
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