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000889652 1001_ $$0P:(DE-HGF)0$$aMendive-Tapia, Eduardo$$b0$$eCorresponding author
000889652 245__ $$aShort period magnetization texture of B20-MnGe explained by thermally fluctuating local moments
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000889652 520__ $$aB20-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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000889652 7001_ $$0P:(DE-HGF)0$$aStaunton, Julie B.$$b3
000889652 7001_ $$0P:(DE-Juel1)130548$$aBlügel, Stefan$$b4
000889652 7001_ $$0P:(DE-Juel1)130805$$aLounis, Samir$$b5
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