تقرير
Tuning skyrmions in B20 compounds by 4d and 5d doping
العنوان: | Tuning skyrmions in B20 compounds by 4d and 5d doping |
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المؤلفون: | Borisov, Vladislav, Xu, Qichen, Ntallis, Nikolaos, Clulow, Rebecca, Shtender, Vitalii, Cedervall, Johan, Sahlberg, Martin, Wikfeldt, Kjartan Thor, Thonig, Danny, Pereiro, Manuel, Bergman, Anders, Delin, Anna, Eriksson, Olle |
سنة النشر: | 2022 |
المجموعة: | Condensed Matter |
مصطلحات موضوعية: | Condensed Matter - Materials Science, Condensed Matter - Strongly Correlated Electrons |
الوصف: | Skyrmion stabilization in novel magnetic systems with the B20 crystal structure is reported here, primarily based on theoretical results. The focus is on the effect of alloying on the 3d sublattice of the B20 structure by substitution of heavier 4d and 5d elements, with the ambition to tune the spin-orbit coupling and its influence on magnetic interactions. State-of-the-art methods based on density functional theory are used to calculate both isotropic and anisotropic exchange interactions. Significant enhancement of the Dzyaloshinskii-Moriya interaction is reported for 5d-doped FeSi and CoSi, accompanied by a large modification of the spin stiffness and spiralization. Micromagnetic simulations coupled to atomistic spin-dynamics and ab initio magnetic interactions reveal a helical ground state and field-induced skyrmions for all these systems. Especially small skyrmions $\sim$50 nm are predicted for Co$_{0.75}$Os$_{0.25}$Si, compared to $\sim$148 nm for Fe$_{0.75}$Co$_{0.25}$Si. Convex-hull analysis suggests that all B20 compounds considered here are structurally stable at elevated temperatures and should be possible to synthesize. This prediction is confirmed experimentally by synthesis and structural analysis of the Ru-doped CoSi systems discussed here, both in powder and in single-crystal forms. Comment: 18 pages, 21 figures, 9 tables |
نوع الوثيقة: | Working Paper |
URL الوصول: | http://arxiv.org/abs/2204.08496 |
رقم الأكسشن: | edsarx.2204.08496 |
قاعدة البيانات: | arXiv |
الوصف غير متاح. |