Author
Listed:
- Rana Saha
(Max Planck Institute of Microstructure Physics)
- Abhay K. Srivastava
(Max Planck Institute of Microstructure Physics
Institute of Physics, Martin Luther University, Halle-Wittenberg)
- Tianping Ma
(Max Planck Institute of Microstructure Physics
Institute of Physics, Martin Luther University, Halle-Wittenberg)
- Jagannath Jena
(Max Planck Institute of Microstructure Physics
Institute of Physics, Martin Luther University, Halle-Wittenberg)
- Peter Werner
(Max Planck Institute of Microstructure Physics)
- Vivek Kumar
(Max Planck Institute for Chemical Physics of Solids)
- Claudia Felser
(Max Planck Institute for Chemical Physics of Solids)
- Stuart S. P. Parkin
(Max Planck Institute of Microstructure Physics
Institute of Physics, Martin Luther University, Halle-Wittenberg)
Abstract
Magnetic anti-skyrmions are one of several chiral spin textures that are of great current interest both for their topological characteristics and potential spintronic applications. Anti-skyrmions were recently observed in the inverse tetragonal Heusler material Mn1.4Pt0.9Pd0.1Sn. Here we show, using Lorentz transmission electron microscopy, that anti-skyrmions are found over a wide range of temperature and magnetic fields in wedged lamellae formed from single crystals of Mn1.4Pt0.9Pd0.1Sn for thicknesses ranging up to ~250 nm. The temperature-field stability window of the anti-skyrmions varies little with thickness. Using micromagnetic simulations we show that this intrinsic stability of anti-skyrmions can be accounted for by the symmetry of the crystal lattice which is imposed on that of the Dzyaloshinskii-Moriya exchange interaction. These distinctive behaviors of anti-skyrmions makes them particularly attractive for spintronic applications.
Suggested Citation
Rana Saha & Abhay K. Srivastava & Tianping Ma & Jagannath Jena & Peter Werner & Vivek Kumar & Claudia Felser & Stuart S. P. Parkin, 2019.
"Intrinsic stability of magnetic anti-skyrmions in the tetragonal inverse Heusler compound Mn1.4Pt0.9Pd0.1Sn,"
Nature Communications, Nature, vol. 10(1), pages 1-7, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-13323-x
DOI: 10.1038/s41467-019-13323-x
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