5
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Large Dzyaloshinskii-Moriya interaction induced by chemisorbed oxygen on a ferromagnet surface

      Read this article at

          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The Dzyaloshinskii-Moriya interaction (DMI) is an antisymmetric exchange interaction that stabilizes chiral spin textures. It is induced by inversion symmetry breaking in noncentrosymmetric lattices or at interfaces. Recently, interfacial DMI has been found in magnetic layers adjacent to transition metals due to the spin-orbit coupling and at interfaces with graphene due to the Rashba effect. We report direct observation of strong DMI induced by chemisorption of oxygen on a ferromagnetic layer at room temperature. The sign of this DMI and its unexpectedly large magnitude—despite the low atomic number of oxygen—are derived by examining the oxygen coverage–dependent evolution of magnetic chirality. We find that DMI at the oxygen/ferromagnet interface is comparable to those at ferromagnet/transition metal interfaces; it has enabled direct tailoring of skyrmion’s winding number at room temperature via oxygen chemisorption. This result extends the understanding of the DMI, opening up opportunities for the chemisorption-related design of spin-orbitronic devices.

          Related collections

          Most cited references44

          • Record: found
          • Abstract: not found
          • Article: not found

          Generalized Gradient Approximation Made Simple

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Real-space observation of a two-dimensional skyrmion crystal.

            Crystal order is not restricted to the periodic atomic array, but can also be found in electronic systems such as the Wigner crystal or in the form of orbital order, stripe order and magnetic order. In the case of magnetic order, spins align parallel to each other in ferromagnets and antiparallel in antiferromagnets. In other, less conventional, cases, spins can sometimes form highly nontrivial structures called spin textures. Among them is the unusual, topologically stable skyrmion spin texture, in which the spins point in all the directions wrapping a sphere. The skyrmion configuration in a magnetic solid is anticipated to produce unconventional spin-electronic phenomena such as the topological Hall effect. The crystallization of skyrmions as driven by thermal fluctuations has recently been confirmed in a narrow region of the temperature/magnetic field (T-B) phase diagram in neutron scattering studies of the three-dimensional helical magnets MnSi (ref. 17) and Fe(1-x)Co(x)Si (ref. 22). Here we report real-space imaging of a two-dimensional skyrmion lattice in a thin film of Fe(0.5)Co(0.5)Si using Lorentz transmission electron microscopy. With a magnetic field of 50-70 mT applied normal to the film, we observe skyrmions in the form of a hexagonal arrangement of swirling spin textures, with a lattice spacing of 90 nm. The related T-B phase diagram is found to be in good agreement with Monte Carlo simulations. In this two-dimensional case, the skyrmion crystal seems very stable and appears over a wide range of the phase diagram, including near zero temperature. Such a controlled nanometre-scale spin topology in a thin film may be useful in observing unconventional magneto-transport effects.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Magnetic skyrmions: advances in physics and potential applications

                Bookmark

                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Science Advances
                Sci. Adv.
                American Association for the Advancement of Science (AAAS)
                2375-2548
                August 14 2020
                August 2020
                August 14 2020
                August 2020
                : 6
                : 33
                : eaba4924
                Affiliations
                [1 ]Physics Department, University of California, Davis, CA 95616, USA.
                [2 ]Depto. Física de Materiales, Universidad Complutense de Madrid, 28040 Madrid, Spain.
                [3 ]Unidad Asociada IQFR(CSIC)-UCM, Madrid E-28040, Spain.
                [4 ]Peter Grünberg Institut and Institute for Advanced Simulation, Forschungszentrum Jülich and JARA, 52425 Jülich, Germany.
                [5 ]Department of Materials Science and Engineering, University of California, Berkeley, CA 94720, USA.
                [6 ]Department of Physics, University of Hamburg, D-20355 Hamburg, Germany.
                [7 ]National Laboratory of Solid State Microstructures, Department of Physics and Collaborative Innovation Center of Advanced Microstructures, Nanjing University, 22 Hankou Road, Nanjing 210093, People’s Republic of China.
                [8 ]Depto. de Física de la Materia Condensada and Condensed Matter Physics Center (IFIMAC), Universidad Autónoma de Madrid, 28049 Madrid, Spain.
                [9 ]NCEM, Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
                [10 ]Physics Department, Georgetown University, Washington, DC 20057, USA.
                Article
                10.1126/sciadv.aba4924
                9eda22e9-7557-4c06-9dc8-67cd5ec603b7
                © 2020

                https://creativecommons.org/licenses/by-nc/4.0/

                History

                Comments

                Comment on this article