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    Robust metastable skyrmions with tunable size in the chiral magnet FePtMo3 N
    (Woodbury, NY : Inst., 2020) Sukhanov, A.S.; Heinemann, A.; Kautzsch, L.; Bocarsly, J.D.; Wilson, S.D.; Felser, C.; Inosov, D.S.
    The synthesis of new materials that can host magnetic skyrmions and their thorough experimental and theoretical characterization are essential for future technological applications. The β-Mn-type compound FePtMo3N is one such novel material that belongs to the chiral space group P4132, where the antisymmetric Dzyaloshinskii-Moriya interaction is allowed due to the absence of inversion symmetry. We report the results of small-angle neutron scattering (SANS) measurements of FePtMo3N and demonstrate that its magnetic ground state is a long-period spin helix with a Curie temperature of 222 K. The magnetic field-induced redistribution of the SANS intensity showed that the helical structure transforms to a lattice of skyrmions at ∼13 mT at temperatures just below TC. Our key observation is that the skyrmion state in FePtMo3N is robust against field cooling down to the lowest temperatures. Moreover, once the metastable state is prepared by field cooling, the skyrmion lattice exists even in zero field. Furthermore, we show that the skyrmion size in FePtMo3N exhibits high sensitivity to the sample temperature and can be continuously tuned between 120 and 210 nm. This offers different prospects in the control of topological properties of chiral magnets. © 2020 authors. Published by the American Physical Society.
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    Field-Angle-Resolved Magnetic Excitations as a Probe of Hidden-Order Symmetry in CeB6
    (College Park, Md. : APS, 2020) Portnichenko, P.Y.; Akbari, A.; Nikitin, S.E.; Cameron, A.S.; Dukhnenko, A.V.; Filipov, V.B.; Shitsevalova, N.Yu.; Čermák, P.; Radelytskyi, I.; Schneidewind, A.; Ollivier, J.; Podlesnyak, A.; Huesges, Z.; Xu, J.; Ivanov, A.; Sidis, Y.; Petit, S.; Mignot, J.-M.; Thalmeier, P.; Inosov, D.S.
    In contrast to magnetic order formed by electrons' dipolar moments, ordering phenomena associated with higher-order multipoles (quadrupoles, octupoles, etc.) are more difficult to characterize because of the limited choice of experimental probes that can distinguish different multipolar moments. The heavy-fermion compound CeB6 and its La-diluted alloys are among the best-studied realizations of the long-range-ordered multipolar phases, often referred to as "hidden order."Previously, the hidden order in phase II was identified as primary antiferroquadrupolar and field-induced octupolar order. Here, we present a combined experimental and theoretical investigation of collective excitations in phase II of CeB6. Inelastic neutron scattering (INS) in fields up to 16.5 T reveals a new high-energy mode above 14 T in addition to the low-energy magnetic excitations. The experimental dependence of their energy on the magnitude and angle of the applied magnetic field is compared to the results of a multipolar interaction model. The magnetic excitation spectrum in a rotating field is calculated within a localized approach using the pseudospin representation for the Γ8 states. We show that the rotating-field technique at fixed momentum can complement conventional INS measurements of the dispersion at a constant field and holds great promise for identifying the symmetry of multipolar order parameters and the details of intermultipolar interactions that stabilize hidden-order phases. © 2020 authors. Published by the American Physical Society.
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    Magnon spectrum of the helimagnetic insulator Cu2OSeO3
    (London : Nature Publishing Group, 2016) Portnichenko, P.Y.; Romhányi, J.; Onykiienko, Y.A.; Henschel, A.; Schmidt, M.; Cameron, A.S.; Surmach, M.A.; Lim, J.A.; Park, J.T.; Schneidewind, A.; Abernathy, D.L.; Rosner, H.; van den Brink, Jeroen; Inosov, D.S.
    Complex low-temperature-ordered states in chiral magnets are typically governed by a competition between multiple magnetic interactions. The chiral-lattice multiferroic Cu2OSeO3 became the first insulating helimagnetic material in which a long-range order of topologically stable spin vortices known as skyrmions was established. Here we employ state-of-the-art inelastic neutron scattering to comprehend the full three-dimensional spin-excitation spectrum of Cu2OSeO3 over a broad range of energies. Distinct types of high- and low-energy dispersive magnon modes separated by an extensive energy gap are observed in excellent agreement with the previously suggested microscopic theory based on a model of entangled Cu4 tetrahedra. The comparison of our neutron spectroscopy data with model spin-dynamical calculations based on these theoretical proposals enables an accurate quantitative verification of the fundamental magnetic interactions in Cu2OSeO3 that are essential for understanding its abundant low-temperature magnetically ordered phases.
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    Fermi surface nesting in several transition metal dichalcogenides
    (Milton Park : Taylor & Francis, 2008) Inosov, D.S.; Zabolotnyy, V.B.; Evtushinsky, D.V.; Kordyuk, A.A.; Büchner, B.; Follath, R.; Berger, H.; Borisenko, S.V.
    By means of high-resolution angle-resolved photoelectron spectroscopy (ARPES), we have studied the fermiology of 2H transition metal dichalcogenide polytypes TaSe2, NbSe2 and Cu0.2NbS 2. The tight-binding model of the electronic structure, extracted from ARPES spectra for all three compounds, was used to calculate the Lindhard function (bare spin susceptibility), which reflects the propensity to charge density wave (CDW) instabilities observed in TaSe2 and NbSe 2. We show that though the Fermi surfaces of all three compounds possess an incommensurate nesting vector in the close vicinity of the CDW wave vector, the nesting and ordering wave vectors do not exactly coincide, and there is no direct relationship between the magnitude of the susceptibility at the nesting vector and the CDW transition temperature. The nesting vector persists across the incommensurate CDW transition in TaSe2 as a function of temperature despite the observable variations of the Fermi surface geometry in this temperature range. In Cu0.2NbS2, the nesting vector is present despite different doping levels, which leads us to expect a possible enhancement of the CDW instability with Cu intercalation in the Cu xNbS2 family of materials.
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    Momentum-resolved superconducting gap in the bulk of Ba1-xK xFe2As2 from combined ARPES and μSR measurements
    (Milton Park : Taylor & Francis, 2009) Evtushinsky, D.V.; Inosov, D.S.; Zabolotnyy, V.B.; Viazovska, M.S.; Khasanov, R.; Amato, A.; Klauss, H.-H.; Luetkens, H.; Niedermayer, Ch.; Sun, G.L.; Hinkov, V.; Lin, C.T.; Varykhalov, A.; Koitzsch, A.; Knupfer, M.; Büchner, B.; Kordyuk, A.A.; Borisenko, S.V.
    Here we present a calculation of the temperature-dependent London penetration depth, λ(T), in Ba1-xKxFe 2As2 (BKFA) on the basis of the electronic band structure (Zabolotnyy et al 2009 Nature 457 569, Zabolotnyy et al 2009 Physica C 469 448) and momentum-dependent superconducting gap (Evtushinsky et al 2009 Phys. Rev. B 79 054517) extracted from angleresolved photoemission spectroscopy (ARPES) data. The results are compared to the direct measurements of λ(T) by muon spin rotation (μSR) (Khasanov et al 2009 Phys. Rev. Lett. 102 187005). The value of λ(T = 0), calculated with no adjustable parameters, equals 270 nm, while the directly measured one is 320 nm; the temperature dependence λ(T) is also easily reproduced. Such agreement between the two completely different approaches allows us to conclude that ARPES studies of BKFA are bulk-representative. Our review of the available experimental studies of the superconducting gap in the new ironbased superconductors in general allows us to state that most of them bear two nearly isotropic gaps with coupling constants 2ΔkBTc = 2.5±1.5 and 7±2.
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    Anisotropic fractal magnetic domain pattern in bulk Mn1.4PtSn
    (Woodbury, NY : Inst., 2020) Sukhanov, A.S.; Zuniga Cespedes, B.E.; Vir, P.; Cameron, A.S.; Heinemann, A.; Martin, N.; Chaboussant, G.; Kumar, V.; Milde, P.; Eng, L.M.; Felser, C.; Inosov, D.S.
    The tetragonal compound Mn1.4PtSn with D2d symmetry recently attracted attention as the first known material that hosts magnetic antiskyrmions, which differ from the skyrmions known so far by their internal structure. The latter have been found in a number of magnets with the chiral crystal structure. In previous works, the existence of antiskyrmions in Mn1.4PtSn was unambiguously demonstrated in real space by means of Lorentz transmission electron microscopy on thin-plate samples (∼100 nm thick). In the present study, we used small-angle neutron scattering and magnetic force microscopy to perform reciprocal- and real-space imaging of the magnetic texture of bulk Mn1.4PtSn single crystals at different temperatures and in applied magnetic field. We found that the magnetic texture in the bulk differs significantly from that of thin-plate samples. Instead of spin helices or an antiskyrmion lattice, we observe an anisotropic fractal magnetic pattern of closure domains in zero field above the spin-reorientation transition temperature, which transforms into a set of bubble domains in high field. Below the spin-reorientation transition temperature the strong in-plane anisotropy as well as the fractal self-affinity in zero field is gradually lost, while the formation of bubble domains in high field remains robust. The results of our study highlight the importance of dipole-dipole interactions in thin-plate samples for the stabilization of antiskyrmions and identify criteria which should guide the search for potential (anti)skyrmion host materials. Moreover, they provide consistent interpretations of the previously reported magnetotransport anomalies of the bulk crystals. © 2020 authors. Published by the American Physical Society. Published by the American Physical Society under the terms of the "https://creativecommons.org/licenses/by/4.0/"Creative Commons Attribution 4.0 International license. Further distribution of this work must maintain attribution to the author(s) and the published article's title, journal citation, and DOI. Open access publication funded by the Max Planck Society.