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Abstract: The physical properties of magnetic topological materials are strongly influenced by their nontrivial band topology coupled with the magnetic structure. Co3Sn2S2 is a ferromagnetic kagome Weyl semimetal displaying giant intrinsic anomalous Hall effect which can be further tuned via elemental doping, such as Ni substitution for Co. Despite significant interest, the exact valency of Co and the magnetic order of the Ni dopants remained unclear. Here, we report a study of Ni-doped Co3Sn2S2 single crystals using synchrotron-based X-ray magnetic circular dichroism (XMCD), X-ray photoelectron emission microscopy (XPEEM), and hard/soft X-ray photoemission spectroscopy (XPS) techniques. We confirm the presence of spin-dominated magnetism from Co in the host material, and also the establishment of ferromagnetic order from the Ni dopant. The oxygen-free photoemission spectrum of the Co 2p core levels in the crystal well resembles that of a metallic Co film, indicating a Co0+ valency. Surprisingly, we find the electron filling in the Co 3d state can reach 8.7–9.0 electrons in these single crystals. Our results highlight the importance of element-specific X-ray spectroscopy in understanding the electronic and magnetic properties that are fundamental to a heavily studied Weyl semimetal, which could aid in developing future spintronic applications based on magnetic topological materials.

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Abstract: We identify a three-dimensional skyrmion side-face state in chiral magnets that consists of a thin layer of modulated surface spirals and an array of phase-locked skyrmion screws. Such chiral spin structures lead to a characteristic X-shaped magnetic diffraction pattern in resonant elastic x-ray scattering, reminiscent of Photo 51 of the DNA double-helix diffraction. By measuring both thin plates and bulk Cu 2 OSeO 3 crystals in the field-in-plane geometry, we unambiguously identify the modulated skyrmion strings by retrieving their chirality and helix angle. The breaking of the translational symmetry along the side faces suppresses the bulk-favored conical state, providing a stabilization mechanism for the skyrmion lattice phase that has been overlooked so far.

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Abstract: We report a comprehensive study on the magnetic ground state of La 1.5 Ca 0.5 Co O 4 combining single crystal neutron diffraction and resonant magnetic x-ray scattering at the Co L 2 , 3 edges. Three single-crystal samples obtained from the same boule were investigated exhibiting magnetic phase transitions from a high-temperature paramagnetic phase to an antiferromagnetic phase at T N ≈ 52 K . Single crystal neutron diffraction reveals that the crystal structure at room temperature shows an orthorhombic A -centered lattice but with a and b axes almost equal in length. The structural phase transition (charge-ordering-like) from the parent tetragonal cell takes place above 523 K into the space group A 2 m m where two nonequivalent compressed and expanded Co O 6 octahedra are ordered showing a checkerboard pattern in the a b plane. The charge segregation between the nonequivalent Co sites is about 0.4(1) electrons. Resonant magnetic x-ray reflections indexed as ( 1 / 4 , 1 / 4 , 0 ) t , ( 1 / 4 , 1 / 4 , 1 ) t , and ( 1 / 4 , 1 / 4 , 1 / 2 ) t in the parent tetragonal cell were observed at low temperature at the Co L 2 , 3 -edge energy range. The resonant spectral shape, with a noticeable absence of any resonant enhancement at the Co L 2 edge, indicates that only Co 2 + -like ions participate in the magnetic ordering. The polarization analysis discloses that the orientation of Co magnetic moments is the same for the three magnetic orders and they are long-range ordered along the diagonal in the a b plane of the parent tetragonal cell with a slight tilt in the c axis. Despite the onset temperatures for the three resonant magnetic reflections being the same, ≈ 55 K , different thermal behavior is observed between ( 1 / 4 , 1 / 4 , 1 / 2 ) t and ( 1 / 4 , 1 / 4 , L ) t ( L = integer ) reflections whose intensities maximize at different temperatures, suggesting the coexistence of two magnetic arrangements. Moreover, the intensity of the ( 1 / 4 , 1 / 4 , 1 / 2 ) t magnetic reflection is at least ten times larger than that of the ( 1 / 4 , 1 / 4 , L ) t ( L = integer ) ones. On the other hand\, neutron diffraction measurements only detect a single type of antiferromagnetic ordering following the propagation vector k = ( 1 / 4 , 1 / 4 , 1 / 2 ) t that involves half of the Co atoms in the unit cell. We conclude that the bulk magnetic order in La 1.5 Ca 0.5 Co O 4 corresponds then to this propagation vector k = ( 1 / 4 , 1 / 4 , 1 / 2 ) t while ( 1 / 4 , 1 / 4 , 0 ) t and ( 1 / 4 , 1 / 4 , 1 ) t magnetic reflections correspond to a minority magnetic phase that must be due to changes in the oxygen stoichiometry near the surface.

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Abstract: The development of high‐density magnetic recording media is limited by superparamagnetism in very small ferromagnetic crystals. Hard magnetic materials with strong perpendicular anisotropy offer stability and high recording density. To overcome the difficulty of writing media with a large coercivity, heat‐assisted magnetic recording was developed, rapidly heating the media to the Curie temperature Tc before writing, followed by rapid cooling. Requirements are a suitable Tc, coupled with anisotropic thermal conductivity and hard magnetic properties. Here, Rh2CoSb is introduced as a new hard magnet with potential for thin‐film magnetic recording. A magnetocrystalline anisotropy of 3.6 MJ m−3 is combined with a saturation magnetization of μ0Ms = 0.52 T at 2 K (2.2 MJ m−3 and 0.44 T at room temperature). The magnetic hardness parameter of 3.7 at room temperature is the highest observed for any rare‐earth‐free hard magnet. The anisotropy is related to an unquenched orbital moment of 0.42 μB on Co, which is hybridized with neighboring Rh atoms with a large spin–orbit interaction. Moreover, the pronounced temperature dependence of the anisotropy that follows from its Tc of 450 K, together with a thermal conductivity of 20 W m−1 K−1, make Rh2CoSb a candidate for the development of heat‐assisted writing with a recording density in excess of 10 Tb in.−2.

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Abstract: The layered van der Waals antiferromagnet MnBi 2 Te 4 has been predicted to combine the band ordering of archetypical topological insulators such as Bi 2 Te 3 with the magnetism of Mn, making this material a viable candidate for the realization of various magnetic topological states. We have systematically investigated the surface electronic structure of MnBi 2 Te 4 (0001) single crystals by use of spin- and angle-resolved photoelectron spectroscopy experiments. In line with theoretical predictions, the results reveal a surface state in the bulk band gap and they provide evidence for the influence of exchange interaction and spin-orbit coupling on the surface electronic structure.