We present comprehensive measurements of the structural, magnetic and electronic properties of layered van-der-Waals ferromagnet VI3 down to low temperatures. Despite belonging to a wellstudied family of transition metal trihalides, this material has received very little attention. We outline, from high-resolution powder x-ray diffraction measurements, a corrected room-temperature crystal structure to that previously proposed and uncover a structural transition at 79 K, also seen in the heat capacity. Magnetization measurements confirm VI3 to be a hard ferromagnet (9.1 kOe coercive field at 2 K) with a high degree of anisotropy, and the pressure dependence of the magnetic properties provide evidence for the two-dimensional nature of the magnetic order. Optical and electrical transport measurements show this material to be an insulator with an optical band gap of 0.67 eV -the previous theoretical predictions of d-band metallicity then lead us to believe VI3 to be a correlated Mott insulator. Our latest band structure calculations support this picture and show good agreement with the experimental data. We suggest VI3 to host great potential in the thriving field of low-dimensional magnetism and functional materials, together with opportunities to study and make use of low-dimensional Mott physics.Two-dimensional van-der-Waals (vdW) magnetic materials have in recent years become the subject of a wide range of intense research 1 . While a large portion of research into two-dimensional materials has centered on graphene, the addition of magnetism into such a system leads to many interesting fundamental questions and opportunities for device applications 2-6 . Particularly for future spintronics applications, semiconducting or metallic materials which exhibit ferromagnetism down to monolayer thickness are an essential ingredient. This has led to a large volume of recent publications on two-dimensional honeycomb ferromagnet CrI 3 7-12 . CrI 3 and VI 3 belong to a wider family of MX 3 transition metal trihalides, with X = Cl, Br, I, which were synthesized in the 60s 13,14 but have since seen little interest until recently 15 . VI 3 is an insulating two-dimensional ferromagnet with a Curie Temperature, T c , given as 55 K and reported to have the layered crystal structure of BiI 3 with space group R-3 [16][17][18] . As shown in a recent review 15 , there is very little available information on VI 3 other than the structure and the expected S = 1 from the 3d 2 configuration of the vanadium sites. Calculations using density functional theory, which additionally yield the exchange constants, have suggested VI 3 to not only remain ferromagnetic down to a single crystalline layer, but to also exhibit Dirac half-metallicity, of interest for spintronic applications 19 .In these vdW materials, hydrostatic pressure forms an extremely powerful tuning parameter. Given the weak mechanical forces between the crystal planes, the application of pressure will dominantly have the effect of pressing the ab planes together, and gradually an...
Mn 3 Sn has recently attracted considerable attention as a magnetic Weyl semimetal exhibiting concomitant transport anomalies at room temperature. The topology of the electronic bands, their relation to the magnetic ground state and their nonzero Berry curvature lie at the heart of the problem. The examination of the full magnetic Hamiltonian reveals otherwise hidden aspects of these unusual physical properties. Here, we report the full spin wave spectra of Mn 3 Sn measured over a wide momentum -energy range by the inelastic neutron scattering technique. Using a linear spin wave theory, we determine a suitable magnetic Hamiltonian which not only explains the experimental results but also stabilizes the low-temperature helical phase, consistent with our DFT calculations. The effect of this helical ordering on topological band structures is further examined using a tight-binding method, which confirms the elimination of Weyl points in the helical phase. Our work provides a rare example of the intimate coupling between the electronic and spin degrees of freedom for a magnetic Weyl semimetal system. 1 arXiv:1811.07549v1 [cond-mat.str-el]
CuAl2O4 is a normal spinel oxide having quantum spin, S=1/2 for Cu is a Jahn-Teller active ion. Thus, we claim that an orbital liquid state is the most likely ground state in CuAl2O4. Of further interest, it also exhibits a large frustration parameter, f = CW/Tm ~67, one of the largest values reported for spinel oxides. Our observations suggest that CuAl2O4 should be a rare example of a frustrated quantum spin glass with a good candidate for an orbital liquid state.
Spin-phonon coupling (SPC) plays a critical role in numerous intriguing phenomena of transition metal oxides (TMOs). In 3d and 4d TMOs, the coupling between spin and lattice degrees of freedom is known to originate from the exchange interaction. On the other hand, the origin of SPC in 5d TMOs remains to be elucidated. To address this issue, we measured the phonon spectra of the 5d pyrochlore iridate Y 2 Ir 2 O 7 using optical spectroscopy. Three infrared-active phonons soften below the Néel temperature of T N ≈ 170 K, indicating the existence of strong SPC. Simulations using density functional theory showed that the coupling is closely related to the Ir-O-Ir bond angle. A tight-binding model analysis reveals that this SPC is mainly mediated by the Dzyaloshinskii-Moriya interaction rather than the usual exchange interaction. We suggest that such unconventional SPC may be realized in other 5d TMOs with non-collinear magnetic order.npj Quantum Materials (2019) 4:17 ; https://doi.
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