No Arabic abstract
The crystal and magnetic structures of stoichiometric ZnCr2Se4 have been investigated using synchrotron X-ray and neutron powder diffraction, muon spin relaxation (muSR) and inelastic neutron scattering. Synchrotron X-ray diffraction shows a spin-lattice distortion from the cubic spinel to a tetragonal I41/amd lattice below TN = 21 K, where powder neutron diffraction confirms the formation of a helical magnetic structure with magnetic moment of 3.04(3) {mu}B at 1.5 K; close to that expected for high-spin Cr3+. MuSR measurements show prominent local spin correlations that are established at temperatures considerably higher (< 100 K) than the onset of long range magnetic order. The stretched exponential nature of the relaxation in the local spin correlation regime suggests a wide distribution of depolarizing fields. Below TN, unusually fast (> 100 {mu}s-1) muon relaxation rates are suggestive of rapid site hopping of the muons in static field. Inelastic neutron scattering measurements show a gapless mode at an incommensurate propagation vector of k = (0 0 0.4648(2)) in the low temperature magnetic ordered phase that extends to 0.8 meV. The dispersion is modelled by a two parameter Hamiltonian, containing ferromagnetic nearest neighbor and antiferromagnetic next nearest neighbor interactions with a Jnnn/Jnn = -0.337.
Mn$_3$O$_4$ is a spin frustrated magnet that adopts a tetragonally distorted spinel structure at ambient conditions and a CaMn$_2$O$_4$-type postspinel structure at high pressure. We conducted both optical measurements and emph{ab} emph{initio} calculations, and systematically studied the electronic band structures of both the spinel and postspinel Mn$_3$O$_4$ phases. For both phases, theoretical electronic structures are consistent with the optical absorption spectra, and display characteristic band-splitting of the conduction band. The band gap obtained from the absorption spectra is 1.91(6) eV for the spinel phase, and 0.94(2) eV for the postspinel phase. Both phases are charge-transfer type insulators. The Mn 3emph{d} $t_2$$_g$ and O 2emph{p} form antibonding orbitals situated at the conduction band with higher energy.
We investigate the magnetic properties of the isostructural spinel-spinel interface of NiMn2O4(NMO)-Fe3O4. Although the magnetic transition temperature of the NMO film is preserved, both bulk and interface sensitive measurements demonstrate that the interface exhibits strong interfacial magnetic coupling up to room temperature. While NMO thin films have a ferrimagnetic transition temperature of 60K, both NiFe2O4 and MnFe2O4 are ferrimagnetic at room temperature. Our experimental results suggest that these magnetic properties arise from a thin interdiffused region of (Fe,Mn,Ni)3O4 at the interface leading to Mn and Ni magnetic properties similar to MnFe2O4 and NiFe2O4.
We report $^{51}$V nuclear magnetic resonance (NMR) studies on single crystals of the multiferroic material FeVO$_4$. The high-temperature Knight shift shows Curie-Weiss behavior, $^{51}K = a/(T + theta)$, with a large Weiss constant $theta approx$ 116 K. However, the $^{51}$V spectrum shows no ordering near these temperatures, splitting instead into two peaks below 65 K, which suggests only short-ranged magnetic order on the NMR time scale. Two magnetic transitions are identified from peaks in the spin-lattice relaxation rate, $1/^{51}T_1$, at temperatures $T_{N1} approx$ 19 K and $T_{N2} approx$ 13 K, which are lower than the estimates obtained from polycrystalline samples. In the low-temperature incommensurate spiral state, the maximum ordered moment is estimated as 1.95${mu}_B$/Fe, or 1/3 of the local moment. Strong low-energy spin fluctuations are also indicated by the unconventional power-law temperature dependence $1/^{51}T_1 propto T^2$. The large Weiss constant, short-range magnetic correlations far above $T_{N1}$, small ordered moment, significant low-energy spin fluctuations, and incommensurate ordered phases all provide explicit evidence for strong magnetic frustration in FeVO$_4$.
Magnetic topological phases of quantum matter are an emerging frontier in physics and material science. Along these lines, several kagome magnets have appeared as the most promising platforms. Here, we explore magnetic correlations in the transition-metal-based kagome magnet TbMn$_{6}$Sn$_{6}$. Our results show that the system exhibits an out-of-plane ferrimagnetic structure $P6/mmm$ (comprised by Tb and Mn moments) with slow magnetic fluctuations in a wide temperature range. These fluctuations exhibit a slowing down below $T_{rm C1}^{*}$ ${simeq}$ 120 K and a slightly modified quasi-static magnetic state is established below $T_{rm C1}$ ${simeq}$ 20 K. A canted variation of the $P6/mmm$ structure is possible, where all moments contribute to a net $c$-axis ferrimagnetic state which exhibits zero net in-plane components. Alternatively, a small incommensurate $k$-vector could arise below $T_{rm C1}$. We further show that the temperature evolution of the anomalous Hall conductivity (AHC) is strongly influenced by the low temperature magnetic crossover. More importantly, the here identified magnetic state seems to be responsible for the large quasi-linear magnetoresistance as well as for the appearance of quantum oscillations, which are related to the quantized Landau fan structure featuring a spin-polarized Dirac dispersion with a large Chern gap. Therefore the exciting perspective of a magnetic system arises in which the topological response can be controlled, and thus explored, over a wide range of parameters.
Ultrasound velocity measurements of the orbitally-frustrated GeCo$_2$O$_4$ reveal unusual elastic instabilities due to the phonon-spin coupling within the antiferromagnetic phase. Shear moduli exhibit anomalies arising from the coupling to short-range ferromagnetic excitations. Diplike anomalies in the magnetic-field dependence of elastic moduli reveal magnetic-field-induced orbital order-order transitions. These results strongly suggest the presence of geometrical orbital frustration which causes novel orbital phenomena within the antiferromagnetic phase.