No Arabic abstract
We report the first detailed investigation of K$_2$MnS$_2$ and K$_2$MnSe$_2$ from the K$_2$MnS$_2$ structure type and their magnetic solid solution K$_2$MnS$_{2-x}$Se$_x$ and find that compounds of this structure type consist of strongly-coupled pseudo-one-dimensional antiferromagnetic chains that collectively represent a frustrated two-dimensional triangular antiferromagnet. Bulk samples of K$_2$MnS$_{2-x}$Se$_x$ with $0 leq x leq 2$ are characterized using X-ray diffraction, neutron diffraction, magnetization and heat capacity measurements. An incommensurate cycloid magnetic structure with a magnetic propagation vector $k = [0.58~0~1]$ is observed for all samples in K$_2$MnS$_{2-x}$Se$_x$, and the ordering is robust despite a 12% increase in cell volume. Geometric frustration of chains results in incommensurability along $a$ and a two-step magnetic transition. The varying geometries accessible in compounds of this structure type are presented as promising avenues to tune frustration.
We report thermodynamic properties, magnetic ground state, and microscopic magnetic model of the spin-1 frustrated antiferromaget Li$_{2}$NiW$_{2}$O$_{8}$ showing successive transitions at $T_{rm N1}simeq 18$ K and $T_{rm N2}simeq 12.5$ K in zero field. Nuclear magnetic resonance and neutron diffraction reveal collinear and commensurate magnetic order with the propagation vector $mathbf k=(frac12,0,frac12)$ below $T_{rm N2}$. The ordered moment of 1.8 $mu_B$ at 1.5 K is directed along $[0.89(9),-0.10(5),-0.49(6)]$ and matches the magnetic easy axis of spin-1 Ni$^{2+}$ ions, which is determined by the scissor-like distortion of the NiO$_6$ octahedra. Incommensurate magnetic order, presumably of spin-density-wave type, is observed in the region between $T_{rm N2}$ and $T_{rm N1}$. Density-functional band-structure calculations put forward a three-dimensional spin lattice with spin-1 chains running along the $[01bar 1]$ direction and stacked on a spatially anisotropic triangular lattice in the $ab$ plane. We show that the collinear magnetic order in Li$_2$NiW$_2$O$_8$ is incompatible with the triangular lattice geometry and thus driven by a pronounced easy-axis single-ion anisotropy of Ni$^{2+}$.
The Raman spectroscopy and AC and DC magnetization of Dy$_{2-x}$Eu$_x$Ti$_2$O$_7$ have been investigated. In Raman Spectroscopy, the systematic shift in all phonon modes with Eu content in Dy$_{2-x}$Eu$_x$Ti$_2$O$_7$ confirms that Dy$^{3+}$ ion is substituted by Eu3+ ions. High concentration of Eu induces the dipolar exchange interactions and crystal-field interactions in Dy$_{2-x}$Eu$_x$Ti$_2$O$_7$. Rich Eu content samples (x=1.8 and 1.9) show the existence of wasp-waisted hysteresis loop and that can be attributed to the coexistence of dipolar field and anisotropy exchange interaction. AC susceptibility shows two single ion spin freezing transitions corresponding to Dy$^{3+}$ and Eu$^{3+}$ ions respectively in x = 1.5, 1.8, 1.9 samples.
The layered {beta}-NaMnO2, a promising Na-ion energy-storage material has been investigated for its triangular lattice capability to promote complex magnetic configurations that may release symmetry restrictions for the coexistence of ferroelectric and magnetic orders. The complexity of the neutron powder diffraction patterns underlines that the routinely adopted commensurate structural models are inadequate. Instead, a single-phase superspace symmetry description is necessary, demonstrating that the material crystallizes in a compositionally modulated q= (0.077(1), 0, 0) structure. Here, Mn3+ Jahn-Teller distorted MnO6 octahedra form corrugated layer stacking sequences of the {beta}-NaMnO2 type, which are interrupted by flat sheets of the {alpha}-like oxygen topology. Spontaneous long-range collinear antiferromagnetic order, defined by the propagation vector k= (1/2, 1/2, 1/2), appears below TN1= 200 K. Moreover, a second transition into a spatially modulated proper-screw magnetic state (k+-q) is established at TN2= 95 K, with an antiferromagnetic order parameter resembling that of a two-dimensional (2D) system. The evolution of 23Na NMR spin-lattice relaxation identifies a magnetically inhomogene-ous state in the intermediate T-region (TN2 <T< TN1), while its strong suppression below TN2 indicates that a spin-gap opens in the excitation spectrum. High-resolution neutron inelastic scattering confirms that the magnetic dynamics are indeed gapped ({Delta}~5 meV) in the low-temperature magnetic phase, while simulations on the basis of the single-mode approximation suggest that Mn-spins residing on ad-jacent antiferromagnetic chains, establish sizable 2D correlations. Our analysis points that novel struc-tural degrees of freedom promote, cooperative magnetism and emerging dielectric properties in this non-perovskite-type of manganite.
The triangular lattice compound TlYbS$_2$ was prepared as large single crystals via a molten flux growth technique using sodium chloride. Anisotropic magnetic susceptibility measurements down to 0.4 K indicate a complete absence of long-range magnetic order. Despite this lack of long-range order, short-range antiferromagnetic interactions are evidenced through broad transitions, suggesting frustrated behavior. Variable magnetic field measurements reveal metamagnetic behavior at temperatures less than 2 K. Complex low temperature field-tunable magnetic behavior, in addition to no observable long-range order down to 0.4 K, suggest that TlYbS$_2$ is a frustrated magnet and a possible quantum spin liquid candidate.
We have systematically studied the magnetic properties of chromium chalcogene compounds FeCr$_2$Se$_{4-x}$Te$_x$. The FeCr2Se4 undergoes antiferromagnetic ordering below 222 K. Substitution of tellurium lowers the antiferromagnetic ordering temperature and leads to short range ferromagnetic cluster behavior towards the tellurium end. Change over from antiferromagnetic to ferrimagnetic like behavior is also reflected in the corresponding transformation from semiconducting to metallic transport behavior. There is a large variation in the Curie-Weiss temperature, effective magnetic moment and ordering temperature (TN / TC) with Te substitution. The electronic band structure calculations suggest antiferromagnetic and ferrimagnetic ground state for the FeCr2Se4 and FeCr2Te4 respectively.