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Register a new userExternal magnetic field effects on a distorted kagome antiferromagnet
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We report bulk magnetization, and elastic and inelastic neutron scattering measurements under an external magnetic field, $H$, on the weakly coupled distorted kagome system, Cu_{2}(OD)_3Cl. Our results show that the ordered state below 6.7 K is a canted antiferromagnet and consists of large antiferromagnetic $ac$-components and smaller ferromagnetic $b$-components. By first-principle calculations and linear spin wave analysis, we present a simple spin hamiltonian with non-uniform nearest neighbor exchange interactions resulting in a system of coupled spin trimers with a single-ion anisotropy that can qualitatively reproduce the spin dynamics of Cu_{2}(OD)_3Cl.
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High-resolution time-of-flight powder neutron diffraction and high-field magnetization were measured to investigate the magnetic structure and existence of a field-induced magnetic phase transition in the distorted kagome antiferromagnet Cs$_2$Cu$_3$SnF$_{12}$. Upon cooling from room temperature, the compound undergoes a structural phase transition at $T_textrm{t}=185$ K from the rhombohedral space group $Rbar{3}m$ with the perfect kagome spin network to the monoclinic space group $P2_1/n$ with the distorted kagome planes. The distortion results in three inequivalent exchange interactions among the $S=1/2$ Cu$^{2+}$ spins that magnetically order below $T_textrm{N}=20.2$ K. Magnetization measured with a magnetic field applied within the kagome plane reveals small in-plane ferromagnetism resulting from spin canting. On the other hand, the out-of-plane magnetization does not show a clear hysteresis loop of the ferromagnetic component nor a prominent anomaly up to 170 T, with the exception of the subtle knee-like bend around 90 T, which could indicate the 1/3 magnetization plateau. The combined analysis using the irreducible representations of the magnetic space groups and magnetic structure refinement on the neutron powder diffraction data suggests that the magnetic moments order in the magnetic space group $P2_1/n$ with the all-in-all-out spin structure, which by symmetry allows for the in-plane canting, consistent with the in-plane ferromagnetism observed in the magnetization.
We present the crystal structure and magnetic properties of Y$_{3}$Cu$_{9}$(OH)$_{19}$Cl$_{8}$, a stoichiometric frustrated quantum spin system with slightly distorted kagome layers. Single crystals of Y$_{3}$Cu$_{9}$(OH)$_{19}$Cl$_{8}$ were grown under hydrothermal conditions. The structure was determined from single crystal X-ray diffraction and confirmed by neutron powder diffraction. The observed structure reveals two different Cu-positions leading to a slightly distored kagome layer in contrast to the closely related YCu$_{3}$(OH)$_{6}$Cl$_{3}$. Curie-Weiss behavior at high-temperatures with a Weiss-temperature $theta_{W}$ of the order of $-100$ K, shows a large dominant antiferromagnetic coupling within the kagome planes. Specific-heat and magnetization measurements on single crystals reveal an antiferromagnetic transition at T$_{N}=2.2$ K indicating a pronounced frustration parameter of $theta_{W}/T_{N}approx50$. Optical transmission experiments on powder samples and single crystals confirm the structural findings. Specific-heat measurements on YCu$_{3}$(OH)$_{6}$Cl$_{3}$ down to 0.4 K confirm the proposed quantum spin-liquid state of that system. Therefore, the two Y-Cu-OH-Cl compounds present a unique setting to investigate closely related structures with a spin-liquid state and a strongly frustrated AFM ordered state, by slightly releasing the frustration in a kagome lattice.
We investigate the magnetism of a previously unexplored distorted spin-1/2 kagome model consisting of three symmetry-inequivalent nearest-neighbor antiferromagnetic Heisenberg couplings and uncover a rich ground state phase diagram even at the classical level. Using analytical arguments and numerical techniques we identify a collinear $vec{Q} = 0$ magnetic phase, two unusual non-collinear coplanar $vec{Q} = (1/3,1/3)$ phases and a classical spin liquid phase with a degenerate manifold of non-coplanar ground states, resembling the jammed spin liquid phase found in the context of a bond-disordered kagome antiferromagnet. We further show with density functional theory calculations that the recently synthesized Y-kapellasite $text{Y}_{text{3}}text{Cu}_{text{9}}text{(OH)}_{text{19}}text{Cl}_{text{8}}$ is a realization of this model and predict its ground state to lie in the region of $vec{Q} = (1/3,1/3)$ order, which remains stable even after inclusion of quantum fluctuation effects within variational Monte Carlo and pseudofermion functional renormalization group. Interestingly, the excitation spectrum of Y-kapellasite lies between that of an underlying triangular lattice of hexagons and a kagome lattice of trimers. The presented model opens a new direction in the study of kagome antiferromagnets.
The magnetic behavior of the compound, Gd3Ru4Al12, which has been reported to crystallize in a hexagonal structure about two decades ago, had not been investigated in the past literature despite interesting structural features (that is, magnetic layers and triangles as well as Kagome-lattice features favouring frustrated magnetism) characterizing this compound. We report here the results of magnetization, heat-capacity, and magnetoresistance studies in the temperature (T) range 1.8-300 K. The results establish that there is a long-range magnetic order of an antiferromagnetic type below (TN= ) 18.5 K, despite a much large value (about 80 K) of paramagnetic Curie temperature with a positive sign characteristic of ferromagnetic interaction. We attribute this to geometric frustration. The most interesting finding is that there is an additional magnetic anomaly below about 55 K before the onset of long range order in the magnetic susceptibility data. Concurrent with this observation, the sign of isothermal entropy change remains positive above TN with a broad peak above TN. This observation indicates the presence of ferromagnetic clusters before the onset of long range magnetic order. Thus, this compound may serve as an example for a situation in which magnetic frustration due to geometrical reasons is faced by competition with such precursor effects. There is also a reversal of the sign of entropy-change in the curves for lower final fields (for H less than 30 kOe) on entering into magnetically ordered state consistent with the entrance into antiferromagnetic state. The magnetoresistance behavior is consistent with above conclusions.
Cu(pz)2(ClO4)2 (with pz denoting pyrazine, C4H4N2) is among the best realizations of a two-dimensional spin-1/2 square-lattice antiferromagnet. Below T_N = 4.21 K, its weak interlayer couplings induce a 3D magnetic order, strongly influenced by external magnetic fields and/or hydrostatic pressure. Previous work, focusing on the [H, T] phase diagram, identified a spin-flop transition, resulting in a field-tunable bicritical point. However, the influence of external pressure has not been investigated yet. Here we explore the extended [p, H, T] phase diagram of Cu(pz)2(ClO4)2 under pressures up to 12 kbar and magnetic fields up to 7.1 T, via magnetometry and 35Cl nuclear magnetic resonance (NMR) measurements. The application of magnetic fields enhances T_XY , the crossover temperature from the Heisenberg to the XY model, thus pointing to an enhancement of the effective anisotropy. The applied pressure has an opposite effect [dT_N/dp = 0.050(8) K/kbar], as it modifies marginally the interlayer couplings, but likely changes more significantly the orbital reorientation and the square-lattice deformation. This results in a remodeling of the effective Hamiltonian, whereby the field and pressure effects compensate each other. Finally, by comparing the experimental data with numerical simulations we estimate T_BKT, the temperature of the Berezinskii-Kosterlitz-Thouless topological transition and argue why it is inaccessible in our case.
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