Spin dynamics of the spin-1/2 kagome lattice antiferromagnet ZnCu3(OH)6Cl2

We have performed thermodynamic and neutron scattering measurements on the S=1/2 kagomé lattice antiferromagnet ZnCu3(OH)6Cl2. The susceptibility indicates a Curie-Weiss temperature of theta CW approximately = -300 K; however, no magnetic order is observed down to 50 mK. Inelastic neutron scattering reveals a spectrum of low energy spin excitations with no observable gap down to 0.1 meV. The specific heat at low-T follows a power law temperature dependence. These results suggest that an unusual spin liquid state with essentially gapless excitations is realized in this kagomé lattice system.     

Magnetic susceptibility of the Kagome antiferromagnet ZnCu3(OH)6Cl2

We analyze the experimental data for the magnetic susceptibility of the material ZnCu3(OH)6Cl2 in terms of the Kagome Lattice Heisenberg model (KLHM), discussing possible role of impurity spins, dilution, exchange anisotropy, and both out-of-plane and in-plane Dzyloshinski-Moriya (DM) anisotropies, with explicit theoretical calculations using the numerical linked cluster method and exact diagonalization. The high-temperature experimental data are well described by the pure Heisenberg model with J=170 K. We show that the sudden upturn in the susceptibility around T=75 K is due to DM interactions. We also observe that at intermediate temperatures, below T=J, our calculated susceptibility for KLHM fits well with a power law T(-0.25).     

Refining the spin Hamiltonian in the spin-1/2 kagome lattice antiferromagnet ZnCu3(OH)6Cl2 using single crystals

We report thermodynamic measurements of the S=1/2 kagome lattice antiferromagnet ZnCu3(OH)6Cl2, a promising candidate system with a spin-liquid ground state. Using single crystal samples, the magnetic susceptibility both perpendicular and parallel to the kagome plane has been measured. A small, temperature-dependent anisotropy has been observed, where χ(z)/χ(p)>1 at high temperatures and χ(z)/χ(p)<1 at low temperatures. Fits of the high-temperature data to a Curie-Weiss model also reveal an anisotropy. By comparing with theoretical calculations, the presence of a small easy-axis exchange anisotropy can be deduced as the primary perturbation to the dominant Heisenberg nearest neighbor interaction. These results have great bearing on the interpretation of theoretical calculations based on the kagome Heisenberg antiferromagnet model to the experiments on ZnCu3(OH)6Cl2.     

Dzyaloshinsky-Moriya anisotropy in the spin-1/2 kagome compound ZnCu3(OH)6Cl2

We report the determination of the Dzyaloshinsky-Moriya interaction, the dominant magnetic anisotropy term in the kagome spin-1/2 compound ZnCu3(OH)6Cl2. Based on the analysis of the high-temperature electron spin resonance (ESR) spectra, we find its main component |Dz|=15(1) K to be perpendicular to the kagome planes. Through the temperature dependent ESR linewidth, we observe a building up of nearest-neighbor spin-spin correlations below approximately 150 K.     

Modified kagome physics in the natural spin-1/2 kagome lattice systems: kapellasite Cu3Zn(OH)6Cl2 and haydeeite Cu3Mg(OH)6Cl2

The recently discovered natural minerals Cu3Zn(OH)6Cl2 and Cu3Mg(OH)6Cl2 are spin 1/2 systems with an ideal kagome geometry. Based on electronic structure calculations, we develop a realistic model which includes couplings across the kagome hexagons beyond the original kagome model that are intrinsic in real kagome materials. Exact diagonalization studies for the derived model reveal a strong impact of these couplings on the magnetic ground state. Our predictions could be compared to and supplied with neutron scattering, thermodynamic data, and NMR data.     

Weak ferromagnetic exchange and anomalous specific heat in ZnCu3(OH)6Cl2

Experimental evidence for a plethora of low energy spin excitations in the spin-1/2 kagome antiferromagnet ZnCu3(OH)6Cl2 may be understandable in terms of an extended Fermi surface of spinons coupled to a U(1) gauge field. We carry out variational calculations to examine the possibility that such a state may be energetically viable. A Gutzwiller-projected wave function reproduces the dimerization of a kagome strip found previously by the density matrix renormalization group. Application to the full kagome lattice shows that the inclusion of a small ferromagnetic next-nearest-neighbor interaction favors a ground state with a spinon Fermi surface.     

Magnetic susceptibility and specific heat of the spin-${\frac{1}{2}}$ Heisenberg model on the kagome lattice and experimental data on ZnCu3(OH)6Cl2

We compute the magnetic susceptibility and specific heat of the spin- Heisenberg model on the kagome lattice with high-temperature expansions and exact diagonalizations. We compare the results with the experimental data on ZnCu₃(OH)₆Cl₂ obtained by Helton et al. [Phys. Rev. Lett. 98, 107204 (2007)]. Down to k_BT/J≃0.2, our calculations reproduce accurately the experimental susceptibility, with an exchange interaction J≃190 K and a contribution of 3.7% of weakly interacting impurity spins. The comparison between our calculations of the specific heat and the experiments indicate that the low-temperature entropy (below ~20 K) is smaller in ZnCu₃(OH)₆Cl₂ than in the kagome Heisenberg model, a likely signature of other interactions in the system.     

63Cu, 35Cl, and 1H NMR in the S=1/2 Kagome lattice ZnCu3(OH)6Cl2

ZnCu(3)(OH)(6)Cl(2) (S=1/2) is a promising new candidate for an ideal Kagome Heisenberg antiferromagnet, because there is no magnetic phase transition down to approximately 50 mK. We investigated its local magnetic and lattice environments with NMR techniques. We demonstrate that the intrinsic local spin susceptibility decreases toward T=0, but that slow freezing of the lattice near approximately 50 K, presumably associated with OH bonds, contributes to a large increase of local spin susceptibility and its distribution. Spin dynamics near T=0 obey a power-law behavior in high magnetic fields.     

Slow magnetic order-order transition in the spin chain antiferromagnet Ca3Co2O6

Using powder neutron diffraction, we have discovered an unusual magnetic order-order transition in the Ising spin chain compound Ca3Co2O6. On lowering the temperature, an antiferromagnetic phase with a propagation vector k=(0.5,-0.5,1) emerges from a higher temperature spin density wave structure with k=(0,0,1.01). This transition occurs over an unprecedented time scale of several hours and is never complete.     

Critical spin dynamics of the 2D quantum Heisenberg antiferromagnets Sr2CuO2Cl2 and Sr2Cu3O4Cl2

We report a neutron scattering study of the long-wavelength dynamic spin correlations in the model two-dimensional S = 1/2 square lattice Heisenberg antiferromagnets Sr2CuO2Cl2 and Sr2Cu3O4Cl2. The characteristic energy scale, omega(0)(T/J), is determined by measuring the quasielastic peak width in the paramagnetic phase over a wide range of temperature ( 0.2 less similarT/J less similar0.7). The obtained values for omega(0)(T/J) agree quantitatively between the two compounds and also with values deduced from quantum Monte Carlo simulations. The combined data show scaling behavior, omega approximately xi(-z), over the entire temperature range with z = 1.0(1), in agreement with dynamic scaling theory.     

Isomeric Cl(2)O(2)(+) and Cl(2)O(2)(-) ions

Charged species structurally related to several isomers of Cl(2)O(2), of considerable importance in atmospheric chemistry, were obtained by chemical ionization (CI) and characterized by collisionally activated dissociation (CAD) mass spectrometry. The ClOClO(+) and [Cl(2)-O(2)](+) species were prepared by positive ion Cl(2)/CI of ClO(2) and O(2), respectively, whereas the ClClO(2)(+) isomer proved an elusive species of considerably lower stability. The ClClO(2)(-) anion was obtained from the negative ion Cl(2)/CI of ClO(2). The formation process, structure and stability of the ions are discussed in connection with available theoretical results and related to the recent preparation of (Cl(2)O(2))(+)SbF(6)(-) and (Cl(2)O(2))(+)Sb(2)F(11)(-) salts in the solid phase. Copyright 1999 John Wiley & Sons, Ltd.     

Critical dynamics of models of the antiferromagnet Cr2O3

The critical dynamics of models of the real antiferromagnet Cr₂O₃ is investigated by the Monte Carlo method. The relaxation times of systems with N = 256, 500, 864, 2048, and 2916 spins are determined using the autocorrelation functions formalism. The values of the dynamic critical index z are calculated based on them.     

Coexistence of long-range order and spin fluctuation in geometrically frustrated clinoatacamite Cu2Cl(OH)3

Muon spin rotation experiments are carried out on clinoatacamite, Cu2Cl(OH)3, which is a new geometrically frustrated system featuring a three-dimensional network of corner-sharing tetrahedral 3d Cu2+ spins. A long-range antiferromagnetic order occurs below 18.1 K with a surprisingly small entropy release of about 0.05Rln2/Cu. Below 6.5 K, the static long-range order transforms abruptly into a metastable state with nearly complete depolarization of muon spins which suggests strong fluctuation. The system then enters a state in which partial long-range order and spin fluctuation coexist down to the lowest experimentally attainable temperature of 20 mK. This work presents a novel system for studying geometric frustration.     

NMR study of guanidinium cation dynamics in C(NH2)3SbCl6

Proton NMR second moment and spin—lattice relaxation times T ₁ and T _1p have been studied for polycrystalline guanidinium hexachloroantimonate C(NH₂)₃SbCl₆ in a wide temperature range. A dynamic inequivalence of two cations has been detected in spite of their crystal-lographical equivalence. Activation parameters for C₃ reorientation and self-diffusion of the more mobile cation have been determined. It was shown that the para–ferroelastic phase transition at 351 K is connected with abrupt changes in the dynamics of the two cations. The weaker, second-order transition at 265 K is thought to be related to a change in the dynamics of one of the cations.     

Three-dimensional ab initio quantum dynamics of the photodesorption of CO from Cr(2)O(3)(0001): stereodynamic effects

Having performed the first three-dimensional ab initio quantum dynamical study of photodesorption from solid surfaces, we gained mechanistic understanding of the rotational alignment observed in the CO/Cr(2)O(3)(0001) system. Our study is based on potential energy surfaces obtained by embedded cluster calculations for both the electronic ground and excited state of the adsorbate substrate complex. Stochastic wave packet calculations demonstrate the importance of the angular degrees of freedom for the microscopic picture of the desorption process in addition to the desorption coordinate.