1,319 research outputs found

    Ferroelectricity from spin supercurrents in LiCuVO4

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    We have studied the magnetic structure of the ferroelectric frustrated spin-1/2 chain material LiCuVO4 in applied electric and magnetic fields using polarized neutrons. A symmetry and mean-field analysis of the data rules out the presence of static Dzyaloshinskii-Moriya interaction, while exchange striction is shown to be negligible by our specific-heat measurements. The experimentally observed magnetoelectric coupling is in excellent agreement with the predictions of a purely electronic mechanism based on spin supercurrents.Comment: 4 pages, 3 figures, final versio

    Haydeeite: a spin-1/2 kagome ferromagnet

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    The mineral haydeeite, alpha-MgCu3(OD)6Cl2, is a S=1/2 kagome ferromagnet that displays long-range magnetic order below TC=4.2 K with a strongly reduced moment. Our inelastic neutron scattering data show clear spin-wave excitations that are well described by a Heisenberg Hamiltonian with ferromagnetic nearest-neighbor exchange J1=-38 K and antiferromagnetic exchange Jd=+11 K across the hexagons of the kagome lattice. These values place haydeeite very close to the quantum phase transition between ferromagnetic order and non-coplanar twelve-sublattice cuboc2 antiferromagnetic order. Diffuse dynamic short-range ferromagnetic correlations observed above TC persist well into the ferromagnetically ordered phase with a behavior distinct from critical scattering

    Evidence of a bond-nematic phase in LiCuVO4

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    Polarized and unpolarized neutron scattering experiments on the frustrated ferromagnetic spin-1/2 chain LiCuVO4 show that the phase transition at HQ of 8 Tesla is driven by quadrupolar fluctuations and that dipolar correlations are short-range with moments parallel to the applied magnetic field in the high-field phase. Heat-capacity measurements evidence a phase transition into this high-field phase, with an anomaly clearly different from that at low magnetic fields. Our experimental data are consistent with a picture where the ground state above HQ has a next-nearest neighbour bond-nematic order along the chains with a fluid-like coherence between weakly coupled chains.Comment: 5 pages, 4 figures. To appear in Phys. Rev. Let

    Electronic structure and magnetic properties of the spin-1/2 Heisenberg system CuSe2O5

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    A microscopic magnetic model for the spin-1/2 Heisenberg chain compound CuSe2O5 is developed based on the results of a joint experimental and theoretical study. Magnetic susceptibility and specific heat data give evidence for quasi-1D magnetism with leading antiferromagnetic (AFM) couplings and an AFM ordering temperature of 17 K. For microscopic insight, full-potential DFT calculations within the local density approximation (LDA) were performed. Using the resulting band structure, a consistent set of transfer integrals for an effective one-band tight-binding model was obtained. Electronic correlations were treated on a mean-field level starting from LDA (LSDA+U method) and on a model level (Hubbard model). In excellent agreement of experiment and theory, we find that only two couplings in CuSe2O5 are relevant: the nearest-neighbour intra-chain interaction of 165 K and a non-frustrated inter-chain coupling of 20 K. From a comparison with structurally related systems (Sr2Cu(PO4)2, Bi2CuO4), general implications for a magnetic ordering in presence of inter-chain frustration are made.Comment: 20 pages, 8 figures, 3 table

    Spin correlations and exchange in square lattice frustrated ferromagnets

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    The J1-J2 model on a square lattice exhibits a rich variety of different forms of magnetic order that depend sensitively on the ratio of exchange constants J2/J1. We use bulk magnetometry and polarized neutron scattering to determine J1 and J2 unambiguously for two materials in a new family of vanadium phosphates, Pb2VO(PO4)2 and SrZnVO(PO4)2, and we find that they have ferromagnetic J1. The ordered moment in the collinear antiferromagnetic ground state is reduced, and the diffuse magnetic scattering is enhanced, as the predicted bond-nematic region of the phase diagram is approached.Comment: 4 pages, 4 figure

    Magnetic-field-induced spin excitations and renormalized spin gap of the underdoped superconductor La1.895_{1.895}Sr0.105_{0.105}CuO4_{4}

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    High-resolution neutron inelastic scattering experiments in applied magnetic fields have been performed on La1.895_{1.895}Sr0.105_{0.105}CuO4_{4} (LSCO). In zero field, the temperature dependence of the low-energy peak intensity at the incommensurate momentum-transfer $\mathbf{Q}^{\ }_{\mathrm{IC}}=(0.5,0.5\pm\delta,0),(0.5\pm\delta,0.5,0)exhibitsananomalyatthesuperconducting exhibits an anomaly at the superconducting T^{\}_{c}$ which broadens and shifts to lower temperature upon the application of a magnetic field along the c-axis. A field-induced enhancement of the spectral weight is observed, but only at finite energy transfers and in an intermediate temperature range. These observations establish the opening of a strongly downward renormalized spin gap in the underdoped regime of LSCO. This behavior contrasts with the observed doping dependence of most electronic energy features.Comment: accepted for publication in Phys. Rev. Let

    NMR relaxation rate in the field-induced octupolar liquid phase of spin-1/2 J1-J2 frustrated chains

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    In the spin-1/2 frustrated chain with nearest-neighbor ferromagnetic exchange J1 and next-nearest-neighbor antiferromagnetic exchange J2 under magnetic field, magnetic multipolar-liquid (quadrupolar, octupolar, and hexadecapolar) phases are widely expanded from the saturation down to a low-field regime. Recently, we have clarified characteristic temperature and field dependence of the NMR relaxation rate 1/T_1 in the quadrupolar phase. In this paper, we examine those of 1/T_1 in the octupolar phase combining field theoretical method with numerical data. The relevance of the results to quasi one-dimensional J1-J2 magnets such as PbCuSO4(OH)2, Rb2Cu2Mo3O12 and Li2ZrCuO4 is shortly discussed.Comment: 6 pages (1 column), 3 figure
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