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L. E. Svistov

Publications and source records attributed to L. E. Svistov.

24 records · Page 2Linked to original sources

NMR study of the high-field magnetic phase of LiCuVO$_4$

We report on NMR studies of the quasi--1D antiferromagnetic $S=1/2$ chain cuprate LiCuVO$_4$, focusing on the high--field spin--modulated phase observed recently in applied magnetic fields $H > H_{\rm c2}$ ($μ_0H_{\rm c2} \approx 7.5$ T). The NMR spectra of $^7$Li and $^{51}$V around the transition from the ordered to the paramagnetic state were measured. It is shown that the spin--modulated magnetic structure forms with ferromagnetic interactions between spins of neighboring chains within the {\bf ab}--plane at low temperatures 0.6 K $ < T < T_{\rm N}$. The best fit provides evidence that the mutual orientation between spins of neighboring {\bf ab}--planes is random. For elevated temperatures $T_{\rm N} < T \lesssim 15$ K, short--range magnetic order occurs at least on the characteristic time scale of the NMR experiment.

cond-mat.mtrl-sci↗

Co-existing chiral and collinear phases in a distorted triangular antiferromagnet

The entire magnetic phase diagram of the quasi two dimensional (2D) magnet on a distorted triangular lattice KFe(MoO4)2 is outlined by means of magnetization, specific heat, and neutron diffraction measurements. It is found that the spin network breaks down into two almost independent magnetic subsystems. One subsystem is a collinear antiferromagnet that shows a simple spin-flop behavior in applied fields. The other is a helimagnet that instead goes through a series of exotic commensurate-incommensurate phase transformations. In the various phases one observes either true 3D order or quasi-2D order. The experimental findings are compared to theoretical predictions found in literature

cond-mat.str-el↗

Spin-modulated quasi-1D antiferromagnet LiCuVO_4

We report on magnetic resonance studies within the magnetically ordered phase of the quasi-1D antiferromagnet LiCuVO_4. Our studies reveal a spin reorientational transition at a magnetic field H_c1 ~ 25 kOe applied within the crystallographical (ab)-plane in addition to the recently observed one at H_c2 \~75 kOe [ M.G. Banks et al., cond-mat/0608554 (2006)]. Spectra of the antiferromagnetic resonance (AFMR) along low-frequency branches can be described in the frame of a macroscopic theory of exchange-rigid planar magnetic structures. These data allow to obtain the anisotropy of the exchange interaction together with a constant of the uniaxial anisotropy. Spectra of 7Li nuclear magnetic resonance (NMR) show that, within the magnetically ordered phase of LiCuVO_4 in the low-field range H < H_c1, a planar spiral spin structure is realized with the spins lying in the (ab)-plane in agreement with neutron scattering studies of B.J. Gibson et al. [Physica B Vol. 350, 253 (2004)]. Based on NMR spectra simulations, the transition at H_c1 can well be described as a spin-flop transition, where the spin plane of the magnetically ordered structure rotates to be perpendicular to the direction of the applied magnetic field. For H > H_c2 ~ 75 kOe, our NMR spectra simulations show that the magnetically ordered structure exhibits a modulation of the spin projections along the direction of the applied magnetic field H.

cond-mat.str-el↗

Magnetic phase diagram, critical behaviour and 2D-3D crossover in a triangular lattice antiferromagnet RbFe(MoO4)2

We have studied the magnetic and thermodynamic properties as well as the NMR spectra of the Heisenberg antiferromagnet RbFe(MoO4)2. The observed temperature dependence of the order parameter, the critical indices and the overall magnetic H-T phase diagram are all in a good agreement with the theoretical predictions for a 2D XY model. The temperature dependence of the specific heat at low temperature demonstrates a crossover from a T^2 law characteristic of a two-dimensional antiferromagnet to a three-dimensional T^3 law.

cond-mat.str-el↗

Quasi two-dimensional antiferromagnet on a triangular lattice RbFe(MoO4)2

RbFe(MoO4)2 is a rare example of a nearly two-dimensional Heisenberg antiferromagnet on a triangular lattice. Magnetic resonance spectra and magnetization curves reveal that the system has a layered spin structure with six magnetic sublattices. The sublattices within a layer are arranged in a triangular manner with the magnetization vectors 120 degree apart. The H-T phase diagram, containing at least five different magnetic phases is constructed. In zero field, RbFe(MoO4)2 undergoes a phase transition at T_N=3.8 K into a non-collinear triangular spin structure with all the spins confined in the basal plane. The application of an in-plane magnetic field induces a collinear spin state between the fields H_c1=47 kOe and H_c2=71 kOe and produces a magnetization plateau at one-third of the saturation moment. Both the ESR and the magnetization measurements also clearly indicate an additional first-order phase transition in a field of 35 kOe. The exact nature of this phase transition is uncertain.

cond-mat.str-el↗

Anisotropic Exchange in LiCuVO$_4$ probed by ESR

We investigated the paramagnetic resonance in single crystals of LiCuVO$_4$ with special attention to the angular variation of the absorption spectrum. To explain the large resonance linewidth of the order of 1 kOe, we analyzed the anisotropic exchange interaction in the chains of edge-sharing CuO$_6$ octahedra, taking into account the ring-exchange geometry of the nearest-neighbor coupling via two symmetric rectangular Cu-O bonds. The exchange parameters, which can be estimated from theoretical considerations, nicely agree with the parameters obtained from the angular dependence of the linewidth. The anisotropy of this magnetic ring exchange is found to be much larger than it is usually expected from conventional estimations which neglect the bonding geometry. Hence, the data yield the evidence that in copper oxides with edge-sharing structures the role of the orbital degrees of freedom is strongly enhanced. These findings establish LiCuVO$_4$ as one-dimensional compound at high temperatures. PACS: 76.30.-v, 76.30.Fc, 75.30.Et

cond-mat.str-el↗