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Incommensurate spin-density-wave order in quasi-one-dimensional metallic antiferromagnet NaV2O4

Hiroshi Nozaki, Jun Sugiyama, Martin Månsson, Masashi Harada, Vladimir Pomjakushin, Vadim Sikolenko, Antonio Cervellino, Bertrand Roessli, and Hiroya Sakurai
Phys. Rev. B 81, 100410(R) – Published 23 March 2010
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Abstract

To clarify the reason for the coexistence of long-range antiferromagnetic order and metallic conductivity for NaV2O4, in which the V ions form quasi-one-dimensional zigzag chains along the b axis, we have performed a neutron-scattering experiment using a powder sample down to 20 K. The analysis of the magnetic powder diffractogram below TN=140K demonstrates the formation of an incommensurate spin-density-wave order with k=(0,0.191,0); the ordered moment was estimated as (0,0,0.77μB) at 20 K.

  • Received 24 February 2010

DOI:https://doi.org/10.1103/PhysRevB.81.100410

©2010 American Physical Society

Authors & Affiliations

Hiroshi Nozaki 1,*, Jun Sugiyama 1, Martin Månsson 2, Masashi Harada 1, Vladimir Pomjakushin 2, Vadim Sikolenko 2, Antonio Cervellino 3, Bertrand Roessli 2, and Hiroya Sakurai 4

  • 1Toyota Central Research and Development Laboratories Inc., Nagakute, Aichi 480-1192, Japan
  • 2Laboratory for Neutron Scattering, ETH Zürich and Paul Scherrer Institut, CH-5232 Villigen PSI, Switzerland
  • 3Swiss Light Source, Paul Scherrer Institut, CH-5232 Villigen PSI, Switzerland
  • 4National Institute for Materials Science, Namiki, Tsukuba, Ibaraki 305-0044, Japan

  • *e1236@mosk.tytlabs.co.jp
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Vol. 81, Iss. 10 — 1 March 2010

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  • Figure 1
    (Color online) Crystal structure of NaV2O4. The V2O4 double chains, i.e., zigzag chains are formed by a network of edge-sharing VO6 octahedra align along the b axis so as to make an irregular hexagonal 1D channel. The Na ions are located in the center of the 1D channel.Reuse & Permissions
  • Figure 2
    (Color online) SR-XRD pattern at T=150K and fit result by Rietveld analysis where the reliability (R) factor was minimized down to 4.96%. The diffraction peaks from the V2O3 phase are also observed. However, since its mass fraction is estimated as 1.3%, the V2O3 phase is eventually ignorable for the present structural and magnetic-structural analyses.Reuse & Permissions
  • Figure 3
    (Color online) T dependences of lattice parameters and unit-cell volume for NaV2O4 obtained by Rietveld analysis. Gray (red online) and black symbols denotes the data taken using He-flow cryostat and liquid N2 cryojet, respectively.Reuse & Permissions
  • Figure 4
    (Color online) (a) NPD patterns obtained at 20 and 150 K, and their difference. At least, four magnetic Bragg peaks are clearly observed and they are indexed by an incommensurate propagation vector with k=(0,0.191,0). (b) Fit result for the NPD pattern obtained at 20 K using a SDW model along the b axis (Γ3,S). (c) T dependence of the normalized square root of the intensity of the magnetic Bragg peak 0qy0. The μ+SR result (muon-spin precession frequency fμ in ZF) is also plotted for comparison; below 120 K, the second highest fμ among the four fμ’s is plotted, as it is continuous to fμ above 120 K. The solid line in (c) represents the T dependence of the BCS gap energy.Reuse & Permissions
  • Figure 5
    (Color online) Magnetic structure of NaV2O4 at 20 K. Small (red) and large (blue) circles correspond to V ions at different sites (V1 and V2). Arrows indicate the direction and magnitude of the V moment. Na and O atoms are not shown for clarity. The average value of the ordered magnetic moment is estimated as 0.49μB/V by integration of Eq. (1) in the whole lattices, although the effective magnetic moment (μeff) was reported as 1.992.70μB/V (Ref. 4).Reuse & Permissions
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