Magnetic correlations and quantum criticality in the insulating antiferromagnetic, insulating spin liquid, renormalized Fermi liquid, and metallic antiferromagnetic phases of the Mott system V2O3

Wei Bao, C. Broholm, G. Aeppli, S. A. Carter, P. Dai, T. F. Rosenbaum, J. M. Honig, P. Metcalf, and S. F. Trevino
Phys. Rev. B 58, 12727 – Published 15 November 1998
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Abstract

Magnetic correlations in all four phases of pure and doped vanadium sesquioxide (V2O3) have been examined by magnetic thermal-neutron scattering. Specifically, we have studied the antiferromagnetic and paramagnetic phases of metallic V2yO3, the antiferromagnetic insulating and paramagnetic metallic phases of stoichiometric V2O3, and the antiferromagnetic and paramagnetic phases of insulating V1.944Cr0.056O3. While the antiferromagnetic insulator can be accounted for by a localized Heisenberg spin model, the long-range order in the antiferromagnetic metal is an incommensurate spin-density wave, resulting from a Fermi surface nesting instability. Spin dynamics in the strongly correlated metal are dominated by spin fluctuations with a “single lobe” spectrum in the Stoner electron-hole continuum. Furthermore, our results in metallic V2O3 represent an unprecedentedly complete characterization of the spin fluctuations near a metallic quantum critical point, and provide quantitative support for the self-consistent renormalization theory for itinerant antiferromagnets in the small moment limit. Dynamic magnetic correlations for ħω<kBT in the paramagnetic insulator carry substantial magnetic spectral weight. However, they are extremely short-ranged, extending only to the nearest neighbors. The phase transition to the antiferromagnetic insulator, from the paramagnetic metal and the paramagnetic insulator, introduces a sudden switching of magnetic correlations to a different spatial periodicity which indicates a sudden change in the underlying spin Hamiltonian. To describe this phase transition and also the unusual short-range order in the paramagnetic state, it seems necessary to take into account the orbital degrees of freedom associated with the degenerate d orbitals at the Fermi level in V2O3.

  • Received 28 April 1998

DOI:https://doi.org/10.1103/PhysRevB.58.12727

©1998 American Physical Society

Authors & Affiliations

Wei Bao*

  • Physics Department, Brookhaven National Laboratory, Upton, New York 11973

C. Broholm

  • Department of Physics and Astronomy, The Johns Hopkins University, Baltimore, Maryland 21218
  • Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland 20899

G. Aeppli

  • NEC, 4 Independence Way, Princeton, New Jersey 08540

S. A. Carter

  • Department of Physics, University of California, Santa Cruz, California 95064

P. Dai

  • Solid State Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831

T. F. Rosenbaum

  • James Franck Institute and Department of Physics, University of Chicago, Chicago, Illinois 60637

J. M. Honig and P. Metcalf

  • Department of Chemistry, Purdue University, West Lafayette, Indiana 47907

S. F. Trevino

  • United States Army Research Laboratory, Adelphi, Maryland 20783
  • Center for Neutron Research, National Institute of Standards and Technology, Gaithersburg, Maryland 20899

  • *Current address: MST-10, Los Alamos National Laboratory, Los Alamos, NM 87545.

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Vol. 58, Iss. 19 — 15 November 1998

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