Orbital-ordering transition in Sr2VO4

Temperature-dependent dc susceptibility and x-ray powder diffraction on a pure tetragonal sample of Sr(2)VO(4) show an antiferromagnetic orbital-ordering transition at T(oo) = 97 K, in which the occupied orbitals lie along the c axis. The unusual broadening of the x-ray Bragg peaks throughout the or...

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Bibliographic Details
Published in:Physical review letters 2007-09, Vol.99 (13), p.136403-136403
Main Authors: Zhou, H D, Conner, B S, Balicas, L, Wiebe, C R
Format: Article
Language:English
Online Access:Get full text
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Summary:Temperature-dependent dc susceptibility and x-ray powder diffraction on a pure tetragonal sample of Sr(2)VO(4) show an antiferromagnetic orbital-ordering transition at T(oo) = 97 K, in which the occupied orbitals lie along the c axis. The unusual broadening of the x-ray Bragg peaks throughout the orbital-ordering transition temperature region indicates that this process occurs in stages, and the onset of short-range orbital ordering occurs at T(1) approximately 122 K. The study of the order parameter associated with this transition by analyzing the spontaneous strain results in a critical exponent beta = 0.35(2) consistent with 3D Heisenberg behavior. These results experimentally confirm the orbital-ordering state in Sr(2)VO(4) predicted by first-principles calculations using combinations of the local-density approximation and the GW method.
ISSN:0031-9007
DOI:10.1103/PhysRevLett.99.136403