Journal
PHYSICAL REVIEW LETTERS
Volume 99, Issue 13, Pages -Publisher
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevLett.99.136403
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Temperature-dependent dc susceptibility and x-ray powder diffraction on a pure tetragonal sample of Sr2VO4 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 approximate to 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 Sr2VO4 predicted by first-principles calculations using combinations of the local-density approximation and the GW method.
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