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LETTER TO THE EDITOR
2002 J. Phys.: Condens. Matter 14 L551-L557 doi: 10.1088/0953-8984/14/28/105
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Abstract.
The structural and magnetic properties of the geometrically
frustrated spinel system CdV2O4 with V3+ (S = 1), whose lattice constant
and oxygen u-parameter
differ significantly from those of isomorphous MgV2O4 and ZnV2O4, have
been explored by means of x-ray diffraction and through measurements of
the magnetization and nuclear magnetic resonance. CdV2O4 undergoes
a cubic–tetragonal structural transition with ct/at = 0.990
as well as a magnetic transition with a jump of the susceptibility at Tc1 = 97
K. Another magnetic anomaly appears at Tc2 = 35 K
which may be a transition to the antiferromagnetic state. The analysis in terms of
the high-temperature series expansion of up to eighth order precisely indicates the
nearest-neighbour exchange-coupling constant for the cubic phase to be J = 44 K. In the vanadium
spinel with S = 1,
the spin-singlet V4-tetramer model with the exchange coupling Jtet inside V4, where
Jtet = 2J,
is applicable at temperatures above T
Jtet:
for CdV2O4 with Jtet ≤Tc1,
all of the susceptibility data for the cubic phase are explained using that
model, while for MgV2O4 and ZnV2O4 with Jtet ≥Tc1,
it is difficult to account for the data for between Jtet and
Tc1.
In this sense, the present bound state may be regarded as pseudotetramers.
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