期刊
PHYSICAL REVIEW B
卷 80, 期 22, 页码 -出版社
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevB.80.220402
关键词
crystal structure; iron; iron compounds; magnetic moments; magnetic structure; multiferroics; neutron diffraction; polarisation; specific heat; spin dynamics
FeVO4 has been studied by heat capacity, magnetic susceptibility, electric polarization and single-crystal neutron-diffraction experiments. The triclinic crystal structure is made of S-shaped clusters of six Fe3+ ions, linked by VO43- groups. Two long-range magnetic ordering transitions occur at T-N1=22 K and T-N2=15 K. Both magnetic structures are incommensurate and below T-N2, FeVO4 becomes weakly ferroelectric coincidentally with the loss of the collinearity of the magnetic structure in a very similar fashion than in the classical TbMnO3 multiferroic material. However we argue that the symmetry considerations and the mechanisms invoked to explain these properties in TbMnO3 do not straightforwardly apply to FeVO4. First, the magnetic structures, even the collinear structure, are all acentric so that ferroelectricity in FeVO4 is not correlated with the fact magnetic ordering is breaking inversion symmetry. Regarding the mechanism, FeVO4 has quenched orbital moments that questions the exact role of the spin-orbit interactions.
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