Internal-strain mediated coupling between polar Bi and magnetic Mn ions in the defect-free quadruple-perovskite BiMn3Mn4O12
Abstract
By means of neutron powder diffraction, we investigated the effect of the polar Bi3+ ion on the magnetic ordering of the Mn3+ ions in BiMn3Mn4O12, the counterpart with quadruple perovskite structure of the simple perovskite BiMnO3. The data are consistent with a noncentrosymmetric spacegroup Im which contrasts the centrosymmetric one I2/m previously reported for the isovalent and isomorphic compound LaMn3Mn4O12, which gives evidence of a Bi3+-induced polarization of the lattice. At low temperature, the two Mn3+ sublattices of the A' and B sites order antiferromagnetically (AFM) in an independent manner at 25 and 55 K, similarly to the case of LaMn3Mn4O12. However, both magnetic structures of BiMn3Mn4O12 radically differ from those of LaMn3Mn4O12. In BiMn3Mn4O12 the moments MA' of the A' sites form an anti-body AFM structure, whilst the moments MB of the B sites result from a large and uniform modulation MB,b along the b-axis of the moments MB,ac in the ac-plane. The modulation is strikingly correlated with the displacements of the Mn3+ ions induced by the Bi3+ ions. Our analysis unveils a strong magnetoelastic coupling between the internal strain created by the Bi3+ ions and the moment of the Mn3+ ions in the B sites. This is ascribed to the high symmetry of the oxygen sites and to the absence of oxygen defects, two characteristics of quadruple perovskites not found in simple ones, which prevent the release of the Bi3+-induced strain through distortions or disorder. This demonstrates the possibility of a large magnetoelectric coupling in proper ferroelectrics and suggests a novel concept of internal strain engineering for multiferroics design.
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