International audienceIn this work, we studied the effect of heterovalent Ca, Sr, Pb, and Ba substitution on the crystal structure, dielectric, local ferroelectric, and magnetic properties of the BiFeO3 multiferroic perovskite. Ceramic solid solutions with the general formula Bi0.7A0.3FeO3 (A is a doping element) were prepared and characterized by x-ray diffraction, dielectric, piezoresponse force microscopy (PFM), and magnetic measurements. It is shown that the crystal structure of the compounds is described within the space group R3c, permitting the spontaneous polarization, whose existence was confirmed by the PFM data. Magnetic properties of the solid solutions are determined by the ionic radius of the substituting element. Experimental results suggest that the increase in the radius of the A-site ion leads to the effective suppression of the spiral spin structure of BiFeO3, resulting in the appearance of net magnetization

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International audienceRelaxor ferroelectrics are a prototypical example of ferroic systems in which interplay between atomic disorder and order parameters gives rise to emergence of unusual properties, including non-exponential relaxations, memory effects, polarization rotations, and broad spectrum of bias- and emperatureinduced phase transitions. Despite more than 40 years of extensive research following the original discovery of ferroelectric relaxors by the Smolensky group, the most basic aspect of these materials - the existence and nature of order parameter - has not been understood thoroughly. Using extensive imaging and spectroscopic studies by variable-temperature and time resolved piezoresponse force microscopy, we fi nd that the observed mesoscopic behavior is consistent with the presence of two effective order parameters describing dynamic and static parts of polarization, respectively. The static component gives rise to rich spatially ordered systems on the 100 nm length scales, and are only weakly responsive to electric fi eld. The surface of relaxors undergoes a mesoscopic symmetry breaking leading to the freezing of polarization fl uctuations and shift of corresponding transition temperature

Bi 1 − x A x Fe O 3 ceramics (A=Ca,Sr,Pb) were sintered by conventional mixed oxide route. The crystallographic structure of all samples is characterized by the rhombohedral symmetry (space group R3c). The existence of switchable ferroelectric polarization is verified by piezoresponse force microscopy that is proven to be a useful technique in semi-insulating ferroelectrics. Magnetic properties of Ca and Sr-doped ceramics are found to reproduce the antiferromagnetic behavior of undoped BiFeO3 without any enhancement of the magnetization. On the contrary, Pb-doped compound demonstrates appearance of a weak ferromagnetism. It is thus shown that Pb doping of BiFeO3 is a promising way for preparing multiferroic materials.

Room-temperature crystal structure, local ferroelectric, and magnetic properties of the Bi1−xGdxFeO3 (x=0.1,0.2,0.3) polycrystalline samples have been investigated by x-ray diffraction, piezoresponse force microscopy, and magnetometry techniques. Performed measurements have revealed a sequence of the composition-driven structural phase transitions R3c→Pn21a (occurs at x∼0.1) and Pn21a→Pnma (takes place within the concentrational range of 0.2<x<0.3). The latter structural transformation is attributed to the substitution-induced suppression of the polar displacements. Gd substitution has been shown to effectively induce the appearance of the spontaneous magnetization, thus indicating a promising way for improving multiferroic properties of antiferromagnetic BiFeO3.