Magnetoelectric (ME) materials combine magnetic and electric polarizabilities in the same phase, offering a basis for developing high-density data storage and spintronic or low-consumption devices owing to the possibility of triggering one property with the other. Such applications require strong interaction between the constitutive properties, a criterion that is rarely met in classical inorganic ME materials at room temperature. We provide evidence of a strong ME coupling in a paramagnetic ferroelectric lanthanide coordination complex with magnetostrictive phenomenon. The properties of this molecular material suggest that it may be competitive with inorganic magnetoelectrics.

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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.