Abstract
In this paper, the relationship between ferroic states and the physicochemical mechanism which governs the (Bi/Pb/La)–O bonds in polycrystalline La doped (0.6)BiFeO3–(0.4)PbTiO3 compounds were investigated. An abrupt change in the symmetries of perovskite-structured samples, from tetragonal (P4mm) to rhombohedral (R3c), occurs with the increase of the La concentration, highlighting the diminishment of the hybridization of the (Bi/Pb)–O bonds when La is added into the solid solution, and the emergence of a characteristic morphotropic phase boundary tuned by doping. A maximum remnant polarization (10 μC/cm2) was observed for low La concentrations (where R3c and P4mm phases coexist), while the maximum remnant magnetization (∼75 × 10−3 emu/g) was observed for highly La concentrated samples. These results show that ferroelectric and weak-ferromagnetic orders are strongly correlated to the structural arrangement, which in turn are directly related to the chemical A–O and B–O bonds (long-range and short-range forces) and with the chemical characteristics of the elements that fulfills the A site of the perovskite structure.
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