Multifunctional oxides - Influence of defects on the ferroic properties

Transition metal oxides exhibit a wealth of physical phenomena, among them ferroic properties such as ferroelasticity, ferroelectricity and ferromagnetism, or their combination in multiferroics. In addition, transition metal oxides are sensitive to the chemical environment via the external partial pressure of oxygen; changes induce stoichiometry deviations, which cause conductivity changes and modify the ferroic characteristics. The present study focuses on SrTiO3, YMnFeO5, and BiFeO3 and correlates local changes due to point and planar defects with changes of the elastic, polarization and magnetic properties. The microscopic interactions are determined by density functional calculations, which yield the basis for more large-scale simulations with effective Hamiltonian approaches. Under oxygen-poor conditions oxygen vacancies in SrTiO3 accumulate in an external electric field and reduce the hardness. In an Sr/O-rich environment the phases SrO(SrTiO3)n are formed, which yield a distinct change of the X-Ray reflectivity due to the regular arrangement of extrinsic SrO(001) stacking faults. YMn2O5 has a series of complex antiferromagnetic phases in coexistence with ferroelectricity. In YFeMnO5, only one commensurable ferrimagnetic phase was found and ferroelectricity is absent. Based on spin-polarized DFT calculations a Heisenberg model yields the coupling constants of the Fe-substituted and the mangenese-only compounds and relates them to crystal-field interactions. BiFeO3 is a rhombohedral multiferroic with several domain wall configurations. Among them, the 109 and 180 walls have a significant change in the component of their polarization perpendicular to the wall; the corresponding step in the
electrostatic potential is consistent with a recent report of electrical conductivity at the domain walls. Changes in the Fe-O-Fe bond angles at the walls change the canting of the Fe magnetic moments which can enhance the local magnetization.