Insights into cationic ordering in Re-based double perovskite oxides.

Cationic ordering in Sr2FeReO6 (SFRO) and Sr2CrReO6 (SCRO) is investigated using magnetic property measurement, atomic-scale imaging, and first-principles calculations. We find that the nature of cationic ordering strongly depends on the host oxides, although they have the same crystal symmetry and chemical formula. Firstly, adding Re is effective to enhance the cationic ordering in SFRO, but makes it worse in SCRO. Secondly, the microscopic structure of antisite (AS) defects, associated with the level of cationic ordering, is also distinguishable; the AS defects in SFRO are clustered in the form of an antiphase-boundary-like feature, while they are randomly scattered in SCRO. Interestingly, we observe that the clustered AS defects deteriorate the ferromagnetism more than the scattered defects. Our findings elevate the importance of the AS defect configuration as well as the amount of defects in terms of magnetic property.

Enhanced polarization by the coherent heterophase interface between polar and non-polar phases.

A piezoelectric composite containing the ferroelectric polar (Bi(Na0.8K0.2)0.5TiO3: f-BNKT) and the non-polar (0.94Bi(Na0.75K0.25)0.5TiO3-0.06BiAlO3: BNKT-BA) phases exhibits synergetic properties which combine the beneficial aspects of each phase, i.e., the high saturated polarization (Ps) of the polar phase and the low coercive field (Ec) of the non-polar phase. To understand the origin of such a fruitful outcome from this type of polar/non-polar heterophase structure, comprehensive studies are conducted, including transmission electron microscopy (TEM) and finite element method (FEM) analyses. The TEM results show that the polar/non-polar composite has a core/shell structure in which the polar phase (core) is surrounded by a non-polar phase (shell). In situ electrical biasing TEM experiments visualize that the ferroelectric domains in the polar core are aligned even under an electric field of ∼1 kV mm(-1), which is much lower than its intrinsic coercive field (∼3 kV mm(-1)). From the FEM analyses, we can find that the enhanced polarization of the polar phase is promoted by an additional internal field at the phase boundary which originates from the preferential polarization of the relaxor-like non-polar phase. From the present study, we conclude that the coherent interface between polar and non-polar phases is a key factor for understanding the enhanced piezoelectric properties of the composite.

Intriguing photo-control of exchange bias in BiFeO3/La2/3Sr1/3MnO3 thin films on SrTiO3 substrates.

To date, electric fields have been widely used to control the magnetic properties of BiFeO3-based antiferromagnet/ferromagnet heterostructures through application of an exchange bias. To extend the applicability of exchange bias, however, an alternative mechanism to electric fields is required. Here, we report the photo-control of exchange bias in BiFeO3/La2/3Sr1/3MnO3 thin films on an SrTiO3 substrate. Through an ex situ pulsed laser deposition technique, we successfully synthesized epitaxial BiFeO3/La2/3Sr1/3MnO3 thin films on SrTiO3 substrates. By measuring magnetoresistance under light illumination, we investigated the effect of light illumination on resistance, exchange bias, and coercive field in BiFeO3/La2/3Sr1/3MnO3 thin films. After illumination of red and blue lights, the exchange bias was sharply reduced compared to that measured in the dark. With increasing light intensity, the exchange bias under red and blue lights initially decreased to zero and then appeared again. It is possible to reasonably explain these behaviors by considering photo-injection from SrTiO3 and the photo-conductivity of La2/3Sr1/3MnO3. This study may provide a fundamental understanding of the mechanism underlying photo-controlled exchange bias, which is significant for the development of new functional spintronic devices.