Structural evolution of epitaxial SrCoOx films near topotactic phase transition

Control of oxygen stoichiometry in complex oxides via topotactic phase transition is an interesting avenue to not only modifying the physical properties, but utilizing in many energy technologies, such as energy storage and catalysts. However, detailed structural evolution in the close proximity of the topotactic phase transition in multivalent oxides has not been much studied. In this work, we used strontium cobaltites (SrCoOx) epitaxially grown by pulsed laser epitaxy (PLE) as a model system to study the oxidation-driven evolution of the structure, electronic, and magnetic properties. We grew coherently strained SrCoO2.5 thin films and performed post-annealing at various temperatures for topotactic conversion into the perovskite phase (SrCoO3-{\delta}). We clearly observed significant changes in electronic transport, magnetism, and microstructure near the critical temperature for the topotactic transformation from the brownmillerite to the perovskite phase. Nevertheless, the overall crystallinity was well maintained without much structural degradation, indicating that topotactic phase control can be a useful tool to control the physical properties repeatedly via redox reactions.Comment: 16 pages, 4 figure

Macroscopic visualization of fast electrochemical reaction of SrCoOx oxygen sponge

Strontium cobaltite (SrCoOx) is known as a material showing fast topotactic electrochemical Redox reaction so-called oxygen sponge. Although atomic scale phenomenon of the oxidation of SrCoO2.5 into SrCoO3 is known, the macroscopic phenomenon has not been clarified yet thus far. Here, we visualize the electrochemical oxidation of SrCoOx macroscopically. SrCoOx epitaxial films with various oxidation states were prepared by the electrochemical oxidation of SrCoO2.5 film into SrCoO3-d film. Steep decrease of both resistivity and the absolute value of thermopower of electrochemically oxidized SrCoOx epitaxial films indicated the columnar oxidation firstly occurred along with the surface normal and then spread in the perpendicular to the normal. Further, we directly visualized the phenomena using the conductive AFM. This macroscopic image of the electrochemical oxidation would be useful to develop a functional device utilizing the electrochemical redox reaction of SrCoOx.Comment: 24 pages, 5 figures, 5 supplementary figure

Strongly coupled phase transition in ferroelectric/correlated electron oxide heterostructures

We fabricated ultrathin ferroelectric/correlated electron oxide heterostructures composed of the ferroelectric Pb(Zr0.2Ti0.8)O3 and the correlated electron oxide (CEO) La0.8Sr0.2MnO3 on SrTiO3 substrates by pulsed laser epitaxy. The hole accumulation in the ultrathin CEO layer was substantially modified by heterostructuring with the ferroelectric layer, resulting in an insulator-metal transition. In particular, our thickness dependent study showed that drastic changes in transport and magnetic properties were strongly coupled to the modulation of charge carriers by ferroelectric field effect, which was confined to the vicinity of the interface. Thus, our results provide crucial evidence that strong ferroelectric field effect control can be achieved in ultrathin (10 nm) heterostructures, yielding at least a 100,000-fold change in resistivity

Growth and characterization of multiferroic BiMnO3_3 thin films

We have grown epitaxial thin films of multiferroic BiMnO$_3$ using pulsed laser deposition. The films were grown on SrTiO$_3$ (001) substrates by ablating a Bi-rich target. Using x-ray diffraction we confirmed that the films were epitaxial and the stoichiometry of the films was confirmed using Auger electron spectroscopy. The films have a ferromagnetic Curie temperature ($T_C$) of 85$\pm$5 K and a saturation magnetization of 1 $\mu_B$/Mn. The electric polarization as a function of electric field ($P-E$) was measured using an interdigital capacitance geometry. The $P-E$ plot shows a clear hysteresis that confirms the multiferroic nature of the thin films.Comment: 4 pages, 4 figures, submitted to J. Appl. Phy