Surface Sr segregation behaviors in a model thin film perovskite cathode for solid oxide fuel cells

Surface cation segregation, strontium (Sr) in particular, has been considered as one of crucial barriers to achieving a fast surface oxygen exchange rate of perovskite oxide electrodes for solid oxide fuel cells (SOFCs). However, the major driving force for the segregation phenomenon still remains unknown, and thus it is also unknown how to maximize the cathode performance. In this work, we fabricated epitaxial thin films of SrTi1-xFexO3-δ (STF) via pulsed laser deposition (PLD) and quantitatively characterized their microstructures, surface chemical compositions and oxygen exchange rates by a range of analysis tools, in this case HR-TEM, HR-XRD, angle resolved X-ray photoelectron spectroscopy (AR-XPS) and electrical conductivity relaxation (ECR). The use of well-defined epitaxial thin films not only guarantees high precision, reproducibility and reliability of the surface properties, but also enables us to control the degree of misfit strain by varying the choice of the substrate and the target composition. This, in combination with density functional theory (DTF) simulation, enabled to reveal a close relationship between the degree of surface Sr segregation and the misfit strain and thereby to identify the governing factors for the Sr segregation phenomenon

Virtual Synchronization for Fast Distributed Cosimulation of Dataflow Task Graphs

Fast distributed cosimulation is a challenging problem for the embedded system design. The main theme of this paper is to increase simulation speed by reducing the frequency of intersimulator communications, reducing the active duration of simulators and utilizing the parallelism of component simulators, which is accomplished by combining event-driven and datadriven simulation methods. The proposed technique is applicable when the simulated tasks follow dataflow execution semantics. Experimental results show that the proposed technique can boost the cosimulation speed significantly compared with the previous conservative approaches

Sr Segregation in Perovskite Oxides: Why It Happens and How It Exists

Among the phenomena related to the surface rearrangement of cations in perovskite-based oxides, A-site cation enrichment, Sr in particular, near the surface has been frequently observed. Upon annealing in an oxidizing atmosphere, Sr is often enriched on the surface as compared with the bulk composition of the material, which eventually forms Sr-rich phases or rearranges the crystal structure of the surface. This Sr segregation changes the structure and composition of the perovskite surfaces and thus affects the stability of the materials and the reactivity with gas phases. In this regard, many studies have been carried out in the field of solid oxide electrochemical cells (SOCs). In this review, we summarize the latest research efforts on Sr segregation in perovskite-based SOC O2 electrodes, with a focus on how excess Sr is present. We then discuss the origins of Sr segregation and suggest strategies for suppressing it to realize high-performance perovskite-based O2 electrodes.11Nsciescopu

Enhanced oxygen exchange of perovskite oxide surfaces through strain-driven chemical stabilization

Surface cation segregation and phase separation, of strontium in particular, have been suggested to be the key reason behind the chemical instability of perovskite oxide surfaces and the corresponding performance degradation of solid oxide electrochemical cell electrodes. However, there is no well-established solution for effectively suppressing Sr-related surface instabilities. Here, we control the degree of Sr-excess at the surface of SrTi0.5Fe0.5O3-delta thin films, a model mixed conducting perovskite O-2-electrode, through lattice strain, which significantly improves the electrode surface reactivity. Combined theoretical and experimental analyses reveal that Sr cations are intrinsically under a compressive state in the SrTi0.5Fe0.5O3-delta lattice and that the Sr-O bonds are weakened by the local pressure around the Sr cation, which is the key origin of surface Sr enrichment. Based on these findings, we successfully demonstrate that when a large-sized isovalent dopant is added, Sr-excess can be remarkably alleviated, improving the chemical stability of the resulting perovskite O-2-electrodes.11Nsciescopu