Cation diffusion was investigated in La_0.6Sr_0.4CoO_3−δ (LSC) thin films on (100) yttria stabilized zirconia in the temperature range 625–800 °C. Isotopic (⁸⁶Sr) and elemental tracers (Fe, Sm) were used to establish diffusion profiles of the cations in bi- and multi-layered thin films. The profiles were analyzed by time of flight-secondary ion mass spectrometry (ToF-SIMS). Grain and grain boundary diffusion coefficients of the cations were determined for LSC thin films with columnar grains – diffusion along grain boundaries is shown to be about three orders of magnitude faster than in grains. This could be verified for thin films with different grain size. A- and B-site cations showed very similar temperature dependencies with activation energies of ∼3.5 eV for bulk and ∼4.1 eV for grain boundary diffusion. The importance of cation diffusivities for surface segregation of Sr and thus for a major degradation mechanism of LSC cathodes in solid oxide fuel cells is discussed.

Real-time MRI of granular dynamics enabled by a joint optimization of imaging hardware, pulse sequences, and sample properties.

With the ongoing digitalization of industry, imaging sensors are becoming increasingly important for industrial process control. In addition to direct imaging techniques such as those provided by video or infrared cameras, tomographic sensors are of interest in the process industry where harsh process conditions and opaque fluids require non-intrusive and non-optical sensing techniques. Because most tomographic sensors rely on complex and often time-multiplexed excitation and measurement schemes and require computationally intensive image reconstruction, their application in the control of highly dynamic processes is often hindered. This article provides an overview of the current state of the art in fast process tomography and its potential for use in industry.

La_0.6Sr_0.4CoO_3−δ thin films of varying thicknesses (20–170 nm) were prepared by pulsed laser deposition on yttria-stabilized zirconia (100) substrates, and their electrochemical electrode performance was correlated with the chemical surface composition and microstructure (e.g. porosity, surface area). The surface cation composition was analyzed by an atomic etching procedure with on-line inductively coupled plasma optical emission spectrometry detection. The surface sensitivity of the method was increased by dynamically switching the etching reagent during the on-line analysis and quantitative results for even the top atomic layer were obtained. A water-soluble Sr-rich surface species could be quantified on top of the LSC films and in combination with electrochemical analysis of the films by impedance spectroscopy an improved understanding of the surface exchange resistance could be obtained. Microstructural features such as the effective porosity of the films became accessible by a combination of these methods.