The La_0.6Sr_0.4Co_0.2Fe_0.8O₃ (LSCF48) cathode material was used as a protective-conducting coating on an interconnect made of Crofer 22 APU ferritic steel intended for application in intermediate-temperature solid oxide fuel cell (IT-SOFC) stacks. The LSCF48 coating was deposited on the surface of the steel via screen-printing followed by appropriate thermal treatment. The oxidation kinetics of the Crofer 22 APU steel—uncoated and coated with LSCF48—approximately obeys the parabolic rate law in air at 1,073 K under isothermal and cyclic oxidation conditions. The oxidation rate for uncoated steel is higher than that for coated steel. SEM–EDS and XRD investigations showed that the LSCF48 coating interacts with the steel during long-term oxidation in the afore-mentioned thermal conditions, and an intermediate multilayer interfacial zone is formed. This intermediate layer leads to lower area specific resistance in air at 1,073 K in comparison to the Crofer 22 APU steel without surface modification.

The effects of prolonged exposure to air at 1073 K on Al20Cr25Nb20Ti20Zr15 and Al20Cr25Nb19Ti20Zr15Y1 (at.%) high-entropy alloys (HEAs) were investigated in this work. Combined scanning electron microscopy and energy-dispersive x-ray spectroscopy (SEM–EDS) analysis revealed that scales containing all major elements in the systems are formed during the oxidation process. Thermogravimetric analysis carried out under the above-mentioned corrosive conditions indicates an initial parabolic kinetics course in the case of the sample with 1 at.% Y addition. However, after a certain period of time, the correlation between mass gain per unit surface area and time becomes linear. In the other case, oxidation proceeds according to the parabolic rate law for the entire process duration. The addition of 1 at.% Y decreases the parabolic rate constants by 1 order of magnitude, thereby improving the chemical stability of the studied Al-Cr-Nb-Ti-Zr system. This is confirmed by visual evaluation, as well as SEM–EDS cross-sectional analysis. Additionally, x-ray diffraction studies indicate that a multiphase oxide scale is formed on the metallic core of both samples. This means that selective oxidation does not occur and all constituent elements took part in the reaction. Taking all of the above into account, it can be concluded that more research is required to fully understand and improve the corrosion resistance of Ti-Al-Cr-Nb-based HEAs.

The objective of this work is to analyse the chemical stability of BaCe_0.85Y_0.15O_3−δ –Ce_0.85Y_0.15O_2−δ (BCY15–YDC15) composite materials at 600 °C and to compare the aforementioned chemical stability with that of pure BCY15. The composite powders were obtained by mixing together powders of BCY15 and YDC15 in the following volume fractions: 90 % BCY15 + 10 % YDC15, 70 % BCY15 + 30 % YDC15, 30 % BCY15 + 70 % YDC15, 20 % BCY15 + 80 % YDC15 and 10 % BCY15 + 90 % YDC15. After that both powders and sintered samples of the BCY15 and the BCY15–YDC15 composites were saturated in two different atmospheres at 600 °C: CO₂/H₂O (3.1 mol% H₂O) and N₂/H₂O (46.8 mol% H₂O). The effects of the previously mentioned atmospheres on the physicochemical properties of the samples were investigated via differential thermal analysis (DTA) combined with thermogravimetric analysis (TG). Furthermore, mass spectrometry was used to analyse the chemical composition of the gases released from the samples during the DTA–TG heating process. The surface and cross-section morphology of the samples were examined by scanning electron microscopy. Moreover, the phase composition of each sample was studied via X-ray Diffraction. From the combined analysis, it can be concluded that the addition of YDC15 in the composite samples leads to an increase in resistance against the corrosive effects of CO₂. Furthermore, it was determined that all samples maintain stability in the presence of H₂O at 600 °C.