Solid oxide cells (SOCs) are highly efficient and environmentally benign devices that can be used to store renewable electrical energy in the form of fuels such as hydrogen in the solid oxide electrolysis cell mode and regenerate electrical power using stored fuels in the solid oxide fuel cell mode. Despite this, insufficient long-term durability over 5–10 years in terms of lifespan remains a critical issue in the development of reliable SOC technologies in which the surface segregation of cations, particularly strontium (Sr) on oxygen electrodes, plays a critical role in the surface chemistry of oxygen electrodes and is integral to the overall performance and durability of SOCs. Due to this, this review will provide a critical overview of the surface segregation phenomenon, including influential factors, driving forces, reactivity with volatile impurities such as chromium, boron, sulphur and carbon dioxide, interactions at electrode/electrolyte interfaces and influences on the electrochemical performance and stability of SOCs with an emphasis on Sr segregation in widely investigated (La,Sr)MnO₃and (La,Sr)(Co,Fe)O_3−δ. In addition, this review will present strategies for the mitigation of Sr surface segregation.Graphic

Selective hydrogenation plays an important role in the chemical industry and has a wide range of applications, including the production of fine chemicals and petrochemicals, pharmaceutical synthesis, healthcare product development, and the synthesis of agrochemicals. Pd-based catalysts have been widely applied for selective hydrogenation due to their unique electronic structure and ability to adsorb and activate hydrogen and unsaturated substrates. However, the exclusive and comprehensive summarization of the size, composition, and surface and interface effect of metal Pd on the performance for selective hydrogenation is still lacking. In this perspective, the research progress on selective hydrogenation using Pd-based catalysts is summarized. The strategies for improving the catalytic hydrogenation performance over Pd-based catalysts are investigated. Specifically, the effects of the size, composition, and surface and interfacial structure of Pd-based catalysts, which could influence the dissociation mode of hydrogen, the adsorption, and the reaction mode of the catalytic substrate, on the performance have been systemically reviewed. Then, the progress on Pd-based catalysts for selective hydrogenation of unsaturated alkynes, aldehydes, ketones, and nitroaromatic hydrocarbons is revealed based on the fundamental principles of selective hydrogenation. Finally, perspectives on the further development of strategies for chemical selective hydrogenation are provided. It is hoped that this perspective would provide an instructive guideline for constructing efficient heterogeneous Pd-based catalysts for various selective hydrogenation reactions.