Journal
CATALYSIS TODAY
Volume 409, Issue -, Pages 87-93Publisher
ELSEVIER
DOI: 10.1016/j.cattod.2022.04.022
Keywords
Epitaxial thin films; Crystallographic orientation engineering; Pulse laser deposition; Oxygen defects; Oxygen reduction reaction (ORR); Solid oxide fuel cells (SOFCs); Oxygen migration channels
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Designing oxide materials with specific crystallographic orientations can significantly enhance the oxygen reduction reaction (ORR) activity. This study demonstrates that the (114)-oriented LSC214 films exhibit much higher ORR activity compared to (001)- and (103)-oriented films, thanks to the exposed oxygen migration channels and increased oxygen vacancies. This research provides a new design strategy to enhance the ORR activity for high-performance energy applications and emphasizes the importance of controlling crystallographic orientation to tune electrocatalytic activity.
Designing oxide materials to achieve the high oxygen reduction reaction (ORR) activity is a key requirement to facilitate the development of energy and environmental applications. Manipulating the crystallographic planes of layered oxides has an impact on determining the electrocatalytic activity. However, the correlation between the ORR kinetics and the crystallographic orientations is not fully understood in a single material system. Here, a superconducting oxide, La1.85Sr0.15CuO4-delta (LSC214) is used to demonstrate that the crystallographic orientation plays a crucial role in controlling the ORR activity. The (114)-oriented epitaxial LSC214 films show dramatically enhanced ORR activity up to two orders of magnitude compared to the (001)- and (103)-oriented LSC214 films. We attribute the enhanced ORR activity of the LSC214 films to both the exposed oxygen migration channels and the increased oxygen vacancies. Our study provides a new design strategy to enhance the ORR activity for highperformance energy applications and illustrates that the control of orientation is a simple means to tune the electrocatalytic activity.
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