Contribution of the Sub-Surface to Electrocatalytic Activity in Atomically Precise La0.7Sr0.3MnO3 Heterostructures

Electrocatalytic reactions are known to take place at the catalyst/electrolyte interface. Whereas recent studies of size-dependent activity in nanoparticles and thickness-dependent activity of thin films imply that the sub-surface layers of a catalyst can contribute to the catalytic activity as well, most of these studies consider actual modification of the surfaces. In this study, the role of catalytically active sub-surface layers was investigated by employing atomic-scale thickness control of the La0.7Sr0.3MnO3 (LSMO) films and heterostructures, without altering the catalyst/electrolyte interface. The activity toward the oxygen evolution reaction (OER) shows a non-monotonic thickness dependence in the LSMO films and a continuous screening effect in LSMO/SrRuO3 heterostructures. The observation leads to the definition of an electrochemically-relevant depth on the order of 10 unit cells. This study on the electrocatalytic activity of epitaxial heterostructures provides new insight in designing efficient electrocatalytic nanomaterials and core-shell architectures.

Automated summary

This study investigates the role of catalytically active sub-surface layers in electrocatalytic reactions by controlling the atomic-scale thickness of LSMO films and heterostructures. The thickness dependence of activity towards the oxygen evolution reaction varies in LSMO films and LSMO/SrRuO3 heterostructures. This research provides new insights for designing efficient electrocatalytic nanomaterials and core-shell architectures.