Tuning electrochemially driven surface transformation in atomically flat LaNiO3 thin films for enhanced water electrolysis

Structure-activity relationships built on descriptors of bulk and bulk-terminated surfaces are the basis for the rational design of electrocatalysts. However, electrochemically driven surface transformations complicate the identification of such descriptors. Here we demonstrate how the as-prepared surface composition of (001)-terminated LaNiO3 epitaxial thin films dictates the surface transformation and the electrocatalytic activity for the oxygen evolution reaction. Specifically, the Ni termination (in the as-prepared state) is considerably more active than the La termination, with overpotential differences of up to 150 mV. A combined electrochemical, spectroscopic and density-functional theory investigation suggests that this activity trend originates from a thermodynamically stable, disordered NiO2 surface layer that forms during the operation of Ni-terminated surfaces, which is kinetically inaccessible when starting with a La termination. Our work thus demonstrates the tunability of surface transformation pathways by modifying a single atomic layer at the surface and that active surface phases only develop for select as-synthesized surface terminations. Structure-activity relationships built on descriptors of surfaces can help to design electrocatalysts, but their identification for electrochemically driven surface transformations is challenging. The composition of LaNiO3 thin film surfaces can now dictate surface transformation and activity of the oxygen evolution reaction.

Automated summary

The composition of LaNiO3 thin film surfaces dictates surface transformation and the activity of the oxygen evolution reaction, with Ni termination being significantly more active than La termination in the initial state. Active surface phases only develop for select as-synthesized surface terminations.