Seawater electrolysis under alkaline conditions is a crucial technology for sustainable hydrogen production. However, achieving the long-term stability of the electrocatalyst remains a significant challenge. In this study, it is demonstrated that surface reconstruction of a transition metal nitride (TMN) can be used to develop a highly stable oxygen evolution reaction (OER) electrocatalyst. Rapid introduction of phosphate groups (PO4 3-) accelerates the in situ surface reconstruction of Ni3FeN, generating a catalyst, with a conductive nitride core and Cl--resistant hydroxide shell that demonstrates outstanding performance, maintaining stability for over 2500 h at 1 A cm-2 current density in alkaline seawater. In situ characterization and density functional theory (DFT) calculations reveal the dynamic evolution of active sites, providing insights into the mechanisms driving long-term stability. This work not only introduces an efficient approach to TMN-based catalyst design but also advances the development of durable electrocatalysts for industrial-scale seawater hydrogen production.
Keywords: durability; electrocatalysis; oxygen evolution reaction; seawater splitting; transition metal nitride.
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