Abstract

<h2>Summary</h2> Transition metal-based nanomaterials represent an emerging class of highly active and low-cost precatalysts for the oxygen evolution reaction (OER) in alkaline electrolyzers. However, most OER precatalysts undergo slow or incomplete self-reconstructions to generate real active sites, which is a time-consuming process for achieving high OER performance. Thus, we report a new class of OER precatalysts that can achieve highly active OER species by a rapid and deep self-reconstruction (denoted by SELF-RECON). The precatalysts with a core-shell structure comprising NiMoO<sub>4</sub> (core) and NiFe/NiFeO<sub>x</sub> nanoparticles in N-doped amorphous carbons (shell) (denoted by NiMoFeO@NC), can realize rapid MoO<sub>4</sub><sup>2−</sup> dissolution and fast formation of NiOOH with Fe incorporation simultaneously. <i>In situ</i> Raman spectroscopy together with electron microscopy, X-ray photoelectron spectroscopy, and electrochemical tests indicate that the obtained NiFeOOH/NiFe-LDH after SELF-RECON behave as the real active species that outperform NiMoFeO@NC, with ultralow overpotentials and extraordinary long-term stability.

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