Abstract

The sluggish oxygen evolution reaction (OER) is one of the major factors limiting the application of water splitting for hydrogen production. This study used a single-stage hydrothermal method to synthesize highly porous FeO-Co3O4 nanoparticles on oxidized graphite (GOX) sheets. The fabrication of FeO-Co3O4@GOX nanoparticles depends on the oxidation time. The optimal catalyst (FeO-Co3O4@GOX-10) showed higher activity toward the OER than Co3O4, FeO-Co3O4, FeO-Co3O4@GOX-5, and FeO-Co3O4@GOX-24. The FeO-Co3O4@GOX-10 catalyst exhibited a low overpotential and small Tafel slope of 0.23 V and 64 mV dec−1, respectively, at a current density of 10 mA cm−2, demonstrating enhanced specific activity and turnover frequency. The optimal catalyst played a synergistic role in accelerating the electron transfer process and accelerating the OER with faradaic efficiency of 95.3%. Moreover, the improved activity of the FeO-Co3O4@GOX-10 catalyst was attributed to enhanced active site exposure, fast charge transfer, and synergistic effect of FeO-Co3O4 and GOX. This study provides a new approach for the development of efficient, stable, and environmentally friendly hybrid catalysts for energy conversion applications.

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