The inherent catalytic efficiency of Fe3O4 nanoparticles (Fe3O4 NPs) for water splitting is unsatisfactory owing to its limited electronic conductivity and inadequate active sites necessary for both oxygen and hydrogen evolution processes (OER and HER). These issues have prompted the investigation of diverse approaches for Fe3O4 NPs, including doping with transition metals. Herein, the Co-doped Fe3O4 NPs were loaded on Ni-foam using a microwave-assisted method, and characterized by various analytical techniques. The electrochemical investigations demonstrated that Co-doped Fe3O4 NPs exhibit exceptional OER and HER performance, with minimal overpotentials of 146 mV and 210 mV at a current density of 10 mA/cm2, in contrast to Fe3O4 NPs, which showed overpotentials of 278 mV and 245 mV at the same current density. Theoretical investigations indicated that Co-doping substantially altered the electronic structure and optimised the active sites of Fe3O4 NPs, hence enhancing overall catalytic efficiency. This study presents an innovative approach for the synthesis of highly efficient, economical electrocatalysts for water splitting, with potential applications in clean energy generation and sustainable hydrogen production.
Saraswat et al. (Wed,) studied this question.
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