4.6 Article

Loose spherical FeOOH/MnO nanoarrays from a simple in situ hydrothermal method for enhanced oxygen evolution electrocatalysis

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DOI: 10.1016/j.colsurfa.2023.131228

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In situ hydrothermal; Heterostructure; Fe-based composites; Low crystallinity; Oxygen evolution reaction

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The loose spherical MnFe bimetal oxide nanoarrays based on nickel foam were successfully synthesized by a simple in situ hydrothermal method. The loose nanoarrays facilitate water adsorption and exposure of active sites, enabling the catalyst to exhibit excellent electrocatalytic OER activity. The low crystal-linity characteristic of the material is favorable for lattice distortion shrinkage, and the formation of Fe/Mn-O sites can accelerate the charge transfer rate, thereby accelerating the OER process. Meanwhile, the strong interaction of electrons between the hetero-structure can adjust the binding energy intensity and enhance the density of states near the Fermi level, improving the electrocatalytic performance.
The development of abundant, low-cost, stable and efficient non-precious metal OER electrocatalysts is of great significance in large-scale water splitting for hydrogen production. Herein, loose spherical (Spherical-like composed of loose nanoarrays) MnFe bimetal oxide nanoarrays based on nickel foam were successfully synthesized by a simple in situ hydrothermal method. The loose nanoarrays facilitate water adsorption and exposure of active sites, enabling the catalyst to exhibit excellent electrocatalytic OER activity in alkaline media with an overpotential of 209 mV and a Tafel slope of 70 mV center dot dec(-1). The addition of Fe greatly improves the electrical conductivity of the composites and the Fe site as the main active site, which together to the enhanced catalytic performance of FeOOH/MnO@NF (FeOOH/MnO In situ growth on Nickel Foam). In addition, the low crystal-linity characteristic of the material is favorable for lattice distortion shrinkage, and the formation of Fe/Mn-O sites can accelerate the charge transfer rate, thereby accelerating the OER process. Meanwhile, the results of density functional theory calculations show that due to the strong interaction of electrons between the hetero-structure, the displacement of the D-band center of the metal atom and the enhanced density of states near the Fermi level can adjust the binding energy intensity, which can affect the OER process, thereby improving the electrocatalytic performance. The findings broaden the exploration avenues of bimetallic oxyhydroxides as materials for water electrolysis and provides a new strategy for energy conversion and storage of sustainable energy.

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