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Abstract
To mitigate the adverse effects of high concentrations of Cl− ions in seawater on electrolysis efficiency, it is essential to develop efficient and stable electrocatalysts. Based on this need, CuCo-ZIF NCs were used as a precursor to synthesize a CuCo-TA@FeOOH heterojunction composites, specifically designed for the oxygen evolution reaction (OER) in alkaline seawater, through a combination of acid etching and a self-growth method. The resulting material exhibits an OER overpotential of 234 mV at 10 mA/cm2 in alkaline freshwater and 256 mV at 10 mA/cm2 in seawater electrolyte. This performance is attributed to synergistic interactions at the heterojunction interfaces, which enhances the specific surface area, offers abundant active sites, and improves mass transfer efficiency, thereby increasing catalytic activity. Moreover, at a current density of 100 mA/cm², it maintains stable performance for up to 300 h without deactivation. This remarkable stability and corrosion resistance stems from the synergistic effect at the CoOOH and FeOOH interface formed during reconstruction, which facilitates electron transfer, optimizes the electronic structure during the reaction process, and effectively suppresses the chlorine evolution reaction (CER). This study offers a valuable reference for the rational design of high-performance electrocatalysts for alkaline seawater oxidation.
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Keywords
CuCo-TA@FeOOH
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heterojunction
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hollow structure
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electrocatalytic seawater oxidation
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oxygen evolution reaction (OER)
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Bo Hu, Yang Cao.
Construction of an efficient CuCo-TA@FeOOH heterojunction for high-performance electrocatalytic seawater oxidation.
Front. Energy, 2025, 19(5): 757-766 DOI:10.1007/s11708-025-1021-5
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