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Achieving efficient and robust seawater oxidation through rational design of V2O3/NiFeP composite
Quan Li1, Qifeng Han1,2, Hehao Zhou3
1College of Chemistry and Materials Science, Sichuan Normal University, Chengdu 610068, Sichuan, China. liquan6688@163.com.
None:
Direct seawater electrolysis has potential in green hydrogen production; however, its anode is susceptible to chloride-induced corrosion, limiting its durability. Herein, using nickel foam (NF) as a catalyst support, we developed a V2O3/NiFeP/NF anode for alkaline seawater oxidation. During the oxygen evolution reaction, NiFeP generates phosphate ions (PO43-), which electrostatically repel chloride ions (Cl-). As a Lewis acid, V2O3 enriches OH- on the surface, thereby enhancing catalytic activity and facilitating Cl- repulsion. At an industrial-scale current density of 1000 mA cm-2, V2O3/NiFeP/NF requires only 335 mV of overpotential and operates stably for 1000 h with negligible degradation and a small amount of active chlorine generation. The membrane electrode assembly electrolyzer, comprising a V2O3/NiFeP/NF anode and a Pt/C/NF cathode, exhibits stable operation at 300 mA cm-2 for 250 h.
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