阳极
化学
生理盐水
无机化学
盐水
铁氰化物
电极
分析化学(期刊)
核化学
环境化学
盐度
生物
内分泌学
海洋学
物理化学
地质学
作者
Wei Liu,Jiage Yu,Marshet Getaye Sendeku,Tianshui Li,Wenqin Gao,Guotao Yang,Yun Kuang,Xiaoming Sun
标识
DOI:10.1002/anie.202309882
摘要
The direct seawater electrolysis at high current density and low overpotential affords an effective strategy toward clean and renewable hydrogen fuel production. However, the severe corrosion of anode as a result of the saturation of Cl- upon continuous seawater feeding seriously hamper the electrolytic process. Herein, cobalt ferricyanide / cobalt phosphide (CoFePBA/Co2 P) anodes with Cap/Pin structure are synthesized, which stably catalyze alkaline saturated saline water oxidation at 200-2000 mA cm-2 over hundreds of hours without corrosion. Together with the experimental findings, the molecular dynamics simulations reveal that PO43- and Fe(CN)63- generated by the electrode play synergistic role in repelling Cl- via electrostatic repulsion and dense coverage, which reduced Cl- adsorption by nearly 5-fold. The novel anionic synergy endow superior corrosion protection for the electrode, and is expected to promote the practical application of saline water electrolysis.
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