Du Jian, Li Zhiheng, Wang Linqin, Ding Yunxuan, Ye Wentao, Yang Wenxing, Sun Licheng
Center of Artificial Photosynthesis for Solar Fuels and Department of Chemistry, School of Science and Research Center for Industries of the Future, Westlake University, 600 Dunyu Road, Hangzhou, Zhejiang Province, 310000, China.
Division of Solar Energy Conversion and Catalysis at Westlake University, Zhejiang Baima Lake Laboratory Co., Ltd., Hangzhou, Zhejiang Province, 310000, China.
Adv Sci (Weinh). 2025 Jun;12(22):e2416661. doi: 10.1002/advs.202416661. Epub 2025 Mar 28.
Hydrogen production through seawater electrolysis is promising but challenging due to severe anode corrosion by chlorine (Cl) ions. Herein, a corrosion-resistant NiFe layered double hydroxide electrode (CAPist-S1) is reported as a high-performance electrocatalyst for seawater oxidation, achieving an industrial-level current density of 1.0 A cm at overpotentials of 200 and 220 mV in alkaline simulated (1 M KOH + 0.5 M NaCl) and natural (1 M KOH + seawater) seawater, respectively, along with extraordinary long-term stability over 9000 h under 1.0 A cm in alkaline natural seawater. A dense NiFe LDH interlayer generated between the NiFe LDH nanosheets and metal substrate is found to efficiently retard the penetration of Cl ions to the substrate surface, improving the resistance to Cl ions corrosion. Furthermore, this dense interlayer is an essential prerequisite for establishing a dynamic equilibrium between Fe leaching and redeposition over the in situ formed FeOOH, and this dynamic equilibrium can in turn stabilize the dense interlayer, maintaining the activity of CAPist-S1 during prolonged electrolysis. Using CAPist-S1 in an anion exchange membrane (AEM) seawater electrolyzer, the obtained electrolyzer stably functions over 700 h at 1.0 A cm under room temperature, indicating promising prospects for industrial seawater electrolysis application.
通过海水电解制氢前景广阔,但由于氯离子对阳极的严重腐蚀,这一过程颇具挑战。在此,我们报道了一种耐腐蚀的镍铁层状双氢氧化物电极(CAPist-S1),它是一种用于海水氧化的高性能电催化剂,在碱性模拟海水(1 M KOH + 0.5 M NaCl)和天然海水(1 M KOH + 海水)中,分别在200和220 mV的过电位下实现了1.0 A cm的工业级电流密度,并且在碱性天然海水中1.0 A cm的电流密度下具有超过9000小时的超长稳定性。研究发现,在镍铁层状双氢氧化物纳米片与金属基底之间生成的致密镍铁层状双氢氧化物中间层能够有效阻碍氯离子渗透到基底表面,提高对氯离子腐蚀的抗性。此外,这种致密中间层是在原位形成的氢氧化铁上建立铁浸出与再沉积动态平衡的必要前提,而这种动态平衡反过来又能稳定致密中间层,在长时间电解过程中保持CAPist-S1的活性。在阴离子交换膜(AEM)海水电解槽中使用CAPist-S1,该电解槽在室温下1.0 A cm的电流密度下稳定运行超过700小时,显示出在工业海水电解应用中的广阔前景。