Anion Exchange Membrane Seawater Electrolysis at 1.0 A cm <sup>−2</sup> With an Anode Catalyst Stable for 9000 H

Hydrogen production through seawater electrolysis is promising but challenging due to severe anode corrosion by chlorine (Cl<sup>-</sup>) 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<sup>-2</sup> 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<sup>-2</sup> 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<sup>-</sup> ions to the substrate surface, improving the resistance to Cl<sup>-</sup> 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<sup>-2</sup> under room temperature, indicating promising prospects for industrial seawater electrolysis application.

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Publication Details

Journal
Advanced Science
Published
2025-03-28
DOI
https://doi.org/10.1002/advs.202416661
Citations
18
Primary Topic
Membrane-based Ion Separation Techniques
Type
article
Field-Weighted Citation Impact
12.13

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article

Anion Exchange Membrane Seawater Electrolysis at 1.0 A cm −2 With an Anode Catalyst Stable for 9000 H

Wenxing Yang, Licheng Sun, Yunxuan Ding, Wentao Ye et al.
18 citations
Advanced Science
Membrane-based Ion Separation Techniques
12.13
article

Anion Exchange Membrane Seawater Electrolysis at 1.0 A cm −2 With an Anode Catalyst Stable for 9000 H

Wenxing Yang, Licheng Sun, Yunxuan Ding, Wentao Ye, Linqin Wang, Zhiheng Li, Jian Du
article en
18 citations

Abstract

Hydrogen production through seawater electrolysis is promising but challenging due to severe anode corrosion by chlorine (Cl<sup>-</sup>) 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<sup>-2</sup> 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<sup>-2</sup> 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<sup>-</sup> ions to the substrate surface, improving the resistance to Cl<sup>-</sup> 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<sup>-2</sup> under room temperature, indicating promising prospects for industrial seawater electrolysis application.

Advanced ScienceVol. 12(22)
Westlake University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 1%
Membrane-based Ion Separation Techniques
12.13
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Anion Exchange Membrane Seawater Electrolysis at 1.0 A cm <sup>−2</sup> With an Anode Catalyst Stable for 9000 H — Wenxing Yang, Licheng Sun, et al. · Advanced Science (2025) | TGRS Research Map | TGRS