Catalyst for Industrial‐Scale Seawater Electrolysis: Inhibit Active Metal Dissolution and Chlorine Corrosion

Alkaline seawater electrolysis is a promising technology for sustainable green hydrogen production. However, active metal dissolution and chlorine-induced corrosion during long-term, industrial-scale operation pose critical challenges to catalyst stability. Here, a surface engineering strategy is reported using phytic acid (PA) as a molecular "armor" to construct highly durable oxygen evolution reaction (OER) catalysts. Comprehensive characterization and density functional theory (DFT) calculations reveal that surface modification with PO<sub>4</sub> <sup>3-</sup> groups not only facilitates surface reconstruction to form NiOOH active sites, but also optimizes the adsorption-desorption dynamics of key reaction intermediates, thereby enhancing catalytic performance. Importantly, the PO<sub>4</sub> <sup>3-</sup> layer suppresses the adsorption of chloride ions at active sites, significantly improving corrosion resistance under harsh seawater conditions. As a result, the catalyst delivers a current density of 100 mA cm<sup>-2</sup> at a low overpotential of 208 mV in alkaline seawater, maintaining stable performance over 1500 h. When integrated as the anode in a proton exchange membrane electrolyzer, it supports operation at 1 A cm<sup>-2</sup> with a cell voltage of only 2.18 V, exhibiting no performance degradation over 500 h.

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Publication Details

Journal
Advanced Science
Published
2025-09-16
DOI
https://doi.org/10.1002/advs.202514301
Citations
4
Primary Topic
Electrochemical Analysis and Applications
Type
article
Field-Weighted Citation Impact
2.06

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article

Catalyst for Industrial‐Scale Seawater Electrolysis: Inhibit Active Metal Dissolution and Chlorine Corrosion

Yong Wan, Yusuke Yamauchi, Yun‐Ze Long, Mang Niu et al.
4 citations
Advanced Science
Electrochemical Analysis and Applications
2.06
article

Catalyst for Industrial‐Scale Seawater Electrolysis: Inhibit Active Metal Dissolution and Chlorine Corrosion

Yong Wan, Yusuke Yamauchi, Yun‐Ze Long, Mang Niu, Yuyang Li, Peng Wang, Jie Zheng, Qiaofu Shi, Jun Zhang
article en
4 citations

Abstract

Alkaline seawater electrolysis is a promising technology for sustainable green hydrogen production. However, active metal dissolution and chlorine-induced corrosion during long-term, industrial-scale operation pose critical challenges to catalyst stability. Here, a surface engineering strategy is reported using phytic acid (PA) as a molecular "armor" to construct highly durable oxygen evolution reaction (OER) catalysts. Comprehensive characterization and density functional theory (DFT) calculations reveal that surface modification with PO<sub>4</sub> <sup>3-</sup> groups not only facilitates surface reconstruction to form NiOOH active sites, but also optimizes the adsorption-desorption dynamics of key reaction intermediates, thereby enhancing catalytic performance. Importantly, the PO<sub>4</sub> <sup>3-</sup> layer suppresses the adsorption of chloride ions at active sites, significantly improving corrosion resistance under harsh seawater conditions. As a result, the catalyst delivers a current density of 100 mA cm<sup>-2</sup> at a low overpotential of 208 mV in alkaline seawater, maintaining stable performance over 1500 h. When integrated as the anode in a proton exchange membrane electrolyzer, it supports operation at 1 A cm<sup>-2</sup> with a cell voltage of only 2.18 V, exhibiting no performance degradation over 500 h.

Advanced ScienceVol. 12(45)
Qingdao University (CN), The University of Queensland (AU), Nagoya University (JP)
Australian National Fabrication Facility, National Natural Science Foundation of China, Qingdao University, Exploratory Research for Advanced Technology
Openalex Percentile: Top 12%
Electrochemical Analysis and Applications
2.06
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