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September 17, 2025Advanced Science25 citationsOpen Access

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

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PWPeng WangJZJie ZhengYLYuyang Li

Key Points

  • The catalyst maintains stable performance over 1500 hours in alkaline seawater, highlighting its durability.
  • Surface modification with PO4 3- significantly improves corrosion resistance and catalytic performance.
  • A current density of 100 mA cm-2 is achieved at a low overpotential of 208 mV, showcasing efficiency.
  • Integrating the catalyst as an anode supports operation at 1 A cm-2 with 2.18 V, indicating its effectiveness.

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 PO4 3- 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 PO4 3- 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-2 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-2 with a cell voltage of only 2.18 V, exhibiting no performance degradation over 500 h.

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Cite This Study

Wang et al. (2025) studied this question.

synapsesocial.com/papers/68d45b1b31b076d99fa5d690https://doi.org/10.1002/advs.202514301
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