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Metal Corrosion and the Efficiency of Corrosion Inhibitors in Less Conductive Media
Published on: November 3, 2018
Self-Inhibiting Corrosion Protection through Dynamic Oxyanion Interfacial Regulation for Industrial Seawater
Minghui Gu1, Yalei Fan2, Jinyu Nie2
1Institute of Advanced Technology, University of Science and Technology of China, Hefei230026, P.R. China.
Abstract:
Direct seawater electrolysis offers a sustainable pathway for large-scale hydrogen production but is fundamentally challenged by chloride-induced corrosion, which rapidly destroys conventional transition-metal electrodes (Ni, Fe, Co, Cu, etc.) within 10 h. Herein, we report a self-inhibiting corrosion protection strategy enabled by a Ni-Fe-Cr-Mo superalloy (Hastelloy C-276) for durable alkaline simulated seawater electrolysis. When combined with the NiFe catalyst, the C-276 alloy substrate significantly improves electrode durability. Under a current density of 1.0 A cm-2, the NiFe/C-276 electrode achieves stable operation over a cumulative testing period of more than 10,800 h in alkaline simulated seawater. Integrated into an anion-exchange membrane (AEM) electrolyzer, the system delivers a current density of 5.0 A cm-2 at 2.01 V and maintains stable operation for over 500 h at 500 mA cm-2. Under the same operating current density, an OER Faradaic efficiency of 99.1% is achieved, with strongly suppressed formation of chlorine-derived byproducts. Detailed characterizations reveal that under anodic conditions, Hastelloy C-276 provides a sustained source of Mo- and Cr-derived oxyanionic species, which accumulate at the positively polarized NiFe oxyhydroxide interface. TOF-SIMS analysis and theoretical calculations further indicate that the resulting oxyanion-enriched interface suppresses chloride adsorption while optimizing the adsorption energetics of OER intermediates. The C-276 substrate therefore functions not only as a corrosion-resistant support but also as a reservoir that sustains interfacial oxyanion regulation during long-term operation. Distinct from conventional passive protection strategies, this work proposes a universal approach for integrating corrosion-resistant substrates with catalytic activity, providing a general framework for designing durable electrochemical systems operating in highly corrosive environments.
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