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Redox-mediated Decoupled Seawater Direct Splitting for H Production

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Journal Nat Commun
Specialty Biology
Date 2024 Oct 14
PMID 39402055
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Abstract

Seawater direct electrolysis (SDE) using renewable energy provides a sustainable pathway to harness abundant oceanic hydrogen resources. However, the side-reaction of the chlorine electro-oxidation reaction (ClOR) severely decreased direct electrolysis efficiency of seawater and gradually corrodes the anode. In this study, a redox-mediated strategy is introduced to suppress the ClOR, and a decoupled seawater direct electrolysis (DSDE) system incorporating a separate O evolution reactor is established. Ferricyanide/ferrocyanide ([Fe(CN)]) serves as an electron-mediator between the cell and the reactor, thereby enabling a more dynamically favorable half-reaction to supplant the traditional oxygen evolution reaction (OER). This alteration involves a straightforward, single-electron-transfer anodic reaction without gas precipitation and effectively eliminates the generation of chlorine-containing byproducts. By operating at low voltages (~1.37 V at 10 mA cm and ~1.57 V at 100 mA cm) and maintaining stability even in a Cl-saturated seawater electrolyte, this system has the potential of undergoing decoupled seawater electrolysis with zero chlorine emissions. Further improvements in the high-performance redox-mediators and catalysts can provide enhanced cost-effectiveness and sustainability of the DSDE system.

Citing Articles

Seawater Membrane Distillation Coupled with Alkaline Water Electrolysis for Hydrogen Production: Parameter Influence and Techno-Economic Analysis.

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Comprehensive Chlorine Suppression: Advances in Materials and System Technologies for Direct Seawater Electrolysis.

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