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Seawater Electrolysis Using All-PGM-Free Catalysts and Cell Components in an Asymmetric Feed AITranslate

Technical University of Berlin;Technical University of Berlin;Technical University of Berlin;Forschungszentrum Jülich, Helmholtz Institut Erlangen-Nürnberg für Erneuerbare Energien;Technical University of Berlin;Technical University of Berlin; North-West University;Technical University of Berlin
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Publisher: ACS
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Abstract AITranslate

In arid coastal zones, direct seawater electrolysis appears particularly intriguing for green hydrogen production. State-of-the-art direct seawater electrolyzers, however, show unsatisfactory performance and rely on large amounts of platinum-group metals (PGMs) in the electrodes or hidden as transport layer coatings. Herein, we report an asymmetric-feed electrolyzer design, in which all cell components consist of PGM-free materials. Cobalt- and nickel-based phosphides/chalcogenides not only serve as active and robust electrocatalysts but also are put forth as porous transport layer (PTL) surface coatings enhancing selective seawater splitting performance. In a systematic design study at the single-cell level, we report the integration of our catalysts and PTLs into a membrane–electrode assembly (MEA) using a customized, terphenyl-based anion-exchange membrane (AEM). The presented entirely PGM-free electrolyzer achieves industrially relevant current densities of up to 1.0 A cm–2 below 2.0 Vcell in standardized alkaline seawater and dry cathode operation.

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DOI:https://doi.org/10.1021/acsenergylett.3c00492

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In arid coastal zones, direct seawater electrolysis appears particularly intriguing for green hydrogen production. State-of-the-art direct seawater electrolyzers, however, show unsatisfactory performance and rely on large amounts of platinum-group metals (PGMs) in the electrodes or hidden as transport layer coatings. Herein, we report an asymmetric-feed electrolyzer design, in which all cell components consist of PGM-free materials. Cobalt- and nickel-based phosphides/chalcogenides not only serve as active and robust electrocatalysts but also are put forth as porous transport layer (PTL) surface coatings enhancing selective seawater splitting performance. In a systematic design study at the single-cell level, we report the integration of our catalysts and PTLs into a membrane–electrode assembly (MEA) using a customized, terphenyl-based anion-exchange membrane (AEM). The presented entirely PGM-free electrolyzer achieves industrially relevant current densities of up to 1.0 A cm–2 below 2.0 Vcell in standardized alkaline seawater and dry cathode operation.

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GB/T 7714-2015 [1] Marvin L. Frisch, Trung Ngo Thanh, Aleks Arinchtein, et al. ACS Energy Letters, 2023(8). DOI:10.1021/acsenergylett.3c00492.
MLA [1] Marvin L. Frisch, et al., ACS Energy Letters, no. 8, 2023, https://doi.org/10.1021/acsenergylett.3c00492.
APA [1] Marvin L. Frisch, Trung Ngo Thanh, Aleks Arinchtein, Linus Hager, Johannes Schmidt, Sven Brückner, Jochen Kerres, & Peter Strasser. (2023). ACS Energy Letters(8). https://doi.org/10.1021/acsenergylett.3c00492
IEEE [1] Marvin L. Frisch, Trung Ngo Thanh, Aleks Arinchtein, Linus Hager, Johannes Schmidt, Sven Brückner, Jochen Kerres, and Peter Strasser, ACS Energy Letters, no. 8, 2023, doi: 10.1021/acsenergylett.3c00492.