Combinatorial Use of Reference Electrodes and DRT for Disentangling AEM Electrolyzer Losses

Anion exchange membrane water electrolyzers (AEMWEs) offer a promising alternative to proton exchange membrane (PEM) electrolyzers, leveraging non-precious-metal catalysts and alkaline electrolytes for cost reduction. However, challenges persist in achieving long-term durability, high current densities, and stable membrane performance. While previous studies have examined AEM development, a comprehensive structural-electrochemical analysis of AEMWE components under prolonged operation remains limited. This study presents a detailed structural and electrochemical characterization of a commercial AEMWE, where its full-cell performance was matched with the intrinsic half-electrode performance through the use of dual reference electrodes. The electrochemical analysis was supported by a thorough tomographic and spectroscopic investigation of each electrode, thereby providing for the first time a complete materials analysis of the commercial NiFeO<sub>x</sub> anode and Raney nickel cathode. Electrochemical characterization using LSV, EIS, and a dual reference electrode setup revealed full-cell performance of 1.0 A cm<sup>-2</sup> at 2.2 V (ambient) and 1.1 A cm<sup>-2</sup> at 2.0 V (60 °C), with an HHV efficiency of 74.5% at 1.0 A cm<sup>-2</sup>. Long-term operation over 1000 h at 1.0 A cm<sup>-2</sup>, 60 °C, in 1.0 M KOH resulted in a substantial polarization resistance increase beyond 230 h, despite an unexpected continuous improvement in MEA performance due to membrane degradation. DRT analysis, coupled with reference electrode studies, was critical in isolating losses. Low-frequency peaks (1.5-25 Hz) were linked to bubble formation, while intermediate-frequency (50-2000 Hz) and high-frequency (>2000 Hz) processes corresponded to charge transfer and ionic transport. The NiFeO<sub>x</sub> anode exhibited better charge transfer, whereas the Raney nickel cathode showed higher polarization resistance.

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Publication Details

Journal
Energy & Fuels
Published
2025-08-15
DOI
https://doi.org/10.1021/acs.energyfuels.5c01799
Citations
4
Primary Topic
Fuel Cells and Related Materials
Type
article
Field-Weighted Citation Impact
2.92

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article

Combinatorial Use of Reference Electrodes and DRT for Disentangling AEM Electrolyzer Losses

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4 citations
Energy & Fuels
Fuel Cells and Related Materials
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article

Combinatorial Use of Reference Electrodes and DRT for Disentangling AEM Electrolyzer Losses

Vanja Subotić, Albert Taureg, Samaneh Daviran, Fabio Dionigi, Jan Van herle, Mounir Mensi, Peter Strasser, Suhas Nuggehalli Sampathkumar, Pascal Schouwink, Philippe Aubin, T.B. Ferriday, Hamza Moussaoui, Khaled Lawand, Arthur Paul Lucien Thévenot
article en
4 citations

Abstract

Anion exchange membrane water electrolyzers (AEMWEs) offer a promising alternative to proton exchange membrane (PEM) electrolyzers, leveraging non-precious-metal catalysts and alkaline electrolytes for cost reduction. However, challenges persist in achieving long-term durability, high current densities, and stable membrane performance. While previous studies have examined AEM development, a comprehensive structural-electrochemical analysis of AEMWE components under prolonged operation remains limited. This study presents a detailed structural and electrochemical characterization of a commercial AEMWE, where its full-cell performance was matched with the intrinsic half-electrode performance through the use of dual reference electrodes. The electrochemical analysis was supported by a thorough tomographic and spectroscopic investigation of each electrode, thereby providing for the first time a complete materials analysis of the commercial NiFeO<sub>x</sub> anode and Raney nickel cathode. Electrochemical characterization using LSV, EIS, and a dual reference electrode setup revealed full-cell performance of 1.0 A cm<sup>-2</sup> at 2.2 V (ambient) and 1.1 A cm<sup>-2</sup> at 2.0 V (60 °C), with an HHV efficiency of 74.5% at 1.0 A cm<sup>-2</sup>. Long-term operation over 1000 h at 1.0 A cm<sup>-2</sup>, 60 °C, in 1.0 M KOH resulted in a substantial polarization resistance increase beyond 230 h, despite an unexpected continuous improvement in MEA performance due to membrane degradation. DRT analysis, coupled with reference electrode studies, was critical in isolating losses. Low-frequency peaks (1.5-25 Hz) were linked to bubble formation, while intermediate-frequency (50-2000 Hz) and high-frequency (>2000 Hz) processes corresponded to charge transfer and ionic transport. The NiFeO<sub>x</sub> anode exhibited better charge transfer, whereas the Raney nickel cathode showed higher polarization resistance.

Energy & FuelsVol. 39(34)
University of Oslo (NO), Graz University of Technology (AT), Technische Universität Berlin (DE), École Polytechnique Fédérale de Lausanne (CH)
Horizon 2020 Framework Programme, Staatssekretariat für Bildung, Forschung und Innovation
Openalex Percentile: Top 8%
Fuel Cells and Related Materials
2.92
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