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GDE Stability in CO2 Electroreduction to Formate: The Role of Ionomer Type and Loading
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    GDE Stability in CO2 Electroreduction to Formate: The Role of Ionomer Type and Loading
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    • Jose Antonio Abarca*
      Jose Antonio Abarca
      Departamento de Ingenierías Química y Biomolecular, Universidad de Cantabria, Avenida de los Castros s/n, Santander 39005, Spain
      *Email: [email protected]
    • Lucas Warmuth
      Lucas Warmuth
      Institute of Catalysis Research and Technology (IKFT), Karlsruhe Institute of Technology (KIT), Hermann-von-Helmholtz-Platz 1, Eggenstein-Leopoldshafen 76344, Germany
    • Alain Rieder
      Alain Rieder
      Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Freiestrasse 3, Bern 3012, Switzerland
      NCCR Catalysis, University of Bern, Freiestrasse 3, Bern 3012, Switzerland
      More by Alain Rieder
    • Abhijit Dutta
      Abhijit Dutta
      Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Freiestrasse 3, Bern 3012, Switzerland
      NCCR Catalysis, University of Bern, Freiestrasse 3, Bern 3012, Switzerland
    • Soma Vesztergom
      Soma Vesztergom
      Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Freiestrasse 3, Bern 3012, Switzerland
      NCCR Catalysis, University of Bern, Freiestrasse 3, Bern 3012, Switzerland
      MTA−ELTE Momentum Interfacial Electrochemistry Research Group, Eötvös Loránd University, Pázmány Péter sétány 1/A, Budapest 1117, Hungary
    • Peter Broekmann*
      Peter Broekmann
      Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, Freiestrasse 3, Bern 3012, Switzerland
      NCCR Catalysis, University of Bern, Freiestrasse 3, Bern 3012, Switzerland
      *Email: [email protected]
    • Angel Irabien
      Angel Irabien
      Departamento de Ingenierías Química y Biomolecular, Universidad de Cantabria, Avenida de los Castros s/n, Santander 39005, Spain
    • Guillermo Díaz-Sainz
      Guillermo Díaz-Sainz
      Departamento de Ingenierías Química y Biomolecular, Universidad de Cantabria, Avenida de los Castros s/n, Santander 39005, Spain
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    ACS Catalysis

    Cite this: ACS Catal. 2025, 15, 11, 8753–8767
    Click to copy citationCitation copied!
    https://doi.org/10.1021/acscatal.5c02052
    Published May 8, 2025
    Copyright © 2025 American Chemical Society

    Abstract

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    The electrochemical reduction of CO2 (ERCO2) to formate is a promising decarbonization strategy, yet the long-term stability of gas diffusion electrodes (GDEs) remains a major bottleneck for large-scale implementation and technoeconomic viability. This study systematically investigates the role of catalyst layer (CL) composition in enhancing GDE performance and durability, focusing on ionomer selection, catalyst-to-ionomer ratio optimization, and the use of additives (such as PTFE) to tune the CL hydrophobicity. As a catalyst, (BiO)2CO3 is used as an active material thanks to its selectivity toward formate. The impact of the ionomer type is evaluated by comparing Nafion, a proton-conducting ionomer, with Sustainion, an anion-conducting ionomer. While Nafion-based GDEs exhibit competitive selectivity toward formate at low ionomer content, with Faradaic efficiencies (FE) around 85%, increasing the ionomer concentration can promote hydrogen evolution reaction (HER), with FEs for H2 even exceeding 60%, due to worsened catalyst distribution and the clogging of CO2 pathways to the active catalyst sites. In contrast, Sustainion-based GDEs effectively suppress HER across all catalyst-to-ionomer ratios, achieving high FEs for formate, in the range of 60–90%. However, even with Sustainion, excessive ionomer loading leads to pore clogging, limited CO2 accessibility, and decreased formate production. To further enhance stability, PTFE is introduced as an additive alongside Sustainion, tuning the hydrophobicity of the CL. By optimizing the amount of PTFE to add, we achieve continuous operation for 24 h, maintaining a high FE for formate (∼85%) and keeping HER below 10%, with formate rates of 8.92 mmol m–2 s–1 and single-pass conversion efficiencies of 5.81%. Stability studies reveal that Nafion- and Sustainion-only GDEs suffer from electrolyte flooding over time, which limits the CO2 transport and accelerates HER. In contrast, flooding can be prevented on PTFE-modified GDEs, enabling permanent catalyst accessibility and preventing high HER rates. These findings underscore the critical role of CL composition in achieving prolonged GDE stability. By leveraging anion-conducting ionomers and optimizing hydrophobicity, this work provides a pathway toward the scalable deployment of ERCO2 in formate technology.

    Copyright © 2025 American Chemical Society

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    Supporting Information

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    The Supporting Information is available free of charge at https://pubs.acs.org/doi/10.1021/acscatal.5c02052.

    • Figures of merit description, XRD and STEM of the catalyst, EIS of different GDE compositions, additional long-term stability results, and SEM/water contact angle characterization (PDF)

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    ACS Catalysis

    Cite this: ACS Catal. 2025, 15, 11, 8753–8767
    Click to copy citationCitation copied!
    https://doi.org/10.1021/acscatal.5c02052
    Published May 8, 2025
    Copyright © 2025 American Chemical Society

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