Metal-oxide phase transition of platinum nanocatalyst below fuel cell open-circuit voltage

The long-term stability of Pt-based catalysts is critical to the reliability of proton exchange membrane fuel cells (PEMFCs), and receives constant attention. However, the current knowledge of Pt oxidation is restricted to unrealistic PEMFC cathode environment or operation, which questions its practical relevance. Herein, Pt oxidation is investigated directly in a PEMFC with stroboscopic operando high energy X-ray scattering. The onset potential for phase transition of the nanoparticles surface from metallic to amorphous electrochemical oxide is observed far below previously reported values, and most importantly, below the open-circuit potential of PEMFC cathode. Such phase transition is shown to impact PEMFC performance and its role on Pt transient dissolution is verified by electrochemical on-line inductively coupled plasma mass spectrometry. By further demonstrating and resolving the limitations of currently employed accelerated stress test protocols in the light of metal-oxide phase transitions kinetics, this picture of Pt oxidation enables new mitigation strategies against PEMFC degradation.

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Publication Details

Journal
Nature Communications
Published
2025-01-22
DOI
https://doi.org/10.1038/s41467-024-55299-3
Citations
24
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
8.72

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article

Metal-oxide phase transition of platinum nanocatalyst below fuel cell open-circuit voltage

Amir Gasmi, Raphaël Chattot, Pierre‐Yves Blanchard, Sara Cavalière et al.
24 citations
Nature Communications
Electrocatalysts for Energy Conversion
8.72
article

Metal-oxide phase transition of platinum nanocatalyst below fuel cell open-circuit voltage

Amir Gasmi, Raphaël Chattot, Pierre‐Yves Blanchard, Sara Cavalière, Deborah J. Jones, Carlos A. Campos‐Roldàn, Jean‐Sébastien Filhol, Jakub Drnec, Isaac Martens, Meryem Ennaji, Morgane Stodel
article en
24 citations

Abstract

The long-term stability of Pt-based catalysts is critical to the reliability of proton exchange membrane fuel cells (PEMFCs), and receives constant attention. However, the current knowledge of Pt oxidation is restricted to unrealistic PEMFC cathode environment or operation, which questions its practical relevance. Herein, Pt oxidation is investigated directly in a PEMFC with stroboscopic operando high energy X-ray scattering. The onset potential for phase transition of the nanoparticles surface from metallic to amorphous electrochemical oxide is observed far below previously reported values, and most importantly, below the open-circuit potential of PEMFC cathode. Such phase transition is shown to impact PEMFC performance and its role on Pt transient dissolution is verified by electrochemical on-line inductively coupled plasma mass spectrometry. By further demonstrating and resolving the limitations of currently employed accelerated stress test protocols in the light of metal-oxide phase transitions kinetics, this picture of Pt oxidation enables new mitigation strategies against PEMFC degradation.

Nature CommunicationsVol. 16(1)
École Nationale Supérieure de Chimie de Montpellier (FR), Centre National de la Recherche Scientifique (FR), Université Toulouse III - Paul Sabatier (FR), Université Fédérale de Toulouse Midi-Pyrénées (FR), Université de Montpellier (FR), European Synchrotron Radiation Facility (FR), Centre Interuniversitaire de Recherche et d’Ingénierie des Matériaux (FR)
Agence Nationale de la Recherche, European Synchrotron Radiation Facility
Openalex Percentile: Top 2%
Electrocatalysts for Energy Conversion
8.72
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