Fe‐N‐C in Proton Exchange Membrane Fuel Cells: Impact of Ionomer Loading on Degradation and Stability

Abstract Fe single atoms in N‐doped C (Fe‐N‐C) present the most promising replacement for carbon‐supported Pt‐based catalysts for the O 2 reduction reaction at the cathode of proton exchange membrane fuel cells (PEMFCs). However, it remains unclear how the I/C ratio affects Fe‐N‐C degradation and the stability of single Fe atom active sites (FeN x ). Here, an accelerated stress test (AST) protocol is combined with emerging electrochemical techniques for a porous Fe‐N‐C in PEMFC with a range of I/C ratios. The PEMFC current density degradation rates are found to be comparable; however, with increased I/C ratio the additional FeN x sites accessed are more stable, as shown by their higher active site stability number (electrons passed per FeN x lost) at the end of the AST protocol. Meanwhile, the initial rate of TOF decay is suppressed with increasing I/C. Electrochemical process changes are studied via distribution of relaxation times analysis. Minor changes in H + and O 2 transport resistance at low current density prove kinetic degradation dominants at high potentials. These findings demonstrate how electrochemical techniques can be combined with stability metrics to determine and deconvolute changes from the active site to device level electrochemical processes in PEMFCs.

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Publication Details

Journal
Advanced Energy Materials
Published
2024-11-13
DOI
https://doi.org/10.1002/aenm.202403920
Citations
8
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.82

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article

Fe‐N‐C in Proton Exchange Membrane Fuel Cells: Impact of Ionomer Loading on Degradation and Stability

Angus Pedersen, Lior Elbaz, Frédéric Maillard, Ifan E. L. Stephens et al.
8 citations
Advanced Energy Materials
Electrocatalysts for Energy Conversion
0.82
article

Fe‐N‐C in Proton Exchange Membrane Fuel Cells: Impact of Ionomer Loading on Degradation and Stability

Angus Pedersen, Lior Elbaz, Frédéric Maillard, Ifan E. L. Stephens, Laëtitia Dubau, Rongsheng Cai, Maria‐Magdalena Titirici, Sarah J. Haigh, Jesús Barrio, Rifael Z. Snitkoff‐Sol, Yan Presman
article en
8 citations

Abstract

Abstract Fe single atoms in N‐doped C (Fe‐N‐C) present the most promising replacement for carbon‐supported Pt‐based catalysts for the O 2 reduction reaction at the cathode of proton exchange membrane fuel cells (PEMFCs). However, it remains unclear how the I/C ratio affects Fe‐N‐C degradation and the stability of single Fe atom active sites (FeN x ). Here, an accelerated stress test (AST) protocol is combined with emerging electrochemical techniques for a porous Fe‐N‐C in PEMFC with a range of I/C ratios. The PEMFC current density degradation rates are found to be comparable; however, with increased I/C ratio the additional FeN x sites accessed are more stable, as shown by their higher active site stability number (electrons passed per FeN x lost) at the end of the AST protocol. Meanwhile, the initial rate of TOF decay is suppressed with increasing I/C. Electrochemical process changes are studied via distribution of relaxation times analysis. Minor changes in H + and O 2 transport resistance at low current density prove kinetic degradation dominants at high potentials. These findings demonstrate how electrochemical techniques can be combined with stability metrics to determine and deconvolute changes from the active site to device level electrochemical processes in PEMFCs.

Advanced Energy MaterialsVol. 15(25)
Institut polytechnique de Grenoble (FR), Centre National de la Recherche Scientifique (FR), Bar-Ilan University (IL), Chinese Academy of Sciences (CN), Tohoku University (JP), University of Manchester (GB), Lanzhou Institute of Chemical Physics (CN), Imperial College London (GB), École Nationale Supérieure des Mines de Paris (FR), Université Savoie Mont Blanc (FR), Université Grenoble Alpes (FR)
Henry Royce Institute, Imperial College London, European Commission, Israel Science Foundation, Ministry of Energy, Israel, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 32%
Electrocatalysts for Energy Conversion
0.82
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