Performance and durability trade-offs in low-iridium catalyst layers for PEM water electrolysis

To deploy proton-exchange membrane (PEM) water electrolyzers at a gigawatt scale, the iridium-specific power density must be reduced to below 0.1 mg Ir W −1 . Significant variability in reported performance and durability benchmarks makes it difficult to define clear pathways for technological improvement. Here, we report a device-level investigation combining multimodal diagnostics with long-term durability testing across four commercial catalysts at loadings from 0.1 to 0.8 mg Ir cm −2 . While all catalysts achieve the 0.1 mg Ir W −2 target, this cannot be met at lower heating value-based efficiencies above 75% through catalyst design alone. Durability testing over 500 and 1,000 h shows that degradation rates decrease with extended operation and that each catalyst exhibits distinct, loading-dependent behavior. Postmortem characterization confirms progressive catalyst crystallization as a primary contributor to kinetic degradation. These findings demonstrate that future deployment targets depend far more on reducing cell resistance and ensuring long-term durability than on advancing intrinsic catalyst activity.

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Publication Details

Journal
Cell Reports Physical Science
Published
2026-07-16
DOI
https://doi.org/10.1016/j.xcrp.2026.103441
Primary Topic
Hybrid Renewable Energy Systems
Type
article
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article

Performance and durability trade-offs in low-iridium catalyst layers for PEM water electrolysis

Heinrich Hartmann, Fabian Scheepers, Nikolai Utsch, Ralf Peters et al.
Cell Reports Physical Science
Hybrid Renewable Energy Systems
article

Performance and durability trade-offs in low-iridium catalyst layers for PEM water electrolysis

Heinrich Hartmann, Fabian Scheepers, Nikolai Utsch, Ralf Peters, Martin Müller, David Aymé-Perrot
article en

Abstract

To deploy proton-exchange membrane (PEM) water electrolyzers at a gigawatt scale, the iridium-specific power density must be reduced to below 0.1 mg Ir W −1 . Significant variability in reported performance and durability benchmarks makes it difficult to define clear pathways for technological improvement. Here, we report a device-level investigation combining multimodal diagnostics with long-term durability testing across four commercial catalysts at loadings from 0.1 to 0.8 mg Ir cm −2 . While all catalysts achieve the 0.1 mg Ir W −2 target, this cannot be met at lower heating value-based efficiencies above 75% through catalyst design alone. Durability testing over 500 and 1,000 h shows that degradation rates decrease with extended operation and that each catalyst exhibits distinct, loading-dependent behavior. Postmortem characterization confirms progressive catalyst crystallization as a primary contributor to kinetic degradation. These findings demonstrate that future deployment targets depend far more on reducing cell resistance and ensuring long-term durability than on advancing intrinsic catalyst activity.

Cell Reports Physical ScienceVol. 7(8)
Total (France) (FR), Forschungszentrum Jülich (DE)
Openalex Percentile: Top 21%
Hybrid Renewable Energy Systems
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