Experimental evaluation shows reduced degradation in proton exchange membranes with tungsten oxides and cerium ions, suggesting a novel approach to durability.
To improve the chemical durability of proton exchange membrane fuel cells (PEMFCs) while imposing minimal performance penalties, the effects of simultaneously incorporating tungsten oxide (WO x ) and cerium (Ce) ions into the membrane are evaluated. Open‐circuit voltage (OCV) hold tests are conducted using Nafion membranes containing Ce ions alone, WO x alone, or both. The combination of Ce 3+ , a hydroxyl radical scavenger, and WO x , a hydrogen peroxide decomposition catalyst with high stability and immobility under acidic conditions, achieves a degradation suppression effect that is consistent with the product of their individual contributions. The distinct mitigation mechanisms of Ce ions and WO x are supported by ex situ H 2 O 2 decomposition experiments and membrane molecular weight analysis. No marked initial performance loss is observed with WO x addition. These results indicate that the use of WO x allows for reduced Ce ion loading and that it mitigates negative effects associated with Ce ion mobility. The combined use of suppressants that target different degradation pathways presents a promising strategy for achieving high membrane durability with minimal performance tradeoffs.
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Shinozaki et al. (2025) studied this question.
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