- By:
- Park, Heemin; Chen, Kate; Min Ahn, Su; Guo, Hengquan; Fujimoto, Cy; Choi, Jong-Ho; Amichi, Lynda ; Kim, Danah; Geol lee, Seung; Wang, Xiaojing; Spendelow, Jacob; Yung Kang, Sun; Bexis, Panagiotis; Joo Park, Eun; Seung kim, Yu
- Journal Name:
- Advanced Materials
- Volume:
- TBD
- Publication Date:
- August 20, 2026
- View DOI Listing:
- https://doi.org/10.1002/adma.74561
Abstract
Reducing reliance on perfluoroalkyl substances (PFAS) in proton-exchange membrane fuel cells requires hydrocarbon ionomers that combine high performance with long-term durability, a persistent challenge in catalyst-layer design. Here, we identify oxidation-driven ionomer-catalyst interfacial degradation as a dominant failure pathway in hydrocarbon ionomer-bonded cathodes and introduce an adsorption-engineering strategy to overcome this limitation. The comparison of a commercial sulfonated poly(phenylene) (Pemion) with structurally engineered sulfonated poly(fluorene)s demonstrated that electrode durability is governed by the interplay between ionomer adsorption strength and resistance to oxidative degradation on carbon-supported Pt catalysts. A poly(fluorene) ionomer with mobile alkyl sulfonic acid groups forms resilient interfaces, delivering 1.28 A cm−2 at 0.65 V under fully humidified H2/air conditions (80°C and 150 kPaabs), comparable to Pemion. After 90,000 accelerated potential cycles, the poly(fluorene)-bonded cathode exhibits significantly improved durability, with only 29% performance loss compared to 58% for Pemion; further molecular refinement reduces the loss to 17%, approaching that of Nafion-bonded cathodes (14%). These findings establish adsorption-engineered ionomer design that decouples interfacial anchoring from oxidative degradation as a general strategy for achieving durable, high-performance PFAS-free PEM fuel cell electrodes.