Document Type

Article

Corresponding Author(s)

Rui Wu(ruiwu0904@uestc.edu.cn)

Abstract

High-loading Pt cathodes are essential for heavy-duty proton exchange membrane fuel cells (PEMFCs) but suffer from a critical trade-off between ionomer sulfonate poisoning and nanoparticle instability. Herein, we report a spatial confinement strategy to encapsulate dense Pt nanoparticles (~51.8 wt%) within Mn/N-co-doped mesoporous carbon nanocages (denoted as Pt-MnNC). This architecture excludes bulky ionomers to create an ionomer-shielded environment against sulfonate poisoning, while Mn-Nx-mediated strong metal-support interactions anchor the Pt nanoparticles to prevent agglomeration and further boost durability. In 5×5 cm2 membrane electrode assembly (MEA) tests, the Pt-MnNC catalyst delivers an exceptional peak power density of 1.26 W·cm-2 at 2.0 A·cm-2. Notably, it exhibits superior durability with only a 20.8% mass activity loss after 30,000 cycles, significantly outperforming commercial Pt/C, which suffers a 61.6% loss. This work provides a robust pathway to decouple ionomer poisoning from catalyst loading, advancing the development of high-power, durable heavy-duty fuel cells.

Graphical Abstract

Keywords

Proton exchange membrane fuel cells, Mesoporous carbon nanocages, Sulfonate poisoning, High-loading

Online Date

6-11-2026

2603242-SI.pdf (5315 kB)

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