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电化学(中英文) ›› 2026, Vol. 32 ›› Issue (9): 2603242.  doi: 10.61558/2993-074X.3618

• 论文 • 上一篇    下一篇

锰-氮-碳纳米笼限域的高密度铂纳米颗粒用于高耐久重载质子交换膜燃料电池

赵磊a,b,#, 曹振明c,#, 左珈瑜a, 杨明亮a, 乔红艳a, 陈俊松a, 吴睿a,*()()   

  1. a 电子科技大学材料与能源学院, 四川 成都 611731
    b 成都工业学院材料与环境工程学院, 四川 成都 611730
    c 中自科技股份有限公司氢能研发中心, 四川 成都 611731
  • 收稿日期:2026-03-24 修回日期:2026-05-23 接受日期:2026-06-11 发布日期:2026-06-11 出版日期:2026-09-28

Dense Platinum Nanoparticles Confined in Mn-N-C Nanocages for Robust Heavy-Duty PEMFCs

Lei Zhaoa,b,#, Zhen-Min Caoc,#, Jia-Yu Zuoa, Ming-Liang Yanga, Hong-Yan Qiaoa, Jun Song Chena, Rui Wua,*()()   

  1. a School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 611731, P.R. China
    b School of Materials and Environmental Engineering, Chengdu Technological University, Chengdu 611730, P.R. China
    c Hydrogen Energy R&D Center, SINOTECH Company Limited, Chengdu 611731, P.R. China
  • Received:2026-03-24 Revised:2026-05-23 Accepted:2026-06-11 Online:2026-06-11 Published:2026-09-28
  • Contact: *Rui Wu, E-mail: ruiwu0904@uestc.edu.cn
  • About author:Author Contributions

    Lei Zhao: Conceptualization, Methodology, Investigation, Writing. Zhen-Min Cao: experiment, data collection. Jia-Yu Zuo: data collection, validation, Data curation. Ming-Liang Yang: Investigation, Visualization. Hong-Yan Qiao: experiment. Jun Song Chen: Supervision, funding acquisition. Rui Wu: Conceptualization, Funding acquisition, Project administration, Resources, Supervision, Writing - review & editing. All authors have read and approved the final version of the manuscript.

    #Lei Zhao and Zhen-Min Cao contributed equally to this work.

摘要:

高负载铂(Pt)阴极催化层是实现重载型质子交换膜燃料电池高性能运行的关键,但其长期面临离聚物磺酸基团毒化与Pt纳米颗粒稳定性难以兼顾的矛盾。本文提出一种空间限域策略,通过将高含量Pt纳米颗粒(约51.8 wt%)封装于锰-氮-碳(Mn-N-C)纳米笼中,构筑了具有离聚物屏蔽微环境的Pt-MnNC催化剂。该介孔笼状结构可有效阻隔离聚物进入其内部,显著降低了磺酸基团对Pt活性位点的吸附毒化;同时,Mn-Nx位点与Pt之间的强金属-载体相互作用能够稳定锚定Pt纳米颗粒,抑制其迁移与团聚。在5 × 5 cm2膜电极测试中,Pt-MnNC催化剂在2.0 A·cm-2电流密度下实现1.26 W·cm-2的峰值功率密度。经过30000次加速老化测试后,其质量活性仅下降20.8%,显著优于商业Pt/C催化剂(衰减61.6%)。研究结果表明,空间限域构筑的离聚物屏蔽微环境能够有效缓解离聚物磺酸基团对Pt的毒化,并协同增强Pt纳米颗粒稳定性,为高功率密度、长寿命重载型质子交换膜燃料电池阴极催化剂的设计提供了新的思路。

关键词: 质子交换膜燃料电池, 介孔碳纳米笼, 磺酸基团毒化, 高载量

Abstract:

High-loading Pt cathodes are essential for heavy-duty proton exchange membrane fuel cells but suffer from a critical trade-off between ionomer sulfonate poisoning and nanoparticles' 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 the 5 × 5 cm2 membrane electrode assembly (MEA) tests, the Pt-MnNC catalyst delivered an exceptional peak power density of 1.26 W·cm-2 at 2.0 A·cm-2. Notably, it exhibited superior durability with only a 20.8% mass activity loss after 30,000 cycles, significantly outperforming commercial Pt/C, which suffered 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.

Key words: Proton exchange membrane fuel cell, Mesoporous carbon nanocage, Sulfonate poisoning, High-loading