质子交换膜燃料电池
化学工程
纳米纤维
材料科学
芳纶
甲基丙烯酸甲酯
膜
阳极
纤维素
色散(光学)
表面改性
碳纳米纤维
聚合物
碳纤维
渗透
高分子化学
膜电极组件
扩散
图层(电子)
质子输运
阴极
碳纳米管
聚酰胺
化学
纳米复合材料
电导率
作者
Bin Wen,Ruyin Ma,Jianbin Chen,Zhou Sha,Jiahao Feizheng,Daliang Guo,Linxin Zhong,Qianyu Sun,Yinchao Xu,Ziyang Chang,Chengliang Duan,Jing Li,Xin Tong
标识
DOI:10.1021/acssuschemeng.5c10511
摘要
As the critical gas diffusion layer in proton exchange membrane fuel cells (PEMFCs), carbon paper (CP) governs the charge transfer, mechanical integrity, and gas/water transport. However, conventional CP struggles to simultaneously optimize permeability, strength, and conductivity, hindered by structural defects from resin expansion and weakened fiber-resin bonds during fabrication. To overcome this, a novel synergistic modifier: aramid nanofibers (ANF) and cellulose nanofibers grafted with methyl methacrylate (CNFM) within the phenolic resin (PF) were used to prepare CP. Investigating ANF:CNFM ratios revealed enhanced PF dispersion stability and modified thermochemical properties. The modified CP exhibited a tunable surface morphology, mechanical strength, in-plane resistivity, and pore characteristics, peaking at ANF:CNFM (3:1). Crucially, this modification inhibited PF methylene bridge fracture, increased polycondensation sites, and fostered a more ordered carbon matrix (reduced ID/IG: 2.12 vs 2.16 unmodified). Assembled PEMFCs with optimized ANF:CNFM (3:1) modified CP achieved a peak power density of 1.34 W·cm–2 (2 N·m, 60 °C anode humidification), surpassing commercial CP by 15.51% (1.16 W·cm–2). Lower mass transport impedance, confirmed by EIS, underscores the superior gas–liquid transport enabled by a tailored pore structure and enhanced mechanical strength, advancing high-performance PEMFCs design.
科研通智能强力驱动
Strongly Powered by AbleSci AI