离聚物
材料科学
催化作用
化学工程
Zeta电位
极化(电化学)
质子交换膜燃料电池
溶剂化
氢铵
溶剂
催化剂载体
泥浆
图层(电子)
复合材料
相(物质)
膜
癸烷
无机化学
电解质
多金属氧酸盐
粒子(生态学)
双金属片
溶剂效应
粒径
作者
Daozeng Yang,Tiankuo Chu,Yuqing Guo,Zheng Zhang,Jue Wang,Weibo Zheng,Daijun Yang,Pingwen Ming,Bo Li
标识
DOI:10.1021/acsami.5c18925
摘要
The catalyst-bound ionomer layer (CBIL) in catalyst slurries consists of surface-adsorbed ionomers and solvent-diffused hydronium ions, where ionomers exhibit solvation diameters spanning tens to hundreds of nanometers with distinct phase-separated structures. This work elucidates how solvent composition and polarity regulate ionomer solvation-induced phase separation, thereby governing the CBIL architecture on catalyst aggregates, slurry network heterogeneity, bimodal pore distribution in coatings, and electrode polarization performance. Key findings reveal that water-rich solvents reduce ionomer exclusion volumes and induce morphological collapse, accompanied by decreased side-chain offset, indicating constrained -SO3H group extension. These changes yield a denser CBIL structure with highly negative surface zeta potentials (<-70 mV), weakening interaggregate network strength. The concurrent main-chain collapse and side-chain curling lower surface sulfur content in catalyst layers, mitigating Pt poisoning risks from the -SO3H groups. Notably, elevated CBIL zeta potentials enhance interaggregate repulsion, effectively suppressing particle overaggregation in coatings and significantly improving the polarization performance of proton exchange membrane fuel cells (PEMFCs).
科研通智能强力驱动
Strongly Powered by AbleSci AI