离聚物
铈
膜
材料科学
磺酸
化学工程
兴奋剂
无机化学
化学
复合材料
高分子化学
聚合物
共聚物
光电子学
生物化学
工程类
作者
Kentaro U. Hansen,Priyamvada Goyal,Jennifer Garland,Andrew R. Crothers,Ahmet Kusoglu
标识
DOI:10.1021/acsapm.4c00827
摘要
Thin-film ionomers, pivotal in the function of fuel-cell catalyst layers (CLs), are undercharacterized compared to their bulk membrane counterparts, especially with respect to cation effects. Cerium cations, used as an additive in fuel-cell membranes, tend to migrate from the membrane into the CL ionomer during operation. This study investigates whether cerium doping of perfluorinated sulfonic acid ionomer changes under confinement (to a nanometer thin film) and affects the hydration behavior. Confinement has a negligible effect on the ionomer's cerium partitioning, yet it reduces the ionomer water uptake. Thus, cerium replaces protons similarly in a membrane or CL ionomer; however, its presence affects the thermodynamics of hydration differently.
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