离聚物
材料科学
质子交换膜燃料电池
化学工程
膜
催化作用
磺酸
膜电极组件
Nafion公司
复合材料
高分子化学
化学
电解质
电化学
有机化学
聚合物
电极
共聚物
物理化学
工程类
生物化学
作者
Jong-Hyeok Park,Beom Seok Kim,Jin‐Soo Park
标识
DOI:10.1016/j.electacta.2022.140680
摘要
In this study, various ionomer dispersions having different equivalent weights, length of side chains, and dispersing solvents have been extensively analyzed to investigate the effect of the microstructure of catalyst layers on the performance of membrane-electrode assembly in proton exchange membrane fuel cells. Five different commercially available perfluorinated sulfonic acid ionomer dispersions have been used to prepare laboratory-made propylene glycol-based ionomer dispersions. The thickness of self-assembled ultra-thin films on silicon wafer for all types of ionomer dispersions has been measured and correlated mainly with the type of dispersing solvents (i.e., water, 2-propanol, and propylene glycol), the length of ionomer side chain, and the wettability. As a result, the short side chain and the propylene glycol-based ionomer dispersions form thicker films due to the smaller average size of their ionomer aggregates. The thick-ionomer wrapped catalyst layers especially prepared by the propylene glycol-based ionomer dispersions result in no influence on activation loss but approximately 42% less Ohmic loss and 43% higher limiting current density in proton exchange membrane fuel cells. In addition, it is confirmed that the slightly higher performance is exhibited as the thickness of ultra-thin ionomer film increases due to the effect of the length of side chains. The catalyst layers with the ionomer film over 100 nm show the higher performance than those below 100 nm. The MEA using Nafion D2020 having hydrophobic surface shows the lower increasing ratio (2.26%) in HFR than the one using Aquivion D98-25BS having hydrophilic surface due to the difference of the water-retaining ability.
科研通智能强力驱动
Strongly Powered by AbleSci AI