对苯二甲酸
金属有机骨架
膜
材料科学
激进的
氧化还原
化学工程
有机化学
核化学
高分子化学
无机化学
化学
吸附
复合材料
聚酯纤维
生物化学
工程类
作者
Kangwei Xu,Supeng Pei,Wei Zhang,Zhiyue Han,Panpan Guan,Li Wang,Yecheng Zou,Han Ding,Xiaojuan Ma,Cai-Di Xu,Feng Liu,Yongming Zhang
标识
DOI:10.1016/j.mtener.2022.101195
摘要
Herein, in order to relieve the chemical degradation of perfluorosulfonic acid (PFSA) membranes without decreasing their proton conductivity, Ce (III)-terephthalic acid metal-organic frameworks (Ce-TPA MOFs) with efficient ·OH radical scavenging efficiency are designed via coordinating the organic antioxidant ligand (TPA) with inorganic radical scavenger (Ce ions). Ce-TPA MOFs with a different weight ratio of 0.5, 1.0, or 2.0% was introduced in PFSA matrix to produce composite membranes. On the one hand, the hydrophilic groups of Ce-TPA MOFs caused better water absorption, which promoted the proton conduction to some extent. Also, the presence of the redox Ce3+/Ce4+ couple, oxygen vacancy, and TPA molecules in Ce-TPA MOFs scavenging ·OH radical together via synergy effect. The optimum peak power density of the PFSA/Ce-TPA1.0 composite membrane at 75 °C under 80% relative humidity was 1086 mW/cm that of pristine PFSA membrane was only 1032 mW/cm. Furthermore, PFSA/Ce-TPA1.0 composite membrane experienced the decay of only 0.31 mV/h during 96 h operation under the same conditions, whereas that of pristine PFSA membrane was 2.20 mV/h. Thus, the PFSA/Ce-TPA membrane was a potential candidate for proton exchange membrane fuel cells.
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