钒
膜
联苯
吡啶
氧化还原
质子交换膜燃料电池
化学
流动电池
兴奋剂
燃料电池
无机化学
化学工程
材料科学
高分子化学
有机化学
电极
物理化学
生物化学
光电子学
工程类
电解质
作者
Ning Shi,Guorui Wang,Qian Wang,Lele Wang,Qingfeng Li,Jingshuai Yang
标识
DOI:10.1016/j.cej.2024.151121
摘要
Both high temperature proton exchange membrane fuel cell (HT-PEMFC) and vanadium redox flow battery (VRFB) are represented as two advanced energy conversion and energy storage devices. They have a same core component of the separator membrane, which still faces several intractable scientific and industrial issues. For HT-PEMFC, the increase in conductivity is normally as the expense of mechanical strength; while for VRFB, the improvement in proton transport always brings in serious vanadium ion crossover. Meanwhile, the membrane also should possess an excellent chemical stability towards the attack by radicals or high valence vanadium ions. The above questions can be well solved by the preparation of triphenylbenzene (TPB) branched poly(biphenyl-4-acetylpyridine) membranes (x%TPB-PBAP), which are synthesized by one-step Friedel-Crafts polymerization. Amounts of alkaline pyridine groups equip x%TPB-PBAP membranes with good phosphoric acid and sulfonic acid absorption capability, resulting in high proton conductivity in both HT-PEMFC and VRFB. Meanwhile, the construction of the branched structure, i.e. a kind of covalently crosslinked network, can improve the mechanical strength and chemical stability. Consequently, the 1.5 %TPB-PBAP membrane displays large potential in both HT-PEMFC and VRFB. A single H2-O2 cell based on the 1.5 %TPB-PBAP/263 %PA membrane shows a peak power density of 1010 mW cm−2 at 180 °C without any back pressure. Meanwhile, the VRFB based on above membrane also depicts better battery efficiencies and cycle durability than that with Nafion 212.
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