膜
共价有机骨架
化学
化学工程
法拉第效率
溶解
双层
阴极
聚丙烯
芘
共价键
阳极
涂层
有机化学
电极
物理化学
工程类
生物化学
作者
Alae Eddine Lakraychi,Erin S. Picton,Yanliang Liang,Devin L. Shaffer,Yan Yao
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-11-06
卷期号:8 (12): 5032-5040
标识
DOI:10.1021/acsenergylett.3c01740
摘要
Organic batteries, while promising due to their abundant elements and minimal environmental impact, often suffer from capacity fade because of the shuttle effect of dissolved redox intermediates. To address this issue, we introduced a bilayer membrane, TpPa@PP, consisting of a 70-nm covalent organic framework (COF) thin film synthesized by interfacial condensation and subsequently deposited on a polypropylene substrate. This membrane allows solvent and ion transport, while rejecting soluble organic intermediates. When paired with pyrene-4,5,9,10-tetraone (PTO), an organic cathode with high capacity but notable dissolution issues, the TpPa@PP membrane effectively blocked the bulky PTO and Li2-PTO species from crossover in an H-type cell, resulting in only a slight decrease in Li-ion flux. Furthermore, the membrane improved the first-cycle Coulombic efficiency. This work offers crucial insights into the membrane design for organic batteries.
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