共轭体系
共价键
电化学
质子
水溶液
共价有机骨架
电解质
聚合物
离域电子
储能
材料科学
纳米技术
化学
离子
电极
化学工程
有机化学
物理化学
功率(物理)
工程类
物理
量子力学
作者
Mingchao Wang,Gang Wang,Naisa Chandrasekhar,Yubin Fu,Sai Manoj Gali,Silvia Paasch,Mao Wang,Haiko Wittkaemper,Christian Papp,Eike Brunner,Shengqiang Zhou,David Beljonne,Hans‐Peter Steinrück,Renhao Dong⧫,Xinliang Feng
标识
DOI:10.1002/anie.202310937
摘要
Electrochemical proton storage plays an essential role in designing next-generation high-rate energy storage devices, e.g., aqueous batteries. Two-dimensional conjugated covalent organic frameworks (2D c-COFs) are promising electrode materials, but their competitive proton and metal-ion insertion mechanisms remain elusive, and proton storage in COFs is rarely explored. Here, we report a perinone-based poly(benzimidazobenzophenanthroline) (BBL)-ladder-type 2D c-COF for fast proton storage in both a mild aqueous Zn-ion electrolyte and strong acid. We unveil that the discharged C-O- groups exhibit largely reduced basicity due to the considerable π-delocalization in perinone, thus affording the 2D c-COF a unique affinity for protons with fast kinetics. As a consequence, the 2D c-COF electrode presents an outstanding rate capability of up to 200 A g-1 (over 2500 C), surpassing the state-of-the-art conjugated polymers, COFs, and metal-organic frameworks. Our work reports the first example of pure proton storage among COFs and highlights the great potential of BBL-ladder-type 2D conjugated polymers in future energy devices.
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