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用于快速质子存储的聚(苯并咪唑并苯并菲咯啉)-梯型二维共轭共价有机框架

Poly(benzimidazobenzophenanthroline)-Ladder-Type Two-Dimensional Conjugated Covalent Organic Framework for Fast Proton Storage.

作者信息

Wang Mingchao, Wang Gang, Naisa Chandrasekhar, Fu Yubin, Gali Sai Manoj, Paasch Silvia, Wang Mao, Wittkaemper Haiko, Papp Christian, Brunner Eike, Zhou Shengqiang, Beljonne David, Steinrück Hans-Peter, Dong Renhao, Feng Xinliang

机构信息

Center for Advancing Electronics Dresden (cfaed) and Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, Mommsenstrasse 4, 01062, Dresden, Germany.

Key Laboratory of Advanced Fuel Cells and Electrolyzers Technology of Zhejiang Province, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, 315201, China.

出版信息

Angew Chem Int Ed Engl. 2023 Nov 13;62(46):e202310937. doi: 10.1002/anie.202310937. Epub 2023 Oct 10.

Abstract

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 (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.

摘要

电化学质子存储在设计下一代高倍率储能装置(如水系电池)中起着至关重要的作用。二维共轭共价有机框架(2D c-COF)是很有前景的电极材料,但其竞争性的质子和金属离子插入机制仍不清楚,且COF中的质子存储很少被研究。在此,我们报道了一种基于苝酮的聚(苯并咪唑并苯并菲咯啉)(BBL)阶梯型2D c-COF,用于在温和的水系锌离子电解质和强酸中快速存储质子。我们发现,由于苝酮中存在大量的π离域,放电后的C-O基团碱性大幅降低,从而赋予2D c-COF对质子独特的亲和力和快速动力学。因此,2D c-COF电极展现出高达200 A g(超过2500 C)的出色倍率性能,超过了目前最先进的共轭聚合物、COF和金属有机框架。我们的工作报道了COF中纯质子存储的首个实例,并突出了BBL阶梯型2D共轭聚合物在未来能源装置中的巨大潜力。

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