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在一个稳健的共价有机框架中具有多个可及的氧化还原活性位点,用于高性能钾存储。

Multiple Accessible Redox-Active Sites in a Robust Covalent Organic Framework for High-Performance Potassium Storage.

机构信息

College of Chemistry and Materials Science, Guangdong Provincial Key Laboratory of Functional Supramolecular Coordination Materials and Applications, Jinan University, Guangzhou 510632, China.

Hefei National Laboratory for Physical Sciences at the Microscale and Department of Applied Chemistry, University of Science and Technology of China, Hefei 230026, China.

出版信息

J Am Chem Soc. 2023 Mar 8;145(9):5105-5113. doi: 10.1021/jacs.2c11264. Epub 2023 Feb 16.

Abstract

Covalent organic framework (COF) materials with porous character and robust structure have significant applied implications for K-ion battery (KIB) anodes, but they are limited by the low reversible capacity and inferior rate capability. Here, based on theoretical calculations, we identified that a porous bulk COF featuring numerous pyrazines and carbonyls in the π-conjugated periodic skeleton could provide multiple accessible redox-active sites for high-performance potassium storage. Its porous structure with a surface-dominated storage mechanism enabled the fast and stable storage of K-ions. Its insolubility in organic electrolytes and small volumetric change after potassiation ensured a robust electrode for stable cycling. As a KIB anode, this bulk COF demonstrated an unprecedentedly outstanding combination of reversible capacity (423 mAh g at 0.1 C), rate capability (185 mAh g at 10 C), and cyclability. The theoretical simulation and comprehensive characterizations confirmed the active sites are contributed by C═O, C═N, and the cation-π effect.

摘要

具有多孔性和稳定结构的共价有机骨架(COF)材料对钾离子电池(KIB)的阳极具有重要的应用意义,但由于可逆容量低和倍率性能差,其应用受到限制。在此,我们通过理论计算,确定了一种具有大量吡嗪和羰基的多孔整体 COF,其在π共轭周期性骨架中具有多个可及的氧化还原活性位点,可为高性能钾存储提供条件。其具有表面主导存储机制的多孔结构能够实现快速稳定的钾离子存储。它不溶于有机溶剂电解质,在钾化后体积变化较小,确保了稳定循环的坚固电极。作为 KIB 的阳极,这种整体 COF 表现出前所未有的卓越可逆容量(在 0.1 C 时为 423 mAh g)、倍率性能(在 10 C 时为 185 mAh g)和循环稳定性。理论模拟和综合特性表征证实,活性位点来自 C=O、C=N 和阳离子-π 作用。

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