Jiang Qiang, Xiong Peixun, Liu Jingjuan, Xie Zhen, Wang Qinchao, Yang Xiao-Qing, Hu Enyuan, Cao Yu, Sun Jie, Xu Yunhua, Chen Long
Department of Chemistry, Institute of Molecular Plus, Tianjin Key Laboratory of Molecular Optoelectronic Science, Tianjin University, Tianjin, 300072, China.
School of Materials Science and Engineering, Key Laboratory of Advanced Ceramics and Machining Technology Tianjin Key Laboratory of Composite and Functional Materials, Tianjin University, Tianjin, 300072, China.
Angew Chem Int Ed Engl. 2020 Mar 23;59(13):5273-5277. doi: 10.1002/anie.201914395. Epub 2020 Jan 28.
Metal-organic framework cathodes usually exhibit low capacity and poor electrochemical performance for Li-ion storage owing to intrinsic low conductivity and inferior redox activity. Now a redox-active 2D copper-benzoquinoid (Cu-THQ) MOF has been synthesized by a simple solvothermal method. The abundant porosity and intrinsic redox character endow the 2D Cu-THQ MOF with promising electrochemical activity. Superior performance is achieved as a Li-ion battery cathode with a high reversible capacity (387 mA h g ), large specific energy density (775 Wh kg ), and good cycling stability. The reaction mechanism is unveiled by comprehensive spectroscopic techniques: a three-electron redox reaction per coordination unit and one-electron redox reaction per copper ion mechanism is demonstrated. This elucidatory understanding sheds new light on future rational design of high-performance MOF-based cathode materials for efficient energy storage and conversion.
由于固有的低导电性和较差的氧化还原活性,金属有机框架阴极在锂离子存储方面通常表现出低容量和较差的电化学性能。现在,通过一种简单的溶剂热法合成了一种具有氧化还原活性的二维铜-对苯醌(Cu-THQ)金属有机框架。丰富的孔隙率和固有的氧化还原特性赋予二维Cu-THQ金属有机框架良好的电化学活性。作为锂离子电池阴极,其具有高可逆容量(387 mA h g)、大比能量密度(775 Wh kg)和良好的循环稳定性,表现出优异的性能。通过综合光谱技术揭示了反应机理:证明了每个配位单元发生三电子氧化还原反应,每个铜离子发生单电子氧化还原反应。这种阐释性的理解为未来合理设计用于高效能量存储和转换的高性能金属有机框架基阴极材料提供了新的思路。