A Redox-Active 2D Metal-Organic Framework for Efficient Lithium Storage with Extraordinary High Capacity

被引:253
作者
Jiang, Qiang [1 ]
Xiong, Peixun [2 ]
Liu, Jingjuan [1 ]
Xie, Zhen [1 ]
Wang, Qinchao [3 ]
Yang, Xiao-Qing [3 ]
Hu, Enyuan [3 ]
Cao, Yu [4 ]
Sun, Jie [4 ]
Xu, Yunhua [2 ]
Chen, Long [1 ]
机构
[1] Tianjin Univ, Dept Chem, Inst Mol Plus, Tianjin Key Lab Mol Optoelect Sci, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Sch Mat Sci & Engn, Key Lab Adv Ceram & Machining Technol, Tianjin Key Lab Composite & Funct Mat, Tianjin 300072, Peoples R China
[3] Brookhaven Natl Lab, Chem Div, Upton, NY 11973 USA
[4] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
2D materials; cathodes; metal-organic framework; energy storage; lithium ion batteries; ELECTRODE MATERIALS; MIXED-VALENCE; MECHANISM; EDGE; SOFT;
D O I
10.1002/anie.201914395
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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(-1)), large specific energy density (775 Wh kg(-1)), 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.
引用
收藏
页码:5273 / 5277
页数:5
相关论文
共 28 条
[1]  
[Anonymous], 2007, ANGEW CHEM, V119, P3323
[2]  
[Anonymous], 2018, ANGEW CHEM, V130, P9024
[3]   Building better batteries [J].
Armand, M. ;
Tarascon, J. -M. .
NATURE, 2008, 451 (7179) :652-657
[4]   Fundamental understanding and practical challenges of anionic redox activity in Li-ion batteries [J].
Assat, Gaurav ;
Tarascon, Jean-Marie .
NATURE ENERGY, 2018, 3 (05) :373-386
[5]   Electronic Conductivity, Ferrimagnetic Ordering, and Reductive Insertion Mediated by Organic Mixed-Valence in a Ferric Semiquinoid Metal-Organic Framework [J].
Darago, Lucy E. ;
Aubrey, Michael L. ;
Yu, Chung Jui ;
Gonzalez, Miguel I. ;
Long, Jeffrey R. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2015, 137 (50) :15703-15711
[6]   Robust and conductive two-dimensional metal-organic frameworks with exceptionally high volumetric and areal capacitance [J].
Feng, Dawei ;
Lei, Ting ;
Lukatskaya, Maria R. ;
Park, Jihye ;
Huang, Zhehao ;
Lee, Minah ;
Shaw, Leo ;
Chen, Shucheng ;
Yakovenko, Andrey A. ;
Kulkarni, Ambarish ;
Xiao, Jianping ;
Fredrickson, Kurt ;
Tok, Jeffrey B. ;
Zou, Xiaodong ;
Cui, Yi ;
Bao, Zhenan .
NATURE ENERGY, 2018, 3 (01) :30-36
[7]   Mixed-valence Li/Fe-based metal-organic frameworks with both reversible redox and sorption properties [J].
Ferey, Gerard ;
Millange, Franck ;
Morcrette, Mathieu ;
Serre, Christian ;
Doublet, Marie-Liesse ;
Greneche, Jean-Marc ;
Tarascon, Jean-Marie .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2007, 46 (18) :3259-3263
[8]   Tunable Redox Chemistry and Stability of Radical Intermediates in 2D Covalent Organic Frameworks for High Performance Sodium Ion Batteries [J].
Gu, Shuai ;
Wu, Shaofei ;
Cao, Lujie ;
Li, Minchan ;
Qin, Ning ;
Zhu, Jian ;
Wang, Zhiqiang ;
Li, Yingzhi ;
Li, Zhiqiang ;
Chen, Jingjing ;
Lu, Zhouguang .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2019, 141 (24) :9623-9628
[9]   Chemistry of the Redox Series from Hexahydroxybenzene to Cyclohexanehexaone [J].
Hettegger, Hubert ;
Hosoya, Takashi ;
Rosenau, Thomas .
CURRENT ORGANIC SYNTHESIS, 2016, 13 (01) :86-100
[10]   Oxygen plasma induced degradation of the surface of poly(styrene), poly(bisphenol-A-carbonate) and poly(ethylene terephthalate) as observed by soft X-ray absorption spectroscopy (NEXAFS) [J].
Koprinarov, I ;
Lippitz, A ;
Friedrich, JF ;
Unger, WES ;
Woll, C .
POLYMER, 1998, 39 (14) :3001-3009