Conductive metal-organic framework with redox metal center as cathode for high rate performance lithium ion battery

被引:141
作者
Gu, Shaonan [1 ,5 ]
Bai, Zhaowen [1 ,2 ]
Majumder, Soumyadip [3 ]
Huang, Baoling [4 ]
Chen, Guohua [1 ]
机构
[1] Hong Kong Polytech Univ, Dept Mech Engn, Hung Hom, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Sch Engn, Environm Engn Program, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[3] Hong Kong Univ Sci & Technol, Dept Chem & Biol Engn, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[4] Hong Kong Univ Sci & Technol, Dept Mech & Aerosp Engn, Kowloon, Clear Water Bay, Hong Kong, Peoples R China
[5] Qilu Univ Technol, Shandong Acad Sci, Sch Chem & Pharmaceut Engn, Key Lab Fine Chem Univ Shandong, Jinan, Shandong, Peoples R China
关键词
Conductive MOF; Redox center; Cathode; High rate performance; GAS-STORAGE; MOF; CU; REDUCTION; OXYGEN; MIL-101(FE); ADSORPTION; ELECTRODES; MECHANISM; SORPTION;
D O I
10.1016/j.jpowsour.2019.04.087
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Exploration of new materials for lithium ion battery is a continuous challenge to meet the increasing demand for energy storage. Herein, a novel conductive metal-organic framework Cu-3(2,3,6,7,10,11-hexahydroxy-triphenylene)(2) (Cu-3(HHTP)(2)) is obtained and tested as cathode active material in lithium ion battery. With a working voltage range of 1.7-3.5 V, Cu-3(HHTP)(2) cathode shows a reversible discharge and charge capacity of similar to 95 mA h g(-1), which is almost equal to its theoretical value. Impressively, this novel cathode also shows highly stable redox cycling performance at the current rate as high as 20C because of its intrinsic electrical conductivity and two dimensional porous structure. Electrochemical properties and chemical analysis of Cu-3(HHTP)(2) reveal that the valence change of copper cations in the framework is responsible for the lithium ions insertion/desertion during redox cycles. The first principle calculation also supports this mechanism.
引用
收藏
页码:22 / 29
页数:8
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