Reduced irreversible capacities of graphene oxide-based anodes used for lithium ion batteries via alkali treatment

被引:20
|
作者
Jiao, Danhua [1 ,2 ]
Xie, Zhengwei [1 ,3 ]
Wan, Qi [1 ]
Qu, Meizhen [1 ]
机构
[1] Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Sichuan, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
[3] Shenzhen New Hengye Battery Technol Co Ltd, Shenzhen 518055, Guangdong, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Irreversible capacity; Graphene oxide; Epoxide group; Ring-opening reaction; THERMAL REDUCTION; FUNCTIONALIZED GRAPHENE; ELECTROCHEMICAL PERFORMANCE; COMPOSITE; GRAPHITE; OXYGEN; SUPERCAPACITOR; EXFOLIATION; MECHANISM; EVOLUTION;
D O I
10.1016/j.jechem.2018.11.018
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The large irreversible capacities of graphene oxide-based anodes hinder commercial applications of GO materials although the high specific capacity of it has been universally accepted. In this paper, GO was treated under alkaline condition and the composite consisting of the modified GO and graphite was used as anode for lithium ion batteries (LIBs), resulting in an improved initial coulombic efficiency. Electrochemical tests also showed that the modified GO/graphite electrode possessed 86.0% of initial coulombic efficiency, which was 15% higher than that of pristine GO/graphite electrode. The species and the content of functional groups were investigated via XPS, FTIR characterizations in detail, which certified that the ring-opening reaction of epoxides under alkaline condition could greatly reduce the irreversible capacity of GO/graphite anode, in addition, the reversible capacity was guaranteed at the same time. This modified GO/graphite electrodes in the LIBs exhibit superior rate capability and long cycle life. The uniqueness of this electrode lied in its chemical stability, which benefits from the transition of epoxide group and unstable functional groups removal. (C) 2018 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
引用
收藏
页码:73 / 81
页数:9
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