Tin indium oxide/graphene nanosheet nanocomposite as an anode material for lithium ion batteries with enhanced lithium storage capacity and rate capability

被引:50
|
作者
Yang, Hongxun [1 ]
Song, Taeseup [2 ]
Lee, Sangkyu [2 ]
Han, Hyungkyu [2 ]
Xia, Fan [2 ]
Devadoss, Anitha [2 ]
Sigmund, Wolfgang [1 ,3 ]
Paik, Ungyu [1 ,2 ]
机构
[1] Hanyang Univ, WCU Dept Energy Engn, Seoul 133791, South Korea
[2] Hanyang Univ, Div Mat Sci Engn, Seoul 133791, South Korea
[3] Univ Florida, Dept Mat Sci & Engn, Gainesville, FL 32606 USA
基金
新加坡国家研究基金会;
关键词
Tin indium oxide; Graphene; Anode; Lithium ion batteries; SNO2/GRAPHENE COMPOSITE; OXIDE COMPOSITE; LI STORAGE; GRAPHENE; NANOCRYSTALS; PERFORMANCE; ELECTRODE; IN2O3;
D O I
10.1016/j.electacta.2012.12.070
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Tin oxide (SnO2) is a promising candidate as an anode for lithium ion batteries because of its high theoretical capacity. However, poor capacity retention caused by large volume changes during cycling, large initial irreversible capacity, and low rate capability frustrate its practical application. We have developed a ternary nanocomposite based on tin indium oxide (SnO2-In2O3) and graphene nanosheet (GNS) synthesized via a facile solvothermal method. The incorporation of In2O3 into SnO2 can improve the electrochemical property of SnO2 and reduce the charge transfer resistance of electrode leading to the enhanced reversible capacity and rate capability. The graphene nanosheet in the composite electrode can accommodate high volume expansion/contraction during cycling resulting in excellent capacity retention. As an anode for lithium ion batteries, the SnO2-In2O3/GNS nanocomposite exhibits a remarkably improved electrochemical performance in terms of lithium storage capacity (962 mAh g(-1) at 60 mA g(-1) rate), initial coulombic efficiency (57.2%), cycling stability (60.8% capacity retention after 50 cycles), and rate capability (393.25 mAh g(-1) at 600 mA g(-1) rate after 25 cycles) compared to SnO2/GNS and pure SnO2-In2O3 electrode. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:275 / 281
页数:7
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