Hydrothermal Self-Assembly Synthesis of Porous SnO2/Graphene Nanocomposite as an Anode Material for Lithium Ion Batteries

被引:3
作者
Liu, Chuntao [1 ,2 ]
Wang, Panpan [3 ]
Du, Chunyu [3 ]
Li, Li [1 ]
Yin, Geping [3 ]
Zuo, Pengjian [3 ]
Cheng, Xinqun [3 ]
机构
[1] Heilongjiang Univ, Sch Chem & Mat Sci, Harbin 150080, Peoples R China
[2] Coll Heilongjiang Prov, Key Lab Chem Engn Proc & Technol High Efficiency, Harbin 150080, Peoples R China
[3] Harbin Inst Technol, Minist Ind & Informat Technol, Key Lab Crit Mat Technol New Energy Convers & Sto, Sch Chem & Chem Engn, Harbin 150001, Peoples R China
关键词
Lithium Ion Batteries; Anode Materials; Graphene; Tin Oxide Nanoparticles; Hydrothermal Self-Assembly; LARGE-SCALE SYNTHESIS; ONE-POT SYNTHESIS; NANOSTRUCTURED MATERIALS; CYCLIC PERFORMANCE; ENERGY-CONVERSION; STORAGE CAPACITY; COMPOSITES; CARBON; OXIDE; NANOPARTICLES;
D O I
10.1166/jnn.2017.13013
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A porous SnO2/graphene nanocomposite is synthesized by the self assembly in a simple one-pot hydrothermal process, which is demonstrated as a high performance anode material for lithium ion batteries. Scanning electron microscopy, transmission electron microscopy and X-ray diffraction indicate that this porous nanocomposite is composed of SnO2 nanoparticles with the size of 10 nm, which are uniformly dispersed on graphene nanosheets. The SnO2/graphene nanocomposite exhibits a reversible capacity of similar to 800 mAh g(-1) at the current density of 250 mA g(-1) and a good rate capacity, which are significantly higher than those of currently commercial graphite anodes. Moreover, the SnO2/graphene nanocomposite displays a superior cycling stability with capacity fade of only 8.8% from the 20th to the 100th cycles at the current density of 250 mA g(-1). The superior electrochemical performance of this nanocomposite is attributed to its highly conductive graphene network, the porous nanostructure, and the well-dispersed SnO2 nanoparticles.
引用
收藏
页码:1877 / 1883
页数:7
相关论文
共 35 条
[1]   Nanostructured materials for advanced energy conversion and storage devices [J].
Aricò, AS ;
Bruce, P ;
Scrosati, B ;
Tarascon, JM ;
Van Schalkwijk, W .
NATURE MATERIALS, 2005, 4 (05) :366-377
[2]   Tin-graphite materials prepared by reduction of SnCl4 in organic medium:: Synthesis, characterization and electrochemical lithiation [J].
Balan, L. ;
Schneider, R. ;
Willmann, P. ;
Billaud, D. .
JOURNAL OF POWER SOURCES, 2006, 161 (01) :587-593
[3]   Nanomaterials for rechargeable lithium batteries [J].
Bruce, Peter G. ;
Scrosati, Bruno ;
Tarascon, Jean-Marie .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (16) :2930-2946
[4]   A facile route to carbon-coated SnO2 nanoparticles combined with a new binder for enhanced cyclability of Li-ion rechargeable batteries [J].
Chou, Shu-Lei ;
Wang, Jia-Zhao ;
Zhong, Chao ;
Rahman, M. M. ;
Liu, Hua-Kun ;
Dou, Shi-Xue .
ELECTROCHIMICA ACTA, 2009, 54 (28) :7519-7524
[5]   In situ polyol-assisted synthesis of nano-SnO2/carbon composite materials as anodes for lithium-ion batteries [J].
Courtel, Fabrice M. ;
Baranova, Elena A. ;
Abu-Lebdeh, Yaser ;
Davidson, Isobel J. .
JOURNAL OF POWER SOURCES, 2010, 195 (08) :2355-2361
[6]   Electrochemical and in situ x-ray diffraction studies of the reaction of lithium with tin oxide composites [J].
Courtney, IA ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (06) :2045-2052
[7]   Ultrafine SnO2 dispersed carbon matrix composites derived by a sol-gel method as anode materials for lithium ion batteries [J].
Gao, Mingxia ;
Chen, Xuan ;
Pan, Hongge ;
Xiang, Liangshun ;
Wu, Fan ;
Liu, Yongfeng .
ELECTROCHIMICA ACTA, 2010, 55 (28) :9067-9074
[8]  
Guo YG, 2008, ADV MATER, V20, P2878, DOI 10.1002/adma.200800627
[9]   Structure and electrochemical performance of nanostructured Fe3O4/carbon nanotube composites as anodes for lithium ion batteries [J].
He, Yang ;
Huang, Ling ;
Cai, Jin-Shu ;
Zheng, Xiao-Mei ;
Sun, Shi-Gang .
ELECTROCHIMICA ACTA, 2010, 55 (03) :1140-1144
[10]   PREPARATION OF GRAPHITIC OXIDE [J].
HUMMERS, WS ;
OFFEMAN, RE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1958, 80 (06) :1339-1339