Carbon-Coated Ordered Mesoporous SnO2 Composite Based Anode Material for High Performance Lithium-Ion Batteries

被引:6
|
作者
Heo, Jungwon [1 ,2 ]
Liu, Ying [1 ,2 ]
Haridas, Anupriya K. [2 ,3 ]
Jeon, Jinwoo [2 ,3 ]
Zhao, Xiaohui [4 ]
Cho, Kwon-Koo [2 ,3 ]
Ahn, Hyo-Jun [2 ,3 ]
Lee, Younki [2 ,3 ]
Ahn, Jou-Hyeon [1 ,2 ,3 ]
机构
[1] Gyeongsang Natl Univ, Dept Chem Engn, Jinju 52828, South Korea
[2] Gyeongsang Natl Univ, Res Inst Green Energy Convergence Technol, Jinju 52828, South Korea
[3] Gyeongsang Natl Univ, Dept Mat Engn & Convergence Technol, Jinju 52828, South Korea
[4] Soochow Univ, Coll Phys Optoelect & Energy, Soochow Inst Energy & Mat Innovat, Suzhou 215006, Peoples R China
基金
新加坡国家研究基金会;
关键词
SBA-15; SnO2; Mesoporous SnO2; Carbon Coating; SILICA; NANOPARTICLES; ARRAYS;
D O I
10.1166/jnn.2018.15688
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently, tin oxide (SnO2) has received significant attention for use as an anode material for next generation lithium-ion batteries (LIBs) owing to its high theoretical capacity (782 mAh g(-1)), which is more than twice of that of the commercialized graphite (372 mAh g(-1)). Several additional advantages, such as low cost, environmental friendliness, easy fabrication and natural abundance improve its promise. Although the theoretical capacity of SnO2 is high, volume expansion during cycling causes issue with cycling stability. In this study, an ordered mesoporous SnO2 was synthesized using a hard template (SBA-15), such that its mesoporous structure can buffer SnO2 particles from cracks caused by volume expansion. It can also allow effective electrolyte infiltration to ensure better reactivity of the active material with Li+ ions. The capacity of synthesized mesoporous SnO2 improved to 218.4 mAh g(-1) compared regular SnO2 nanoparticles (69.6 mAh g(-1)) after 50 cycles at a rate of 0.1 C. Furthermore, carbon-coated mesoporous SnO2 enhanced capacity retention upon cycling (844.6 mAh g(-1) after 50 cycles at 0.1 C) by insulating and preventing the cracking of the active material during lithiation and delithiation.
引用
收藏
页码:6415 / 6421
页数:7
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