材料科学
碳热反应
阳极
碳化
碳纤维
电化学
化学工程
离子
惰性气体
锂(药物)
水热碳化
芯(光纤)
纳米结构
锂离子电池的纳米结构
壳体(结构)
电极
纳米技术
惰性
复合材料
扫描电子显微镜
化学
有机化学
碳化物
复合数
物理化学
内分泌学
工程类
医学
作者
Xiaoyuan Yu,Siyuan Yang,Baohua Zhang,Dan Shao,Xiaoting Dong,Yueping Fang,Ze-Sheng Li,Shaoyi Wang
摘要
A new low-flow-rate inert atmosphere strategy has been demonstrated for the synthesis of perfect SnO2@carbon core-shell nanochains (SCNCs) by carbonization of an SnO2@carbonaceous polysaccharide (CPS) precursor at a relatively high temperature. This strategy results in the thorough carbonization of CPS whilst avoiding the carbothermal reduction of SnO2 at 700 °C. It has been investigated that a moderate carbon content contributes to the 1-D growth of SCNCs, and the thickness of the carbon shell can be easily manipulated by varying the hydrothermal treatment time in the precursor process. Such a unique nanochain architecture could afford a very high lithium storage capacity as well as resulting in a desirable cycling performance. SCNCs with about 8 nm carbon shell synthesized by optimized routes were demonstrated for optimal electrochemical performances. More than 760 mAh g¬1 of reversible discharge capacity was achieved at a current density of 300 mA g−1, and above 85% retention can be obtained after 100 charge-discharge cycles. TEM analysis of electrochemically-cycled electrodes indicates that the structural integrity of the SnO2@carbon core-shell nanostructure is retained during electrochemical cycling, contributing to the good cycleability demonstrated by the robust carbon shell.
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