Xiaoyuan YuSiyuan YangBaohua ZhangDan ShaoXianming DongYueping FangZe‐Sheng LiHongqiang Wang
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.
Jun LiuWen LiArumugam Manthiram
Xiaowei LiShenglin XiongJingfa LiXin LiangJiazhao WangJing BaiYitai Qian
Julien SouriceArnaud BordesAdrien BoulineauJohn P. AlperSylvain FrangerAxelle QuinsacAurélie HabertY. LeconteÉric De VitoWilly PorcherCécile ReynaudNathalie Herlin‐BoimeCédric Haon
Lei YuNing DuWei LiuHao WuDeren Yang
Hongwen ChenYangdan LuHangjian ZhuYichuan GuoRui HuRabia KhatoonLingxiang ChenYu‐Jia ZengJiao LeiJianxing LengJianguo Lü