阳极
材料科学
碳纤维
锂(药物)
电池(电)
二氧化碳
硅
负二氧化碳排放
离子
化学工程
锂离子电池
二氧化硅
纳米技术
无机化学
电极
化学
复合材料
复合数
固碳
有机化学
冶金
功率(物理)
物理化学
内分泌学
工程类
物理
医学
量子力学
作者
Yaguang Zhang,Ning Du,Yifan Chen,Yangfan Lin,Jinwei Jiang,Yuanhong He,Lei Yu,Deren Yang
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2018-01-01
卷期号:10 (12): 5626-5633
被引量:48
摘要
Si/C composite is one of the most promising candidate materials for next-generation lithium-ion battery anodes. Herein, we demonstrate the novel structure of carbon cages encapsulating porous Si synthesized by the reaction between magnesium silicide (Mg2Si) and carbon dioxide (CO2) and subsequent acid washing. Benefitting from the in situ deposition through magnesiothermic reduction of CO2, the carbon cage seals the inner Si completely and shows higher graphitization than that obtained from the decomposition of acetylene. After removing MgO, pores are created, which can accommodate the volume change of the Si anode during the charge/discharge process. As the anode material for lithium-ion batteries, the porous Si/C electrode shows a charge capacity of ∼1124 mA h g-1 after 100 cycles with 86.4% capacity retention at the current density of 0.4 A g-1. When the current density increases to 1.6 and 3.2 A g-1, the capacity can still be maintained at ∼860 and ∼460 mA h g-1, respectively. The prominent cycling and rate performance is contributed by the built-in space for Si expansion, static carbon cages that prevent penetration of electrolyte and stabilize the solid electrolyte interface (SEI) outside, and fast charge transport by the novel structure.
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