材料科学
阳极
无定形固体
纳米复合材料
离子
电极
分层(地质)
纳米结构
化学工程
体积热力学
硅
体积膨胀
碳纤维
无定形碳
复合材料
纳米技术
光电子学
复合数
结晶学
古生物学
俯冲
量子力学
化学
生物
物理化学
医学
工程类
内科学
物理
构造学
作者
Rusheng Fu,Keli Zhang,Remo Proietti Zaccaria,Heran Huang,Yonggao Xia,Zhaoping Liu
出处
期刊:Nano Energy
[Elsevier]
日期:2017-09-01
卷期号:39: 546-553
被引量:113
标识
DOI:10.1016/j.nanoen.2017.07.040
摘要
SiOx owing to high reversible capacity and moderate volume expansion has been attracting a lot of attention as state-of-the-art anodes for the next generation of Li-ion batteries. However, poor cycling performance and poor rate capability, respectively associated with detrimental volume expansion and insulative amorphous SiO2, are still challenging issues which need to be addressed for the actual employment as anodes for Li-ion batteries. In this regard, here we design, synthesize, characterize and test carbon coated sheet-like SiO1.1 nanocomposites formed by Si-nanodomains confined inside amorphous SiO2 (nano-Si/a-SiO2). As a proof-of-concept, we achieve sheet-like SiOx nanocomposites via in-situ transformation of delaminated siloxene. In particular, self-prepared siloxene with oxygen-inserted Si6 rings terminated with H and OH ligands is prepared by delamination of CaSi2 in dilute HCl. Importantly, the resulting carbon coated nano-Si/a-SiO2 material shows enhanced reaction kinetics and structural stability leading to 946 mAh g−1 capacity at 0.15 A g−1. Intriguingly, 38.0% (~360 mAh g−1) of the maximum capacity is maintained even at 7.5 A g−1, corresponding to a remarkable less than 3 min charge/discharge time. Finally, the electrode shows merely 24% of volume expansion and minor cracks with capacity retention of 92% after 300 cycles at 7.5 A g−1.
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