阳极
材料科学
空隙(复合材料)
硅
离子
电极
阴极
电化学
功率密度
纳米技术
化学工程
复合材料
光电子学
化学
物理化学
量子力学
物理
工程类
功率(物理)
有机化学
作者
Xiangyu Bi,Tianyu Tang,Xingwang Shi,Xuhui Ge,Weiwei Wu,Zhiya Zhang,Jun Wang
出处
期刊:Small
[Wiley]
日期:2022-08-12
卷期号:18 (37)
被引量:25
标识
DOI:10.1002/smll.202200796
摘要
The core-void@shell architecture shows great advantages in enhancing cycling stability and high-rate performance of Si-based anodes. However, it is usually synthesized by template methods which are complex and environmentally unfriendly and would lead to low-efficiency charge and mass exchange because of the single-point van der Waals contact between the Si core and the shell. Here, a facile and benign one-step method to synthesize multi-Si-void@SiO2 structure, where abundant void spaces exist between multiple Si cores that are multi-point attached to a SiO2 shell through strong chemical bonding, is reported. The corresponding electrode exhibits highly stable cycling stability and excellent electrochemical performance. After 200 cycles at a current density of 0.1 A g-1 and then another 200 cycles at 1.2 A g-1 , the electrode outputs a specific capacity of 1440 mAh g-1 . Even at 2.0 A g-1 , it outputs a specific capacity as high as 1182 mAh g-1 . Such an anode can match almost all the cathode materials presently used in lithium-ion batteries. These results demonstrate the multi-Si-void@SiO2 as a promising anode to be used in future commercial lithium-ion batteries of high energy density and high power density.
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