阳极
材料科学
动力学
离子
锂(药物)
化学工程
复合材料
空隙(复合材料)
电极
化学
有机化学
工程类
内分泌学
物理
物理化学
医学
量子力学
作者
Fei Wang,Bo Wang,Ting‐Ting Ruan,Tiantian Gao,Rensheng Song,Fan Jin,Yu Zhou,Dianlong Wang,Huan Liu,Shi Xue Dou
出处
期刊:ACS Nano
[American Chemical Society]
日期:2019-10-07
卷期号:13 (10): 12219-12229
被引量:142
标识
DOI:10.1021/acsnano.9b07241
摘要
Silicon (Si), a promising candidate for next-generation lithium-ion battery anodes, is still hindered by its volume change issue for (de)lithiation, thus resulting in tremendous capacity fading. Designing carbon-modified Si materials with a void-preserving structure (Si@void@C) can effectively solve this issue. The preparation of Si@void@C, however, usually depended on template-based routes or chemical vapor deposition, which involve toxic reagents, tedious operation processes, and harsh conditions. Here, a facile templateless approach for preparing Si@void@C materials is reported through controlling the growth kinetics of resin, without the use of toxic hydrofluoric acid or harsh conditions. This approach allows great flexibility in tuning the crucial parameters of Si@void@C, such as the carbon shell thickness, the reserved void size, and the number of Si cores coated by a carbon shell. The optimized Si@void@C delivers a large specific capacity (1993.2 mAh g–1 at 0.1 A g–1), excellent rate performance (799.4 mAh g–1 at 10.0 A g–1), and long cycle life (73.5% capacity retention after 1000 cycles at 2.0 A g–1). In addition, a full cell fabricated with a Si@void@C anode and commercial LiFePO4 cathode also displays an impressive cycling performance.
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