材料科学
阳极
碳热反应
石墨
锂(药物)
碳纤维
电解质
阴极
热冲击
化学工程
无定形碳
纳米技术
无定形固体
电极
复合材料
化学
复合数
结晶学
医学
碳化物
物理化学
工程类
内分泌学
作者
Chang-Hyun Cho,Wonyeop Jeong,Chang-Ha Lim,Jae-Kook Yoon,Chris Yeajoon Bon,Kap Seung Yang,Min‐Sik Park
出处
期刊:Carbon
[Elsevier]
日期:2024-08-10
卷期号:229: 119542-119542
被引量:1
标识
DOI:10.1016/j.carbon.2024.119542
摘要
We present a cost-effective synthesis process for producing a carbon-coated nano-Si@Graphite (n-Si@G-C) anode, in which nano-sized Si (n-Si) particles (∼50 nm in size) are anchored onto natural graphite particles by a carbothermal shock through microwave induction. During the carbothermal shock process, graphite undergoes a fast increase in temperature resulting in micron-sized Si (m-Si) particles (∼4 μm in size) to undergo stress fractures due to rapid thermal expansion. This process leads to the formation of abundant n-Si particles onto graphite particles. Subsequently, a thin carbon shell is introduced by a wet-coating process combined with a thermal decomposition of coal-tar pitch. The amorphous carbon shell offers multiple functionalities: i) preventing direct exposure of n-Si particles to the electrolyte, ii) accommodating their volume expansion, and iii) maintaining electron conduction pathways. The resulting n-Si@G-C anode allows a high reversible capacity (500.8 mAh g−1) as well as fast-charging characteristics. When utilized in a full-cell configured with a commercial-grade LiNi0.8Co0.1Mn0.1O2 cathode, it achieves a notable reduction in charging time (approximately 10.1 min@80 % state of charge). After 300 cycles, a high capacity retention (71.3 %) can be retained under 3C charging. Moreover, the distinctive structural features of the n-Si@G-C anode effectively suppress undesirable Li plating.
科研通智能强力驱动
Strongly Powered by AbleSci AI