材料科学
阳极
硅
碳纤维
化学工程
制作
熔盐
多孔硅
硅烷
电池(电)
涂层
多孔性
纳米技术
聚丙烯腈
图层(电子)
复合数
聚二甲基硅氧烷
多孔介质
液体燃料
碳纳米纤维
集电器
电极
作者
Yida Wang,Xiaoyan Cui,Renwei Liao,Yun Xia,Wenrui Hu,Zhenjia Xu,Haiyun Zhou,Yanqing Wang,Jianqiang Chen
出处
期刊:Small
[Wiley]
日期:2026-09-10
卷期号:: e75724-e75724
摘要
ABSTRACT The structures of silicon‑embedded porous carbon feature unique pore‑confinement effects and serve as highly promising configurations for silicon‑carbon anodes. However, conventional preparation technologies based on silicon sources have obvious technical shortcomings that limit the fabrication and industrial application of such composite anodes. Among them, the CVD process using silane as a precursor carries high safety risks and can easily lead to pore clogging of carbon matrices and aggregation of silicon particles. This work employs chemically stable and highly wettable polydimethylsiloxane (PDMS) as the liquid silicon source, employs biomass‐derived porous carbon as a host matrix, and synthesizes silicon‐embedded porous carbon anode materials through in situ low‐temperature molten salt reduction (denoted as SiNPs@PC). SiNPs@PC exhibits a reversible capacity of up to 1209 mAh g −1 after 100 cycles at 0.1 A g −1 . Subsequently, coating SiNPs@PC with an ionic‐liquid‐derived carbon layer yields SiNPs@PC1_ILs3, which delivers enhanced cycling stability and retains 82.7% of its initial capacity after 2000 long‐term cycles at 5 A g −1 . The in situ preparation strategy using liquid silicon source offers comprehensive advantages over CVD method in the safety, operability and cost of process.
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