阳极
硅
材料科学
锂(药物)
碳纤维
离子
对偶(语法数字)
缓冲器(光纤)
化学工程
纳米技术
复合材料
光电子学
电极
化学
复合数
电气工程
有机化学
物理化学
医学
艺术
文学类
工程类
内分泌学
作者
Xiaowen Jiang,Lin Sun,Yuyan Lu,Hongyu Wang,Jingwen Shi,Liduo Yang,Lei Zhang,Rongguan Lv,Jin Zhong
标识
DOI:10.1016/j.jpowsour.2024.234331
摘要
Silicon-carbon (Si/C) composite materials have been proven to be one of the most promising anode materials for the next generation of lithium-ion batteries (LIBs) due to their high theoretical capacity. However, the substantial volume changes during alloying/dealloying processes have posed significant challenges to the working lifespan of Si-based anodes. In this study, we designed a dual-carbon-layer-structured Si composite anode material (DCS-Si). Using ladderlike polysilsesquioxanes as a precursor, we employed a zinc thermal reaction to internally reduce the Si–O–Si framework to Si0. Simultaneously, the phenyl groups directly connected to Si atoms served as a carbon source for the internally dense coating layer. The obtained product underwent further coating controllable pyrolysis reactions to form an external carbon coating layer. As anode for LIBs, DCS-Si delivered a reversible specific capacity exceeding 1000 mAh g−1. Even after 1350 cycles at a current density of 0.3 A g−1, the specific capacity remained above 500 mAh g−1. Moreover, even under a high current density of 3 A g−1, after nearly 1000 cycles, the capacity retention rate still exceeded 70%. Further testing of the full cell also indicated that DCS-Si is a highly promising high-energy-density anode, with potential applications in future commercial lithium-ion batteries.
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