阳极
锂(药物)
材料科学
离子
碳纤维
相(物质)
锂离子电池的纳米结构
对偶(语法数字)
化学工程
纳米技术
化学
复合材料
电极
复合数
工程类
物理化学
医学
艺术
文学类
有机化学
内分泌学
作者
Yulin Fu,Dongxia Li,Xiangfeng Sun,Yuxin Xue,Yuanhao Shi,Zhiqi Li,Chongxian Luo,Qiong Lin,Xuefeng Gui,Kai Xu
出处
期刊:Small
[Wiley]
日期:2024-05-21
卷期号:20 (38): e2403070-e2403070
被引量:15
标识
DOI:10.1002/smll.202403070
摘要
Among silicon-based anode family for Li-ion battery technology, SiOx, a nonstoichiometric silicon suboxide holds the potential for significant near-term commercial impact. In this context, this study mainly focuses on demonstrating an innovative SiOx@C anode design that adopts a pre-lithiation strategy based on in situ pyrolysis of Li-salt of silsesquioxane trisilanolate without the need for lithium metal or active lithium compounds and creates dual carbon encapsulation of SiOC nanodomains by simply one-step thermal treatment. This ingenious design ensures the pre-lithiation process and pre-lithiation material with high-environmental stability. Moreover, phenyl-rich organosiloxane clusters and polyacrylonitrile polymers are expected to serve as internal and external carbon source, respectively. The formation of an interpenetrating and continuous carbon matrix network would not only synergistically offer an improved electrochemical accessibility of active sites but also alleviate the volume expansion effect during cycling. As a result, this new type of anode delivered a high reversible capacity, remarkable cycle stability as well as excellent high-rate capability. In particular, the L2-SiOx@C material has a high initial coulomb efficienc of 80.4% and, after 500 cycles, a capacity retention as high as 97.5% at 0.5 A g-1 with a reversible specific capacity of 654.5 mA h g-1.
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