聚酰亚胺
阳极
硅氧烷
锂(药物)
材料科学
硅
电解质
共聚物
聚合物
化学工程
电化学
氧化物
纳米技术
电极
复合材料
光电子学
化学
图层(电子)
工程类
内分泌学
物理化学
医学
冶金
作者
Wei Tan,Bo Liang,Menghao Chen,Hang Xiao,He Xian,Wenjie Yang,Jianghuai Hu,Ke Zeng,Gang Yang
标识
DOI:10.1016/j.cej.2024.153822
摘要
Silicon is considered as a promising electrode materials for the next generation of lithium-ion batteries. However, it's commercial applications are hindered by significant volume changes. In this study, copolyimide binders with adjustable rigidity and flexibility were synthesized through simple copolymerization. The rigid segments containing adenine groups (p-APA) provide excellent mechanical strength and interface interaction, while flexible segments containing siloxane bonds and alkane chains (DS-NH2) can buffer volume changes through enhanced mobility and topological entanglement of molecular segments. Optimizing the copolymerization ratio helps minimize damage to the silicon electrode structure and stabilizes solid electrolyte interphase (SEI) growth. Compared to the rigid polyimide binders, rigid-flexible coupling strategy improves cycling stability, remaining a capacity of 2170 mAh/g at 2 A/g after 200 cycles and exhibiting stable cycling for over 750 cycles with a capacity limitation of 1500 mAh/g. The high mass loading silicon anodes, micron-sized silicon oxide electrodes and the full cells also exhibit favorable electrochemical performance. This research provides valuable insights for designing high-performance aromatic polymer binders for high energy density lithium-ion batteries.
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