聚酰亚胺
材料科学
阳极
锂(药物)
阴极
硅
化学工程
纳米技术
电极
物理化学
光电子学
图层(电子)
医学
工程类
内分泌学
化学
作者
Wei Tan,Bo Liang,Hang Xiao,Menghao Chen,Wenjie Yang,Xian He,Jianghuai Hu,Ke Zeng,Gang Yang
标识
DOI:10.1021/acsami.5c05284
摘要
Micrometer-sized silicon–carbon (Si/C) anode materials with high capacity represent one of the most promising alternatives for achieving a high energy density in lithium-ion batteries. The development of binders that effectively interact with Si/C active materials is crucial for ensuring the stability of the Si/C electrodes. In this study, a water-processable multifunctional copolyimide binder (denoted as SPI-x) comprising three molecular modules was designed. The adenine modules within the molecular chain serve to facilitate hydrogen bonding with the silicon surface of Si/C as well as promote π–π interactions with the carbon surface. These dual interfacial interactions contribute significantly to the stability of the electrode structure. Furthermore, lithium sulfonate groups (Li+ transport module) and flexible segments (entropic elasticity module) enhance lithium ion transport and accommodate volume expansion, respectively. Electrodes incorporating this multifunctional binder exhibited excellent cycling stability and rate performance: after 400 cycles at 0.5 A g–1, a capacity of 825.2 mAh g–1 was achieved with a retention of 93.1%. At 2.0 A g–1, the electrode maintained a high capacity of 701.6 mAh g–1. Full cells assembled with a LiNi0.5Co0.2Mn0.3O2 cathode demonstrated a capacity of 150.4 mAh g–1, with a retention of 92.7% after 300 cycles. This work provides key insights into the development of multifunctional binders for high-energy, long-life lithium-ion batteries.
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