Molecular Modularized Co-Polyimide as a Water-Processable Multifunctional Binder for High-Performance Si/C Anodes in Lithium-Ion Batteries
Wei Tan, Bo Liang, Hang Xiao, Menghao Chen, Wenjie Yang, Xian He, Jianghuai Hu, Ke Zeng, Gang Yang
Abstract
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 LiNi 0.5 Co 0.2 Mn 0.3 O 2 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.