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Modeling Li-ion concentration distribution and stress of porous electrode particles considering binder and direct particle contact

材料科学 复合材料 粒子(生态学) 电极 压力(语言学) 接触面积 多孔性 离子 联轴节(管道) 扩散 接触力学 有限元法 化学 结构工程 热力学 语言学 海洋学 哲学 物理 有机化学 物理化学 工程类 地质学
作者
Yang Wu,Zhansheng Guo
出处
期刊:Journal of energy storage [Elsevier BV]
卷期号:44: 103315-103315 被引量:17
标识
DOI:10.1016/j.est.2021.103315
摘要

• A fully coupled model of porous electrodes with influence of binder and direct particle contact was developed. • The direct contact between particles will hinder Li-ion insertion, and the blocking effect could stronger than that of the binder. • The compressive stress in the area covered by the binder was much smaller than the compressive stress in the area of direct contact between the AM particles. • The binder is most likely to debond at the edge of the particle-binder interface. During electrochemical cycling, stresses in porous electrode particles arise primarily due to the development of Li-concentration gradients and direct contact between particles, which cause a deterioration in the performance of Li-ion battery electrodes. A model for simulating the effects of binders and direct contact between particles on the Li-ion concentration and stress distribution of active material (AM) particles is proposed in this work. The Li-ion concentration and contact stress of a unidirectional coupling model and a fully coupled model are compared. The influence of binders and the influence of direct contact between particles on the concentration profile and stress distribution are numerically investigated. The simulations show that the direct contact between particles hindered Li-ion insertion, and its blocking effect was stronger than that of the binder. The compressive stress in the area covered by the binder was much smaller than the compressive stress in the area of direct contact between the AM particles. The binder is most likely to debond at the edge of the particle-binder interface. The developed model and results could lay the foundation for studying the contact-diffusion-stress coupling behavior of porous electrode particles.
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