多物理
材料科学
电极
电解质
电池(电)
锂离子电池
电化学
粒子(生态学)
复合材料
电化学动力学
离子
纳米技术
有限元法
化学
热力学
物理
地质学
物理化学
功率(物理)
有机化学
海洋学
作者
Yasir Ali,Imran Shah,Tariq Amin Khan,Noman Iqbal
出处
期刊:Energies
[Multidisciplinary Digital Publishing Institute]
日期:2023-08-05
卷期号:16 (15): 5823-5823
被引量:1
摘要
Understanding the electrochemical and mechanical degradations inside the electrodes of lithium-ion battery is crucial for the design of robust electrodes. A typical lithium-ion battery electrode consists of active particles enclosed with conductive binder and an electrolyte. During the charging and discharging process, these adjacent materials create a mechanical confinement which suppresses the expansion and contraction of the particles and affects overall performance. The electrochemical and mechanical response mutually affect each other. The particle level expansion/contraction alters the electrochemical response at the electrode level. In return, the electrode level kinetics affect the stress at the particle level. In this paper, we developed a multiphysics–multiscale model to analyze the electrochemical and mechanical responses at both the particle and cell level. The 1D Li-ion battery model is fully coupled with 2D representative volume element (RVE) model, where the particles are covered in binder layers and bridged through the binder. The simulation results show that when the binder constraint is incorporated, the particles achieve a lower surface state of charge during charging. Further, the cell charging time increases by 7.4% and the discharge capacity reduces by 1.4% for 1 C-rate charge/discharge. In addition, mechanical interaction creates inhomogeneous stress inside the particle, which results in particle fracture and particle–binder debonding. The developed model will provide insights into the mechanisms of battery degradation for improving the performance of Li-ion batteries.
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