分离器(采油)
材料科学
电解质
阳极
电化学
离子电导率
电极
化学工程
离子
离子键合
电化学动力学
锂离子电池
介电谱
电池(电)
阴极
复合材料
化学
热力学
工程类
物理
物理化学
功率(物理)
有机化学
作者
Daniel Sauerteig,Nina Hanselmann,Arno Arzberger,Holger Reinshagen,Svetlozar Ivanov,Andreas Bund
标识
DOI:10.1016/j.jpowsour.2017.12.044
摘要
The intercalation and aging induced volume changes of lithium-ion battery electrodes lead to significant mechanical pressure or volume changes on cell and module level. As the correlation between electrochemical and mechanical performance of lithium ion batteries at nano and macro scale requires a comprehensive and multidisciplinary approach, physical modeling accounting for chemical and mechanical phenomena during operation is very useful for the battery design. Since the introduced fully-coupled physical model requires proper parameterization, this work also focuses on identifying appropriate mathematical representation of compressibility as well as the ionic transport in the porous electrodes and the separator. The ionic transport is characterized by electrochemical impedance spectroscopy (EIS) using symmetric pouch cells comprising LiNi1/3Mn1/3Co1/3O2 (NMC) cathode, graphite anode and polyethylene separator. The EIS measurements are carried out at various mechanical loads. The observed decrease of the ionic conductivity reveals a significant transport limitation at high pressures. The experimentally obtained data are applied as input to the electrochemical-mechanical model of a prismatic 10 Ah cell. Our computational approach accounts intercalation induced electrode expansion, stress generation caused by mechanical boundaries, compression of the electrodes and the separator, outer expansion of the cell and finally the influence of the ionic transport within the electrolyte.
科研通智能强力驱动
Strongly Powered by AbleSci AI