电池电极材料的电学、化学、热学和力学响应耦合连续介质模型中插层驱动孔隙率效应

Zhenlin Wang, Jason B. Siegel, K. Garikipati
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引用次数: 8

摘要

我们提出了电池材料中静电、化学、热和机械过程的耦合连续谱公式。我们的处理方法适用于宏观尺度,在宏观尺度上,电极可以被建模为由活性颗粒组成的多孔材料,这些活性颗粒由粘合剂粘合在一起,并由电解质灌注。从该领域常见的描述开始,根据离子的反应输运偏微分方程,静电学的经典泊松方程的变体和热方程,我们将力学添加到问题中。我们的主要贡献是模拟孔隙度的演化,这是由插层、热膨胀和机械应力引起的应变的结果。认识到潜在的大局部变形,我们已经确定了有限应变框架。我们提出了一个详细的计算研究的动态演变孔隙率的影响,对离子分布,静电势场,充放电循环和机械力在电池中产生。
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Intercalation driven porosity effects in coupled continuum models for the electrical, chemical, thermal and mechanical response of battery electrode materials
We present a coupled continuum formulation for the electrostatic, chemical, thermal and mechanical processes in battery materials. Our treatment applies on the macroscopic scale, at which electrodes can be modelled as porous materials made up of active particles held together by binders and perfused by the electrolyte. Starting with the description common to the field, in terms of reaction-transport partial differential equations for ions, variants of the classical Poisson equation for electrostatics, and the heat equation, we add mechanics to the problem. Our main contribution is to model the evolution of porosity as a consequence of strains induced by intercalation, thermal expansion and mechanical stresses. Recognizing the potential for large local deformations, we have settled on the finite strain framework. We present a detailed computational study of the influence of the dynamically evolving porosity, upon ion distribution, electrostatic potential fields, charge-discharge cycles and mechanical force generated in the cell.
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