Evolution of stress within a spherical insertion electrode particle under potentiostatic and galvanostatic operation

被引:419
作者
Cheng, Yang-Tse [1 ]
Verbrugge, Mark W. [2 ]
机构
[1] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA
[2] Gen Motors Res & Dev Ctr, Mat & Proc Lab, Warren, MI 48090 USA
基金
美国国家科学基金会;
关键词
Stress; Strain energy; Diffusion; Galvanostatic; Potentiostatic; Battery; MODELING LITHIUM INTERCALATION; CHEMICAL STRESSES; BATTERY CHARGER; HOLLOW CYLINDER; ION BATTERIES; DIFFUSION; GENERATION; CELL; MICROELECTRODES; OPTIMIZATION;
D O I
10.1016/j.jpowsour.2009.01.021
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Lithium ion battery electrode materials generally experience significant volume changes during charging and discharging caused by concentration changes within the host particles. Electrode failure, in the form of fracture or decrepitation, may occur as a result of a highly localized stress, strain energy, and stress cycles overtime. In this paper,we develop analytic expressions for the evolution of stress and strain energy within a spherically shaped electrode element under either galvanostatic (constant Current) or potentiostatic (constant potential) operation when irreversible phenomena are dominated by solute diffusion resistance within host particles. We show that stresses and strain energy can evolve quite differently under potentiostatic vs. galvanostatic control. The findings of this work suggest the possibility of developing new battery charging strategies that minimize stress and strain energy and thus prolong battery life. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:453 / 460
页数:8
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