Kinetic study of low temperature capacity fading in Li-ion cells

被引:29
|
作者
Singer, Jan Patrick [1 ]
Birke, Kai Peter [1 ]
机构
[1] Univ Stuttgart, Inst Photovolta, Elect Energy Storage Syst, Pfaffenwaldring 47, D-70569 Stuttgart, Germany
关键词
Chemical diffusion coefficient; Activation energy; Activation factor; Lithium-ion cells; Capacity fade; Low temperature; Pseudo-OCV; LIFEPO4;
D O I
10.1016/j.est.2017.07.002
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Lithium-ion cells show a reversible capacity fade at low C-rates (C/10) at temperatures below T = 0 degrees C. This phenomenon cannot solely been explained by temperature induced impedance raise and the formation of solid electrolyte interphases any more. We investigate four different cell chemistries at temperatures T = 25, 0, -10 and -20 degrees C. All measurements are carried out on full cells. The activation energies and especially the ratio of anodic and cathodic activation energies have the highest impact on capacity fading at low C-rates. For quantification of the ratio, we define an activation factor between anodic and the cathodic activation energies. We derive temperature and activation energy behavior on basis of the Butler-Volmer equation for increasing internal voltages and polarization. High activation energies causes high energy demand for activation polarization and an earlier reach of cut-off voltages. If the negative and positive electrode are well balanced with respect to activation energies, the internal voltages which are induced at electrodes boundary layers (electrochemical double layer) are small and the pseudo open circuit voltages lower. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:129 / 136
页数:8
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