电镀(地质)
剥离(纤维)
锂(药物)
扩散
电极
离子
分析化学(期刊)
化学
电压
工作(物理)
材料科学
热力学
电气工程
复合材料
物理
色谱法
物理化学
医学
有机化学
工程类
地球物理学
内分泌学
作者
Simon E. J. O’Kane,Ian D. Campbell,M. Waseem Marzook,Gregory J. Offer,Monica Marinescu
标识
DOI:10.1149/1945-7111/ab90ac
摘要
The main barrier to fast charging of Li-ion batteries at low temperatures is the risk of short-circuiting due to lithium plating. In-situ detection of Li plating is highly sought after in order to develop fast charging strategies that avoid plating. It is widely believed that Li plating after a single fast charge can be detected and quantified by using a minimum in the differential voltage (DV) signal during the subsequent discharge, which indicates how much lithium has been stripped. In this work, a pseudo-2D physics-based model is used to investigate the effect on Li plating and stripping of concentration-dependent diffusion coefficients in the active electrode materials. A new modelling protocol is also proposed, in order to distinguish the effects of fast charging, slow charging and Li plating/stripping. The model predicts that the DV minimum associated with Li stripping is in fact a shifted and more abrupt version of a minimum caused by the stage II-stage III transition in the graphite negative electrode. Therefore, the minimum cannot be used to quantify stripping. Using concentration-dependent diffusion coefficients yields qualitatively different results to previous work. This knowledge casts doubt on the utility of DV analysis for detecting Li plating.
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