阳极
锂(药物)
电极
材料科学
电化学
介电谱
阴极
石墨
锂离子电池
化学
化学工程
电池(电)
电解质
容量损失
降级(电信)
分析化学(期刊)
复合材料
色谱法
电气工程
工程类
内分泌学
物理化学
功率(物理)
物理
量子力学
医学
作者
Wenlong Xie,Rong He,Xinlei Gao,Xinghu Li,Huizhi Wang,Xinhua Liu,Xiaoyu Yan,Shichun Yang
标识
DOI:10.1016/j.electacta.2021.138979
摘要
Cycle aging of commercial 2.5 Ah 18650 cylindrical lithium-ion batteries with LiNi0.8Co0.1Mn0.1O2(NCM)/graphite chemistry is investigated at different charging rates. The cells charged at 1C-3C follow a similar aging path, and the degradation mechanisms under 2C and 3C charging are characterized by non-destructive electrochemical techniques and post-mortem analyses. Electrochemical impedance spectroscopy measurements indicate that the impedance rise of cells is primarily attributed to the increase of charge transfer resistance. Post mortem analyses reveal that the side reactions on NCM cathode are secondary particle cracking and transition metal dissolution, and anode degradation is caused by the growth of solid-electrolyte interface layer and the lithium plating. Voltage fitting analyses of 3C charging demonstrate that the main degradation mode is the insufficient active lithium that is available for intercalation/deintercalation in highly-lithiated anodes. Quantitative analyses of the individual electrodes based on differential voltage curves identify that loss of lithium inventory (LLI) contributes the dominant aging mode to full cell, followed by loss of active material of delithiated negative electrode (LAMdeNE) and LAM of lithiated negative electrode (LAMliNE), while LAM of positive electrode (LAMPE) exerts a minor effect. Accurate identification of the battery degradation mechanisms cycling under fast charging conditions helps to provide guidance for charging optimization.
科研通智能强力驱动
Strongly Powered by AbleSci AI