材料科学
阳极
锂(药物)
淡出
原位
石墨
容量损失
离子
同步加速器
阴极
化学工程
磷酸铁锂
自行车
电化学
复合材料
电极
化学
物理化学
核物理学
计算机科学
医学
操作系统
有机化学
考古
历史
内分泌学
工程类
物理
作者
Qi Liu,Yadong Liu,Fan Yang,Hao He,Xianghui Xiao,Yang Ren,Wenquan Lu,Eric A. Stach,Jian Sheng Xie
标识
DOI:10.1021/acsami.7b13060
摘要
In situ high-energy synchrotron XRD studies were carried out on commercial 18650 LiFePO 4 cells at different cycles to track and investigate the dynamic, chemical, and structural changes in the course of long-term cycling to elucidate the capacity fading mechanism. The results indicate that the crystalline structural deterioration of the LiFePO 4 cathode and the graphite anode is unlikely to happen before capacity fades below 80% of the initial capacity. Rather, the loss of the active lithium source is the primary cause for the capacity fade, which leads to the appearance of inactive FePO 4 that is proportional to the absence of the lithium source. Our in situ HESXRD studies further show that the lithium-ion insertion and deinsertion behavior of LiFePO 4 continuously changed with cycling. For a fresh cell, the LiFePO 4 experienced a dual-phase solid-solution behavior, whereas with increasing cycle numbers, the dynamic change, which is characteristic of the continuous decay of solid solution behavior, is obvious. The unpredicted dynamic change may result from the morphology evolution of LiFePO 4 particles and the loss of the lithium source, which may be the cause of the decreased rate capability of LiFePO 4 cells after long-term cycling.
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