材料科学
阴极
降级(电信)
石墨
电池(电)
离子键合
离子
电化学
化学工程
插层(化学)
纳米技术
复合材料
无机化学
电子工程
电极
电气工程
化学
物理
工程类
量子力学
物理化学
功率(物理)
有机化学
作者
Yu Tang,Xingyu Wang,Jincan Ren,Bowen Chen,Zhiyong Huang,Wei Wang,Yalan Huang,Bing-Hao Zhang,Si Lan,Zhanglong He,Qi Liu,Hao He
出处
期刊:Rare Metals
[Springer Science+Business Media]
日期:2023-11-18
卷期号:43 (1): 41-50
被引量:15
标识
DOI:10.1007/s12598-023-02454-2
摘要
Abstract Lithium‐ion batteries (LIBs) with extreme fast charging (XFC) capability are considered an effective way to alleviate range anxiety for electric vehicle (EV) buyers. Owing to the high ionic and electronic conductivity of LiNi x Co y Mn z O 2 ( x + y + z = 1, NCM) cathodes, the inevitable Li plating of graphite in NCM | graphite cell is usually identified as a key bottleneck for XFC LIBs. However, the capacity decay mechanism of cathode materials under XFC has not been fully investigated. In this work, three typical NCM cathode materials with different Ni fractions were chosen and their electrochemical performances under XFC associated with structural evolution were investigated. A faster capacity decay of NCMs under XFC conditions is observed, especially for Ni‐rich NCMs. In‐situ X‐ray diffraction (XRD) reveals that the multiple c ‐axis parameters appear at the high‐voltage regions in Ni‐rich NCMs, which is probably triggered by the larger obstruction of Li (de)intercalation. Particularly, NCMs with moderate Ni fraction also present a similar trend under XFC conditions. This phenomenon is more detrimental to the structural and morphological stability, resulting in a faster capacity decay than that under low current charging. This work provides new insight into the degradation mechanism of NCMs under XFC conditions, which can promote the development of NCM cathode materials with XFC capability.
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