阳极
石墨
锂(药物)
传质
碳纤维
电池(电)
离子
材料科学
储能
电化学
锂离子电池
化学工程
纳米技术
化学
电极
功率(物理)
热力学
冶金
复合材料
色谱法
物理化学
有机化学
物理
内分泌学
工程类
复合数
医学
作者
Yin Zhao,Yulong Fu,Yue Meng,Zhi Wang,Junhao Liu,Xuzhong Gong
标识
DOI:10.1016/j.cej.2023.148047
摘要
Natural graphite (NG) with ordered carbon layers has the advantage of a green and low-cost preparation process, which makes it a suitable candidate for lithium-ion battery (LIB) materials in the field of energy storage. However, the co-embedding of solvated lithium ions (Li+) and the slow mass transfer rate of Li+ in NG anodes result in poor cycle life and low-rate performance, severely restricting their application in large-scale energy storage and power batteries. Remarkable modification methods of NG anodes have been discussed in literature, but most of them ignored the mass transfer of Li+ in NG anodes. This review highlights the effect of Li+ mass transfer on the stability of carbon layers and the performance under low-temperature and rapid-charge conditions and summarizes some potential methods to improve the Li+ mass transfer in graphite interfaces and bulk phases to provide a new perspective on the development of NG anodes.
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