电解质
石墨
阳极
锂(药物)
动力学
锂钴氧化物
材料科学
阴极
化学
无机化学
电极
分析化学(期刊)
锂离子电池
物理化学
电池(电)
热力学
有机化学
复合材料
功率(物理)
医学
内分泌学
量子力学
物理
作者
T. Richard Jow,Michelle Marx,Jan L. Allen
出处
期刊:ECS transactions
[The Electrochemical Society]
日期:2011-03-21
卷期号:33 (23): 1-13
被引量:10
摘要
In examining the Li+ charge transfer kinetics at the graphite anode and the lithium nickel cobalt aluminum oxide, LiNi0.80Co0.15Al0.05O2 (NCA), cathode in a complete cell, we found that the activation energy, Ea, for the charge transfer at the graphite/electrolyte interface is about 68 kJ/mol, which is consistent with the recently reported values. However, the Ea for the charge transfer at the NCA/electrolyte interface is about 50 kJ/mol, which is lower than that at the graphite anode. With desolvation as the predominate step for limiting the kinetics and both of the electrodes were subject to the same electrolyte, the difference in Ea suggests that the Ea is influenced greatly with respect to the nature of electrode materials and their associated SEIs. This is further confirmed by the examination of the LiFePO4 (LFP)/electrolyte and the graphite/electrolyte interfaces using a LFP/graphite complete cell.
科研通智能强力驱动
Strongly Powered by AbleSci AI