Elucidation of Side Reactions in Lithium-ion Batteries with Electrolyte Decomposition Products via Overdischarge for Li[Li1/3Ti5/3]O4/Li[Li0.1Al0.1Mn1.8]O4 Cells with an Imbalanced State-of-Charge

被引:2
作者
Nakamura, Taichi [1 ]
Ariyoshi, Kingo [1 ,2 ]
机构
[1] Osaka City Univ, Grad Sch Engn, Dept Appl Chem & Bioengn, 3-3-138 Sugimoto, Sumiyoshi, Osaka 5588585, Japan
[2] Osaka Metropolitan Univ, Grad Sch Engn, Dept Chem & Bioengn, 3-3-138 Sugimoto, Sumiyoshi, Osaka 5588585, Japan
关键词
Lithium-ion Battery; Capacity Fading; Side Reaction; Crosstalk Reaction; QUATERNARY ONIUM SALTS; LI-ION; REACTION CURRENTS; CAPACITY LOSS; INSERTION; DEGRADATION;
D O I
10.5796/electrochemistry.23-00004
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A major factor in the capacity fading of lithium-ion batteries is the imbalance in the state-of-charge (SOC) between the positive and negative electrodes, which is caused by the difference in the side-reaction current between the two electrodes. Therefore, it is crucial to understand these side reactions to extend battery life. There are two types of side-reaction current, I-SR: "intrinsic"-I-SR results from electrolyte decomposition, while "additional"-I-SR results from the reaction of decomposition products. The "additional"-ISR is closely related to crosstalk reactions. In this study, we conducted overdischarge tests on Li[Li1/3Ti5/3]O-4 (LTO)/Li[Li0.1Al0.1Mn1.8]O-4 (LAMO) cells with the SOC of the positive and negative electrodes intentionally imbalanced to understand the nature of the "additional"-ISR. While the cell capacity initially increased after the overdischarge, the recovered capacity decreased in subsequent cycles. This phenomenon can be explained well by a side-reaction model that considers the oxidant generated in the cell due to overdischarge, which indicates that the concentrations of oxidants and reductants in the cell are important for the I-SR.
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页数:7
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