Thermal Behavior of Solid Electrolyte Interphase Films Deposited on Graphite Electrodes with Different States-of-Charge

被引:26
|
作者
Park, Hosang [1 ,2 ]
Yoon, Taeho [1 ,2 ]
Kim, Youngjin [1 ,2 ]
Lee, Jae Gil [1 ,2 ]
Kim, Jongjung [1 ,2 ]
Kim, Hyun-seung [1 ,2 ]
Ryu, Ji Heon [3 ]
Kim, Jae Jeong [1 ,2 ]
Oh, Seung M. [1 ,2 ]
机构
[1] Seoul Natl Univ, Dept Chem & Biol Engn, Seoul 151744, South Korea
[2] Seoul Natl Univ, Inst Chem Proc, Seoul 151744, South Korea
[3] Korea Polytech Univ, Grad Sch Knowledge Based Technol & Energy, Siheung Si, South Korea
基金
新加坡国家研究基金会;
关键词
LITHIUM-ION BATTERY; NEGATIVE ELECTRODE; SURFACE; INTERCALATION; STABILITY; REACTIVITY; MECHANISM; ANODES; SEI;
D O I
10.1149/2.0431506jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The thermal degradation of surface films (solid electrolyte interphase, SEI) and their repairing behaviors are examined on graphite electrodes that have different states-of-charge (SOC). In detail, a fully passivating SEI layer is generated in advance and then stored at 85 degrees C for a prolonged time. The surface films (SEI) are thermally degraded upon high-temperature exposure. The damaged films are repaired by electrolyte decomposition and concomitant film deposition, during which Li+ ions/electrons are supplied from the graphite electrodes, which appears as an increase in the open-circuit voltage (OCV) of the graphite electrodes. The repaired surface films show a comparable passivating ability along with a similar morphology and chemical composition to that of the initial SEI layers. The degradation/repairing continues until the graphite electrodes are fully de-lithiated (OCV = 3.0 V vs. Li/Li+). Once the graphite electrodes are fully de-lithiated, the damaged surface films cannot be repaired because the Li+ ions/electrons are exhausted in the graphite electrodes. Because of the incomplete repairing, the graphite surface becomes poorly covered by surface films, which leads to a loss of passivating ability. (C) The Author(s) 2015. Published by ECS. All rights reserved.
引用
收藏
页码:A892 / A896
页数:5
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