多收费
热失控
电解质
碳酸乙烯酯
阳极
放热反应
阴极
锂(药物)
化学
无机化学
材料科学
化学工程
电池(电)
电极
有机化学
热力学
物理化学
功率(物理)
内分泌学
工程类
物理
医学
作者
Takahisa Ohsaki,Takashi Kishi,Takashi Kuboki,Norio Takami,Nao Shimura,Yuichi Sato,M. Sekino,Asako Satoh
标识
DOI:10.1016/j.jpowsour.2005.03.105
摘要
Overcharge reaction was studied in detail using 650 mAh prismatic hermetically sealed lithium-ion batteries with LiCoO2 cathodes, graphitic carbon anodes and ethylene carbonate/ethyl methyl carbonate (EC/EMC) electrolytes. Several varieties of gases (CO2, CO, H2, CH4, C2H6 and C2H4) were evolved in the overcharge reaction. The amount of gas increased with the increase in the cell temperature and rose rapidly at the end of the overcharge. In particular, the amount of CO2 gas produced by the oxidation of the electrolyte at the cathode increased markedly. The exothermic oxidation reaction of the electrolyte was accelerated at the temperature above 60 °C, causing the cell temperature to increase rapidly thereafter. The heating tests of the overcharged anode samples enclosed in cylindrical cell cases with EC/EMC electrolytes resulted in thermal runaways. In contrast, the overcharged cathodes tested in the same manner showed no thermal runaway. The thermal runaway reaction during overcharge was caused by the violent reaction between the overcharged anode (deposited lithium) and the electrolyte solvent at high temperature that was the result of the rapid exothermic reaction of the delithiated cathode and the electrolyte.
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