热失控
分离器(采油)
电解质
阳极
电极
锂(药物)
材料科学
化学工程
分析化学(期刊)
量热法
阴极
离子
热的
化学
色谱法
热力学
有机化学
物理
工程类
内分泌学
物理化学
功率(物理)
医学
电池(电)
作者
Daniel P. Abraham,E.P. Roth,Robert Kostecki,K.A. McCarthy,Scott MacLaren,D.H. Doughty
标识
DOI:10.1016/j.jpowsour.2006.04.088
摘要
The inherent thermal instability of lithium-ion cells is a significant impediment to their widespread commercialization for hybrid-electric vehicle applications. Cells containing conventional organic electrolyte-based chemistries are prone to thermal runaway at temperatures around 180 °C. We conducted accelerating rate calorimetry measurements on high-power 18650-type lithium-ion cells in an effort to decipher the sequence of events leading to thermal runaway. In addition, electrode and separator samples harvested from a cell that was heated to 150 °C then air-quenched to room temperature were examined by microscopy, spectroscopy, and diffraction techniques. Self-heating of the cell began at 84 °C. The gases generated in the cell included CO2 and CO, and smaller quantities of H2, C2H4, CH4, and C2H6. The main changes on cell heating to 150 °C were observed on the anode surface, which was covered by a thick layer of surface deposits that included LiF and inorganic and organo-phosphate compounds. The sources of gas generation and the mechanisms leading to the formation of compounds observed on the electrode surfaces are discussed.
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