电解质
电极
锂(药物)
化学
电极电位
半电池
参比电极
标准电极电位
分析化学(期刊)
反应速率
工作电极
催化作用
物理化学
有机化学
医学
内分泌学
作者
Nupur Nikkan Sinha,Thomas H. Marks,Hannah Dahn,Aaron Smith,J. C. Burns,D. J. Coyle,J. J. Dahn,J. R. Dahn
摘要
Active lithium in the negative electrode of a Li-ion cell reacts with electrolyte to form an ever-thickening solid electrolyte interphase. The rate of this reaction can be monitored as a function of temperature, time and electrode potential using storage and symmetric cell studies. Using the soft carbon, petroleum coke, as a model negative electrode material, experiments measuring the open circuit voltage (OCV) change with time of Li/coke cells were made to measure the rate of loss of active lithium. The capacity loss with cycle number or time of coke/coke symmetric cells was also used to measure the rate of Li loss. The results on over 100 test cells show that: 1) the reaction rate decreases by about a factor of 2–4 as the electrode potential increases from 0.005 to 1.0 V; 2) the reaction rate increases approximately 3–10 fold between 30 and 60°C depending on the electrode potential; 3) The reaction rates are within a factor of two, and may be the same, for electrodes at OCV or undergoing cycling; 4) the reaction rate is larger when vinylene carbonate (VC) is present in the electrolyte at 30°C for all potentials and times studied and 5) the reaction rate is about two times smaller in the presence of VC at 60°C for potentials above 0.4 V. A significant number of further experiments are required to develop accurate theoretical models of the reactivity of intercalated lithium with electrolyte as a function of time, temperature and potential.
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