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首页> 外文期刊>Science in China, Series B. Chemistry >LiCoO2 electrode/electrolyte interface of Li-ion batteries investigated by electrochemical impedance spectroscopy
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LiCoO2 electrode/electrolyte interface of Li-ion batteries investigated by electrochemical impedance spectroscopy

机译:锂离子电池的LiCoO2电极/电解质界面的电化学阻抗谱研究

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摘要

The storage behavior and the first delithiation of LiCoO2 electrode in 1 mol/L LiPF6-EC:DMC:DEC electrolyte were investigated by electrochemical impedance spectroscopy(EIS).It has found that,along with the increase of storage time,the thickness of SEI film increases,and some organic carbonate lithium compounds are formed due to spontaneous reactions occurring between the LiCoO2 electrode and the electrolyte.When electrode potential is changed from 3.8 to 3.95 V,the reversible breakdown of the resistive SEI film occurs,which is attributed to the reversible dissolution of the SEI film component.With the increase of electrode potential,the thickness of SEI film increases rapidly above 4.2 V,due to overcharge reactions.The inductive loop observed in impedance spectra of the LiCoO2 electrode in Li/LiCoO2 cells is attributed to the formation of a Li_(1-x)CoO2/LiCoO2 concentration cell.Moreover,it has been demonstrated that the lithium-ion insertion-deinsertion in LiCoO2 hosts can be well described by both Langmuir and Frumkin insertion isotherms,and the symmetry factor of charge transfer has been evaluated at 0.5.
机译:通过电化学阻抗谱(EIS)研究了LiCoO2电极在1 mol / L LiPF6-EC:DMC:DEC电解质中的储存行为和首次脱锂。发现,随着储存时间的增加,SEI的厚度增加LiCoO2电极与电解质之间发生自发反应,导致膜厚增加,并形成了一些有机碳酸锂化合物。当电极电位从3.8 V变为3.95 V时,发生了SEI电阻膜的可逆击穿,这是由于SEI膜组分的可逆溶解。随着电极电位的增加,由于过充电反应,SEI膜的厚度在4.2 V以上迅速增加。 Li_(1-x)CoO2 / LiCoO2浓度池的形成。此外,已经证明,LiCoO2主体中的锂离子插入-插入可以很好地解决。由Langmuir和Frumkin插入等温线确定,电荷转移的对称系数估计为0.5。

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