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In situ scanning tunneling microscopy studies of the SEI formation on graphite electrodes for Li+-ion batteries

机译:原位扫描隧道显微镜的研究SEI在石墨电极上形成李+离子电池

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The SEI-formation on graphitic electrodes operated as an Li+-ion battery anode in a standard 1 M LiPF6 EC/DMC (1 : 1) electrolyte has been studied in situ by EC-STM. Two different modes of in situ study were applied, one, which allowed to follow topographic and crystallographic changes (solvent cointercalation, graphite exfoliation, SEI precipitation on the HOPG basal plane) of the graphite electrode during SEI-formation, and the second, which gave an insight into the SEI precipitation on the HOPG basal plane in real time. From the in situ EC-STM studies, not only conclusions about the SEI-topography could be drawn, but also about the formation mechanism and the chemical composition, which strongly depend on the electrode potential. It was shown that above 1.0 V vs. Li/Li+ the SEI-formation is still reversible, since the molecular structure of the solvent molecules remains intact during an initial reduction step. During further reduction, the molecular structures of the solvents are destructed, which causes the irreversible charge loss. The STM studies were completed by electrochemical methods, like cyclic voltammetry, the potentiostatic intermittent titration technique and charge/discharge tests of MCMB electrodes.
机译:SEI-formation石墨电极操作作为一个李+离子电池阳极在标准1 MLiPF6 EC / DMC(1: 1)电解液进行了研究由EC-STM原位。研究应用,允许地形和晶体变化(溶剂cointercalation、石墨剥落,SEI降水的石墨基底平面)石墨电极在SEI-formation,其次,这给一个洞察SEI降水在石墨基底平面的时间。结论SEI-topography可能画,但也形成机制和化学成分的强烈依赖电极电位。高于1.0 V和李/李+ SEI-formation仍可逆的,因为的分子结构在一个溶剂分子仍然完好无损减少初始步骤。溶剂的分子结构被破坏,导致不可逆的的损失。循环伏安法等电化学方法的电压稳定器的间歇滴定技术和MCMB的充电/放电测试电极。

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