化学
电解质
相间
锂(药物)
电极
介电谱
二甲醚
X射线光电子能谱
三甘醇
电化学
表征(材料科学)
无机化学
金属锂
乙醚
纳米技术
物理化学
医学
内分泌学
材料科学
生物
遗传学
作者
Shizhao Xiong,Yan Diao,Xiaobin Hong,Yingchao Chen,Kai Xie
标识
DOI:10.1016/j.jelechem.2014.02.014
摘要
The electrochemical behavior, chemical composition and the topography of the solid electrolyte interphase (SEI) on lithium electrodes cycling in ether-based electrolytes are investigated using X-ray photoelectron spectroscopy (XPS), scanning probe microscopy (SPM) and electrochemical impedance spectroscopy (EIS). Electrolytes with ethers (1,2-Dimethoxyethane (DME), Diethylene glycol dimethyl ether (DG) and Triethylene glycol dimethyl ether (TEGDME)) are employed to understand the effect of ether/alkyl moieties ratio on the formation of the SEI films. The cycling behavior and impedance spectra of the symmetrical cells show that the stability and property of those SEI films depend on the selection of the solvent. The results indicate that DG and TEGDME based electrolytes lead to a higher resistance for lithium ion migration through the SEI film. Combined with XPS spectra and depth profile, different chemical composition and depth profile distribution for those SEI films are observed. This difference could be attributed to the decomposition of the electrolytes with different ethers. The height images and phase images obtained from SPM show that the decomposition of the three solvents on lithium metal is active after the immersion of the lithium electrodes in electrolytes. In contrast, the decomposition of TFSI− from lithium salt is more active during the cycling of the cells.
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