环丁砜
溶解
分解
电解质
沉积(地质)
无机化学
X射线光电子能谱
电化学
化学
钝化
锂(药物)
化学工程
图层(电子)
有机化学
电极
溶剂
物理化学
沉积物
古生物学
医学
工程类
生物
内分泌学
作者
Yosuke Ugata,Ryoichi Tatara,Toshihiko Mandai,Kazuhide Ueno,Masayoshi Watanabe,Kaoru Dokko
出处
期刊:ACS applied energy materials
[American Chemical Society]
日期:2021-02-11
卷期号:4 (2): 1851-1859
被引量:23
标识
DOI:10.1021/acsaem.0c02961
摘要
Li deposition and dissolution in highly concentrated electrolytes consisting of sulfolane (SL) and two amide-type Li salts, LiN(SO2CF3)2 (LiTFSA) and LiN(SO2F)2 (LiFSA), were investigated. The chronopotentiometry test of Li/Cu cells containing these two electrolytes demonstrated that the reversibility of Li deposition/dissolution and the cycling performance were better in the LiFSA/SL electrolyte than in the LiTFSA/SL electrolyte. Gas analysis with electrochemical mass spectroscopy revealed that the SL molecules were reduced to form tetrahydrothiophene (THT) and butane in the LiTFSA/SL electrolyte during Li deposition. In contrast, these side reactions were significantly suppressed in the LiFSA/SL electrolyte. The X-ray photoelectron spectroscopy analysis for the deposited Li in the LiTFSA/SL electrolyte suggests that Li2O and sulfurous compounds were formed on the Li surface by the reductive decomposition of SL. For the LiFSA/SL electrolyte, the LiF-rich passivation layer derived from the FSA anion could effectively suppress further decomposition of SL, resulting in highly reversible Li deposition and dissolution.
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