电解质
材料科学
锂(药物)
电池(电)
容量损失
碳酸锂
碳酸二乙酯
离子
无机化学
碳酸盐
锂离子电池
碳酸二甲酯
化学工程
碳酸乙烯酯
有机化学
电极
物理化学
冶金
催化作用
化学
热力学
离子键合
医学
功率(物理)
物理
工程类
内分泌学
作者
Florian Gebert,Neeha Gogoi,Dumindu P. Siriwardena,Andrew J. Naylor
标识
DOI:10.1002/admi.202400535
摘要
Abstract 1,1,1‐trifluoroethyl methyl carbonate (FEMC) is a popular non‐flammable solvent for lithium‐ion battery electrolytes, although its high irreversible capacity means it can only be used with film‐forming additives like fluoroethylene carbonate (FEC). This work studies the origin of the high irreversible capacity of FEMC‐containing cells. Scanning electron microscopy and Raman spectroscopy of graphite anodes after charging and discharging in an FEMC electrolyte show evidence of significant physical and chemical graphite degradation, likely caused by solvent co‐intercalation, which is probably responsible for a large portion of the capacity loss. X‐ray photoelectron spectroscopy analysis of the anodes shows very low graphite signals, a sign of graphite degradation, formation of a thick solid electrolyte interphase (SEI), or both. When a small amount of FEC is added to FEMC, co‐intercalation does not occur. FEC reduction occurs at a higher potential versus Li/Li + than FEMC co‐intercalation. It also forms a significantly different and thinner SEI containing more carbon, less fluorine, and no apparent FEMC decomposition products.
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