聚碳酸酯
电解质
锂(药物)
阳极
傅里叶变换红外光谱
化学工程
电化学
化学
碳酸二甲酯
电池(电)
锂离子电池
X射线光电子能谱
材料科学
电极
有机化学
催化作用
物理化学
功率(物理)
医学
量子力学
内分泌学
工程类
物理
作者
K. Uta Schwenke,Sophie Solchenbach,Julien Demeaux,Brett L. Lucht,Hubert A. Gasteiger
摘要
Additives such as vinylene carbonate (VC) and fluoroethylene carbonate (FEC) are commonly added to lithium-ion battery electrolytes in order to form a solid electrolyte interphase (SEI) on the anode, suppressing continuous solvent reduction. In this work, we directly compare VC and FEC by analyzing the SEI with FTIR and XPS, and the evolved gases with on-line electrochemical mass spectrometry (OEMS) in different model systems. Since both additives evolve mainly CO2 during formation, the effect of CO2 as an additive is compared to the addition of VC and FEC. While Li2CO3 is as expected the main SEI compound found due to the added CO2, surprisingly no CO was detected in the gas phase of such cells. Based on FTIR, NMR and OEMS analyses of cells filled with 13C labeled CO2, we suggest a mechanism explaining the beneficial effects of CO2 and hence also of CO2 evolving additives in lithium-ion battery cells. While the generation of polycarbonate from FEC or VC reduction is observed, the generation of Li2CO3 may be as important as the generation of polycarbonate.
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