Effects of 3,5-bis(trifluoromethyl)benzeneboronic acid as an additive on electrochemical performance of propylene carbonate-based electrolytes for lithium ion batteries

被引:32
作者
Wang, B. [1 ,2 ]
Qu, Q. T. [1 ,2 ]
Xia, Q. [1 ,2 ]
Wu, Y. P. [1 ,2 ]
Li, X. [3 ]
Gan, C. L. [3 ]
van Ree, T. [4 ]
机构
[1] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
[2] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[3] Guotai Huarong Chem New Mat Co Ltd, Zhangjiagang, Jiangsu Prov, Peoples R China
[4] Univ Venda, Dept Chem, ZA-0950 Thohoyandou, South Africa
基金
新加坡国家研究基金会;
关键词
Lithium ion batteries; Cycleability; Film-forming; Solid electrolyte interface (SEI); 3,5-Bis(trifluoromethyl)benzeneboronic acid;
D O I
10.1016/j.electacta.2008.06.070
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The effects of 3,5-bis(trifluoromethyl)benzeneboronic acid (BA) as a new film-forming additive have been theoretically and experimentally studied for a graphite (CMS) electrode in propylene carbonate-based (PC) electrolyte for lithium ion batteries. Calculation based on the density functional theory (DFT) method suggests that the energy of the LUMO (the lowest unoccupied molecular orbital) of BA is lower than that of PC, consistent with the results of cyclic voltammograms that BA is reduced before PC. SEM, FT-IR and XPS measurements show that the reduced products of BA contribute in part to the effective SEI film on the graphite electrode surface. Discharge-charge measurements indicate that the addition of BA can effectively prevent the decomposition and the co-intercalation of PC, and lithium ions can reversibly intercalate into and deintercalate from the graphite electrode. These results show that addition of BA improves the electrochemical performance of graphite in PC-based electrolyte. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:816 / 820
页数:5
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