Solvation of the fluorine containing anions and their lithium salts in propylene carbonate and dimethoxyethane

被引:29
|
作者
Chaban, Vitaly [1 ,2 ]
机构
[1] Univ Fed Sao Paulo, Inst Ciencia & Tecnol, BR-12231280 Sao Jose Dos Campos, SP, Brazil
[2] Univ So Calif, Dept Chem, Los Angeles, CA 90089 USA
关键词
Propylene carbonate; Dimethoxyethane; Hexafluorophosphate; Molecular dynamics; PM7-MD; Semiempirical; Structure; Tetrafluoroborate; REACTIVE FORCE-FIELD; NDDO APPROXIMATIONS; MOLECULAR-DYNAMICS; PM6; METHOD; ELECTROLYTE; OPTIMIZATION; PARAMETERS; INTERFACE; DENSITY; REAXFF;
D O I
10.1007/s00894-015-2717-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Electrolyte solutions based on the propylene carbonate (PC)-dimethoxyethane (DME) mixtures are of significant importance and urgency due to emergence of lithium-ion batteries. Solvation and coordination of the lithium cation in these systems have been recently attended in detail. However, analogous information concerning anions (tetrafluoroborate, hexafluorophosphate) is still missed. This work reports PM7-MD simulations (electronic-structure level of description) to include finite-temperature effects on the anion solvation regularities in the PC-DME mixture. The reported result evidences that the anions appear weakly solvated. This observation is linked to the absence of suitable coordination sites in the solvent molecules. In the concentrated electrolyte solutions, both BF4- and PF6- prefer to exist as neutral ion pairs (LiBF4, LiPF6).
引用
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页数:8
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