Ion speciation of lithium hexafluorophosphate in dimethyl carbonate solutions: an infrared spectroscopy study

被引:41
|
作者
Fulfer, Kristen D. [1 ]
Kuroda, Daniel G. [2 ]
机构
[1] Ctr Coll Danville, Chem Program, Danville, KY 40422 USA
[2] Louisiana State Univ, Dept Chem, Baton Rouge, LA 70803 USA
关键词
ETHYLENE CARBONATE; PROPYLENE CARBONATE; SOLVATION STRUCTURE; SOLVENT INTERACTION; SALT CONTENT; ELECTROLYTES; LIPF6; LI+; DYNAMICS; CONDUCTIVITY;
D O I
10.1039/c8cp03315c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Solutions of lithium hexafluorophosphate (LiPF6) in linear organic carbonates play a significant role in the portable energy storage industry. However, many questions remain about the solution structure at the molecular-level. An atomic characterization of these solutions is important for determining their structure-property relations, which will allow for the rational design of new and improved lithium ion based energy storage technologies. In this study, a combination of infrared spectroscopies and density functional theory calculations was used to investigate the speciation of the lithium ion (free ion, solvent separated ion pair, contact ion pairs, and aggregates) in dimethyl carbonate solutions having concentrations ranging from 1 M to 3 M. The experimental data shows that at typical battery electrolyte concentrations the lithium ion exists predominantly as free ions and solvent separated ion pairs, but charged contact ion pairs are also present in small concentrations. In contrast, at high concentrations the lithium ion is present in aggregates, but a noticeable fraction remains present as free ions.
引用
收藏
页码:22710 / 22718
页数:9
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