锂离子在非水混合溶剂中优先溶剂化的13c核磁共振估计

K. Matsubara, Rie Kaneuchi, Noriko Maekita
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引用次数: 44

摘要

测定了含1 mol dm-3 LiPF6的有机电解质溶液在丙酸甲酯(MP) -碳酸甲酯(EMC)、N,N-二甲基乙酰胺(DMA) -碳酸丙烯(PC)和MP -丙酸乙酯(EP)三种二元混合溶剂体系中的13C NMR谱。有电解质和没有电解质的溶剂的化学位移的差异归因于溶剂与锂离子的配位。表征各混合溶剂体系配位能力的归一化配位位移大小依次为:MP>EMC、DMA>PC和MP>EP。推导了二元混合溶剂中锂离子第一配位层溶剂比的方程。在1:1体积组成下,MP-EMC的估计比率为1.6,DMA-PC为15,MP-EP为1.3。
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13 C NMR estimation of preferential solvation of lithium ions in non-aqueous mixed solvents
The 13C NMR spectra of organic electrolyte solutions containing 1 mol dm-3 LiPF6 in the three binary mixed solvent systems, methyl propionate (MP)–ethyl methyl carbonate (EMC), N,N-dimethylacetamide (DMA)–propylene carbonate (PC) and MP–ethyl propionate (EP) were measured at various solvent compositions. The difference in the chemical shifts of a solvent with and without the electrolyte was attributed to the coordination of the solvent to the lithium ion. The order of the normalized coordination shift which represents the coordinating ability for each mixed solvent system was MP>EMC, DMA>PC and MP>EP. An equation was derived which estimates the solvent ratio in the first coordination shell of the lithium ion in the binary mixed solvents for any solvent composition. The estimated ratio at a 1:1 volume composition was 1.6 for MP–EMC, 15 for DMA–PC and 1.3 for MP–EP.
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