Natural abundance 17O nuclear magnetic resonance and computational modeling studies of lithium based liquid electrolytes

JOURNAL OF POWER SOURCES

卷:285

Article

Deng, Xuchu^1,2  Hu, Mary Y.¹  Wei, Xiaoliang¹  Wang, Wei¹  Chen, Zhong²  Liu, Jun¹  Hu, Jian Zhi¹ 

[1] Pacific NW Natl Lab, JCESR, Richland, WA 99352 USA

[2] Xiamen Univ, Dept Elect Sci, Xiamen, Peoples R China

关键词: Natural abundance O-17 NMR;    Chemical shift calculation;    Ethylene carbonate;    Propylene carbonate;    Ethyl methyl carbonate;    Solvation structure;   

DOI  :  10.1016/j.jpowsour.2015.03.091

来源: Elsevier

【 摘 要 】

Natural abundance O-17 NMR measurements were conducted on electrolyte solutions conisting of Li [CF3SO2NSO2CF3] (LiTFSI) dissolved in the solvents of ethylene carbonate (EC), propylene carbonate (PC), ethyl methyl carbonate (EMC), and their mixtures at various concentrations. It was observed that O-17 chemical shifts of solvent molecules change with the concentration of LiTFSI. The chemical shift displacements of carbonyl oxygen are evidently greater than those of ethereal oxygen, strongly indicating that Li+ ion is coordinated with carbonyl oxygen rather than ethereal oxygen. To understand the detailed molecular interaction, computational modeling of O-17 chemical shifts was carried out on proposed solvation structures. By comparing the predicted chemical shifts with the experimental values, it is found that a Li+ ion is coordinated with four double bond oxygen atoms from EC, PC, EMC and TFSI- anion. In the case of excessive amount of solvents of EC, PC and EMC the Li+ coordinated solvent molecules are undergoing quick exchange with bulk solvent molecules, resulting in average O-17 chemical shifts. Several kinds of solvation structures are identified, where the proportion of each structure in the liquid electrolytes investigated depends on the concentration of LiTFSI. (C) 2015 Elsevier B.V. All rights reserved.

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