Determining the Composition of Carbonate Solvent Systems Used in Lithium-Ion Batteries without Salt Removal

In this work, two methods were investigated for determining the composition of carbonate solvent systems used in lithium-ion (Li-ion) battery electrolytes. One method was based on comprehensive two-dimensional gas chromatography with electron ionization time-of-flight mass spectrometry (GC×GC/EI TOF...

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Bibliographic Details
Main Authors: Mohammad Parhizi, Louis Edwards Caceres-Martinez, Brent A. Modereger, Hilkka I. Kenttämaa, Gozdem Kilaz, Jason K. Ostanek
Format: Article
Language:English
Published: MDPI AG 2022-04-01
Series:Energies
Subjects:
Online Access:https://www.mdpi.com/1996-1073/15/8/2805
Description
Summary:In this work, two methods were investigated for determining the composition of carbonate solvent systems used in lithium-ion (Li-ion) battery electrolytes. One method was based on comprehensive two-dimensional gas chromatography with electron ionization time-of-flight mass spectrometry (GC×GC/EI TOF MS), which often enables unknown compound identification by their electron ionization (EI) mass spectra. The other method was based on comprehensive two-dimensional gas chromatography with flame ionization detection (GC×GC/FID). Both methods were used to determine the concentrations of six different commonly used carbonates in Li-ion battery electrolytes (i.e., ethylene carbonate (EC), propylene carbonate (PC), dimethyl carbonate (DMC), diethyl carbonate (DEC), ethyl methyl carbonate (EMC), and vinylene carbonate (VC) in model compound mixtures (MCMs), single-blind samples (SBS), and a commercially obtained electrolyte solution (COES). Both methods were found to be precise (uncertainty < 5%), accurate (error < 5%), and sensitive (limit of detection <0.12 ppm for FID and <2.7 ppm for MS). Furthermore, unlike the previously reported methods, these methods do not require removing lithium hexafluorophosphate salt (LiPF<sub>6</sub>) from the sample prior to analysis. Removal of the lithium salt was avoided by diluting the electrolyte solutions prior to analysis (1000-fold dilution) and using minimal sample volumes (0.1 µL) for analysis.
ISSN:1996-1073