4.8 Article

Effect of overcharge on Li(Ni0.5Mn0.3Co0.2)O2 cathodes: NMP-soluble binder. II - Chemical changes in the anode

Journal

JOURNAL OF POWER SOURCES
Volume 385, Issue -, Pages 156-164

Publisher

ELSEVIER
DOI: 10.1016/j.jpowsour.2017.12.015

Keywords

Lithium-ion battery; Overcharge; SEI layer

Funding

  1. U.S. Department of Energy, Office of Energy Efficiency and Renewable Energy, Vehicle Technologies Office
  2. DOE Office of Science by UChicago Argonne, LLC [DE-AC02-06CH11357]
  3. U.S. Department of Energy (DOE), Office of Energy Efficiency and Renewable Energy, Vehicle Technologies Office, Applied Battery Research
  4. U.S. Department of Energy [DE-AC05-00OR22725]
  5. U.S. Department of Energy's National Nuclear Security Administration (NNSA) [DE-NA0003525]

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Cells based on nickel manganese cobalt oxide (NMC)/graphite electrodes, which contained polyvinylidene difluoride (PVDF) binders in the electrodes, were systematically charged to 100, 120, 140, 160, 180, and 250% state of charge (SOC). Characterization of the anodes by inductively-coupled-plasma mass spectrometry (ICP-MS), X-ray photoelectron spectroscopy (XPS), and high-performance liquid chromatography coupled with electrospray ionization mass spectrometry (HPLC-ESI-MS) showed several extent-of-overcharge-dependent trends. The concentrations (by wt) of nickel, manganese, and cobalt in the negative electrode increased with SOC, but the metals remained in the same ratio as that of the positive. Electrolyte reaction products, such as LiF:LiPO3, increased with overcharge, as expected. Three organic products were found by HPLC-ESI-MS. From an analysis of the mass spectra, two of these compounds seem to be organophosphates, which were formed by the reaction of polymerized electrolyte decomposition products and PF3 or O = PF3. Their concentration tended to reach a constant ratio. The third was seen at 250% SOC only.

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