4.5 Article

Alkyl Substitution Effect on Oxidation Stability of Sulfone-Based Electrolytes

Journal

CHEMELECTROCHEM
Volume 3, Issue 5, Pages 790-797

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/celc.201500550

Keywords

alkyl substitution; high-voltage lithium-ion batteries; oxidation stability; quantum chemistry; sulfone-based electrolytes

Funding

  1. U.S. Department of Energy, Vehicle Technologies Office
  2. U.S. Department of Energy by UChicago Argonne, LLC [DE-AC02-06CH11357]

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Organic sulfone compounds have been widely used as high-voltage electrolytes for lithium-ion batteries for decades. However, owing to the complexity of the synthesis of new sulfones, only a few commercially available sulfones have been studied. In this paper, we report the synthesis of new sulfone compounds with various substituent groups and the impact of the substituent group on the oxidation stability of sulfones. Electrochemical floating tests using a 5 V LiNi0.5Mn1.5O4 spinel cathode and density functional theory calculations showed that the cyclopentyl-substituted sulfone McPS suffered from oxidation instability, starting from 4.9 V versus Li+/Li, as observed by the large leakage currents. On the other hand, the isopropyl-substituted sulfone MiPS and tetramethylene substituted sulfone TMS showed much improved oxidation stability under identical testing conditions. The substitution structure of the sulfone plays a significant role in the determination of its oxidative stability and should first be considered for the development of new sulfone-based electrolytes for high-voltage, high-energy lithium-ion batteries.

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