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Nambu, N., Ohtsuki, K., Mutsuga, H., Suzuki, Y., Takehara, M., Ue, M. and Sasaki, Y. (2012) Use of Monofluorinated Ethyl Propionates as Solvents for Lithium Secondary Batteries. Electrochemistry, 80, 746-748.
http://dx.doi.org/10.5796/electrochemistry.80.746

has been cited by the following article:

• TITLE: Physical and Electrolytic Properties of Monofluorinated Ethyl Acetates and Their Application to Lithium Secondary Batteries

  AUTHORS: Noritoshi Nambu, Yukio Sasaki

  KEYWORDS: Monofluorinated Organic Solvent, Carboxylate, Position Isomerism, Electrolytic Properties, Discharge Capacity, Lithium Secondary Battery

  JOURNAL NAME: Open Journal of Metal, Vol.5 No.1, April 30, 2015

  ABSTRACT: Ethyl acetate (EA) shows low viscosity for its relative permittivity. Monofluorinated organic solvents exert the polar effect on the various properties. We have investigated the effect of position isomerism on the physical and electrochemical properties of two monofluorinated carboxylates: 2-fluoroethyl acetate (2FEA) and ethyl fluoroacetate (EFA). Relative permittivity of 2FEA was lower than that of EFA, whereas viscosity of 2FEA was higher. Electrolytic conductivity of a LiPF6 solution in 2FEA was lower than that in EFA, but higher than that in EA at high temperatures. The use of 2FEA as a co-solvent improved cycling efficiency and suppressed fading of discharge capacity of a Li|LiCoO2 coin cell at high cycle numbers.