TY - JOUR
T1 - Transport properties of electrolyte solution comprising LiPF6, ethylene carbonate, and propylene carbonate
AU - Uchida, Satoshi
AU - Sakaebe, Hikari
AU - Takeichi, Nobuhiko
N1 - Funding Information:
A part of the present study was financially supported by the New Energy and Industrial Technology Development Organization (NEDO) under RISING2 project (JPNP16001), Japan. We thank professor M. Kunimoto of WASEDA University for his kind advice in interpretation of the Raman spectra.
Publisher Copyright:
© The Author(s) 2021.
PY - 2021
Y1 - 2021
N2 - In this study, we experimentally measure the viscosity, η, and ionic conductivity, σ, of 1 mol kg-1 LiPF6 dissolved in a binary solvent of ethylene carbonate (EC) and propylene carbonate (PC) by varying the EC content from 0 to 60 vol%. Replacing EC with PC does not significantly influence on the mechanism of flow and ionic conduction. The state of solvent solvating to Li+ is analyzed using Raman spectra and 13C-NMR; the quantitative analysis suggests that the preference of EC in the Li+ solvation shell is almost similar to that of PC. The diffusion coefficient, D, of each species, Li+, PF6-, EC, and PC, is determined by pulse-gradient spin-echo NMR. In the electrolyte system dealt in this study, the molar conductivity is dominated by only the D of the charge carriers. The hydrodynamic Stokes radius of all constituent species is expressed in terms of D and η using the Stokes–Einstein relation.
AB - In this study, we experimentally measure the viscosity, η, and ionic conductivity, σ, of 1 mol kg-1 LiPF6 dissolved in a binary solvent of ethylene carbonate (EC) and propylene carbonate (PC) by varying the EC content from 0 to 60 vol%. Replacing EC with PC does not significantly influence on the mechanism of flow and ionic conduction. The state of solvent solvating to Li+ is analyzed using Raman spectra and 13C-NMR; the quantitative analysis suggests that the preference of EC in the Li+ solvation shell is almost similar to that of PC. The diffusion coefficient, D, of each species, Li+, PF6-, EC, and PC, is determined by pulse-gradient spin-echo NMR. In the electrolyte system dealt in this study, the molar conductivity is dominated by only the D of the charge carriers. The hydrodynamic Stokes radius of all constituent species is expressed in terms of D and η using the Stokes–Einstein relation.
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U2 - 10.5796/electrochemistry.21-00069
DO - 10.5796/electrochemistry.21-00069
M3 - Article
AN - SCOPUS:85114137714
VL - 89
SP - 439
EP - 446
JO - Electrochemistry
JF - Electrochemistry
SN - 1344-3542
IS - 5
ER -