posted on 2020-07-28, 22:14authored byNishani
Kanchana Jayakody, Carla C. Fraenza, Steven G. Greenbaum, David Ashby, Bruce S. Dunn
We
have investigated the charge transport dynamics of a novel solid-like
electrolyte material based on mixtures of the ionic liquid (IL) 1-butyl-3-methylimidazolium
bis(trifluoromethylsulfonyl)imide ([BMIM] TFSI) and various concentrations
of lithium salt bis(trifluoromethylsulfonyl)imide (LiTFSI) confined
within a SiO2 matrix, prepared via a sol–gel method.
The translational diffusion coefficients of BMIM+, TFSI–, and Li+ in ILs and confined ILs (ionogels,
IGs) with different concentrations of lithium salt have been measured
at variable temperatures, covering the 20–100 °C range,
using nuclear magnetic resonance (NMR) pulsed field gradient diffusion
spectroscopy. The mobility of BMIM+, TFSI–, and Li+ was found to increase with the [BMIM] TFSI/LiTFSI
ratio, exhibiting an almost liquid-like mobility in IGs. Additionally,
the effect of confinement on IL rotational dynamics has been analyzed
by measuring 1H, 19F, and 7Li spin–lattice
relaxation rate dispersions of IGs at different temperatures, using
fast field-cycling NMR relaxometry. The analysis of the experimental
data was performed assuming the existence of two fractions of the
liquid: a bulk fraction (at least several ionic radii from the silica
particles) and a surface fraction (close to the silica particles)
and using two different models based on translational and rotational
diffusion and reorientation mediated by translational displacements.
The existence and weighting of these two fractions of ions were obtained
from the direct diffusion measurements. The results show that the
ion dynamics slowed only modestly under confinement, which evidences
that IGs preserve IL transport properties, and this behavior is an
encouraging indication for using IGs as a solid electrolyte for Li+ batteries.