Lithium batteries
rely crucially on fast charge and mass
transport
of Li+ in the electrolyte. For liquid and polymer electrolytes
with added lithium salts, Li+ couples to the counter-anion
to form ionic clusters that produce inefficient Li+ transport
and lead to Li dendrite formation. Quantification of Li+ transport in glycerol–salt electrolytes via NMR experiments
and MD simulations reveals a surprising Li+-hopping mechanism.
The Li+ transference number, measured by ion-specific electrophoretic
NMR, can reach 0.7, and Li+ diffusion does not correlate
with nearby ion motions, even at high salt concentration. Glycerol’s
high density of hydroxyl groups increases ion dissociation and slows
anion diffusion, while the close proximity of hydroxyls and anions
lowers local energy barriers, facilitating Li+ hopping.
This system represents a bridge between liquid and inorganic solid
electrolytes, thus motivating new molecular designs for liquid and
polymer electrolytes to enable the uncorrelated Li+-hopping
transport needed for fast-charging and all-solid-state batteries.