Skip to main content
Open Access Publications from the University of California

UC Berkeley

UC Berkeley Previously Published Works bannerUC Berkeley

Effect of monomer structure on ionic conductivity in a systematic set of polyester electrolytes


Polymer electrolytes may enable the next generation of lithium ion batteries with improved energy density and safety. Predicting the performance of new ion-conducting polymers is difficult because ion transport depends on a variety of interconnected factors which are affected by monomer structure: Interactions between the polymer chains and the salt, extent of dissociation of the salt, and dynamics in the vicinity of ions. In an attempt to unravel these factors, we have conducted a systematic study of the dependence of monomer structure on ionic conductivity, σ, and glass transition temperature, Tg, using electrolytes composed of aliphatic polyesters and lithium bis(trifluoromethanesulfonyl) imide (LiTFSI) salt. The properties of these electrolytes were compared to those of poly(ethylene oxide) (PEO), a standard polymer electrolyte for lithium batteries. We define a new measure of salt concentration, ρ, the number of lithium ions per unit length of the monomer backbone. This measure enables collapse of the dependence of both the σ and Tg on salt concentration for all polymers (polyesters and PEO). Analysis based on the Vogel-Tammann-Fulcher (VTF) equation reveals the effect of different oxygen atoms on ion transport. The VTF fits were used to factor out the effect of segmental motion in order to clarify the relationship between molecular structure and ionic conductivity. While the conductivity of the newly-developed polyesters was lower than that of PEO, our study provides new insight into the relationship between ion transport and monomer structure in polymer electrolytes.

Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.

Main Content
For improved accessibility of PDF content, download the file to your device.
Current View