Enhanced Li+ migration in solid polymer electrolyte driven by anion-containing polymer-chains

Abstract

Li-ion batteries with solid polymer electrolytes (SPEs) are safer than conventional liquid electrolytes due to the absence of highly flammable liquid electrolytes. However, their performance is limited by the poor Li+ transport in SPEs at room temperature. Anion-containing polymer-chains incorporated SPEs (ASPEs) are therefore developed to enhance Li+ diffusion kinetics. Herein, we propose a novel and feasible strategy to incorporate the anion-containing polymer-chains, such as lithiated perfluorinated sulfonic acid (PFSA), into polyvinylidene fluoride (PVDF) polymer-based SPEs. The immobile anion groups from the PFSA-chains impede the migration of mobile anion groups dissociated from the Li salt. The transference number is thus raised from ∼0.3 to 0.52 with the introduction of anion-containing polymer-chains into SPEs. The electrostatic repulsion among anion-containing chains also reduces the close chain stacking and brings 159% increase in the ionic conductivity to 0.83 × 10−3 S/cm at 30 °C in contrast with the pure PVDF-based SPE. In addition, LiFeO4/Li batteries with ASPEs exhibit 55% capacity boost at 0.5 C in contrast to the capacity of batteries with pure-PVDF SPEs, and also offer more than 1000 charge/discharge cycles. Our research findings potentially offer a facile strategy to design thermal stable SPEs with superior Li+ transport behaviors towards developing high-performance SPEs-based batteries.