Suppression of potasside reaction in localized high concentration electrolytes utilizing fluorine-substituted benzene as bifunctional additive for potassium-metal batteries

Abstract

Localized high-concentration electrolytes (LHCEs) have unique solvation structures that do not affect the original salt–solvent coordination from highly concentrated electrolytes. LHCEs enable a wide electrochemical voltage window and mitigate the extensive dendritic growth of metallic anodes. However, in K metal batteries, LHCE undergoes undesirable side reactions because of potasside (K−), triggering aggressive chemistry with a diluent, represented as hydrofluoroethers (HFEs), eventually resulting in poor cycle life. In this study, 1, 3, 5-trifluorobenzene (TFB) was introduced as a functional additive to prevent the parasitic K− reaction. The three symmetrically substituted fluorines prevented TFB from disrupting the as-formed solvation structure of LHCE located in the outer sphere. This characteristic increases the reaction energy barrier between K− and HFE, suppressing the deterioration of the metal anode by adding only 3 wt.% of TFB in LHCE. Moreover, TFB preferentially decomposes at each electrode because of its molecular energy level and increases the reversibility of the cell, reducing unnecessary consumption of electrolytes with a stable interface. This study discusses a novel method to prevent the K− reaction at the electrolyte level and the utilization of LHCE in K batteries to pursue higher energy densities, sustaining the advantage of using a metal anode.