电解质
聚合物电解质
电导率
材料科学
电介质
离子
聚合物
化学工程
离子电导率
复合材料
化学
有机化学
电极
物理化学
工程类
光电子学
作者
Zachary W. Brotherton,James T. Bamford,Benjamin J. Pedretti,Seamus D. Jones,Rachel A. Segalman,Nathaniel A. Lynd
标识
DOI:10.1021/acsapm.4c03379
摘要
The implementation of energy-dense lithium metal anodes in lithium batteries requires an electrolyte material that enables rapid and selective cation motion and low anion mobility. Although single-ion-conducting polymer electrolytes are selective, they typically exhibit conductivity values several orders of magnitude lower than liquid and neutral polymer electrolytes. In this report, we investigate the effects of blending single-ion-conducting polymer electrolytes (i.e., metal salts with a macromolecular polyfunctional anion) with neutral polymer hosts on the conductivity and ionic motion. With the goal of improving ionic conductivity without overly mobilizing anions, two comb-branched copolymers, with high and low ion-content poly[(lithium 3-[(trifluoromethane) sulfonamidosulfonyl]propyl methacrylate)- co -(poly(ethylene glycol methyl ether acrylate))], were blended with either poly[(ethylene oxide)- co -(allyl glycidyl ether)] or poly(cyanoethyl glycidyl ether) at various polyelectrolyte loadings. These blends are miscible over a wide range of compositions and increase the conductivity of the single-ion-conducting polyelectrolyte by up to 2 orders of magnitude. Neither the glass-transition temperature nor dielectric constant correlates strongly to conductivity in these systems. Instead, the overall Li:O ratio of the blend influences conductivity and exhibits an maximum at ca. 0.05. Finally, we investigated ion mobility through limiting current fraction of Li + ions and observed fractions up to 0.92 with ca. 0.75 for the most conductive blends.
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