电解质
俘获
聚合物
聚合物电解质
导电体
快离子导体
材料科学
无机化学
高分子化学
化学
物理化学
有机化学
电极
离子电导率
复合材料
生物
生态学
作者
Yichen Xue,Haitao Zhao,Xiaoyu Zhou,Huandi Zhang,Zehua Zhao,Xiaowei Shi,Junpeng Liu,Jiamei Liu,Lei Li
标识
DOI:10.1021/acsaem.5c00106
摘要
Solid polymer electrolytes (SPEs) confront the major challenge of low ionic conductivity. The Li+ local coordination environment in SPEs affects the ionic conductivity. Herein, a highly ionic conductive SPE is designed and experimentally realized via governing the Li+ local coordination environment through 4-acetylphenylboronic acid (APBA). The –OH functional groups in APBA react with F atoms in the PVDF-HFP polymer chain segment and O atoms in TFSI– to form the OH···F hydrogen bond and the OH···O hydrogen bond. This weakens the Li+ local coordination with PVDF-HFP and TFSI–, facilitating more free-Li+ release and strengthening the molecular dynamics of Li+. This variation results in the greatly increased Li+ ionic conductivity from 0.63 × 10–4 to 2.39 × 10–4 S/cm of SPE with APBA at 25 °C. This electrolyte makes the symmetric cells full cells with promising electrochemical performance. The strategy provided here is helpful for the development of highly ionic conductive SPEs.
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