材料科学
电解质
超分子聚合物
超分子化学
锂(药物)
离子电导率
化学工程
聚合物
离子
电导率
离子键合
聚合物电解质
超分子组装
金属
纳米技术
对偶(语法数字)
金属锂
氢
无机化学
路易斯酸
氢键
硼酸
离子液体
离子运输机
组合化学
设计要素和原则
快离子导体
水溶液中的金属离子
双重角色
作者
Xue Wang,Yaohan Chen,Nannan Zhang,Xinrui Chai,Zhen Yu,Xiaofeng Li,Shenghai Li
标识
DOI:10.1021/acsami.5c13909
摘要
Poly(ethylene oxide) (PEO)-based polymer electrolytes exhibit great potential for application in all-solid-state batteries. However, the insufficient Li + transport efficiency has hindered the large-scale development of PEO. To address these challenges, we introduced a dual supramolecular interaction strategy for the preparation of PEO-based electrolytes, where tetrafluoroterephthalonitrile (TFTPN) complexes with Li + and phenylenediboronic acid (PBA) as anion capturer were engaged. Through the synergistic effects of Lewis acid–base interactions between TFTPN and Li +, and hydrogen bonding-derived anchoring for bis(trifluoromethylsulfonyl)imide (TFSI – ) anion by boronic acid moieties in PBA, the Li + transport efficiency was significantly enhanced with ionic conductivity of 6.14 × 10 –4 S cm –1 and Li + transference number of 0.6 at 50 °C (1.01 × 10 –4 S cm –1 at 25 °C). PEO-TFTPN-PBA-based cell enabled a maximum discharge specific capacity of 130.7 mAh g –1 at 2 C, and a high retention rate of 81.7% after 200 cycles. This study will provide an effective approach and a synergistic material design strategy for leveraging dynamic supramolecular interactions within PEO-based solid polymer electrolytes.
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