电解质
化学
离子电导率
离子液体
化学工程
阳极
极限抗拉强度
离子强度
离子键合
聚合物
溶剂
韧性
涂层
超分子化学
电化学
超级电容器
高分子化学
过电位
无机化学
离子
化学键
作者
Zuyang Hu,Zixin Han,Haoxin Liu,Xiaolong Jiang,Kai Bai,Shengyang Huang,Zican Yang,Minghui Ye,Yongchao Tang,Yufei Zhang,Xiaoqing Liu,Zhipeng Wen,Ho Seok Park,Chengchao Li
摘要
Interfacial stress accumulation and dendrite penetration constitute the fundamental origins of cycle life degradation in solid-state zinc ion batteries, necessitating polymer electrolytes with both high mechanical strength and high toughness. Nevertheless, constructing double-high-polymer electrolytes through molecular design to enhance dynamic interface compliance remains a persistent challenge. In this study, to achieve long-term stabilized Zn chemistry, a supramolecular ionic liquid gel electrolyte was developed by a solvent exchange process through noncovalent interaction, which consists of PVA and ionic liquid (IL, Bmim[ZnBr3]/Bmim[ZnCl3]). The stable supramolecular effect (Br–H bond and H-bond) of IL endows the electrolyte with high strength (2.22 MPa tensile strength, more than 1200% deformation) and high toughness (1900.74 MJ/m3), and the long-term cycle life of the anode (over 2000 h) can be achieved through the unique stress dissipation mechanism. Besides, the polyanionic groups ([ZnBr3]−) of IL activate the −OH site activity of PVA by changing the distribution of electrons, which enhance binding of Zn2+ to the site, realizing a high Zn2+ transference number (0.61) and ionic conductivity (0.739 mS cm–1). In addition, the low water content and Br–-rich chemical environment contribute to the formation of [IBr2]− polyhalide via interhalogen nucleophilic interactions, stabilizing the realization of the iodine four-electron reaction (0.2 A g–1, 4000 cycles).
科研通智能强力驱动
Strongly Powered by AbleSci AI