金属锂
聚合物电解质
电池(电)
纳米技术
锂(药物)
材料科学
电解质
能量密度
稀缺
储能
导电聚合物
快离子导体
高能
锂电池
聚合物
计算机科学
电化学储能
作者
Xiong Shui,Xiangchun Zhuang,Q Chen,Peihao Yan,Lixin Qiao,Yu Ma,Jianbing Shen,Xiaohe Jiang,Shitao Wang,Kai Chen,Jun Ma,Shanmu Dong,G Xu,Zili Cui,Ling Wang,Xinhong Zhou,Guanglei Cui
摘要
Lithium metal batteries (LMBs) have been extensively studied due to their high energy density; however, their practical application is limited by the scarcity of lithium resources. Emerging mono- and multivalent cation-based metal batteries offer promising alternatives that may overcome this limitation owing to their high abundance. Nevertheless, the development of these batteries using conventional liquid electrolytes (LEs) faces challenges such as safety concerns, parasitic reactions and dendrite formation. Replacing LEs with polymer electrolytes (PEs) can significantly improve battery safety and interfacial compatibility. Among various PEs, single-ion conducting polymer electrolytes (SICPEs) are particularly attractive due to their high cation transference numbers, flexibility, and easy processability. Despite this, systematic strategies for immobilizing anions across different battery systems remain insufficiently discussed and summarized. In addition, the design of SICPEs often depends on experimental trial and error, and the prevalent use of fluorine-containing components in their molecular structures raises significant environmental concerns. This review provides a comprehensive summary of strategies for developing anion-immobilizing SICPEs, highlighting the similarities and differences of different SICPEs for lithium and other emerging battery systems. Finally, we outline existing challenges and future research directions to inspire innovative solutions for tailoring SICPE properties and advancing their practical applications.
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