材料科学
电解质
法拉第效率
溶剂化
桥接(联网)
电化学
离子电导率
纳米技术
化学工程
储能
锂(药物)
电导率
聚氨酯
聚合物
复合材料
锂离子电池
离子键合
堆积
电池(电)
极化(电化学)
电化学电池
分子间力
多尺度建模
离子
纳米材料
超级电容器
自放电
电化学储能
工作(物理)
材料设计
金属锂
弹性模量
科技与社会
作者
S. W. Wang,Wenqing Sun,Bo Zhang,Jiazhu Guan,Tong Wu,Fangqi Zhan,Dalin Wang,Shoubin Zhou,Qi Wang,Zhong Jin,Wen‐Yong Lai
摘要
ABSTRACT The escalating demand for lithium‐based batteries has underscored the urgency to address safety and environmental risks associated with conventional electrolytes. To mitigate these challenges, we propose a fluorine‐free electrolyte architecture leveraging tailored solvent‐polymer elastic bridging. This design encapsulated LiBOB‐based F‐free localized high‐concentration electrolyte within an elaborately synthesized zwitterionic polyurethane combining rigid‐flexible molecular motifs. The chain‐solvent elastic bridging strategy reconstructs the solvation environment through selective Li + ‐solvent coordination, while modulates weak intermolecular interactions in the polymer backbone to guide ion transport and further improve mechanical properties. Thus, the resultant fluorine‐free electrolyte achieves an extremely high lithium‐ion transference number of 0.95, high room‐temperature ionic conductivity of 1.3 mS cm − 1 and high fracture strength of 1.1 MPa. These advancements synergize with the formation of an inorganic boride‐rich interfacial layer, enabling Li||Li symmetric cells to sustain plating/stripping of 1000 h. Moreover, solid‐state full cells achieve superior performance; for instance, the Li|| NCM622 (10 mg cm −2 ) cell exhibits an average capacity of 1.6 mAh cm − 2 (140 mAh g −1 ) and a coulombic efficiency of 99.4% over 200 cycles, and a pouch cell also achieves a capacity of 1600 mAh. This work pioneers electrolyte design innovation through molecular solvent‐polymer synergy and macroscopic electrochemical integration, enabling sustainable fluorine‐free energy storage commercialization.
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