材料科学
电解质
离子电导率
锂(药物)
化学工程
电导率
极限抗拉强度
溶剂
铸造
聚合
离子
同种类的
金属
电化学
表征(材料科学)
金属锂
离子键合
导电体
电阻率和电导率
电极
工作(物理)
离子强度
离子液体
无机化学
复合材料
自愈水凝胶
作者
Yinlin Luo,Huguo Zhou,Shuangshuang Han,Zhenzhen Zhao,欣然 葛,Danning Liu,Xinmiao Hu,Yu Wang,Benkai Liu,Hongfa Xiang,Weiwei Ping
摘要
ABSTRACT In situ polymerization electrolytes hold great promise for high‐energy‐density lithium‐metal batteries but often require additional separators due to their limited mechanical strength. Here, inspired by “glassy gels”, we developed a free‐standing glass gel electrolyte by introducing tributylmethylphosphonium dimethyl phosphate ([P 4441 ] [DMP]) into a poly(acrylic acid) (PAA) matrix. Strong non‐covalent interactions between [P 4441 ] [DMP] and PAA chains generate a tough and homogeneous network while enabling efficient ion transport. The resulting glass gel electrolyte exhibits an ionic conductivity of 2.2 mS cm −1 , a Li + transference number of 0.59, a tensile strength of 30 MPa, and an elongation of up to 700%. The solvent‐toughened scaffold effectively confines the liquid electrolyte and mitigates parasitic reactions with Li metal. Consequently, Li||Li symmetric cells achieve stable cycling for 1900 h at 3 mA cm −2 with an areal capacity of 3 mAh cm −2 . Li//NCM811 cells retain 90% of their capacity after 420 cycles, while Li//LiCoO 2 cells exhibit stable cycling for over 290 cycles at 1 C with a cutoff voltage of 4.6 V. This work provides a robust strategy for designing free‐standing electrolytes for high‐energy‐density lithium‐metal batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI