材料科学
电解质
化学工程
离子电导率
锂(药物)
过电位
热稳定性
多孔性
快离子导体
聚合物
环氧乙烷
复合材料
电化学
电极
化学
工程类
物理化学
内分泌学
医学
共聚物
作者
Dongmei Dai,Xinxin Zhou,Pengyao Yan,Zhuangzhuang Zhang,Liang Wang,Yaru Qiao,Canhui Wu,Haowen Li,Weitao Li,Mengmin Jia,Bao Li,Dai‐Huo Liu
标识
DOI:10.1021/acsami.3c17251
摘要
Lithium batteries have been widely used in our daily lives for their high energy density and long-term stability. However, their safety problems are of paramount concern for consumers, which restricts their scale applications. Gel polymer electrolytes (GPEs) compensate for the defects of liquid leakage and lower ionic conductivity of solid electrolytes, which have attracted a lot of attention. Herein, a 3D interconnected highly porous structural gel electrolyte was prepared with alginate dressing as a host material, poly(ethylene oxide) (PEO), and a commercial liquid electrolyte. With rich polar functional groups and (CH2-CH2-O) segments on the polymer matrix, the transportation of Li+ is faster and uniform; thus, the formations of lithium dendrite were significantly inhibited. The cycle stability of symmetrical Li||Li batteries with modified composite electrolytes (SAA) is greatly improved, and the overpotential remains stable after more than 1000 h. Meanwhile, under the same conditions, the cycle performance of batteries with unmodified electrolytes is inferior and overpotentials are nearly 1 V after 100 h. Additionally, the capacity retention of Li||LiFePO4 with SAA is more than 95% after 200 cycles, while those of the others declined sharply. The alginate dressing-based GPEs can greatly enhance the mechanical and thermal stability of PEO-based GPEs, which provides an environmentally friendly avenue for gel electrolytes' applications in lithium batteries.
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