电解质
聚合
纳米纤维
材料科学
化学工程
复合数
离子电导率
聚合物
锂(药物)
电化学
单体
溶解
离子键合
高分子化学
化学
离子
纳米技术
复合材料
电极
有机化学
物理化学
工程类
医学
内分泌学
作者
Zhichuan Shen,Jiawei Zhong,Jiahong Chen,Wenhao Xie,Kun Yang,Yuhan Lin,Jinbiao Chen,Zhicong Shi
标识
DOI:10.1016/j.cclet.2022.03.093
摘要
Gel polymer electrolytes (GPEs) are promising alternatives to liquid electrolytes applied in high-energy-density batteries. Here superior SiO2 nanofiber composite gel polymer electrolytes (SNCGPEs) are developed via in-situ ionic ring-opening polymerization of 1,3-dioxolane (DOL) monomers in SiO2 nanofiber membrane (PDOL-SiO2) for lithium metal batteries. The oxygen atoms of PDOL together with Si-O of SiO2 construct a more efficient channel for Li+ migration. Consequently, the lithium ion transference number (tLi+) and ionic conductivity (σ) at 30 °C of PDOL-SiO2 are 0.80 and 1.68 × 10−4 S/cm separately. PDOL-SiO2 manifests the electrochemical decomposition potentials of 4.90 V. At 0.5 mA/cm2, Li|PDOL-SiO2|Li cell shows a steady cycling performance for nearly 1400 h. LFP|PDOL-SiO2|Li battery can steadily cycle at 0.5 C with a capacity retention rate of 89% after 200 cycles. While cycling at 2 C, the capacity retention rate can maintain at 78% after 300 cycles. This contribution provides a innovative strategy for accelerating Li+ transportation via designing PDOL molecular chains throughout the SiO2 nanofiber framework, which is crucial for high-energy-density LMBs.
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