材料科学
电解质
化学工程
膜
甲基丙烯酸酯
离子电导率
高分子化学
锂(药物)
聚合物
热稳定性
复合数
电极
复合材料
聚合
化学
物理化学
生物化学
医学
工程类
内分泌学
作者
Huihui Gan,Shaoqiao Li,Yong Zhang,Li‐Ping Yu,Jirong Wang,Zhigang Xue
出处
期刊:Langmuir
[American Chemical Society]
日期:2021-07-02
卷期号:37 (27): 8270-8280
被引量:14
标识
DOI:10.1021/acs.langmuir.1c01035
摘要
Herein, composite membranes based on a single-ion conducting polymer electrolyte (SIPE) and poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) were prepared by an electrospinning technology. The SIPE with hydrogen bonding was obtained via reversible addition–fragmentation chain transfer (RAFT) copolymerization of 2-(3-(6-methyl-4-oxo-1,4-dihydropyrimidin-2-yl)ureido)ethyl methacrylate (UPyMA), poly(ethylene glycol) methyl ether methacrylate (PEGMA), and lithium 4-styrenesulfonyl (phenylsulfonyl) imide (SSPSILi). The obtained composite membrane exhibited a highly porous network structure, superior thermal stability (>300 °C), and high mechanical strength (17.3 MPa). The fabricated SIPE/PVDF-HFP composite membrane without lithium salts possessed a high ionic conductivity of 2.78 × 10–5 S cm–1 at 30 °C, excellent compatibility with the lithium metal electrode, and high lithium-ion transference number (0.89). The symmetric Li//Li cell exhibited a superior cycle performance without short circuit, indicating the generation of a stable interface between SIPE and the lithium metal electrode during the process of lithium plating/stripping, which could inhibit lithium dendrite growth in lithium metal batteries (LMBs). The Li//LiFePO4 cell also exhibited superior cycle life and excellent rate capability at 60 or 25 °C. In consequence, the composite membrane exhibits a considerable future prospect for advanced LMBs.
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