电解质
固化(化学)
聚合物
阴极
氧气
锂(药物)
材料科学
化学工程
无机化学
化学
高分子化学
电极
有机化学
复合材料
医学
物理化学
工程类
内分泌学
作者
Mingming Cui,Hong Sun,Zhichao Xue,Qiang Li,Tianyu Zhang,Qunying Kang
标识
DOI:10.1021/acsaem.4c02643
摘要
Using gel polymer electrolytes (GPEs) instead of liquid electrolytes is a sensible and effective strategy for safety reasons. A GPE membrane was prepared by UV-curing using poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) as the polymer substrate material and an optimized ratio. The GPE membrane exhibited good flexibility and a higher ionic conductivity (σ = 0.63 mS cm–1). The RuO2@C/GPE/Li (abbreviated as S-GPE) battery is employed to demonstrate the electrochemical performance of GPE. The battery exhibits an Rct of 255.9 Ω, accompanied by a lack of cycle stability, with a cycle life of only 110 h. The results indicate that it is challenging to enhance the battery’s overall performance by solely improving the internal transfer performance of the electrolyte and ignoring the high interface impedance caused by the “solid–solid” contact at the electrolyte–electrode interface. Based on these findings, a straightforward one-step method is adopted to combine GPE with the air cathode by in situ photopolymerization and assemble it into RuO2@C-GPE/Li (abbreviated as I-GPE) battery used to demonstrate the electrochemical performance of the integrated GPE. The Rct value of the battery is 89.66 Ω, with a notable improvement in cycle stability. The battery’s cycle life is 940 h, which is 8.5 times that of the sandwich structure lithium–oxygen battery. The results indicate that preparing an integrated GPE by in situ photopolymerization of the electrolyte electrode is a straightforward and effective method to improve poor interfacial compatibility and can provide a theoretical basis for subsequent in-depth research.
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