材料科学
电解质
混溶性
化学工程
热重分析
热稳定性
聚合物
差示扫描量热法
膜
相位反转
离子电导率
锂离子电池
高分子化学
电极
复合材料
电池(电)
化学
工程类
物理
物理化学
功率(物理)
热力学
量子力学
生物化学
作者
Neethu T. M. Balakrishnan,Akhila Das,Jarin Joyner,M. J. Jabeen Fatima,Leya Rose Raphael,Abhilash Pullanchiyodan,Prasanth Raghavan
标识
DOI:10.1016/j.mtchem.2023.101407
摘要
A novel approach to enhance the miscibility of polyvinylidene difluoride (PVdF)/polymethyl methacrylate (PMMA) blend polymer electrolyte is introduced by in-situ polymerization of methyl methacrylate monomers in PVdF matrix. The phase inversion membrane of PVdF/PMMA blend exhibits uniform microporous structure with high porosity, better electrolyte uptake (413%), retention, and lower contact angle. The structural characterization of the membranes is analyzed with Fourier transform infrared spectroscopy. The thermal stability is examined by thermogravimetric analysis and differential scanning calorimetry. The miscibility of the blend is confirmed from examining the blend solution for 100 days. The optimized blend electrolyte system with 50 wt% of the PMMA (gel polymer electrolyte [GPE-50]) reveals better ionic conductivity of 5.2 mS/cm at room temperature. The GPE is capable to establish high anodic stability up to 4.8 V vs. Li/Li+ and a better electrode compatibility. The initial discharge capacity observed for the Li/LiFePO4 cell with GPE-50 is about 162 mAh/g at 0.1C at 25 °C with 95% of cathode utilization of the material. The device-level evaluation ensures that the GPE with good charge–discharge performance and stable cycling can be used for future lithium-ion batteries.
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