C. Revathy, V. R. Sunitha, Rex Joseph, S. Radhakrishnan
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引用次数: 0
Abstract
Mixed solid polymer electrolyte (MSPE) systems show interesting ion conduction behavior that can be exploited for practical charge storage device applications. This study focuses on the MSPE system containing Polyethylene Oxide (PEO1: Mw = 1 106 g/mol), (PEO2: Mw = 1 105 g/mol), Poly(methyl methacrylate) (PMMA: Mw = 1.5 104 g/mol) in various weight proportions with a constant concentration of the lithium perchlorate salt. The dependence of ionic conductivity on temperature follows the Arrhenius behavior. The complex dielectric permittivity and electric modulus results reveal the sensitivity of these parameters to film composition and structural changes. X-ray Diffraction (XRD), Differential Scanning Calorimetry (DSC) and Fourier Transform Infrared Spectroscopy (FTIR) studies confirm significant changes in the crystallinity of the MSPE system. Bandgap studies further confirm the structural disorder in MSPE films induced due to the blending of the polymers. Sample (S2) with composition 96 wt% PEO1–2 wt% PEO2–2 wt% PMMA at 303 K exhibited an optimum conductivity of 1.91 10−4 S/cm and achieved a low activation energy of 0.3 eV which is correlated to the other parameters studied.
混合固体聚合物电解质(MSPE)系统显示出有趣的离子传导行为,可以用于实际的电荷存储器件应用。本研究的重点是MSPE体系含有聚氧化物(PEO1: Mw = 1 × $$ \times $$ 106 g/mol), (PEO2: Mw = 1 × $$ \times $$ 105 g/mol),聚甲基丙烯酸甲酯(PMMA:Mw = 1.5 × $$ \times $$ 104 g/mol),以不同的重量比例与恒定浓度的高氯酸锂盐。离子电导率对温度的依赖遵循阿伦尼乌斯行为。复合介电常数和电模量的结果揭示了这些参数对薄膜组成和结构变化的敏感性。x射线衍射(XRD)、差示扫描量热法(DSC)和傅里叶变换红外光谱(FTIR)研究证实了MSPE体系结晶度的显著变化。带隙研究进一步证实了聚合物共混引起的MSPE薄膜结构紊乱。样品(S2),成分为96 wt% PEO1–2 wt% PEO2–2 wt% PMMA at 303 K exhibited an optimum conductivity of 1.91 × $$ \times $$ 10−4 S/cm and achieved a low activation energy of 0.3 eV which is correlated to the other parameters studied.
期刊介绍:
The Journal of Applied Polymer Science is the largest peer-reviewed publication in polymers, #3 by total citations, and features results with real-world impact on membranes, polysaccharides, and much more.