Mg2+ conducting polymer gel electrolytes: physical and electrochemical investigations
Autor: | C. Maheshwaran, Kuldeep Mishra, Deepak Kumar, D. K. Kanchan |
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Rok vydání: | 2020 |
Předmět: |
Materials science
Magnesium General Chemical Engineering General Engineering General Physics and Astronomy chemistry.chemical_element 02 engineering and technology Electrolyte Dielectric 010402 general chemistry 021001 nanoscience & nanotechnology 01 natural sciences 0104 chemical sciences Differential scanning calorimetry Chemical engineering chemistry General Materials Science Fourier transform infrared spectroscopy 0210 nano-technology Ion transport number Trifluoromethanesulfonate Magnesium ion |
Zdroj: | Ionics. 26:2969-2980 |
ISSN: | 1862-0760 0947-7047 |
DOI: | 10.1007/s11581-020-03459-y |
Popis: | In this work, magnesium ion conducting polymer gel electrolytes based on PVdF-HFP and EC/DEC have been prepared using solution casting technique. Physical and electrochemical investigations have been carried out with a view to understand the effect of magnesium triflate salt concentration within the polymer gel electrolyte. The physical investigations include X-ray diffraction, scanning electron microscopy, differential scanning calorimetry, and Fourier transform infrared spectroscopy measurements to probe changes in structural/morphological, thermal, and spectroscopic properties. In order to investigate the dielectric behavior of the electrolyte system, real part of the permittivity and dielectric loss are discussed as a function of frequency, salt concentration, as well as temperature. The modulus behavior of the electrolyte system has been studied by plotting the real and imaginary part as a function of frequency and temperature. The reported Mg2+ ion conducting electrolyte offers predominant ionic character with total ion transport number close to unity. Perhaps these magnesium ion conducting polymer gel electrolytes are suitable for application in electrochemical device, especially in magnesium-based batteries. |
Databáze: | OpenAIRE |
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