Electrochemical characterization of poly(vinylidenefluoride)-zinc triflate gel polymer electrolyte and its application in solid-state zinc batteries

Kumar, G. Girish ; Sampath, S. (2003) Electrochemical characterization of poly(vinylidenefluoride)-zinc triflate gel polymer electrolyte and its application in solid-state zinc batteries Solid State Ionics, 160 (3-4). pp. 289-300. ISSN 0167-2738

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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S01672...

Related URL: http://dx.doi.org/10.1016/S0167-2738(03)00209-1

Abstract

Gel polymer electrolyte (GPE) films comprising of poly(vinylidenefluoride), propylene carbonate, ethylene carbonate and zinc trifluoromethane sulfonate are prepared and characterized. The composition of GPE is optimized to contain minimum liquid components with a maximum specific conductivity of 3.94×10-3 S cm-1 at (25±1) °C. A detailed investigation on the properties such as ionic conductivity, transport number, electrochemical stability window, reversibility of Zn/Zn2+ couple and Zn/gel electrolyte interfacial stability have been carried out. The ionic conductivity follows a VTF behaviour with an activation energy of about 0.0014 eV. Cationic transport number varies from 0.51 at 25°C to 0.18 at 70°C. Several cells have been assembled with GPE as the electrolyte, zinc as the anode, γ-MnO2 as the cathode and their charge-discharge behaviour followed. Capacity values of 105, 82, 64 and 37 mAh/g of MnO2 have been achieved at 10, 50, 100 and 200 µA/cm2 discharge current densities, respectively. The discharge capacity values are almost constant for about 55 cycles for all values of current densities. Cyclic voltammetric study of MnO2 electrode in Zn/GPE/MnO2 cell clearly shows intercalation/deintercalation of Zn2+.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Gel Polymer Electrolyte; Poly(vinylidenefluoride); Zinc Triflate; γ-MnO2; Rechargeable Battery; AC Impedance; Zn/GPE Interface
ID Code:57337
Deposited On:26 Aug 2011 08:00
Last Modified:26 Aug 2011 08:00

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