1. Ionic liquid supported chitosan-g-SPA as a biopolymer-based single ion conducting solid polymer electrolyte for energy storage devices.
- Author
-
Tiwari R, Parwati K, Verma DK, Kumar D, Yadav S, Rai R, Kumar K, Adhikary P, and Krishnamoorthi S
- Subjects
- Electric Power Supplies, Acrylic Resins chemistry, Biopolymers chemistry, Temperature, Polymers chemistry, Ions chemistry, Electric Capacitance, Chitosan chemistry, Ionic Liquids chemistry, Electric Conductivity, Electrolytes chemistry
- Abstract
This article discusses the preparation of different grades of single-ion conducting quasi-solid polymer electrolytes (q-SPE) material (Chit-g-SPA-IL) based on biopolymer (chitosan), polyacrylic acid and DBU-acetate (DBUH
+ AcO- ) ionic liquid. Chit-SPA-60 %-IL exhibited the highest conductivity within the range of 10-4 S/cm. TGA analysis demonstrated the stability of electrolytes up to a temperature of 120 °C. SEM-EDS analysis unveiled the porous nature of the electrolyte and even distribution of ions throughout the matrix. It exhibited an electrochemical stability window (EWS) of 2.53 V with significant current density and an ionic transference number (ITN) of ~99.9 %. The temperature-dependent conductivity established an Arrhenius-type conduction mechanism with an activation energy of 0.149 eV for ion movement within the electrolyte matrix. The AC conductivity analysis emphasized the time-temperature independence of the ionic conduction mechanism. Dielectric analysis highlighted the capacitive nature of the electrolyte, underlining its substantial capacitance, while modulus studies indicated minimal influence from the electrode-electrolyte interface. Chit-SPA-60 %-IL at 30 °C included a self-diffusion coefficient of 4.57 × 10-5 m2 /s, ionic mobility of 1.75 × 10-3 m2 /Vs, and drift ionic velocity of 0.44 m/s. These findings makes SPE as a promising candidate for sodium-ion-based energy storage devices., Competing Interests: Declaration of competing interest The authors declare no conflicts of interest., (Copyright © 2024 Elsevier B.V. All rights reserved.)- Published
- 2024
- Full Text
- View/download PDF