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Synthesis of polyaniline nanomaterials for an effective supercapacitor applications

Melese Yalew Ayalew, Endrias Adane Bekele, Fekadu Melak, Lodrick Makokha Wangatia, Olu Emmanuel Femi, Tessera Alemneh Wubieneh, Addisu Alemayehu Assegie, Getinet Y. Ashebir, Delele Worku Ayele, Ababay Ketema Worku, Minbale Admas Teshager, Tadele Ageru Alemu, Solomon Demiss Negedu

2024Materials Research Express9 citationsDOIOpen Access PDF

Abstract

Abstract Polyaniline-based materials have been widely used for supercapacitors due to their outstanding properties, such as high specific capacitance, excellent electrochemical properties, and ease of synthesis methods; however, the short-cycle stability of PANI-based supercapacitors and swelling and shrinking of polymeric structures limit their commercialization. Herein, we synthesized polyaniline (PANI) nanomaterials, which meet high specific capacitance through the chemical oxidative polymerization of aniline with ammonium persulfate (APS) in aqueous salicylic acid. The electrode materials were characterized using UV–vis, TGA, SEM, XRD, BAS-50 W potentiostat, and FTIR instrumentations. The electrical conductivity of the prepared materials was analyzed and found to be relatively high. The electrochemical supercapacitance performance of PANI nanomaterials was characterized using cyclic voltammetry. The polyaniline nanomaterials with a [salicylic acid]/[aniline] molar ratio of 0.8 showed a maximum specific capacitance of 688.5 Fg-1 at a scan rate of 50 mV s −1 . Polyaniline nanomaterials were found to exhibit better specific capacitance when compared to bulk polyanilines. Thus, PANI nanomaterials have been found to be a promising alternative for supercapacitor applications.

Topics & Concepts

PolyanilineSupercapacitorNanomaterialsNanotechnologyMaterials sciencePolyaniline nanofibersChemistryElectrochemistryPolymerComposite materialElectrodePhysical chemistryPolymerizationConducting polymers and applicationsSupercapacitor Materials and FabricationElectrochemical sensors and biosensors
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