Issue 14, 2017

Synthesis and electrochemical evaluation of the PANI/δ-MnO2 electrode for high performing asymmetric supercapacitors

Abstract

A comprehensive analysis of the effect of in situ polymerization of polyaniline (PANI) on hydrothermally synthesized Birnessite-type MnO2 (δ-MnO2) flowers on the structural, surface, morphological, and electrochemical properties is presented in this article. The PANI–MnO2 electrodes showed ∼170% higher specific capacitance than pure MnO2; the factors contributing to this enhancement are systematically investigated and discussed. The PANI modification enabled the inactive surface of the MnO2 to be electrochemically active and reduced the characteristic resistances and charge relaxation time. Furthermore, the PANI modification improved the composite conductivity and resulted in (i) reduction of surface pseudocapacitance from 87% (MnO2) to 54% (PANI–MnO2) and (ii) improvement of active charge contribution from 42% (MnO2) to 46% (PANI–MnO2). The mechanism of these changes is discussed. Furthermore, asymmetric (PANI–MnO2//AC and PANI–MnO2//OMC) and symmetric (AC//AC and OMC//OMC) (where AC is activated carbon and OMC is mesoporous carbon) supercapacitors are fabricated in coin cell casing and their charge storage properties are evaluated. Impressive increase in energy storage is observed; however, their properties varied according to the porosity of the carbon electrode. Results from this study provide a better understanding of the charge storage behaviour of polymer coated metal oxide electrodes with a varied choice of carbons in asymmetric supercapacitors.

Graphical abstract: Synthesis and electrochemical evaluation of the PANI/δ-MnO2 electrode for high performing asymmetric supercapacitors

Supplementary files

Article information

Article type
Paper
Submitted
27 Feb 2017
Accepted
12 Jun 2017
First published
12 Jun 2017

New J. Chem., 2017,41, 6574-6584

Synthesis and electrochemical evaluation of the PANI/δ-MnO2 electrode for high performing asymmetric supercapacitors

I. I. Misnon and R. Jose, New J. Chem., 2017, 41, 6574 DOI: 10.1039/C7NJ00679A

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