Binderless synthesis of nanoknotnet-like cobalt oxide for supercapacitor application

Transition metal oxides have promising candidates for supercapacitors application owing to its excellent theoretical capacitance, eco-friendly and good redox reaction feature. In this work, Nano-knotnet type cobalt oxide as an electrode material has been synthesized by a cost-effective and simple ch...

Full description

Saved in:
Bibliographic Details
Published inMaterials today : proceedings Vol. 43; pp. 2663 - 2667
Main Authors Gaikwad, Sanjay L., Angre, Ankita P., Naik, Vishal A., Pargaonkar, Jyotsna G., Patil, Priya A., Chandekar, Kamlesh V., Chavan, Archana U., Gaikar, Paresh S.
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.01.2021
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Transition metal oxides have promising candidates for supercapacitors application owing to its excellent theoretical capacitance, eco-friendly and good redox reaction feature. In this work, Nano-knotnet type cobalt oxide as an electrode material has been synthesized by a cost-effective and simple chemical bath deposition (CBD) method for supercapacitors application. The structural and morphological studies of these electrode materials were evaluated by using X-ray diffraction (XRD) and scanning electron microscopy (SEM) respectively. XRD studies showed that the cobalt oxide thin films were well-crystallized, pure, and face-centered cubic phases with average crystallite size 29.64 nm. The electrochemical behaviour of the cobalt oxide electrodes was characterized by using cyclic voltammetry (CV) and galvanostatic charge/discharge (GCD) in 1 M NaOH aqueous electrolyte. GCD exhibited the maximum specific capacitance 322 F g−1 at a current density of 1 mA cm−2 with 84.16% retention of the specific capacitance value after 10 mA cm−2 current density. The CV and GCD measurements demonstrated binderless cobalt oxide is a promising electrode for supercapacitors application.
ISSN:2214-7853
2214-7853
DOI:10.1016/j.matpr.2020.04.081