Abstract

This study demonstrates successful synthesis of nanoflower-like birnessite δ-MnO2 materials through a simple and effective hydrothermal technique. Characterization of the flower-like materials grown at various dwell times were carried out by employing scanning electron microscopy (SEM), X-ray diffractometry (XRD), Brunauer-Emmett-Teller (BET) and Barrett–Joyner–Halenda (BJH) models, and electrochemical analysis to understand the effect of different growth time on their morphological, structural, surface area along with pore size distribution and electrochemical characteristics as electrodes for electrochemical capacitors. Attention is mainly based on electrochemical assessment of the as-synthesized materials with an insight into some neutral aqueous electrolytes, mainly lithium sulphate (1 M Li2SO4) and sodium sulphate (1 M Na2SO4) solutions as potential medium owing to their non-corrosive nature, cost-effectiveness, electrochemical stability and environmentally friendliness. Significant charge propagation, with a high specific capacitance of 387.1 F g-1 was achieved for the half-cell electrode in 1 M Li2SO4 alongside excellent cycling stability for up to 5 000 cycles performed at 3 A g-1 specific current. A comprehensive electrochemical assessment is performed to understanding the relationship between solvated and diffused ions of the neutral electrolytes that could result in fast charge storage kinetics as well as high specific capacitance.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.