Published 2023 | Version v1
Journal article

Efficient electrochemical performance of the RGO/SrO nanorods prepared by the hydrothermal method

  • 1. Department of Materials Science and Nanotechnology, Yogi Vemana University, 516005, YSR Kadapa, Andhra Pradesh (India)

Description

The reduced graphene oxide-strontium oxide nanorods (RGO/SrO NRs) were prepared by using simple, eco-friendly hydrothermal synthesis methods. The synthesized composite powder of RGO/SrO NRs was characterized and confirmed by using different X-ray powder diffraction (XRD), Elemental mapping, and transmission electron microscopy (TEM) characterization techniques. From TEM analysis, strontium oxide morphologies in nanorod type structure were uniformly decorated on a graphene sheet. The electrochemical performance of confirmed individual SrO NRs and RGO/SrO NRs is a potential candidate for an electrode material in supercapacitors. They were studied in three different molar concentrations of KOH electrolyte solution and tested in different techniques such as cyclic voltammetry (CV), charge-discharge (GCD), electrochemical impedance spectroscopy (EIS), and cycling stability in the aqueous three electrolyte method. It was observed that the better electrochemical performance of individual SrO NRs and novel binary nanocomposite RGO/SrO NRs could be affected 6 M KOH electrolyte solution than the 1 and 3 M KOH electrolyte solution. The RGO/SrO NRs show higher specific capacitance (Csp) of about 271 Fg1 at 0.5 Ag1 current density and exhibits lower solution resistance (Rs) value of about 1.12 Ω in the 6 M KOH electrolyte solution. The capacitance retention of the RGO/SrO NRs in 6 M KOH is about 89.14% for continuous 1000 cycles than in 1 and 3 M KOH electrolyte solution.

Availability note (English)

Available from: http://dx.doi.org/10.1007/s00339-023-06610-4

Additional details

Identifiers

Publishing Information

Journal Title
Applied Physics. A, Materials Science and Processing (Print)
Journal Volume
129
Journal Issue
4
Journal Page Range
vp.
ISSN
0947-8396
CODEN
APAMFC

Optional Information

Notes
AID: 303