Abstract

This research aimed to synthesize non-uniform nanosheet-like tungstate oxide (WO3) using a simple hydrothermal process, which would result in an effective and environment-friendly material for use in supercapacitors (SCs). The resulting materials are thoroughly examined using physio-chemical techniques. The supercapacitive properties of the WO3–Ni-Foam (NF) were examined using 1 M KOH, NaOH, and LiOH electrolytes and further, the electrochemical performance of the WO3–NF electrode was assessed by changing the concentration of KOH electrolytes from 1 to 4 M respectively. The WO3–NF electrode demonstrated the highest specific capacity (Csp) of 70 mAh/g and capacitance (Cs) of 563 F/g with a high energy density of 16 Wh/kg, and power density of 281 W/kg in 2 M KOH electrolyte respectively. Additionally, the WO3–NF electrode showed excellent Columbic efficiency of 98% and long-term capacitive retention of 88% over 5000 cycles in 2 M KOH electrolyte. Additionally, the effect of redox additive (0.01 M of potassium ferrocyanide) improves the electrochemical performance of WO3–NF; the Csp and Cs values were 137 mAh/g, 618 F/g and 100 mAh/g, 800 F/g at 5 mV/s and 5 mA/cm2, respectively. Furthermore, the WO3–NF electrode exhibits good stability retention of 94% over the 2000 cycles. The electrochemical performance of WO3 nanosheets for energy storage applications was improved by this straightforward hydrothermal method and evaluating the effect of redox additive electrolyte.

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.