Issue 8, 2018

Synthesis of Au-V2O5 composite nanowires through the shape transformation of a vanadium(iii) metal complex for high-performance solid-state supercapacitors

Abstract

A simple redox transformation between a vanadium(III) metal complex and gold(III) chloride aided by a cost-effective modified hydrothermal procedure has been adopted for the synthesis of Au-V2O5 composite nanowires. The stability of pseudocapacitive electrode materials in acidic electrolytes is a major challenge. However, the synthesized Au-V2O5 composite nanowires are stable in acidic electrolyte when compared to the precursor component, V2O5. Electrochemical measurement shows a specific capacitance of 419 F g−1 at 1 A g−1 current density in 0.5 M H2SO4 solution for the synthesized composite nanowires. However, the precursor component V2O5 shows a lower specific capacitance under identical conditions. The synthesized composite nanowires, as a pseudocapacitive electrode material, respond to a wide range of working potential windows (+1.6 V), resulting in maximum energy and power densities of 53.33 W h kg−1 and 3.85 kW kg−1 respectively. Moreover, the Au-V2O5 nanowires show high cyclic stability (89% specific capacitance retention) for up to 5000 consecutive charge–discharge (CD) cycles at 10 A g−1 constant current density, due to the composite formation by redox transformation, which reflects the stability of the composite in acidic electrolyte.

Graphical abstract: Synthesis of Au-V2O5 composite nanowires through the shape transformation of a vanadium(iii) metal complex for high-performance solid-state supercapacitors

Supplementary files

Article information

Article type
Research Article
Submitted
09 Apr 2018
Accepted
24 May 2018
First published
24 May 2018

Inorg. Chem. Front., 2018,5, 1836-1843

Synthesis of Au-V2O5 composite nanowires through the shape transformation of a vanadium(III) metal complex for high-performance solid-state supercapacitors

S. Rudra, A. K. Nayak, R. Chakraborty, P. K. Maji and M. Pradhan, Inorg. Chem. Front., 2018, 5, 1836 DOI: 10.1039/C8QI00325D

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