Issue 45, 2024

Cobalt phosphate nanorod bundles for efficient supercapacitor and oxygen evolution reaction applications and their temperature dependence

Abstract

Developing highly stable, low-cost, and efficient electrode materials for supercapacitor and oxygen evolution reactions is a challenging issue in energy storage and generation technology to meet the demand for sustainable and clean energy. Herein, cobalt phosphates in comparison with cobalt oxides were synthesized using a successive ionic layer adsorption and reaction (SILAR) method on a nickel foam substrate with different crystallization temperatures, and their supercapacitor and oxygen evolution reaction performances were studied. The nanorod bundles of cobalt phosphate electrodes prepared at 150 °C delivered an excellent specific charge storage capacity of 1512 F g−1 (681 C g−1) at a current density of 5 mA cm−2, which is higher than that of cobalt oxide (1103.9 F g−1 (496 C g−1)). They are highly stable for more than 2000 charge–discharge cycles with a coulombic efficiency of 93%. Furthermore, the same electrodes exhibited enhanced electrocatalytic behaviour for the oxygen evolution reaction (OER) with an overpotential of 359 mV at a current density of 30 mA cm−2, lowest Tafel slope of 60 mV dec−1 and stability of 20 hours. Enhanced reaction kinetics are attributed to the high electrochemical surface area with a Cdl of 594 μF and improved electronic conductivity. The above results indicated that cobalt phosphate is one of the most efficient electrode materials for the OER and supercapacitors.

Graphical abstract: Cobalt phosphate nanorod bundles for efficient supercapacitor and oxygen evolution reaction applications and their temperature dependence

Supplementary files

Article information

Article type
Paper
Submitted
23 Aug 2024
Accepted
18 Oct 2024
First published
04 Nov 2024

New J. Chem., 2024,48, 19113-19124

Cobalt phosphate nanorod bundles for efficient supercapacitor and oxygen evolution reaction applications and their temperature dependence

S. M. Nikam, S. H. Sutar, S. D. Jituri, A. I. Inamdar and S. H. Mujawar, New J. Chem., 2024, 48, 19113 DOI: 10.1039/D4NJ03712J

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