Issue 72, 2017, Issue in Progress

Bifunctional electro-catalytic performances of CoWO4 nanocubes for water redox reactions (OER/ORR)

Abstract

In this paper, we report the synthesis of cube shaped nanoparticles of CoWO4 (∼30 nm) by molten salts and their bifunctional electro-catalytic activities in water redox reactions for oxygen evolution and oxygen reduction reactions (OER and ORR). Bifunctional performances of CoWO4 nano-cubes are explored for water electrolysis in an alkaline medium (1.0 M KOH) vs. reversible hydrogen electrode (RHE) under various atmospheres (N2, air and O2). Low overpotential (η10 = 0.45 V) of CoWO4 nano-cubes is accomplished at the current density of 10 mA cm−2. Tafel polarization curves (potential vs. log current density) reveal relatively lower slope values for OER (∼82 mV dec−1) and ORR (∼68 mV dec−1) compared to previous reports. Stability test of electrode materials has been performed using chrono-amperometry (CA) at fixed potential for 500 seconds. Kinetics and mobility of electrons have also been studied during the water redox reactions. Stable nature and enhanced bifunctional electro-catalytic performances of earth abundant CoWO4 electrodes could be used as the replacement of expensive electroactive noble electrode materials (Pt, Ir, Ru etc.) for water electrolysis (OER and ORR) in near future.

Graphical abstract: Bifunctional electro-catalytic performances of CoWO4 nanocubes for water redox reactions (OER/ORR)

Article information

Article type
Paper
Submitted
30 Jun 2017
Accepted
18 Sep 2017
First published
25 Sep 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 45615-45623

Bifunctional electro-catalytic performances of CoWO4 nanocubes for water redox reactions (OER/ORR)

Saad M. AlShehri, J. Ahmed, T. Ahamad, P. Arunachalam, T. Ahmad and A. Khan, RSC Adv., 2017, 7, 45615 DOI: 10.1039/C7RA07256B

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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