4.7 Article

Enhanced electrochemical activity of Co3O4/Co9S8 heterostructure catalyst for water splitting

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 47, Issue 72, Pages 30970-30980

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2021.11.124

Keywords

Cobalt sulfide; Cobalt oxide; Heterostructures; Water oxidation; Oxygen evolution reaction

Funding

  1. King Khalid University, Abha, Saudi Arabia [RGP.2/179/42]

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This study synthesized Co3O4, Co9S8, and their heterostructure Co3O4/Co9S8 as water oxidation catalysts, and found that the Co3O4/Co9S8 heterostructure showed excellent electrocatalytic activity at low onset potential, along with good long-term stability and a low Tafel slope.
The dearth of efficient, robust, and economical electrocatalysts for water oxidation is dubiously the key obstacle for renewable energy devices, so synthesis of efficient, and cost-effective metal-based water oxidation catalysts is vital. Herein, Co3O4, Co9S8 catalysts and their heterostructure Co3O4/Co9S8 were synthesized and evaluated as water oxidation electrocatalysts. The characterization of Co3O4, Co9S8, and Co3O4/Co9S8 electrocatalysts was performed using Fourier transform infrared spectroscopy, scanning electron micro-scopy and X-ray diffraction techniques. The heterostructure Co3O4/Co9S8 (1.46 V) exhibited water oxidation electrocatalysis at extremely low onset potential compared to Co3O4 (1.58 V), and Co9S8 (1.48 V) catalysts. A 281 mV overpotential required to attain a current density of 50 mA cm(-2) in alkaline solution (1 M KOH), outperforming most of Co-based benchmark electrocatalysts. Further, the Co3O4/Co9S8 heterojunction demonstrated catalytic activity with small Tafel slope of 37 mV dec(-1). The finding of electrochemical studies involving controlled potential electrolysis and long-term stability are projected to steer the future advancement in constructing efficient, economical, stable, and earth-abundant metal-based water oxidation catalysts. (c) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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