Electrochemically Deposited Amorphous Cobalt–Nickel-Doped Copper Oxide as an Efficient Electrocatalyst toward Water Oxidation Reaction

Production of hydrogen through water splitting is one of the green and the most practical solutions to cope with the energy crisis and greenhouse effect. However, oxygen evolution reaction (OER) being a sluggish step, the use of precious metal-based catalysts is the main impediment toward the viabil...

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Published inACS omega Vol. 6; no. 30; pp. 19419 - 19426
Main Authors Asghar, Muhammad Adeel, Ali, Abid, Haider, Ali, Zaheer, Muhammad, Nisar, Talha, Wagner, Veit, Akhter, Zareen
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 03.08.2021
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Summary:Production of hydrogen through water splitting is one of the green and the most practical solutions to cope with the energy crisis and greenhouse effect. However, oxygen evolution reaction (OER) being a sluggish step, the use of precious metal-based catalysts is the main impediment toward the viability of water splitting. In this work, amorphous copper oxide and doped binary- and ternary-metal oxides (containing CoII, NiII, and CuII) have been prepared on the surface of fluorine-doped tin oxide by a facile electrodeposition route followed by thermal treatment. The fabricated electrodes have been employed as efficient binder-free OER electrocatalysts possessing a high electrochemical surface area due to their amorphous nature. The cobalt–nickel-doped copper oxide (ternary-metal oxide)-based electrode showed promising OER activity with a high current density of 100 mA cm–2 at 1.65 V versus RHE that escalates to 313 mA cm–2 at 1.76 V in alkaline media at pH 14. The high activity of the ternary-metal oxide-based electrode was further supported by a smaller semicircle in the Nyquist plot. Furthermore, all metal-oxide-based electrodes offered high stability when tested for continuous production of oxygen for 50 h. This work highlights the synthesis of efficient and cost-effective amorphous metal-based oxide catalysts to execute electrocatalytic OER employing an electrodeposition approach.
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ISSN:2470-1343
2470-1343
DOI:10.1021/acsomega.1c01251