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A Low Charge Transfer Resistance CuO Composite for Efficient Oxygen Evolution Reaction in Alkaline Media
Univ Sindh Jamshoro, Pakistan.
Linköping University, Department of Science and Technology, Physics, Electronics and Mathematics. Linköping University, Faculty of Science & Engineering.
Mehran Univ Engn & Technol, Pakistan.
Mehran Univ Engn & Technol, Pakistan.
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2021 (English)In: Journal of Nanoscience and Nanotechnology, ISSN 1533-4880, E-ISSN 1533-4899, Vol. 21, no 4, p. 2613-2620Article in journal (Refereed) Published
Abstract [en]

An efficient, simple, environment-friendly and inexpensive cupric oxide (CuO) electrocatalyst for oxygen evolution reaction (OER) is demonstrated. CuO is chemically deposited on the porous carbon material obtained from the dehydration of common sugar. The morphology of CuO on the porous carbon material is plate-like and monoclinic crystalline phase is confirmed by powder X-ray diffraction. The OER activity of CuO nanostructures is investigated in 1 M KOH aqueous solution. To date, the proposed electrocatalyst has the lowest possible potential of 1.49 V versus RHE (reversible hydrogen electrode) to achieve a current density of 20 mA/cm(2) among the. CuO based electrocatalysts and has Tafel slope of 115 mV dec(-1). The electrocatalyst exhibits an excellent long-term stability for 6 hours along with significant durability. The enhanced catalytic active centers of CuO on the carbon material are due to the porous structure of carbon as well as strong coupling between CuO-C. The functionalization of metal oxides or other related nanostructured materials on porous carbon obtained from common sugar provides an opportunity for the development of efficient energy conversion and energy storage systems.

Place, publisher, year, edition, pages
AMER SCIENTIFIC PUBLISHERS , 2021. Vol. 21, no 4, p. 2613-2620
Keywords [en]
Carbon Material; CuO; Oxygen Evolution Reaction; Alkaline Media
National Category
Materials Chemistry
Identifiers
URN: urn:nbn:se:liu:diva-174121DOI: 10.1166/jnn.2021.19091PubMedID: 33500083OAI: oai:DiVA.org:liu-174121DiVA, id: diva2:1537457
Available from: 2021-03-15 Created: 2021-03-15 Last updated: 2024-11-12

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