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Promoted glucose electrooxidation at Ni(OH)(2)/graphene layers exfoliated facilely from carbon waste material

Nowadays, the glucose electro-oxidation reaction (GOR) is considered one of the most important solutions for environmental pollution. The GOR is the anodic reaction in direct glucose fuel cells and hybrid water electrolysis. In this study, the GOR is boosted using a carbon support modified with Ni(O...

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Autores principales: Abdelrahim, Ahmed M., Abd El-Moghny, Muhammad G., El-Shakre, Mohamed E., El-Deab, Mohamed S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830938/
https://www.ncbi.nlm.nih.gov/pubmed/36712643
http://dx.doi.org/10.1039/d2ra07309a
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author Abdelrahim, Ahmed M.
Abd El-Moghny, Muhammad G.
El-Shakre, Mohamed E.
El-Deab, Mohamed S.
author_facet Abdelrahim, Ahmed M.
Abd El-Moghny, Muhammad G.
El-Shakre, Mohamed E.
El-Deab, Mohamed S.
author_sort Abdelrahim, Ahmed M.
collection PubMed
description Nowadays, the glucose electro-oxidation reaction (GOR) is considered one of the most important solutions for environmental pollution. The GOR is the anodic reaction in direct glucose fuel cells and hybrid water electrolysis. In this study, the GOR is boosted using a carbon support modified with Ni(OH)(2) as a non-precious catalyst. The carbon support, with in situ generated graphene nanosheets having a large surface area, grooves, and surface functional groups, is prepared via a simple electrochemical treatment of the carbon rods of an exhausted zinc-carbon battery. Ni(OH)(2) is electrodeposited on the surface of the functionalized exfoliated graphite rod (FEGR) via the dynamic hydrogen bubbling technique (DHBT) and tested for GOR. The thus-prepared Ni(OH)(2)/FEGR electrode is characterized by SEM, mapping EDX, HR-TEM, XRD, and XPS characterization tools. Ni(OH)(2)/FEGR displays an onset potential of 1.23 V vs. the reversible hydrogen electrode (RHE) and attains high current densities at lower potentials. Additionally, Ni(OH)(2)/FEGR showed prolonged stability toward GOR by supporting a constant current over a long electrolysis time. The enhanced catalytic performance is attributed to the superb ionic and electronic conductivity of the catalyst. Importantly, ionic conductivity increased, due to (i) a large surface area of in situ generated graphene layers, (ii) enhanced distribution of active material during deposition using DHBT, and (iii) increased hydrophilicity of the underlying substrate. Therefore, the Ni(OH)(2)/FEGR electrode can be used efficiently for GOR as a low-cost catalyst, achieving low onset potential and high current densities at low potentials.
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spelling pubmed-98309382023-01-26 Promoted glucose electrooxidation at Ni(OH)(2)/graphene layers exfoliated facilely from carbon waste material Abdelrahim, Ahmed M. Abd El-Moghny, Muhammad G. El-Shakre, Mohamed E. El-Deab, Mohamed S. RSC Adv Chemistry Nowadays, the glucose electro-oxidation reaction (GOR) is considered one of the most important solutions for environmental pollution. The GOR is the anodic reaction in direct glucose fuel cells and hybrid water electrolysis. In this study, the GOR is boosted using a carbon support modified with Ni(OH)(2) as a non-precious catalyst. The carbon support, with in situ generated graphene nanosheets having a large surface area, grooves, and surface functional groups, is prepared via a simple electrochemical treatment of the carbon rods of an exhausted zinc-carbon battery. Ni(OH)(2) is electrodeposited on the surface of the functionalized exfoliated graphite rod (FEGR) via the dynamic hydrogen bubbling technique (DHBT) and tested for GOR. The thus-prepared Ni(OH)(2)/FEGR electrode is characterized by SEM, mapping EDX, HR-TEM, XRD, and XPS characterization tools. Ni(OH)(2)/FEGR displays an onset potential of 1.23 V vs. the reversible hydrogen electrode (RHE) and attains high current densities at lower potentials. Additionally, Ni(OH)(2)/FEGR showed prolonged stability toward GOR by supporting a constant current over a long electrolysis time. The enhanced catalytic performance is attributed to the superb ionic and electronic conductivity of the catalyst. Importantly, ionic conductivity increased, due to (i) a large surface area of in situ generated graphene layers, (ii) enhanced distribution of active material during deposition using DHBT, and (iii) increased hydrophilicity of the underlying substrate. Therefore, the Ni(OH)(2)/FEGR electrode can be used efficiently for GOR as a low-cost catalyst, achieving low onset potential and high current densities at low potentials. The Royal Society of Chemistry 2023-01-10 /pmc/articles/PMC9830938/ /pubmed/36712643 http://dx.doi.org/10.1039/d2ra07309a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Abdelrahim, Ahmed M.
Abd El-Moghny, Muhammad G.
El-Shakre, Mohamed E.
El-Deab, Mohamed S.
Promoted glucose electrooxidation at Ni(OH)(2)/graphene layers exfoliated facilely from carbon waste material
title Promoted glucose electrooxidation at Ni(OH)(2)/graphene layers exfoliated facilely from carbon waste material
title_full Promoted glucose electrooxidation at Ni(OH)(2)/graphene layers exfoliated facilely from carbon waste material
title_fullStr Promoted glucose electrooxidation at Ni(OH)(2)/graphene layers exfoliated facilely from carbon waste material
title_full_unstemmed Promoted glucose electrooxidation at Ni(OH)(2)/graphene layers exfoliated facilely from carbon waste material
title_short Promoted glucose electrooxidation at Ni(OH)(2)/graphene layers exfoliated facilely from carbon waste material
title_sort promoted glucose electrooxidation at ni(oh)(2)/graphene layers exfoliated facilely from carbon waste material
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9830938/
https://www.ncbi.nlm.nih.gov/pubmed/36712643
http://dx.doi.org/10.1039/d2ra07309a
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