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Effect of carbon support on the activity of monodisperse Co(45)Pt(55) nanoparticles for oxygen evolution in alkaline media
Oxygen evolution reaction (OER) represents the efficiency-limiting reaction in water electrolyzers, metal-air batteries, and unitized regenerative fuel cells. To achieve high-efficiency OER in alkaline media, we fabricated three novel electrocatalysts by the assembly of as-prepared Co(45)Pt(55) allo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441667/ https://www.ncbi.nlm.nih.gov/pubmed/37608866 http://dx.doi.org/10.3389/fchem.2023.1244148 |
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author | Andrić, Stevan Milikić, Jadranka Sevim, Melike Santos, Diogo M. F. Šljukić, Biljana |
author_facet | Andrić, Stevan Milikić, Jadranka Sevim, Melike Santos, Diogo M. F. Šljukić, Biljana |
author_sort | Andrić, Stevan |
collection | PubMed |
description | Oxygen evolution reaction (OER) represents the efficiency-limiting reaction in water electrolyzers, metal-air batteries, and unitized regenerative fuel cells. To achieve high-efficiency OER in alkaline media, we fabricated three novel electrocatalysts by the assembly of as-prepared Co(45)Pt(55) alloy nanoparticles (NPs) on three different carbon-based support materials: reduced graphene oxide (CoPt/rGO), mesoporous graphitic carbon nitride (CoPt/mpg-CN), and commercial Ketjenblack carbon (CoPt/KB). Voltammetry studies revealed that CoPt/rGO electrocatalyst provided lower OER overpotentials accompanied by higher currents and specific current density values than the other two studied materials. Moreover, CoPt/rGO outperformed commercial CoPt/C electrocatalysts in terms of notably higher specific current densities. Additionally, it was found that CoPt/rGO electrocatalyst activity increases with increasing temperature up to 85°C, as suggested by the increase in the exchange current density. Electrochemical impedance spectroscopy studies of three electrocatalysts in OER revealed similar charge transfer resistance, although CoPt/rGO provided a higher current density. The main issue observed during long-term chronoamperometry and chronopotentiometry studies is the materials’ instability under OER polarization conditions, which is still to be tackled in future work. |
format | Online Article Text |
id | pubmed-10441667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104416672023-08-22 Effect of carbon support on the activity of monodisperse Co(45)Pt(55) nanoparticles for oxygen evolution in alkaline media Andrić, Stevan Milikić, Jadranka Sevim, Melike Santos, Diogo M. F. Šljukić, Biljana Front Chem Chemistry Oxygen evolution reaction (OER) represents the efficiency-limiting reaction in water electrolyzers, metal-air batteries, and unitized regenerative fuel cells. To achieve high-efficiency OER in alkaline media, we fabricated three novel electrocatalysts by the assembly of as-prepared Co(45)Pt(55) alloy nanoparticles (NPs) on three different carbon-based support materials: reduced graphene oxide (CoPt/rGO), mesoporous graphitic carbon nitride (CoPt/mpg-CN), and commercial Ketjenblack carbon (CoPt/KB). Voltammetry studies revealed that CoPt/rGO electrocatalyst provided lower OER overpotentials accompanied by higher currents and specific current density values than the other two studied materials. Moreover, CoPt/rGO outperformed commercial CoPt/C electrocatalysts in terms of notably higher specific current densities. Additionally, it was found that CoPt/rGO electrocatalyst activity increases with increasing temperature up to 85°C, as suggested by the increase in the exchange current density. Electrochemical impedance spectroscopy studies of three electrocatalysts in OER revealed similar charge transfer resistance, although CoPt/rGO provided a higher current density. The main issue observed during long-term chronoamperometry and chronopotentiometry studies is the materials’ instability under OER polarization conditions, which is still to be tackled in future work. Frontiers Media S.A. 2023-08-07 /pmc/articles/PMC10441667/ /pubmed/37608866 http://dx.doi.org/10.3389/fchem.2023.1244148 Text en Copyright © 2023 Andrić, Milikić, Sevim, Santos and Šljukić. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Andrić, Stevan Milikić, Jadranka Sevim, Melike Santos, Diogo M. F. Šljukić, Biljana Effect of carbon support on the activity of monodisperse Co(45)Pt(55) nanoparticles for oxygen evolution in alkaline media |
title | Effect of carbon support on the activity of monodisperse Co(45)Pt(55) nanoparticles for oxygen evolution in alkaline media |
title_full | Effect of carbon support on the activity of monodisperse Co(45)Pt(55) nanoparticles for oxygen evolution in alkaline media |
title_fullStr | Effect of carbon support on the activity of monodisperse Co(45)Pt(55) nanoparticles for oxygen evolution in alkaline media |
title_full_unstemmed | Effect of carbon support on the activity of monodisperse Co(45)Pt(55) nanoparticles for oxygen evolution in alkaline media |
title_short | Effect of carbon support on the activity of monodisperse Co(45)Pt(55) nanoparticles for oxygen evolution in alkaline media |
title_sort | effect of carbon support on the activity of monodisperse co(45)pt(55) nanoparticles for oxygen evolution in alkaline media |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441667/ https://www.ncbi.nlm.nih.gov/pubmed/37608866 http://dx.doi.org/10.3389/fchem.2023.1244148 |
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