In-situ spectroelectrochemical study of highly active Ni-based foam electrocatalysts for hydrogen evolution reaction
Descripción del Articulo
Green hydrogen is a valuable energy source able to overcome the environmental issues generated by fossil fuel consumption. In this regard, large-scale production of green hydrogen could be achieved by anion exchange membrane water electrolyzer (AEMWE). However, highly electroactive, and low-cost cat...
| Autores: | , , , , |
|---|---|
| Formato: | artículo |
| Fecha de Publicación: | 2023 |
| Institución: | Universidad Tecnológica del Perú |
| Repositorio: | UTP-Institucional |
| Lenguaje: | español |
| OAI Identifier: | oai:repositorio.utp.edu.pe:20.500.12867/7234 |
| Enlace del recurso: | https://hdl.handle.net/20.500.12867/7234 https://doi.org/10.1016/j.apcatb.2023.122930 |
| Nivel de acceso: | acceso abierto |
| Materia: | Spectroelectrochemical Electrocatalysis Nickel foam Hydrogen production https://purl.org/pe-repo/ocde/ford#1.04.00 |
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| dc.title.es_PE.fl_str_mv |
In-situ spectroelectrochemical study of highly active Ni-based foam electrocatalysts for hydrogen evolution reaction |
| title |
In-situ spectroelectrochemical study of highly active Ni-based foam electrocatalysts for hydrogen evolution reaction |
| spellingShingle |
In-situ spectroelectrochemical study of highly active Ni-based foam electrocatalysts for hydrogen evolution reaction Bazán Aguilar, Antony Yamir Spectroelectrochemical Electrocatalysis Nickel foam Hydrogen production https://purl.org/pe-repo/ocde/ford#1.04.00 |
| title_short |
In-situ spectroelectrochemical study of highly active Ni-based foam electrocatalysts for hydrogen evolution reaction |
| title_full |
In-situ spectroelectrochemical study of highly active Ni-based foam electrocatalysts for hydrogen evolution reaction |
| title_fullStr |
In-situ spectroelectrochemical study of highly active Ni-based foam electrocatalysts for hydrogen evolution reaction |
| title_full_unstemmed |
In-situ spectroelectrochemical study of highly active Ni-based foam electrocatalysts for hydrogen evolution reaction |
| title_sort |
In-situ spectroelectrochemical study of highly active Ni-based foam electrocatalysts for hydrogen evolution reaction |
| author |
Bazán Aguilar, Antony Yamir |
| author_facet |
Bazán Aguilar, Antony Yamir García, Gonzalo Pastor, Elena Rodríguez, José Luis Baena-Moncada, Angélica María |
| author_role |
author |
| author2 |
García, Gonzalo Pastor, Elena Rodríguez, José Luis Baena-Moncada, Angélica María |
| author2_role |
author author author author |
| dc.contributor.author.fl_str_mv |
Bazán Aguilar, Antony Yamir García, Gonzalo Pastor, Elena Rodríguez, José Luis Baena-Moncada, Angélica María |
| dc.subject.es_PE.fl_str_mv |
Spectroelectrochemical Electrocatalysis Nickel foam Hydrogen production |
| topic |
Spectroelectrochemical Electrocatalysis Nickel foam Hydrogen production https://purl.org/pe-repo/ocde/ford#1.04.00 |
| dc.subject.ocde.es_PE.fl_str_mv |
https://purl.org/pe-repo/ocde/ford#1.04.00 |
| description |
Green hydrogen is a valuable energy source able to overcome the environmental issues generated by fossil fuel consumption. In this regard, large-scale production of green hydrogen could be achieved by anion exchange membrane water electrolyzer (AEMWE). However, highly electroactive, and low-cost catalysts for hydrogen evolution reaction (HER) are critical to executing AEMWE. With this end in view, a straightforward route is revealed to improve the catalytic performance toward the HER of commercial and low-cost Ni foam electrodes. Indeed, an oxyhydroxide nickel-based surface was obtained after a facile and low-cost anhydrous etching procedure of the raw material. The novel catalyst reveals an onset potential for the HER of ca. 10.0 mV (vs. RHE), which is very close to the thermodynamic value, and an increment of the catalytic efficiency towards the HER. Furthermore, differential electrochemical mass spectrometry (DEMS) and Raman spectroelectrochemistry (Raman-SEC) were employed to get insight into the reaction kinetics and mechanism of the HER at catalysts in alkaline medium. |
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2023 |
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2023-08-01T18:55:48Z |
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2023-08-01T18:55:48Z |
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2023 |
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1873-3883 |
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https://hdl.handle.net/20.500.12867/7234 |
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Applied Catalysis B: Environmental |
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https://doi.org/10.1016/j.apcatb.2023.122930 |
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1873-3883 Applied Catalysis B: Environmental |
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https://hdl.handle.net/20.500.12867/7234 https://doi.org/10.1016/j.apcatb.2023.122930 |
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spa |
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spa |
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Applied Catalysis B: Environmental;vol. 336 |
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http://creativecommons.org/licenses/by/4.0/ |
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Elsevier |
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NL |
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Repositorio Institucional - UTP Universidad Tecnológica del Perú |
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Bazán Aguilar, Antony YamirGarcía, GonzaloPastor, ElenaRodríguez, José LuisBaena-Moncada, Angélica María2023-08-01T18:55:48Z2023-08-01T18:55:48Z20231873-3883https://hdl.handle.net/20.500.12867/7234Applied Catalysis B: Environmentalhttps://doi.org/10.1016/j.apcatb.2023.122930Green hydrogen is a valuable energy source able to overcome the environmental issues generated by fossil fuel consumption. In this regard, large-scale production of green hydrogen could be achieved by anion exchange membrane water electrolyzer (AEMWE). However, highly electroactive, and low-cost catalysts for hydrogen evolution reaction (HER) are critical to executing AEMWE. With this end in view, a straightforward route is revealed to improve the catalytic performance toward the HER of commercial and low-cost Ni foam electrodes. Indeed, an oxyhydroxide nickel-based surface was obtained after a facile and low-cost anhydrous etching procedure of the raw material. The novel catalyst reveals an onset potential for the HER of ca. 10.0 mV (vs. RHE), which is very close to the thermodynamic value, and an increment of the catalytic efficiency towards the HER. 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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).