Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis

Autores
Jaramillo Hernández, Camilo; Seijas Da Silva, Alvaro; Vert, Vicente B.; Mizrahi, Martin Daniel; Leyva Pérez, Antonio; Abellán, Gonzalo
Año de publicación
2025
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Alkaline water electrolysis (AWE) is a promising hydrogen production method but faces challenges with the sluggish oxygen evolution reaction (OER), which requires high voltages. Nickel-based layered hydroxides (LHs) are effective earth-abundant OER catalysts, though Fe incorporation from electrolyte impurities significantly enhances their performance. This study systematically examines Fe impurity incorporation in Ni-based LH phases: α-Ni-LH, β-Ni-LH, and NiAl- and NiFe-layered double hydroxides (LDHs). Two incorporation methods were explored: a standard electrolyte purification process and an electrochemical activation approach. Electrochemical activation is more effective, and expanded phases have more affinity to allocate Fe. Incorporation experiments suggest a partial transformation of NiAl into NiFe-like LDH, which exhibits a superior electrocatalytic performance. Spectroscopical techniques suggest that the Fe incorporated in the NiAl LDH could be structural due to synergy with the concomitant leaching of Al in the electrolyte. For pristine NiFe-LDH, these treatment strategies proved ineffective, suggesting that such approaches are unsuitable for optimized compositions. Furthermore, the process is highly dependent on the Fe impurity concentration in the electrolyte. This work highlights the role of the initial LH phase in determining structural Fe incorporation, providing insights for designing efficient electrodes in AWE. It also emphasizes the need for strict control of the electrolyte to optimize catalyst performance.
Fil: Jaramillo Hernández, Camilo. Universidad de Valencia. Instituto de Ciencia Molecular.;
Fil: Seijas Da Silva, Alvaro. Universidad de Valencia. Instituto de Ciencia Molecular.;
Fil: Vert, Vicente B.. Universidad de Valencia. Instituto de Ciencia Molecular.;
Fil: Mizrahi, Martin Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina. Universidad Nacional de La Plata. Facultad de Ingeniería. Departamento de Ciencias Básicas; Argentina
Fil: Leyva Pérez, Antonio. Universidad Politécnica de Valencia. Instituto de Tecnología de Materiales. Departamento Ingeniería Mecanica y Materiales; España
Fil: Abellán, Gonzalo. Universidad de Valencia. Instituto de Ciencia Molecular.;
Materia
Fe Incorporation
LDH
ELECTROCHEMISTRY
XANES-EXAFS
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/282006

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network_name_str CONICET Digital (CONICET)
spelling Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution ElectrocatalysisJaramillo Hernández, CamiloSeijas Da Silva, AlvaroVert, Vicente B.Mizrahi, Martin DanielLeyva Pérez, AntonioAbellán, GonzaloFe IncorporationLDHELECTROCHEMISTRYXANES-EXAFShttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1Alkaline water electrolysis (AWE) is a promising hydrogen production method but faces challenges with the sluggish oxygen evolution reaction (OER), which requires high voltages. Nickel-based layered hydroxides (LHs) are effective earth-abundant OER catalysts, though Fe incorporation from electrolyte impurities significantly enhances their performance. This study systematically examines Fe impurity incorporation in Ni-based LH phases: α-Ni-LH, β-Ni-LH, and NiAl- and NiFe-layered double hydroxides (LDHs). Two incorporation methods were explored: a standard electrolyte purification process and an electrochemical activation approach. Electrochemical activation is more effective, and expanded phases have more affinity to allocate Fe. Incorporation experiments suggest a partial transformation of NiAl into NiFe-like LDH, which exhibits a superior electrocatalytic performance. Spectroscopical techniques suggest that the Fe incorporated in the NiAl LDH could be structural due to synergy with the concomitant leaching of Al in the electrolyte. For pristine NiFe-LDH, these treatment strategies proved ineffective, suggesting that such approaches are unsuitable for optimized compositions. Furthermore, the process is highly dependent on the Fe impurity concentration in the electrolyte. This work highlights the role of the initial LH phase in determining structural Fe incorporation, providing insights for designing efficient electrodes in AWE. It also emphasizes the need for strict control of the electrolyte to optimize catalyst performance.Fil: Jaramillo Hernández, Camilo. Universidad de Valencia. Instituto de Ciencia Molecular.;Fil: Seijas Da Silva, Alvaro. Universidad de Valencia. Instituto de Ciencia Molecular.;Fil: Vert, Vicente B.. Universidad de Valencia. Instituto de Ciencia Molecular.;Fil: Mizrahi, Martin Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina. Universidad Nacional de La Plata. Facultad de Ingeniería. Departamento de Ciencias Básicas; ArgentinaFil: Leyva Pérez, Antonio. Universidad Politécnica de Valencia. Instituto de Tecnología de Materiales. Departamento Ingeniería Mecanica y Materiales; EspañaFil: Abellán, Gonzalo. Universidad de Valencia. Instituto de Ciencia Molecular.;American Chemical Society2025-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/282006Jaramillo Hernández, Camilo; Seijas Da Silva, Alvaro; Vert, Vicente B.; Mizrahi, Martin Daniel; Leyva Pérez, Antonio; et al.; Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis; American Chemical Society; Inorganic Chemistry; 64; 48; 11-2025; 23360-233760020-1669CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.inorgchem.5c02786info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.inorgchem.5c02786info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-03-11T11:58:04Zoai:ri.conicet.gov.ar:11336/282006instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982026-03-11 11:58:04.9CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis
title Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis
spellingShingle Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis
Jaramillo Hernández, Camilo
Fe Incorporation
LDH
ELECTROCHEMISTRY
XANES-EXAFS
title_short Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis
title_full Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis
title_fullStr Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis
title_full_unstemmed Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis
title_sort Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis
dc.creator.none.fl_str_mv Jaramillo Hernández, Camilo
Seijas Da Silva, Alvaro
Vert, Vicente B.
Mizrahi, Martin Daniel
Leyva Pérez, Antonio
Abellán, Gonzalo
author Jaramillo Hernández, Camilo
author_facet Jaramillo Hernández, Camilo
Seijas Da Silva, Alvaro
Vert, Vicente B.
Mizrahi, Martin Daniel
Leyva Pérez, Antonio
Abellán, Gonzalo
author_role author
author2 Seijas Da Silva, Alvaro
Vert, Vicente B.
Mizrahi, Martin Daniel
Leyva Pérez, Antonio
Abellán, Gonzalo
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Fe Incorporation
LDH
ELECTROCHEMISTRY
XANES-EXAFS
topic Fe Incorporation
LDH
ELECTROCHEMISTRY
XANES-EXAFS
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.3
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Alkaline water electrolysis (AWE) is a promising hydrogen production method but faces challenges with the sluggish oxygen evolution reaction (OER), which requires high voltages. Nickel-based layered hydroxides (LHs) are effective earth-abundant OER catalysts, though Fe incorporation from electrolyte impurities significantly enhances their performance. This study systematically examines Fe impurity incorporation in Ni-based LH phases: α-Ni-LH, β-Ni-LH, and NiAl- and NiFe-layered double hydroxides (LDHs). Two incorporation methods were explored: a standard electrolyte purification process and an electrochemical activation approach. Electrochemical activation is more effective, and expanded phases have more affinity to allocate Fe. Incorporation experiments suggest a partial transformation of NiAl into NiFe-like LDH, which exhibits a superior electrocatalytic performance. Spectroscopical techniques suggest that the Fe incorporated in the NiAl LDH could be structural due to synergy with the concomitant leaching of Al in the electrolyte. For pristine NiFe-LDH, these treatment strategies proved ineffective, suggesting that such approaches are unsuitable for optimized compositions. Furthermore, the process is highly dependent on the Fe impurity concentration in the electrolyte. This work highlights the role of the initial LH phase in determining structural Fe incorporation, providing insights for designing efficient electrodes in AWE. It also emphasizes the need for strict control of the electrolyte to optimize catalyst performance.
Fil: Jaramillo Hernández, Camilo. Universidad de Valencia. Instituto de Ciencia Molecular.;
Fil: Seijas Da Silva, Alvaro. Universidad de Valencia. Instituto de Ciencia Molecular.;
Fil: Vert, Vicente B.. Universidad de Valencia. Instituto de Ciencia Molecular.;
Fil: Mizrahi, Martin Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina. Universidad Nacional de La Plata. Facultad de Ingeniería. Departamento de Ciencias Básicas; Argentina
Fil: Leyva Pérez, Antonio. Universidad Politécnica de Valencia. Instituto de Tecnología de Materiales. Departamento Ingeniería Mecanica y Materiales; España
Fil: Abellán, Gonzalo. Universidad de Valencia. Instituto de Ciencia Molecular.;
description Alkaline water electrolysis (AWE) is a promising hydrogen production method but faces challenges with the sluggish oxygen evolution reaction (OER), which requires high voltages. Nickel-based layered hydroxides (LHs) are effective earth-abundant OER catalysts, though Fe incorporation from electrolyte impurities significantly enhances their performance. This study systematically examines Fe impurity incorporation in Ni-based LH phases: α-Ni-LH, β-Ni-LH, and NiAl- and NiFe-layered double hydroxides (LDHs). Two incorporation methods were explored: a standard electrolyte purification process and an electrochemical activation approach. Electrochemical activation is more effective, and expanded phases have more affinity to allocate Fe. Incorporation experiments suggest a partial transformation of NiAl into NiFe-like LDH, which exhibits a superior electrocatalytic performance. Spectroscopical techniques suggest that the Fe incorporated in the NiAl LDH could be structural due to synergy with the concomitant leaching of Al in the electrolyte. For pristine NiFe-LDH, these treatment strategies proved ineffective, suggesting that such approaches are unsuitable for optimized compositions. Furthermore, the process is highly dependent on the Fe impurity concentration in the electrolyte. This work highlights the role of the initial LH phase in determining structural Fe incorporation, providing insights for designing efficient electrodes in AWE. It also emphasizes the need for strict control of the electrolyte to optimize catalyst performance.
publishDate 2025
dc.date.none.fl_str_mv 2025-11
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/282006
Jaramillo Hernández, Camilo; Seijas Da Silva, Alvaro; Vert, Vicente B.; Mizrahi, Martin Daniel; Leyva Pérez, Antonio; et al.; Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis; American Chemical Society; Inorganic Chemistry; 64; 48; 11-2025; 23360-23376
0020-1669
CONICET Digital
CONICET
url http://hdl.handle.net/11336/282006
identifier_str_mv Jaramillo Hernández, Camilo; Seijas Da Silva, Alvaro; Vert, Vicente B.; Mizrahi, Martin Daniel; Leyva Pérez, Antonio; et al.; Fe Incorporation in Ni-Based Layered Hydroxides: Implications for Oxygen Evolution Electrocatalysis; American Chemical Society; Inorganic Chemistry; 64; 48; 11-2025; 23360-23376
0020-1669
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.inorgchem.5c02786
info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.inorgchem.5c02786
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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