Cobalt hexacyanoferrate: compound stoichiometry, infrared spectroelectrochemistry and photoinduced electron transfer
- Autores
- Lezna, Reynaldo Oscar; Romagnoli, Roberto; Tacconi, Norma R. de; Rajeshwar, Krishnan
- Año de publicación
- 2002
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The cobalt hexacyanoferrate system, Mh [FeB(CN)6]l, (where M is an alkali metal cation, and the subscripts h, k, and l are stoichiometric coefficients, and A and B are the formal oxidation states of the Co and Fe metal sites in the structure) was shown to contain a rich series of compounds that are inter-linked through various redox processes (involving both electron and cation transfer) either in the dark or under the near-infrared (IR) activation. These processes were studied by a combined use of cyclic voltammetry, in situ IR spectroelectrochemistry (using both intensity or potential modulation), and ex situ X-ray photoelectron spectroscopy.
Centro de Investigación y Desarrollo en Tecnología de Pinturas - Materia
-
Química
cobalt
spectroelectrochemistry - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-nd/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/170893
Ver los metadatos del registro completo
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Cobalt hexacyanoferrate: compound stoichiometry, infrared spectroelectrochemistry and photoinduced electron transferLezna, Reynaldo OscarRomagnoli, RobertoTacconi, Norma R. deRajeshwar, KrishnanQuímicacobaltspectroelectrochemistryThe cobalt hexacyanoferrate system, Mh [FeB(CN)6]l, (where M is an alkali metal cation, and the subscripts h, k, and l are stoichiometric coefficients, and A and B are the formal oxidation states of the Co and Fe metal sites in the structure) was shown to contain a rich series of compounds that are inter-linked through various redox processes (involving both electron and cation transfer) either in the dark or under the near-infrared (IR) activation. These processes were studied by a combined use of cyclic voltammetry, in situ IR spectroelectrochemistry (using both intensity or potential modulation), and ex situ X-ray photoelectron spectroscopy.Centro de Investigación y Desarrollo en Tecnología de Pinturas2002info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf3612-3621http://sedici.unlp.edu.ar/handle/10915/170893enginfo:eu-repo/semantics/altIdentifier/doi/10.1021/jp013991rinfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:45:26Zoai:sedici.unlp.edu.ar:10915/170893Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:45:26.339SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Cobalt hexacyanoferrate: compound stoichiometry, infrared spectroelectrochemistry and photoinduced electron transfer |
title |
Cobalt hexacyanoferrate: compound stoichiometry, infrared spectroelectrochemistry and photoinduced electron transfer |
spellingShingle |
Cobalt hexacyanoferrate: compound stoichiometry, infrared spectroelectrochemistry and photoinduced electron transfer Lezna, Reynaldo Oscar Química cobalt spectroelectrochemistry |
title_short |
Cobalt hexacyanoferrate: compound stoichiometry, infrared spectroelectrochemistry and photoinduced electron transfer |
title_full |
Cobalt hexacyanoferrate: compound stoichiometry, infrared spectroelectrochemistry and photoinduced electron transfer |
title_fullStr |
Cobalt hexacyanoferrate: compound stoichiometry, infrared spectroelectrochemistry and photoinduced electron transfer |
title_full_unstemmed |
Cobalt hexacyanoferrate: compound stoichiometry, infrared spectroelectrochemistry and photoinduced electron transfer |
title_sort |
Cobalt hexacyanoferrate: compound stoichiometry, infrared spectroelectrochemistry and photoinduced electron transfer |
dc.creator.none.fl_str_mv |
Lezna, Reynaldo Oscar Romagnoli, Roberto Tacconi, Norma R. de Rajeshwar, Krishnan |
author |
Lezna, Reynaldo Oscar |
author_facet |
Lezna, Reynaldo Oscar Romagnoli, Roberto Tacconi, Norma R. de Rajeshwar, Krishnan |
author_role |
author |
author2 |
Romagnoli, Roberto Tacconi, Norma R. de Rajeshwar, Krishnan |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
Química cobalt spectroelectrochemistry |
topic |
Química cobalt spectroelectrochemistry |
dc.description.none.fl_txt_mv |
The cobalt hexacyanoferrate system, Mh [FeB(CN)6]l, (where M is an alkali metal cation, and the subscripts h, k, and l are stoichiometric coefficients, and A and B are the formal oxidation states of the Co and Fe metal sites in the structure) was shown to contain a rich series of compounds that are inter-linked through various redox processes (involving both electron and cation transfer) either in the dark or under the near-infrared (IR) activation. These processes were studied by a combined use of cyclic voltammetry, in situ IR spectroelectrochemistry (using both intensity or potential modulation), and ex situ X-ray photoelectron spectroscopy. Centro de Investigación y Desarrollo en Tecnología de Pinturas |
description |
The cobalt hexacyanoferrate system, Mh [FeB(CN)6]l, (where M is an alkali metal cation, and the subscripts h, k, and l are stoichiometric coefficients, and A and B are the formal oxidation states of the Co and Fe metal sites in the structure) was shown to contain a rich series of compounds that are inter-linked through various redox processes (involving both electron and cation transfer) either in the dark or under the near-infrared (IR) activation. These processes were studied by a combined use of cyclic voltammetry, in situ IR spectroelectrochemistry (using both intensity or potential modulation), and ex situ X-ray photoelectron spectroscopy. |
publishDate |
2002 |
dc.date.none.fl_str_mv |
2002 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo 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://sedici.unlp.edu.ar/handle/10915/170893 |
url |
http://sedici.unlp.edu.ar/handle/10915/170893 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1021/jp013991r |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-nd/4.0/ Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) |
eu_rights_str_mv |
openAccess |
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http://creativecommons.org/licenses/by-nc-nd/4.0/ Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0) |
dc.format.none.fl_str_mv |
application/pdf 3612-3621 |
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SEDICI (UNLP) - Universidad Nacional de La Plata |
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