Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces
- Autores
- Bhattacharyya, Dhritiman; Videla, Pablo Ernesto; Cattaneo, Mauricio; Batista, Victor S.; Lian, Tianquan; Kubiak, Clifford P.
- Año de publicación
- 2021
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- External control of chemical processes is a subject of widespread interest in chemical research, including control of electrocatalytic processes with significant promise in energy research. The electrochemical double-layer is the nanoscale region next to the electrode/electrolyte interface where chemical reactions typically occur. Understanding the effects of electric fields within the electrochemical double layer requires a combination of synthesis, electrochemistry, spectroscopy, and theory. In particular, vibrational sum frequency generation (VSFG) spectroscopy is a powerful technique to probe the response of molecular catalysts at the electrode interface under bias. Fundamental understanding can be obtained via synthetic tuning of the adsorbed molecular catalysts on the electrode surface and by combining experimental VSFG data with theoretical modelling of the Stark shift response. The resulting insights at the molecular level are particularly valuable for the development of new methodologies to control and characterize catalysts confined to electrode surfaces. This Perspective article is focused on how systematic modifications of molecules anchored to surfaces report information concerning the geometric, energetic, and electronic parameters of catalysts under bias attached to electrode surfaces.
Fil: Bhattacharyya, Dhritiman. University of Emory; Estados Unidos
Fil: Videla, Pablo Ernesto. University of Yale; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Cattaneo, Mauricio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina
Fil: Batista, Victor S.. University of Yale; Estados Unidos
Fil: Lian, Tianquan. University of Emory; Estados Unidos
Fil: Kubiak, Clifford P.. University of California at San Diego; Estados Unidos - Materia
-
VIBRATIONAL STARK SHIFT SPECTROSCOPY
MOLECULAR CATALYSTS
INFLUENCE OF ELCTRIC FIELDS
ELECTRODE SURFACE - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/147393
Ver los metadatos del registro completo
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Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfacesBhattacharyya, DhritimanVidela, Pablo ErnestoCattaneo, MauricioBatista, Victor S.Lian, TianquanKubiak, Clifford P.VIBRATIONAL STARK SHIFT SPECTROSCOPYMOLECULAR CATALYSTSINFLUENCE OF ELCTRIC FIELDSELECTRODE SURFACEhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1External control of chemical processes is a subject of widespread interest in chemical research, including control of electrocatalytic processes with significant promise in energy research. The electrochemical double-layer is the nanoscale region next to the electrode/electrolyte interface where chemical reactions typically occur. Understanding the effects of electric fields within the electrochemical double layer requires a combination of synthesis, electrochemistry, spectroscopy, and theory. In particular, vibrational sum frequency generation (VSFG) spectroscopy is a powerful technique to probe the response of molecular catalysts at the electrode interface under bias. Fundamental understanding can be obtained via synthetic tuning of the adsorbed molecular catalysts on the electrode surface and by combining experimental VSFG data with theoretical modelling of the Stark shift response. The resulting insights at the molecular level are particularly valuable for the development of new methodologies to control and characterize catalysts confined to electrode surfaces. This Perspective article is focused on how systematic modifications of molecules anchored to surfaces report information concerning the geometric, energetic, and electronic parameters of catalysts under bias attached to electrode surfaces.Fil: Bhattacharyya, Dhritiman. University of Emory; Estados UnidosFil: Videla, Pablo Ernesto. University of Yale; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Cattaneo, Mauricio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; ArgentinaFil: Batista, Victor S.. University of Yale; Estados UnidosFil: Lian, Tianquan. University of Emory; Estados UnidosFil: Kubiak, Clifford P.. University of California at San Diego; Estados UnidosRoyal Society of Chemistry2021-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/147393Bhattacharyya, Dhritiman; Videla, Pablo Ernesto; Cattaneo, Mauricio; Batista, Victor S.; Lian, Tianquan; et al.; Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces; Royal Society of Chemistry; Chemical Science; 12; 30; 7-2021; 10131-101492041-65202041-6539CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1039/D1SC01876Kinfo:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2021/SC/D1SC01876Kinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T15:37:20Zoai:ri.conicet.gov.ar:11336/147393instacron: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:34982025-10-15 15:37:20.513CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces |
title |
Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces |
spellingShingle |
Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces Bhattacharyya, Dhritiman VIBRATIONAL STARK SHIFT SPECTROSCOPY MOLECULAR CATALYSTS INFLUENCE OF ELCTRIC FIELDS ELECTRODE SURFACE |
title_short |
Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces |
title_full |
Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces |
title_fullStr |
Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces |
title_full_unstemmed |
Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces |
title_sort |
Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces |
dc.creator.none.fl_str_mv |
Bhattacharyya, Dhritiman Videla, Pablo Ernesto Cattaneo, Mauricio Batista, Victor S. Lian, Tianquan Kubiak, Clifford P. |
author |
Bhattacharyya, Dhritiman |
author_facet |
Bhattacharyya, Dhritiman Videla, Pablo Ernesto Cattaneo, Mauricio Batista, Victor S. Lian, Tianquan Kubiak, Clifford P. |
author_role |
author |
author2 |
Videla, Pablo Ernesto Cattaneo, Mauricio Batista, Victor S. Lian, Tianquan Kubiak, Clifford P. |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
VIBRATIONAL STARK SHIFT SPECTROSCOPY MOLECULAR CATALYSTS INFLUENCE OF ELCTRIC FIELDS ELECTRODE SURFACE |
topic |
VIBRATIONAL STARK SHIFT SPECTROSCOPY MOLECULAR CATALYSTS INFLUENCE OF ELCTRIC FIELDS ELECTRODE SURFACE |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
External control of chemical processes is a subject of widespread interest in chemical research, including control of electrocatalytic processes with significant promise in energy research. The electrochemical double-layer is the nanoscale region next to the electrode/electrolyte interface where chemical reactions typically occur. Understanding the effects of electric fields within the electrochemical double layer requires a combination of synthesis, electrochemistry, spectroscopy, and theory. In particular, vibrational sum frequency generation (VSFG) spectroscopy is a powerful technique to probe the response of molecular catalysts at the electrode interface under bias. Fundamental understanding can be obtained via synthetic tuning of the adsorbed molecular catalysts on the electrode surface and by combining experimental VSFG data with theoretical modelling of the Stark shift response. The resulting insights at the molecular level are particularly valuable for the development of new methodologies to control and characterize catalysts confined to electrode surfaces. This Perspective article is focused on how systematic modifications of molecules anchored to surfaces report information concerning the geometric, energetic, and electronic parameters of catalysts under bias attached to electrode surfaces. Fil: Bhattacharyya, Dhritiman. University of Emory; Estados Unidos Fil: Videla, Pablo Ernesto. University of Yale; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina Fil: Cattaneo, Mauricio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina Fil: Batista, Victor S.. University of Yale; Estados Unidos Fil: Lian, Tianquan. University of Emory; Estados Unidos Fil: Kubiak, Clifford P.. University of California at San Diego; Estados Unidos |
description |
External control of chemical processes is a subject of widespread interest in chemical research, including control of electrocatalytic processes with significant promise in energy research. The electrochemical double-layer is the nanoscale region next to the electrode/electrolyte interface where chemical reactions typically occur. Understanding the effects of electric fields within the electrochemical double layer requires a combination of synthesis, electrochemistry, spectroscopy, and theory. In particular, vibrational sum frequency generation (VSFG) spectroscopy is a powerful technique to probe the response of molecular catalysts at the electrode interface under bias. Fundamental understanding can be obtained via synthetic tuning of the adsorbed molecular catalysts on the electrode surface and by combining experimental VSFG data with theoretical modelling of the Stark shift response. The resulting insights at the molecular level are particularly valuable for the development of new methodologies to control and characterize catalysts confined to electrode surfaces. This Perspective article is focused on how systematic modifications of molecules anchored to surfaces report information concerning the geometric, energetic, and electronic parameters of catalysts under bias attached to electrode surfaces. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-07 |
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/11336/147393 Bhattacharyya, Dhritiman; Videla, Pablo Ernesto; Cattaneo, Mauricio; Batista, Victor S.; Lian, Tianquan; et al.; Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces; Royal Society of Chemistry; Chemical Science; 12; 30; 7-2021; 10131-10149 2041-6520 2041-6539 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/147393 |
identifier_str_mv |
Bhattacharyya, Dhritiman; Videla, Pablo Ernesto; Cattaneo, Mauricio; Batista, Victor S.; Lian, Tianquan; et al.; Vibrational stark shift spectroscopy of catalysts under the influence of electric fields at electrode–solution interfaces; Royal Society of Chemistry; Chemical Science; 12; 30; 7-2021; 10131-10149 2041-6520 2041-6539 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1039/D1SC01876K info:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2021/SC/D1SC01876K |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Royal Society of Chemistry |
publisher.none.fl_str_mv |
Royal Society of Chemistry |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
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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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13.22299 |