Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid

Autores
Melchionna, Michele; Bracamonte, Maria Victoria; Giuliani, Angela; Nasi, Lucia; Montini, Tiziano; Tavagnacco, Claudio; Bonchio, Marcella; Fornasiero, P; Prato, Maurizio
Año de publicación
2018
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Direct conversion of carbon dioxide to formic acid at thermodynamic equilibrium is an advantage of enzymatic catalysis, hardly replicated by synthetic analogs, but of high priority for carbon-neutral energy schemes. The bio-mimetic potential of totally inorganic Pd@TiO2 nanoparticles is envisioned herein in combination with Single Walled Carbon NanoHorns (SWCNHs). The high surface nano-carbon entanglement templates a wide distribution of "hard-soft" bimetallic sites where the small Pd nanoparticles (1.5 nm) are shielded within the TiO2 phase (Pd@TiO2), while being electrically wired to the electrode by the nanocarbon support. This hybrid electrocatalyst activates CO2 reduction to formic acid at near zero overpotential in the aqueous phase (onset potential at E < -0.05 V vs. RHE, pH = 7.4), while being able to evolve hydrogen via sequential formic acid dehydrogenation. The net result hints at a unique CO2 "circular catalysis" where formic acid versus H2 selectivity is addressable by flow-reactor technology.
Fil: Melchionna, Michele. Università degli Studi di Trieste; Italia
Fil: Bracamonte, Maria Victoria. Università degli Studi di Trieste; Italia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina
Fil: Giuliani, Angela. Università degli Studi di Trieste; Italia
Fil: Nasi, Lucia. Istituto Dei Materiali Per L'elettronica Ed Il Magnetismo; Italia
Fil: Montini, Tiziano. Università degli Studi di Trieste; Italia
Fil: Tavagnacco, Claudio. Università degli Studi di Trieste; Italia
Fil: Bonchio, Marcella. Università di Padova; Italia
Fil: Fornasiero, P. Università degli Studi di Trieste; Italia
Fil: Prato, Maurizio. Università degli Studi di Trieste; Italia
Materia
PD NANOPARTICLES
CARBON NANOHORNS
CO2 REDUCTION
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/91195

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spelling Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acidMelchionna, MicheleBracamonte, Maria VictoriaGiuliani, AngelaNasi, LuciaMontini, TizianoTavagnacco, ClaudioBonchio, MarcellaFornasiero, PPrato, MaurizioPD NANOPARTICLESCARBON NANOHORNSCO2 REDUCTIONhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Direct conversion of carbon dioxide to formic acid at thermodynamic equilibrium is an advantage of enzymatic catalysis, hardly replicated by synthetic analogs, but of high priority for carbon-neutral energy schemes. The bio-mimetic potential of totally inorganic Pd@TiO2 nanoparticles is envisioned herein in combination with Single Walled Carbon NanoHorns (SWCNHs). The high surface nano-carbon entanglement templates a wide distribution of "hard-soft" bimetallic sites where the small Pd nanoparticles (1.5 nm) are shielded within the TiO2 phase (Pd@TiO2), while being electrically wired to the electrode by the nanocarbon support. This hybrid electrocatalyst activates CO2 reduction to formic acid at near zero overpotential in the aqueous phase (onset potential at E < -0.05 V vs. RHE, pH = 7.4), while being able to evolve hydrogen via sequential formic acid dehydrogenation. The net result hints at a unique CO2 "circular catalysis" where formic acid versus H2 selectivity is addressable by flow-reactor technology.Fil: Melchionna, Michele. Università degli Studi di Trieste; ItaliaFil: Bracamonte, Maria Victoria. Università degli Studi di Trieste; Italia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; ArgentinaFil: Giuliani, Angela. Università degli Studi di Trieste; ItaliaFil: Nasi, Lucia. Istituto Dei Materiali Per L'elettronica Ed Il Magnetismo; ItaliaFil: Montini, Tiziano. Università degli Studi di Trieste; ItaliaFil: Tavagnacco, Claudio. Università degli Studi di Trieste; ItaliaFil: Bonchio, Marcella. Università di Padova; ItaliaFil: Fornasiero, P. Università degli Studi di Trieste; ItaliaFil: Prato, Maurizio. Università degli Studi di Trieste; ItaliaRoyal Society of Chemistry2018-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/91195Melchionna, Michele; Bracamonte, Maria Victoria; Giuliani, Angela; Nasi, Lucia; Montini, Tiziano; et al.; Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid; Royal Society of Chemistry; Energy & Environmental Science; 11; 6; 6-2018; 1571-15801754-56921754-5706CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2018/EE/C7EE03361Cinfo:eu-repo/semantics/altIdentifier/doi/10.1039/C7EE03361Cinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:54:33Zoai:ri.conicet.gov.ar:11336/91195instacron: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:34982025-09-29 09:54:33.431CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid
title Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid
spellingShingle Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid
Melchionna, Michele
PD NANOPARTICLES
CARBON NANOHORNS
CO2 REDUCTION
title_short Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid
title_full Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid
title_fullStr Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid
title_full_unstemmed Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid
title_sort Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid
dc.creator.none.fl_str_mv Melchionna, Michele
Bracamonte, Maria Victoria
Giuliani, Angela
Nasi, Lucia
Montini, Tiziano
Tavagnacco, Claudio
Bonchio, Marcella
Fornasiero, P
Prato, Maurizio
author Melchionna, Michele
author_facet Melchionna, Michele
Bracamonte, Maria Victoria
Giuliani, Angela
Nasi, Lucia
Montini, Tiziano
Tavagnacco, Claudio
Bonchio, Marcella
Fornasiero, P
Prato, Maurizio
author_role author
author2 Bracamonte, Maria Victoria
Giuliani, Angela
Nasi, Lucia
Montini, Tiziano
Tavagnacco, Claudio
Bonchio, Marcella
Fornasiero, P
Prato, Maurizio
author2_role author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv PD NANOPARTICLES
CARBON NANOHORNS
CO2 REDUCTION
topic PD NANOPARTICLES
CARBON NANOHORNS
CO2 REDUCTION
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Direct conversion of carbon dioxide to formic acid at thermodynamic equilibrium is an advantage of enzymatic catalysis, hardly replicated by synthetic analogs, but of high priority for carbon-neutral energy schemes. The bio-mimetic potential of totally inorganic Pd@TiO2 nanoparticles is envisioned herein in combination with Single Walled Carbon NanoHorns (SWCNHs). The high surface nano-carbon entanglement templates a wide distribution of "hard-soft" bimetallic sites where the small Pd nanoparticles (1.5 nm) are shielded within the TiO2 phase (Pd@TiO2), while being electrically wired to the electrode by the nanocarbon support. This hybrid electrocatalyst activates CO2 reduction to formic acid at near zero overpotential in the aqueous phase (onset potential at E < -0.05 V vs. RHE, pH = 7.4), while being able to evolve hydrogen via sequential formic acid dehydrogenation. The net result hints at a unique CO2 "circular catalysis" where formic acid versus H2 selectivity is addressable by flow-reactor technology.
Fil: Melchionna, Michele. Università degli Studi di Trieste; Italia
Fil: Bracamonte, Maria Victoria. Università degli Studi di Trieste; Italia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina
Fil: Giuliani, Angela. Università degli Studi di Trieste; Italia
Fil: Nasi, Lucia. Istituto Dei Materiali Per L'elettronica Ed Il Magnetismo; Italia
Fil: Montini, Tiziano. Università degli Studi di Trieste; Italia
Fil: Tavagnacco, Claudio. Università degli Studi di Trieste; Italia
Fil: Bonchio, Marcella. Università di Padova; Italia
Fil: Fornasiero, P. Università degli Studi di Trieste; Italia
Fil: Prato, Maurizio. Università degli Studi di Trieste; Italia
description Direct conversion of carbon dioxide to formic acid at thermodynamic equilibrium is an advantage of enzymatic catalysis, hardly replicated by synthetic analogs, but of high priority for carbon-neutral energy schemes. The bio-mimetic potential of totally inorganic Pd@TiO2 nanoparticles is envisioned herein in combination with Single Walled Carbon NanoHorns (SWCNHs). The high surface nano-carbon entanglement templates a wide distribution of "hard-soft" bimetallic sites where the small Pd nanoparticles (1.5 nm) are shielded within the TiO2 phase (Pd@TiO2), while being electrically wired to the electrode by the nanocarbon support. This hybrid electrocatalyst activates CO2 reduction to formic acid at near zero overpotential in the aqueous phase (onset potential at E < -0.05 V vs. RHE, pH = 7.4), while being able to evolve hydrogen via sequential formic acid dehydrogenation. The net result hints at a unique CO2 "circular catalysis" where formic acid versus H2 selectivity is addressable by flow-reactor technology.
publishDate 2018
dc.date.none.fl_str_mv 2018-06
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/11336/91195
Melchionna, Michele; Bracamonte, Maria Victoria; Giuliani, Angela; Nasi, Lucia; Montini, Tiziano; et al.; Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid; Royal Society of Chemistry; Energy & Environmental Science; 11; 6; 6-2018; 1571-1580
1754-5692
1754-5706
CONICET Digital
CONICET
url http://hdl.handle.net/11336/91195
identifier_str_mv Melchionna, Michele; Bracamonte, Maria Victoria; Giuliani, Angela; Nasi, Lucia; Montini, Tiziano; et al.; Pd@TiO2/carbon nanohorn electrocatalysts: Reversible CO2 hydrogenation to formic acid; Royal Society of Chemistry; Energy & Environmental Science; 11; 6; 6-2018; 1571-1580
1754-5692
1754-5706
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2018/EE/C7EE03361C
info:eu-repo/semantics/altIdentifier/doi/10.1039/C7EE03361C
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
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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