Ultrafast interface charge separation in carbon nanodot-nanotube hybrids

Detalhes bibliográficos
Autor(a) principal: Sciortino, Alice
Data de Publicação: 2021
Outros Autores: Ferrante, Francesco, Gonçalves, Gil, Tobias, Gerard, Popescu, Radian, Gerthsen, Dagmar, Mauro, Nicolò, Giammona, Gaetano, Buscarino, Gianpiero, Gelardi, Franco M., Agnello, Simonpietro, Cannas, Marco, Duca, Dario, Messina, Fabrizio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/32705
Resumo: Carbon dots are an emerging family of zero-dimensional nanocarbons behaving as tunable light harvesters and photoactivated charge donors. Coupling them to carbon nanotubes, which are well-known electron acceptors with excellent charge transport capabilities, is very promising for several applications. Here, we first devised a route to achieve the stable electrostatic binding of carbon dots to multi- or single-walled carbon nanotubes, as confirmed by several experimental observations. The photoluminescence of carbon dots is strongly quenched when they contact either semiconductive or conductive nanotubes, indicating a strong electronic coupling to both. Theoretical simulations predict a favorable energy level alignment within these complexes, suggesting a photoinduced electron transfer from dots to nanotubes, which is a process of high functional interest. Femtosecond transient absorption confirms indeed an ultrafast (<100 fs) electron transfer independent of nanotubes being conductive or semiconductive in nature, followed by a much slower back electron transfer (≈60 ps) from the nanotube to the carbon dots. The high degree of charge separation and delocalization achieved in these nanohybrids entails significant photocatalytic properties, as we demonstrate by the reduction of silver ions in solution. The results are very promising in view of using these "all-carbon" nanohybrids as efficient light harvesters for applications in artificial photocatalysis and photosynthesis.
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spelling Ultrafast interface charge separation in carbon nanodot-nanotube hybridsCarbon nanodotsCarbon nanotubesUltrafast electron transferPump probe spectroscopyCarbon dots are an emerging family of zero-dimensional nanocarbons behaving as tunable light harvesters and photoactivated charge donors. Coupling them to carbon nanotubes, which are well-known electron acceptors with excellent charge transport capabilities, is very promising for several applications. Here, we first devised a route to achieve the stable electrostatic binding of carbon dots to multi- or single-walled carbon nanotubes, as confirmed by several experimental observations. The photoluminescence of carbon dots is strongly quenched when they contact either semiconductive or conductive nanotubes, indicating a strong electronic coupling to both. Theoretical simulations predict a favorable energy level alignment within these complexes, suggesting a photoinduced electron transfer from dots to nanotubes, which is a process of high functional interest. Femtosecond transient absorption confirms indeed an ultrafast (<100 fs) electron transfer independent of nanotubes being conductive or semiconductive in nature, followed by a much slower back electron transfer (≈60 ps) from the nanotube to the carbon dots. The high degree of charge separation and delocalization achieved in these nanohybrids entails significant photocatalytic properties, as we demonstrate by the reduction of silver ions in solution. The results are very promising in view of using these "all-carbon" nanohybrids as efficient light harvesters for applications in artificial photocatalysis and photosynthesis.American Chemical Society2022-10-20T00:00:00Z2021-10-20T00:00:00Z2021-10-20info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/vnd.openxmlformats-officedocument.wordprocessingml.documenthttp://hdl.handle.net/10773/32705eng1944-824410.1021/acsami.1c16929Sciortino, AliceFerrante, FrancescoGonçalves, GilTobias, GerardPopescu, RadianGerthsen, DagmarMauro, NicolòGiammona, GaetanoBuscarino, GianpieroGelardi, Franco M.Agnello, SimonpietroCannas, MarcoDuca, DarioMessina, Fabrizioinfo:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T12:02:43Zoai:ria.ua.pt:10773/32705Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:04:10.788796Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Ultrafast interface charge separation in carbon nanodot-nanotube hybrids
title Ultrafast interface charge separation in carbon nanodot-nanotube hybrids
spellingShingle Ultrafast interface charge separation in carbon nanodot-nanotube hybrids
Sciortino, Alice
Carbon nanodots
Carbon nanotubes
Ultrafast electron transfer
Pump probe spectroscopy
title_short Ultrafast interface charge separation in carbon nanodot-nanotube hybrids
title_full Ultrafast interface charge separation in carbon nanodot-nanotube hybrids
title_fullStr Ultrafast interface charge separation in carbon nanodot-nanotube hybrids
title_full_unstemmed Ultrafast interface charge separation in carbon nanodot-nanotube hybrids
title_sort Ultrafast interface charge separation in carbon nanodot-nanotube hybrids
author Sciortino, Alice
author_facet Sciortino, Alice
Ferrante, Francesco
Gonçalves, Gil
Tobias, Gerard
Popescu, Radian
Gerthsen, Dagmar
Mauro, Nicolò
Giammona, Gaetano
Buscarino, Gianpiero
Gelardi, Franco M.
Agnello, Simonpietro
Cannas, Marco
Duca, Dario
Messina, Fabrizio
author_role author
author2 Ferrante, Francesco
Gonçalves, Gil
Tobias, Gerard
Popescu, Radian
Gerthsen, Dagmar
Mauro, Nicolò
Giammona, Gaetano
Buscarino, Gianpiero
Gelardi, Franco M.
Agnello, Simonpietro
Cannas, Marco
Duca, Dario
Messina, Fabrizio
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Sciortino, Alice
Ferrante, Francesco
Gonçalves, Gil
Tobias, Gerard
Popescu, Radian
Gerthsen, Dagmar
Mauro, Nicolò
Giammona, Gaetano
Buscarino, Gianpiero
Gelardi, Franco M.
Agnello, Simonpietro
Cannas, Marco
Duca, Dario
Messina, Fabrizio
dc.subject.por.fl_str_mv Carbon nanodots
Carbon nanotubes
Ultrafast electron transfer
Pump probe spectroscopy
topic Carbon nanodots
Carbon nanotubes
Ultrafast electron transfer
Pump probe spectroscopy
description Carbon dots are an emerging family of zero-dimensional nanocarbons behaving as tunable light harvesters and photoactivated charge donors. Coupling them to carbon nanotubes, which are well-known electron acceptors with excellent charge transport capabilities, is very promising for several applications. Here, we first devised a route to achieve the stable electrostatic binding of carbon dots to multi- or single-walled carbon nanotubes, as confirmed by several experimental observations. The photoluminescence of carbon dots is strongly quenched when they contact either semiconductive or conductive nanotubes, indicating a strong electronic coupling to both. Theoretical simulations predict a favorable energy level alignment within these complexes, suggesting a photoinduced electron transfer from dots to nanotubes, which is a process of high functional interest. Femtosecond transient absorption confirms indeed an ultrafast (<100 fs) electron transfer independent of nanotubes being conductive or semiconductive in nature, followed by a much slower back electron transfer (≈60 ps) from the nanotube to the carbon dots. The high degree of charge separation and delocalization achieved in these nanohybrids entails significant photocatalytic properties, as we demonstrate by the reduction of silver ions in solution. The results are very promising in view of using these "all-carbon" nanohybrids as efficient light harvesters for applications in artificial photocatalysis and photosynthesis.
publishDate 2021
dc.date.none.fl_str_mv 2021-10-20T00:00:00Z
2021-10-20
2022-10-20T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/32705
url http://hdl.handle.net/10773/32705
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1944-8244
10.1021/acsami.1c16929
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dc.format.none.fl_str_mv application/vnd.openxmlformats-officedocument.wordprocessingml.document
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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