Ultrafast interface charge separation in carbon nanodot-nanotube hybrids
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , , , , |
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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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 |
format |
article |
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 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/embargoedAccess |
eu_rights_str_mv |
embargoedAccess |
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 instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
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 |
repository.mail.fl_str_mv |
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1799137697312276480 |