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Ultrafast Interface Charge Separation in Carbon Nanodot–Nanotube Hybrids

[Image: see text] 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 s...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8532113/
https://www.ncbi.nlm.nih.gov/pubmed/34609127
http://dx.doi.org/10.1021/acsami.1c16929
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author 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_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_sort Sciortino, Alice
collection PubMed
description [Image: see text] 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 pubmed-85321132021-10-22 Ultrafast Interface Charge Separation in Carbon Nanodot–Nanotube Hybrids 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 ACS Appl Mater Interfaces [Image: see text] 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. American Chemical Society 2021-10-05 2021-10-20 /pmc/articles/PMC8532113/ /pubmed/34609127 http://dx.doi.org/10.1021/acsami.1c16929 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle 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
Ultrafast Interface Charge Separation in Carbon Nanodot–Nanotube Hybrids
title 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_short Ultrafast Interface Charge Separation in Carbon Nanodot–Nanotube Hybrids
title_sort ultrafast interface charge separation in carbon nanodot–nanotube hybrids
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8532113/
https://www.ncbi.nlm.nih.gov/pubmed/34609127
http://dx.doi.org/10.1021/acsami.1c16929
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