TY - JOUR
T1 - Ultrafast Interface Charge Separation in Carbon Nanodot-Nanotube Hybrids
AU - Buscarino, Gianpiero
AU - Agnello, Simonpietro
AU - Mauro, Nicolò
AU - Gelardi, Franco Mario
AU - Sciortino, Alice
AU - Duca, Dario
AU - Cannas, Marco
AU - Giammona, Gaetano
AU - Messina, Fabrizio
AU - Ferrante, Francesco
PY - 2021
Y1 - 2021
N2 - 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.
AB - 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.
KW - carbon nanodots
KW - carbon nanohybrids
KW - carbon nanotubes
KW - pump probe spectroscopy
KW - ultrafast electron transfer
KW - carbon nanodots
KW - carbon nanohybrids
KW - carbon nanotubes
KW - pump probe spectroscopy
KW - ultrafast electron transfer
UR - http://hdl.handle.net/10447/522368
M3 - Article
SN - 1944-8244
VL - 13
SP - 49232
EP - 49241
JO - ACS APPLIED MATERIALS & INTERFACES
JF - ACS APPLIED MATERIALS & INTERFACES
ER -