Disentangling the respective roles of the surface and core structures in the photocycle of carbon nanodots is a critical open problem in carbon nanoscience. While the need of passivating carbon dot surfaces to obtain efficiently emitting nanoparticles is very well-known in the literature, it is unclear if passivation introduces entirely new surface emitting states, or if it stabilizes existing states making them fluorescent. In this multi-technique femtosecond spectroscopy study, the relaxation dynamics of non-luminescent (non-passivated) carbon dots are directly compared with their luminescent (passivated) counterparts. Non-passivated dots are found to host emissive states, albeit very short-lived and practically incapable of steady-state fluorescence. In contrast, the passivation procedure gives birth to a distinctive new manifold of emitting states, localized on the surface of the dots, and capable of intense, tunable, long-lived fluorescence. It turns out that these surface states are instantaneously populated by photo-excitation, and their subsequent dynamics are entirely independent of core electronic transitions. The experiments reveal the lack of any crosstalk between core- and surface states, at least for certain common types of carbon dots, and open a new perspective on the mechanisms by which surface passivation governs the fluorescence properties of these nanoparticles.

Sciortino A., Gazzetto M., Soriano M.L., Cannas M., Cardenas S., Cannizzo A., et al. (2019). Ultrafast spectroscopic investigation on fluorescent carbon nanodots: the role of passivation. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 21(30), 16459-16467 [10.1039/c9cp03063h].

Ultrafast spectroscopic investigation on fluorescent carbon nanodots: the role of passivation

Sciortino A.;Cannas M.;Messina F.
2019-08-14

Abstract

Disentangling the respective roles of the surface and core structures in the photocycle of carbon nanodots is a critical open problem in carbon nanoscience. While the need of passivating carbon dot surfaces to obtain efficiently emitting nanoparticles is very well-known in the literature, it is unclear if passivation introduces entirely new surface emitting states, or if it stabilizes existing states making them fluorescent. In this multi-technique femtosecond spectroscopy study, the relaxation dynamics of non-luminescent (non-passivated) carbon dots are directly compared with their luminescent (passivated) counterparts. Non-passivated dots are found to host emissive states, albeit very short-lived and practically incapable of steady-state fluorescence. In contrast, the passivation procedure gives birth to a distinctive new manifold of emitting states, localized on the surface of the dots, and capable of intense, tunable, long-lived fluorescence. It turns out that these surface states are instantaneously populated by photo-excitation, and their subsequent dynamics are entirely independent of core electronic transitions. The experiments reveal the lack of any crosstalk between core- and surface states, at least for certain common types of carbon dots, and open a new perspective on the mechanisms by which surface passivation governs the fluorescence properties of these nanoparticles.
14-ago-2019
Sciortino A., Gazzetto M., Soriano M.L., Cannas M., Cardenas S., Cannizzo A., et al. (2019). Ultrafast spectroscopic investigation on fluorescent carbon nanodots: the role of passivation. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 21(30), 16459-16467 [10.1039/c9cp03063h].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/368067
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