We report a detailed study on the optical properties of Au279(SR)84 using steady-state and transient absorption measurements to probe its metallic nature, timedependent density functional theory (TDDFT) studies to correlate the optical spectra, and density of states (DOS) to reveal the factors governing the origin of the collective surface plasmon resonance (SPR) oscillation. Au279 is the smallest identified gold nanocrystal to exhibit SPR. Its optical absorption exhibits SPR at 510 nm. Powerdependent bleach recovery kinetics of Au279 suggests that electron dynamics dominates its relaxation and it can support plasmon oscillations. Interestingly, TDDFT and DOS studies with different tail group residues (−CH3 and −Ph) revealed the important role played by the tail groups of ligands in collective oscillation. Also, steady-state and timeresolved absorption for Au36, Au44, and Au133 were studied to reveal the molecule-to-metal evolution of aromatic AuNMs. The optical gap and transient decay lifetimes decrease as the size increases.

Au279(SR)84: The Smallest Gold Thiolate Nanocrystal That Is Metallic and the Birth of Plasmon

Stener, Mauro
Membro del Collaboration Group
;
Fortunelli, Alessandro
Membro del Collaboration Group
;
2018-01-01

Abstract

We report a detailed study on the optical properties of Au279(SR)84 using steady-state and transient absorption measurements to probe its metallic nature, timedependent density functional theory (TDDFT) studies to correlate the optical spectra, and density of states (DOS) to reveal the factors governing the origin of the collective surface plasmon resonance (SPR) oscillation. Au279 is the smallest identified gold nanocrystal to exhibit SPR. Its optical absorption exhibits SPR at 510 nm. Powerdependent bleach recovery kinetics of Au279 suggests that electron dynamics dominates its relaxation and it can support plasmon oscillations. Interestingly, TDDFT and DOS studies with different tail group residues (−CH3 and −Ph) revealed the important role played by the tail groups of ligands in collective oscillation. Also, steady-state and timeresolved absorption for Au36, Au44, and Au133 were studied to reveal the molecule-to-metal evolution of aromatic AuNMs. The optical gap and transient decay lifetimes decrease as the size increases.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11368/2938836
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