Issue 9, 2016

Excited state nonadiabatic dynamics of bare and hydrated anionic gold clusters Au3[H2O]n (n = 0–2)

Abstract

We present a joint theoretical and experimental study of excited state dynamics in pure and hydrated anionic gold clusters Au3[H2O]n (n = 0–2). We employ mixed quantum-classical dynamics combined with femtosecond time-resolved photoelectron spectroscopy in order to investigate the influence of hydration on excited state lifetimes and photo-dissociation dynamics. A gradual decrease of the excited state lifetime with the number of adsorbed water molecules as well as gold cluster fragmentation quenching by two or more water molecules are observed both in experiment and in simulations. Non-radiative relaxation and dissociation in excited states are found to be responsible for the excited state population depletion. Time constants of these two processes strongly depend on the number of water molecules leading to the possibility to modulate excited state dynamics and fragmentation of the anionic cluster by adsorption of water molecules.

Graphical abstract: Excited state nonadiabatic dynamics of bare and hydrated anionic gold clusters Au3−[H2O]n (n = 0–2)

Article information

Article type
Paper
Submitted
22 Jul 2015
Accepted
07 Oct 2015
First published
08 Oct 2015

Phys. Chem. Chem. Phys., 2016,18, 6411-6419

Author version available

Excited state nonadiabatic dynamics of bare and hydrated anionic gold clusters Au3[H2O]n (n = 0–2)

P. G. Lisinetskaya, C. Braun, S. Proch, Y. D. Kim, G. Ganteför and R. Mitrić, Phys. Chem. Chem. Phys., 2016, 18, 6411 DOI: 10.1039/C5CP04297F

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