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Issue 45, 2018
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Nucleation and growth of gold nanoparticles initiated by nanosecond and femtosecond laser irradiation of aqueous [AuCl4]

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Abstract

Irradiation of aqueous [AuCl4] with 532 nm nanosecond (ns) laser pulses produces monodisperse (PDI = 0.04) 5 nm Au nanoparticles (AuNPs) without any additives or capping agents via a plasmon-enhanced photothermal autocatalytic mechanism. Compared with 800 nm femtosecond (fs) laser pulses, the AuNP growth kinetics under ns laser irradiation follow the same autocatalytic rate law, but with a significantly lower sensitivity to laser pulse energy. The results are explained using a simple model for simulating heat transfer in liquid water and at the interface with AuNPs. While the extent of water superheating with the ns laser is smaller compared to the fs laser, its significantly longer duration can provide sufficient energy to dissociate a small fraction of the [AuCl4] present, resulting in the formation of AuNPs by coalescence of the resulting Au atoms. Irradiation of initially formed AuNPs at 532 nm results in plasmon-enhanced superheating of water, which greatly accelerates the rate of thermal dissociation of [AuCl4] and accounts for the observed autocatalytic kinetics. The plasmon-enhanced heating under ns laser irradiation fragments the AuNPs and results in nearly uniform 5 nm particles, while the lack of particles' heating under fs laser irradiation results in the growth of the particles as large as 40 nm.

Graphical abstract: Nucleation and growth of gold nanoparticles initiated by nanosecond and femtosecond laser irradiation of aqueous [AuCl4]−

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Supplementary files

Article information


Submitted
19 Sep 2018
Accepted
01 Nov 2018
First published
02 Nov 2018

Phys. Chem. Chem. Phys., 2018,20, 28465-28475
Article type
Paper
Author version available

Nucleation and growth of gold nanoparticles initiated by nanosecond and femtosecond laser irradiation of aqueous [AuCl4]

C. J. Rodrigues, J. A. Bobb, M. G. John, S. P. Fisenko, M. S. El-Shall and K. M. Tibbetts, Phys. Chem. Chem. Phys., 2018, 20, 28465
DOI: 10.1039/C8CP05774E

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