Photochemical reduction of aqueous
Ag+ and [AuCl4]− into alloy
Au–Ag nanoparticles
(Au–Ag NPs) with intense laser pulses is a green synthesis
approach that requires no toxic chemical reducing agents or stabilizers;
however size control without capping agents still remains a challenge.
Hydrated electrons produced in the laser plasma can reduce both [AuCl4]− and Ag+ to form NPs, but hydroxyl
radicals (OH·) in the plasma inhibit Ag NP formation by promoting
the back-oxidation of Ag0 into Ag+. In this
work, femtosecond laser reduction is used to synthesize Au–Ag
NPs with controlled compositions by adding the OH· scavenger
isopropyl alcohol (IPA) to precursor solutions containing KAuCl4 and AgClO4. With sufficient IPA concentration,
varying the precursor ratio enabled control over the Au–Ag
NP composition and produced alloy NPs with average sizes less than
10 nm and homogeneous molar compositions of Au and Ag. By investigating
the kinetics of Ag+ and [AuCl4]− coreduction, we find that the reduction of [AuCl4]− into Au–Ag NPs occurs before most of the Ag+ is incorporated, giving us insight into the mechanism of
Au–Ag NP formation.