The mechanism of the Brust–Schiffrin gold nanoparticle synthesis has been investigated through the use of ion transfer voltammetry at the water/1,2-dichloroethane (DCE) solution interface, combined with X-ray absorption fine structure (XAFS) of the reaction between [AuCl4]− and thiol (RSH) in homogeneous toluene (TL) solution. Ion transfer calculations indicate the formation of [AuCl2]− at RSH/Au ratios from 0.2–2 with a time-dependent variation observed over several days. At RSH/Au ratios above 2 and after time periods greater than 24 h, the formation of Au(I)SR is also observed. The relative concentrations of reaction products observed at the liquid/liquid interface are in excellent agreement with those observed by XAFS for the corresponding reaction in a single homogeneous phase. BH4– ion transfer reactions between water and DCE indicate that the reduction of [AuCl4]− or [AuCl2]− to Au nanoparticles by BH4– proceeds in the bulk organic phase. On the other hand, BH4– was unable to reduce the insoluble [Au(I)SR]n species to Au nanoparticles. The number and size of the nanoparticles formed was dependent on the concentration ratio of RSH/Au, as well as the experimental duration because of the competing formation of the [Au(I)SR]n precipitate. Higher concentrations of nanoparticles, with diameters of 1.0–1.5 nm, were formed at RSH/Au ratios from 1 to 2.
CORE (COnnecting REpositories)
CORE (COnnecting REpositories)