Phase-transfer and size-dependent film formation of gold nanoparticles

Abstract

In this article, prefunctionalized polyoxometalate, γ-[SiW 10O 36(HSC 3H 6Si) 2O] 4−, {[POM(SH) 2] 4−} capped Au nanoparticles were synthesized successfully in N,N′-dimethylformamide (DMF). The thiol group of [POM(SH) 2] 4− provides a capping shell around Au nanoparticles. Zeta potential measurements showed that [POM(SH) 2] 4− coated nanoparticles were negatively charged in DMF. A novel method for transferring Au nanoparticles from DMF solution into non-polar organic solvent cyclohexane was developed. Charge neutralization using CTAB enables concentrating nanoparticle dispersion in cyclohexane which is a prerequisite for transfer and for successful three-dimensional self-assembly. The dispersed particles were stable for at least 45 days. After the phase-transfer, Au nanoparticles could be separated out from the cyclohexane phase in the form of a powder. The hydrophobic particles thus prepared are stable and are readily dispersed in solvent like toluene without further surface treatment. We also report extension of this wet-chemical method to make films by spontaneous assembly of passivated Au nanoparticles at the DMF/H 2O–cyclohexane liquid interface. The particle size information and collective self-assembling properties of the [POM(SH) 2] 4−/CTAB capped Au nanoparticles and film were evaluated by TEM, XRD and FTIR spectroscopy.