Abstract
Abstract Gold nanoparticle formation was found from tetrachloroaurate(III) in the presence of Good’s Buffers, such as 2-morpholinoethanesulfonic acid (MES) and 2-[4-(2-hydroxyethyl)-1-piperazinyl]ethanesulfonic acid (HEPES), which are used widely in laboratories for studies of analytical, inorganic, physical, and bio-chemistry as well as biology. The obtained gold nanoparticles were examined by Ultraviolet–Visible Spectroscopy (UV–vis), Dynamic Light Scattering (DLS) and Electrophoretic Light Scattering (ELS) in an aqueous system and by transmission electron microscopy (TEM) for particle morphologies. UV–vis spectra showed absorption maxima at ∼530 and ∼750 nm, depending on the buffer reagents and their concentration, pH, and ionic strength. The size and the surface zeta potential of the formed nanoparticles were 23 to 73 nm and −30 to −12 mV, respectively. The TEM pictures clearly indicated the formation of finely dispersed, chained, or aggregated gold nanoparticles, depending on the experimental conditions. The mechanism of gold nanoparticle formation was studied by the measurements of cyclic voltammetry (CV) and electron spin resonance (ESR). MES and HEPES showed a positive anodic peak at approximately +800 mV vs Ag/AgCl electrode, which indicated that these buffering agents have mild reducing ability. ESR results indicated the generation of nitrogen-centered cationic free radicals from these Good’s Buffers in the presence of Au(III), resulting in the formation of gold nanoparticles. A reaction mechanism is proposed.
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