Affiliation:
1. Flinders Institute for Nanoscale Science and Technology College of Science and Engineering Flinders University Adelaide SA 5042 Australia
2. School of Environmental and Life Sciences The University of Newcastle Callaghan NSW 2308 Australia
3. Physics Department, Faculty of Science Taibah University Almadinah Almunawarrah 42353 Saudi Arabia
Abstract
Controlling the size and morphology of gold nanoparticles occurs in the absence of added reducing agents or other excipients such as surfactants, on UV irradiation (λ 254 nm) of aqueous auric acid (H[AuCl4]) in a thin film of liquid in a vortex fluidic device (VFD) within a rapidly rotating tilted quartz tube. This involves contact electrification (CE), which occurs at the solid−liquid interface with the oxidation of water photoinduced, forming the hydroxyl radical, OH•. In air, the redox couple is reduction of 3O2 to the superoxide radical anion, O2−•, which then reduces Au3+ to elemental gold, as does other reactive oxygen species present, competing with CE reduction of Au3+. The resulting nanogold structures effectively mold the different high‐shear topological fluid flows in the VFD, being isolated as ultrathin 2D sheets, prisms, hierarchical structures comprising nanoparticles embedded within these sheets, and rosette and tubular structures, depending on the VFD processing parameters and the concentration of auric acid. Processing under a nitrogen atmosphere while UV irradiated affords mainly 2D gold through the above reduction of Au3+. The findings establish a paradigm for VFD processing in water involving photo‐CE, generating hydrogen peroxide and hydrogen gas with the surfaces of the gold nanoparticles pristine.
Funder
Australian Research Council