Selectivity in Ligand Functionalization of Photocatalytic Metal Oxide Nanoparticles for Phase Transfer and Self-assembly Applications

Abstract

Functionalization of photocatalytic metal oxide nanoparticles of TiO2, ZnO, WO3 and CuO with amine-terminated (oleylamine) and thiol-terminated (1-dodecanethiol) alkyl chained ligands was studied under ambient conditions. A high selectivity was observed in the binding specificity of a ligand towards nanoparticles of these different oxides. It was observed that oleylamine binds stably to only TiO2 and WO3, while 1-dodecanethiol binds stably only to ZnO and CuO. Similarly, polar to non-polar solvent phase transfer of TiO2 and WO3 nanoparticles could be achieved by using oleylamine, but not by 1-dodecanethiol, while the contrary holds for ZnO and CuO. The surface chemistry of ligand functionalized nanoparticles was probed by ATR-FTIR spectroscopy, that enabled to elucidate the occupation of the ligands at the active sites. The photo-stability of the ligands on the nanoparticle surface was determined by the photocatalytic self-cleaning properties of the material. While TiO2 and WO3 degrade the ligands within 24 hours under both UV and visible light, ligands on ZnO and CuO remain unaffected. The gathered insights are also highly relevant from an application point of view. As an example, since the ligand functionalized nanoparticles are hydrophobic in nature, they can thus be self-assembled at the air-water interface, for obtaining nanoparticle films with demonstrated photocatalytic as well as anti-fogging properties.