We
study plasmonic control of photocatalytic properties of metal
oxides and the ways they influence interaction of quantum dots with
metallic nanostructures. For this, gold nanostructures are coated
with ultrathin layers of metal oxides (Al, Cu, Cr, or Ti oxide) and
then covered with CdSe/ZnS quantum dots. The results show how the
photocatalytic properties of such metal oxides are renormalized by
plasmon near fields. In the cases of Al, Cr, and Ti oxides, the results
mostly indicate the direct impact of plasmon fields via enhancement
of optical excitations of the quantum dots. For the case of Cu oxide,
however, the outcomes are found to be quite unique. In the absence
of the plasmonic structures, such an oxide (CuO) presents highly active
photocatalytic processes, leading to complete annihilation of the
quantum dot emission. In the presence of the metallic nanostructures,
the emission of such quantum dots is revived, offering an ultrafast
decay process (∼112 ps). These results indicate that in the
case of CuO, the plasmonic metal oxide-induced photocatalytic processes
include not only direct impact of plasmon near fields on the optical
excitations of quantum dots but also the enhancement of interband
transitions in CuO nanoparticles. The effects of energy transfer from
quantum dots to metallic nanostructures and its equalization with
Purcell effects on such processes are discussed.