Using electrostatic self-assembly and electrostatic nanotemplating,
a quaternary nanostructured system consisting of zinc oxide nanoparticles,
gold nanoparticles, poly[3-(potassium-4-butanoate)thiophene-2,5-diyl]
(PT), and methyltrioctylammonium chloride (MTOA) (PT–MTOA–ZnO–Au)
was designed for aqueous photocatalysis. The PT–MTOA hollow
sphere aggregates served as an electrostatic template for both individual
inorganic nanoparticles controlling their morphology, stabilizing
the nanoparticles, and acting as a photosensitizer. The hybrid structures
included spherical ZnO nanoparticles with a diameter of d = 2.6 nm and spherical Au nanoparticles with d =
6.0 nm embedded in PT–MTOA hollow spheres with a hydrodynamic
radius of R
H = 100 nm. The ZnO nanoparticles
acted as the main catalyst, while the Au nanoparticles acted as the
cocatalyst. As a photocatalytic model reaction, the dye degradation
of methylene blue in aqueous solution using the full spectral range
from UV to visible light was tested. The photocatalytic activity was
optimized by varying the Zn and Au loading ratios and was substantially
enhanced regarding the components; for example, it was increased by
about 61% using PT–MTOA–ZnO–Au compared to the
composite without gold particles. A photocatalytic mechanism of the
methylene blue degradation was proposed when catalyzed by these multicomponent
nano-objects. Thus, a simple procedure of templating two different
nanoparticle species within the same cocatalytically active template
has been demonstrated, which can be extended to other inorganic particles,
making a variety of task-specific catalysts accessible.