We
demonstrate experimental evidence of the effect of surface plasmon
resonance of noble metal nanoparticles (NPs) on the activity of a
well-known biomedicinal drug in the proximity of a semiconductor having
a wide band gap for enhanced photodynamic therapy (PDT) efficacy.
We have chosen riboflavin (Rf) (or vitamin B2) as a model
photosensitizer, attached with ZnO NPs and further attached with gold
(Au) NP-decorated ZnO to increase the efficiency. The synthesized
nanohybrids are characterized with the help of different microscopic,
optical spectroscopic, and density functional theory (DFT)-based techniques.
The DFT and time-dependent DFT-based calculations validate the experimental
findings. A detailed ultrafast spectroscopic study has been carried
out further to study the excited-state charge dynamics in the interface
of the nanohybrids. The occurrence of a Förster resonance energy
transfer (FRET) between Rf and Au has been found to be the key reason
for the increased efficiency in the Rf–ZnO–Au nanohybrid
over the Rf–ZnO one. The dipolar coupling between Au and Rf
in the Rf–ZnO–Au nanohybrid further facilitates the
generation of reactive oxygen species (ROS) in comparison to Rf–ZnO
under blue-light irradiation. The greater efficiency in ROS generation
by the Rf–ZnO–Au nanohybrid has been utilized for antimicrobial
action against methicillin-resistant S. aureus (MRSA). Overall, the present study highlights the dual sensitization
for achieving enhanced electron injection efficiency in the Rf–ZnO–Au
nanohybrid in order to use it as an antibacterial agent that could
be translated in PDT.