The
improvement of the solar efficiency of photocatalytic materials
is important for solar driven environmental remediation and solar
energy harvesting applications. Photoelectrochemical characterization
of nitrogen and fluorine codoped titanium dioxide (N,F-TiO2) was used to probe the mechanism of visible light activity. The
spectral photocurrent response under visible irradiation did not correlate
with the optical absorption spectrum of the N,F-TiO2; however,
open-circuit photopotential measurements provided better correlation
to the optical absorption spectra. These observations suggest that
electrons excited to the conduction band from the N-induced midgap
state are rapidly trapped by defect levels below the conduction band.
Reactive oxygen species (ROS) can be produced via the reduction of
molecular oxygen by conduction band electrons leading to the oxidative
degradation of organic pollutants, and singlet oxygen may play a role.
If there is no loss in the band gap activity, as compared to undoped
titania, then any additional visible light activity may give an overall
improvement in the solar efficiency. The photocurrent response should
not be used as a direct measure of photocatalytic activity for doped
titania as the oxygen reduction pathway is vitally important for the
generation of ROS, whereas hole transfer from dopant midgap states
may not be so critical.
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