A p-type Si(111)/n-TiO2(110) heterojunction photodetector
device has been fabricated for broad spectral range detection. An
environmentally friendly NaCl assisted hydrothermal route was employed
for synthesizing an n-type TiO2(110) hierarchical nanostructure
powder. A 1 μm thick film of TiO2 was then deposited
by spin coating on the top of p-type Si(111). The role of NaCl in
tuning both anionic (oxygen vacancy) and cationic (Ti mono- and divacancy,
Ti interstitials) defects has been investigated. The vacancies posed
a significant effect on photoresponse and junction characteristics
of the device, viz., dark current, barrier height, photosensitivity,
detectivity, and photoresponse gain. The TiO2 n-type layer
fabricated at higher NaCl concentrations has been found to exhibit
maximum responsivity of ∼550 A/W, gain of ∼2.00, specific
detectivity of ∼1.27 × 1011 Jones, and fast
response and recovery times of 38 and 43 ms, respectively. The device
has been highly repeatable (for 12 cycles) with a stability of 60
days. These have been ascribed to the exciton, formed at the bridged
oxygen adjacent to the Ti vacancy at the (110) surface. We have also
resolved that the charge carrier–phonon interaction facilitates
exciton stabilization, while the charge transfer across the interface
follows the adiabatic process. To explain the variation of device
performance with defects, a mathematical model has been proposed to
correlate the device responsivity to the different vacancies.