Owing to their excellent
hydrogen surface susceptibility, TiO2 thin films have been
proven worthy of sensing hydrogen. However,
these sensors work best at temperatures of 150–400 °C,
with poor selectivity and a low response at room temperature. In this
context, the novelty of this paper includes an investigation of the
critical role of electrode fabrication that is found to significantly
define the surface as well as the performance of a sensor. Sensors
prepared with optimized conditions showed the best sensor response
(S
R) of ∼1.58 × 107 toward
10 000 ppm H2 with excellent linearity (R-square ∼ 0.98 for 300–10 000 ppm)
at room temperature (∼20 °C). In addition, the said sensor
showed a response time of ∼125 s with full baseline recovery
and a selectivity factors (S
F) of ∼1754,
2456, and 4723 to 1000 ppm of interfering reducing gases CH4, CO, and NH3, respectively, at 100 °C. At room temperature,
the selectivity factor (for 300 ppm H2) of the sensor is
∼3.41 to 90% RH and ∼37.35 to 250 ppm oxygen, 200 ppm
CO, and 1600 ppm CO2. Last but not least, our X-ray diffraction,
X-ray photoelectron spectroscopy, and electrical transport characteristics
enabled us to explain the high sensing mechanism on the basis of the
estimated grain size, the quantitative atomic composition, the barrier
at the Pt/TiO2 interface, and the thermal activation energy
(also known as the intergranular barrier height) of the thin films.