Layered two-dimensional
transition metal dichalcogenides, due to
their semiconducting nature and large surface-to-volume ratio, have
created their own niche in the field of gas sensing. Their large recovery
time and accompanied incomplete recovery result in inferior sensing
properties. Here, we report a composite-based strategy to overcome
these issues. In this study, we report a facile double-step synthesis
of a MoS
2
/SnO
2
composite and its successful
use as a superior room-temperature ammonia sensor. Contrary to the
pristine nanosheet-based sensors, the devices made using the composite
display superior gas sensing characteristics with faster response.
Specifically, at room temperature (30° C), the composite-based
sensor exhibited excellent sensitivity (10%) at an ammonia concentration
down to 0.4 ppm along with the response and recovery times of 2 and
10 s, respectively. Moreover, the device also exhibited long-term
durability, reproducibility, and selectivity toward ammonia against
hydrogen sulfide, methanol, ethanol, benzene, acetone, and formaldehyde.
Sensor devices made on quartz and alumina substrates with different
roughnesses have yielded almost an identical response, except for
slight variations in response and recovery transients. Further, to
shed light on the underlying adsorption energetics and selectivity,
density functional theory simulations were employed. The improved
response and enhanced selectivity of the composite were explicitly
discussed in terms of adsorption energy. Lowdin charge analysis was
performed to understand the charge transfer mechanism between NH
3
, H
2
S, CH
3
OH, HCHO, and the underlying
MoS
2
/SnO
2
composite surface. The long-term durability
of the sensor was evident from the stable response curves even after
2 months. These results indicate that hydrothermally synthesized MoS
2
/SnO
2
composite-based gas sensors can be used as
a promising sensing material for monitoring ammonia gas in real fields.