Noble-metal-decorated
metal oxide sensors have shown promising
gas-sensing properties. However, the optimal dispersion of metal particles
on a semiconductor is still challenging for most sensing materials.
In this study, Co3O4 nanocubes (NCs) and Pt-supported
Co3O4 NCs were prepared as sensing materials
for acetone gas detection. Transmission electron microscopy and X-ray
diffraction were used to examine the structure and exposed facets
of Co3O4 NCs. As a result, the Co3O4 NCs were identified as the single-crystalline phase
of spinel Co3O4, and each surface exposed the
{100} plane. To examine the cocatalytic effect of Pt combined with
Co3O4 NCs on the sensing performance, Pt nanoparticles
were photodeposited on Co3O4 (Pt–Co3O4 NCs). The Pt–Co3O4 NC-based sensor provided a higher p-type response than the Co3O4 NC sensor in the detection of 500 ppb acetone
at 200 °C, with the highest response of 3.1 (R
g/R
a). The enhanced performance
of the Pt–Co3O4 NCs is caused by the
exposed {100} planes of Co3O4, in addition to
the loaded Pt nanoparticles. The sensor with Co3O4 NCs has a larger neck diameter and hole accumulation layer at the
interface than that with Co3O4 nanospheres and
thus provides a wide channel for charge carriers, resulting in better
gas-sensing responses and high selectivity toward acetone over other
volatile compounds. Moreover, the Pt nanoparticles stimulate O2 dissociation on the Co3O4 surface,
thus increasing the concentration of chemisorbed oxygen species by
the spillover effect. Thus, the incorporation of Pt with Co3O4 NCs promotes the sensitivity of the material in the
detection of acetone gas and also enhances the selectivity. This study
highlights the possibility of the rapid deposition of metal nanoparticles
for the improvement of gas sensors.