The development of mobile, noninvasive, and portable
sensor technologies
for diagnostics and emission control is highly demanded. For that
purpose, laser carbonization is studied as a tool to produce responsive
carbon materials from inexpensive organic precursors for the room-temperature
selective detection of volatile organic compounds (VOCs) applicable
in future sensor array-based devices. To increase the response of
intrinsically low-responsive laser-patterned carbons (LP-C) to analytes
in the gas phase, we tested carbonization in the presence of nanoscale
ZnO precursors in primary inks. Following the addition of a zinc salt,
Zn(NO3)2, a noticeable 43-fold increase in the
sensor response (ΔR/R
0 = −21.5% toward 2.5% acetone) was achieved. This effect
is explained by a significant increase in the measurable surface area
up to ∼700 m2·g–1 due to
the carbothermic reduction supported by the in situ formation of ZnO
nanoparticles. Varying Zn concentrations or the addition of as-prepared
ZnO nanorods lead to different surface properties like the surface
area, porosity, and polarity of LP-C. A predominant effect of the
surface polarity on the selectivity toward different analytes of the
sensors during physisorption, e.g., acetone vs toluene, was identified
and tested. The best-performing LP-C sensors were finely characterized
by transmission/scanning electron microscopies and X-ray photoelectron/energy-dispersive
X-ray/Raman spectroscopies.