Herein, a highly sensitive volatile organic compound
(VOC) gas
sensor is demonstrated using immobilized ionic liquid (IL), 1-butyl-3-methylimidazolium
hexafluorophosphate, onto surfaces functionalized by the quaternary
ammonium group −N+R, −COOH, and −NH2, i.e., N+–IL, COOH–IL,
and NH2–IL, respectively. These functional groups
ensure highly tunable interactions between the IL and surfaces, efficiently
modulating the electrical resistance of the immobilized IL upon exposure
to acetone and toluene. The immobilized IL to both acetone and toluene
displays significant electronic resistance changes at a concentration
of 150 ppm, falling in the order NH2–IL > N+–IL > COOH–IL for acetone while COOH–IL
> NH2–IL > N+–IL for toluene.
A better gaseous sensing ability is achieved in COOH–IL for
toluene than acetone, while this does not hold in the case of NH2–IL and N+–IL surfaces because of
the completely different ion structuring of the IL at these functionalized
surfaces. The accelerated ion mobility in the IL that is immobilized
onto functionalized surfaces is also responsible for the strong gaseous
sensing response, which is demonstrated further by the atomic force
microscopy-measured smaller friction coefficient. This is highly encouraging
and suggests that ILs can be immobilized by a network formed by surface
functionalization to easily and cheaply detect VOCs at ppm concentrations.