Plasma-assisted catalysis represents
an alternative solution to
pollution abatement. To be viable, a thorough understanding of plasma–catalyst
synergisms must be gained, specifically establishing links between
the gas-phase, gas–surface interface, and resulting material
properties. Optical emission spectroscopy provides insights into the
impact of Pt and zeolite catalysts on plasma species densities, energetics,
reaction kinetics, and plasma–catalyst configurations within
N2O plasmas. The role of material structure on gas-phase
chemistry is revealed through the use of Pt catalysts with two morphologies
and size scaling. The concentration of excited-state NO substantially
decreased at high powers with Pt nanopowder or microstructured zeolites.
All catalytic materials significantly decreased N2 vibrational
temperatures, with little impact on rotational temperatures. Conversely,
Pt materials had a limited effect on vibrational temperatures of NO;
however, Pt powder enhanced NO decomposition within a two-stage system
over the single-stage system. Material characterization revealed that
the plasma effectively poisons Pt materials, resulting in poorer performance.