CO and byproduct formation during CO2 reduction in dielectric barrier discharges

• Published in: Journal of applied physics 2014-09, Vol.116 (12)
• Main Authors: Brehmer, F., Welzel, S., van de Sanden, M. C. M., Engeln, R.
• Format: Article
• Language: English
• Subjects: ABSORPTION SPECTROSCOPY; Applied physics; Atomic oxygen; CARBON DIOXIDE; CARBON MONOXIDE; Charge transfer; CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY; Dielectric barrier discharge; DIELECTRIC MATERIALS; DIFFUSION BARRIERS; DISSOCIATION; ENERGY EFFICIENCY; Energy of dissociation; EV RANGE; Gas temperature; Infrared absorption; Infrared cameras; MIXING RATIO; MOLECULES; OXYGEN; PLASMA; Plasmas (physics); Reaction mechanisms; RECOMBINATION; REDUCTION; STOICHIOMETRY; SURFACES; Temperature; TEMPERATURE DEPENDENCE; Wall temperature
• ISSN: 0021-8979; 1089-7550
• DOI: 10.1063/1.4896132

The dissociation of CO2 and the formation of CO, O3, and O2 were studied in a dielectric barrier discharge (DBD) at atmospheric pressure by means of ex-situ infrared absorption spectroscopy. CO mixing ratios of 0.1%–4.4% were determined for specific injected energies between 0.1 and 20 eV per molecule (0.3–70 kJ/l). A lower limit of the gas temperature of 320–480 K was estimated from the wall temperature of the quartz reactor as measured with an infrared camera. The formation of CO in the DBD could be described as function of the total number of transferred charges during the residence time of the gas in the active plasma zone. An almost stoichiometric CO:O2 ratio of 2:1 was observed along with a strongly temperature dependent O3 production up to 0.075%. Although the ideal range for an efficient CO2 dissociation in plasmas of 1 eV per molecule for the specific injected energy was covered, the energy efficiency remained below 5% for all conditions. The present results indicate a reaction mechanism which is initiated by electron impact processes followed by charge transfer reactions and non-negligible surface enhanced O and CO recombination. While electron-driven CO2 dissociation is relatively energy inefficient by itself, fast O recombination and the low gas temperatures inhibit the synergistic reuse of atomic oxygen in a secondary CO2 + O dissociation step.