This work explores the effect of O2 addition on CO2 dissociation and on the vibrational kinetics of CO2 and CO under various non-equilibrium plasma conditions. A self-consistent model, previously validated for pure CO2 discharges, is further extended by adding the vibrational kinetics of CO, including electron impact excitation and de-excitation (e-V), vibration-to-translation relaxation (V-T) and vibration-to-vibration energy exchange (V-V) processes. The vibrational kinetics considered include levels up to v = 10 for CO and up to v1 = 2 and v2 = v3 = 5, respectively for the symmetric stretch, bending and asymmetric stretch modes of CO2, and accounts for e-V, V-T in collisions between CO, CO2 and O2 molecules and O atoms and V-V processes involving all possible transfers involving CO2 and CO molecules. The kinetic scheme is validated by comparing the model predictions with recent experimental data measured in a DC glow discharge, operating at pressures in the range 0.4 - 5 Torr (53.33 - 666.66 Pa). The experimental results show a lower vibrational temperature of the different modes of CO2 and a decreased dissociation fraction of CO2 when O2 is added to the plasma but an increase of the vibrational temperature of CO. On the one hand, the simulations suggest that the former effect is the result of the stronger V-T energy-transfer collisions with O atoms which leads to an increase of the relaxation of the CO2 vibrational modes; On the other hand, two main mechanisms contribute to the lower CO2 dissociation fraction with increased O2 content in the mixture: the back reaction, CO(a3Πr) + O2 → CO2 + O and the recombinative detachment O- + CO → e + CO2.

This work presents a reaction mechanism for oxygen plasmas, i.e. a set of reactions and corresponding rate coefficients that are validated against benchmark experiments. The kinetic scheme is validated in a DC glow discharge for gas pressures of 0.2–10 Torr and currents of 10–40 mA, using the 0D LisbOn KInetics (LoKI) simulation tool and available experimental data. The comparison comprises not only the densities of the main species in the discharge - O2(X3Σ− g), O2(a1Δg), O2(b1Σ+ g ) and O(3P) - but also the self-consistent calculation of the reduced electric field and the gas temperature. The main processes involved in the creation and destruction of these species are identified. Moreover, the results show that the oxygen atoms play a dominant role in gas heating, via recombination at the wall and quenching of O2(X3Σ− g, v) vibrations and O2 electronically-excited states. It is argued that the development and validation of kinetic schemes for plasma chemistry should adopt a paradigm based on the comparison against standard validation tests, as it is done in electron swarm validation of cross sections.

Vibrational excitation represents an efficient channel to drive the dissociation of CO2 in a non-thermal plasma. Its viability is investigated in low-pressure pulsed discharges, with the intention of selectively exciting the asymmetric stretching mode, leading to stepwise excitation up to the dissociation limit of the molecule. Gas heating is crucial for the attainability of this process, since the efficiency of vibration-translation relaxation strongly depends on temperature, creating a feedback mechanism that can ultimately thermalize the discharge. Indeed, recent experiments demonstrated that the timeframe of vibration-translation non-equilibrium is limited to a few milliseconds at ca. 6 mbar, and shrinks to the μs-scale at 100 mbar. With the aim of backtracking the origin of gas heating in pure CO2 plasma, we perform a kinetic study to describe the energy transfers under typical non-thermal plasma conditions. The validation of our kinetic scheme with pulsed glow discharge experiments enables to depict the gas heating dynamics. In particular, we pinpoint the role of vibration-vibration-translation relaxation in redistributing the energy from asymmetric to symmetric levels of CO2, and the importance of collisional quenching of CO2 electronic states in triggering the heating feedback mechanism in the sub-millisecond scale. This latter finding represents a novelty for the modelling of low-pressure pulsed discharges and we suggest that more attention should be paid to it in future studies. Additionally, O atoms convert vibrational energy into heat, speeding up the feedback loop. The efficiency of these heating pathways, even at relatively low gas temperature and pressure, underpins the lifetime of vibration-translation non-equilibrium and suggests a redefinition of the optimal conditions to exploit the “ladder-climbing” mechanism in CO2 discharges.

This work explores the effect of N2 addition on CO2 dissociation and on the vibrational kinetics of CO2 and CO under various non-equilibrium plasma conditions. A self-consistent kinetic model, previously validated for pure CO2 and CO2-O2 discharges, is further extended by adding the kinetics of N2. The vibrational kinetics considered include levels up to v = 10 for CO, v = 59 for N2 and up to v 1 = 2 and v 2 = v 3 = 5, respectively for the symmetric stretch, bending and asymmetric stretch modes of CO2, and account for electron-impact excitation and de-excitation (e-V), vibration-to-translation (V-T) and vibration-to-vibration energy exchange (V-V) processes. The kinetic scheme is validated by comparing the model predictions with recent experimental data measured in a DC glow discharge operating in pure CO2 and in CO2-N2 mixtures, at pressures in the range 0.6 - 4 Torr (80.00 - 533.33 Pa) and a current of 50 mA. The experimental results show a higher vibrational temperature of the different modes of CO2 and CO and an increased dissociation fraction of CO2, that can reach values as high as 70 %, when N2 is added to the plasma. On the one hand, the simulations suggest that the former effect is the result of the CO2-N2 and CO-N2 V-V transfers and the reduction of quenching due to the decrease of atomic oxygen concentration; on the other hand, the dilution of CO2 and dissociation products, CO and O2, reduces the importance of back reactions and contributes to the higher CO2 dissociation fraction with increased N2 content in the mixture, while the N2(B3Πg) electronically excited state further enhances the CO2 dissociation.

This work focuses on the comparison between a zero-dimensional (0D) global model (LoKI) and a one-dimensional (1D) radial fluid model for the positive column of oxygen DC glow discharges in a tube of 1 cm inner radius at pressures between 0.5 Torr and 10 Torr. The data used in the two models are the same, so that the difference between the models is reduced to dimensionality. A good agreement is found between the two models on the main discharge parameters (gas temperature, electron density, reduced electric field and dissociation fraction), with relative differences below 5%. The agreement on other species average number densities, charged and neutral, is slightly worse, with relative differences increasing with pressure from 11% at 0.5 Torr to 57% at 10 Torr. The success of the 0D global model in describing these plasmas through volume averaged quantities decreases with pressure, due to pressure-driven narrowing of radial profiles. Hence, in the studied conditions, we recommend the use of volume-averaged models only in the pressure range up to 10 Torr.