Optical emission and absorption spectroscopy of argon 2p-1s transitions (Paschen notation) combined with collisional-radiative (CR) modeling of argon 2p states are developed and used to determine the neutral gas temperature, the Ar 1s number density, and the electron temperature along a microwave argon plasma column at atmospheric pressure. The CR model, designed specifically for atmospheric-pressure and optically thick plasma conditions, is fully detailed and validated by comparing the relative line emission intensities of argon 2p-to-1s transitions measured experimentally with the ones predicted by the CR model using the electron temperature as the only adjustable parameter. Subsequently, the neutral gas temperature (∼1300–1600 K; obtained from the broadening of argon 2p2-1s2 and 2p3-1s2 emission lines), the Ar 1s5 number density (1–2 × 1018 m−3; obtained from absorption spectroscopy of the argon 2p9-1s5 transition using a tunable laser diode), and the electron temperature (∼1.4 eV; obtained from the comparison between the measured and simulated 2p-to-1s emission line intensities) are reported as a function of the axial distance along the microwave plasma column. The values and behaviors reveal a good agreement with those reported in previous experimental and modeling studies.
The influence of the input voltage frequency (35 and 150 kHz), interelectrode gap (1 and 2 mm) and precursor concentration (250, 350, and 450 ppm) on the electron temperature (Te), number density of metastable Ar atoms (n(Ar m )), and discharge current density (proportional to the electron density ne) is studied in an argon-ethyl lactate dielectric barrier discharge (DBD). An argon-ammonia Penning mixture is also considered as reference. These results are correlated to the chemistry (XPS, IR) and topography (AFM) of the ethyl-lactate-based plasma polymer coatings. Low Te values from 0.3 to 0.5 eV were obtained for all discharges. This observation, in addition to resemblances with the Ar-NH3 mixture, suggested that the ionization kinetics of ethyl lactate-based discharges is driven by Penning reactions. Among the investigated parameters, the dissipated power obtained through changes of the excitation frequency had the largest impact on both the coatings properties and the discharge behavior.
A combination of optical emission spectroscopy and collisional-radiative modelling is used to determine the time-resolved electron temperature (assuming Maxwellian electron energy distribution function) and number density of Ar 1s states in atmospheric pressure Ar-based dielectric barrier discharges in presence of either NH3 or ethyl lactate. In both cases, Te values were higher early in the discharge cycle (around 0.8 eV), decreased down to about 0.35 eV with the rise of the discharge current, and then remained fairly constant during discharge extinction. The opposite behaviour was observed for Ar 1s states, with cycle-averaged values in the 10 17 m −3 range. Based on these findings, a link was established between the discharge ionization kinetics (and thus the electron temperature) and the number density of Ar 1s state.
By comparing time-resolved optical emission spectroscopy measurements and the predictions of a collisional-radiative model, the evolutions of electron temperature (Te) and number density of argon metastable atoms (n(Ar m)) were determined in argon-ethyl lactate dielectric barrier discharges. The influence of a square pulse power supply on Te, n(Ar m), and the discharge current is evaluated and correlated to the chemistry and the topography of the plasma-deposited coatings. Pulsed discharges were found to have shorter (100 ns) but stronger (1 A) current peaks and higher electron temperatures (0.7 eV) than when using a 35 kHz sinusoidal power supply (2 µs, 30 mA, 0.3 eV). The n(Ar m) values seemed rather stable around 10 11 cm-3 with a sinus power supply. On the contrary, with a pulse power supply with long time off (i.e. time without discharge) between each pulse, a progressive increase of n(Arm) from 10 11 cm-3 up to 10 12-10 13 cm-3 was observed. When the time off was reduced, these increases were measured in sync with the current peak. The chemical composition of the coatings was not significantly affected by using a pulse signal whereas the topography was strongly influenced and led to powder formations when reducing the time off.
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