30th ICPIG, August 28th - September 2nd , 2011, Belfast, UK Topic number B5 Influence of helium admixture on charged particle dynamics in an electronegative oxygen capacitively coupled plasma A. Greb1 , K. Niemi1 , D. O’Connell1 , T. Gans1 1 Centre for Plasma Physics, Queen’s University Belfast, BT7 1NN, Belfast, Northern Ireland, UK The influence of helium admixture on an electronegative oxygen capacitively coupled plasma is investigated by means of a one-dimensional numerical fluid model with semi-kinetic treatment of electrons. This model is operated at 100 Pa with a sinusoidal driving voltage at a frequency of 13.56 MHz and is solved self-consistently for each individual RF-cycle. The − change in the spatial profiles of dominant charged particles (O+ 2 , O , e) as well as the electronegativity are analysed under variation of the helium admixture. Discharge excitation dynamics, in particular of the atomic oxygen line λ = 844 nm (3 P −3 S ) are investigated and compared to those observed from pure oxygen capacitively coupled plasma experiments. The simulations show that additional helium in the oxygen discharge acts as inhibitor for excitation mechanisms during the phase of sheath collapse. solid: 0% helium dashed: 99% helium 1.0 Normalised densiity 1. Introduction To model the capacitively coupled plasma a hybrid model was applied. There, the electron transport coefficients and reaction rates for electron impact collisions are simulated kinetically in advance [1], whereas the densities of the accounted species as well as the electric field are simulated with a fluid approach. The simulations are performed in O2 gas with variable He admixture at a constant pressure of 100 Pa. For simplicity reasons, the simulations are done in an one-dimensional domain across the discharge gap of the capacitively coupled plasma. A total of 9 species are accounted for in the model. These species are electrons (e), the background gases oxygen (O2 ) and helium (He), oxygen molecular ions (O2+ ) and atomic oxygen negative ions (O− ), helium metastable atoms (He∗ ), helium ions (He+ ), helium molecular ions (He+ 2) and helium excimers (He∗2 ). The incorporated oxygen ion species were particularly chosen because of experimental results [2, 3]. There, their densities have been measured by a photo detachment technique and were found as the most dominant species under the given conditions. A comparable chemical reaction scheme for the helium species used in this work can be found in the literature [4]. The self-consistent model is closed by the boundary conditions for each considered species, by the potential and mean electron energy. + O 0.8 2 0.6 e 0.4 0.2 - O 0.0 0 10 20 30 40 Position (mm) Fig. 1: Time averaged spatial profiles of O− , O+ 2 and electrons for two different helium admixtures at U0 ≈ 300 V and p = 100 Pa. 2. Influence of He admixture 2.1. Spatial profiles The spatial profiles of the dominant charged − particles (O+ 2 , O , e) are obtained from a converged solution along the symmetry axis of the discharge and are shown in figure 1. The profiles of the heavy particles remain static for all times, however, the electron density profile shows a temporal variation due to their higher mobility, which was then time averaged. In figure 1 all density profiles were normalised to the maximum density of the dominant positive ion O+ 2 for each corresponding helium admixture. It can be observed that the atomic oxygen negative ion spatial profile exhibits a maximum within the centre of the bulk for a high helium admixture (99%), whereas it shows a broader 30th ICPIG, August 28th - September 2nd , 2011, Belfast, UK Topic number B5 0.70 electronegativity 0.65 0.55 n O - /n e 0.60 0.50 0.45 0.40 0 20 40 60 80 100 He fraction (%) Fig. 2: Electronegativity as a function of the helium admixture at constant power P = 0.1 W/cm2 and p = 100 Pa. double peaked profile near the electrodes for less He admixture. Furthermore, the O− density decays with a higher gradient in the electrode region than the electrons but never exceeds the electron density. This is due to the dominant production and destruction mechanisms. Generally, the spatial variation of electrons entails a corresponding variation of the O− density, since the latter is only generated by electron collisions in the model. However, in the bulk region the destruction of O− exceeds the production due to collisions with O2 (1 ∆), which is assumed to be the main collision partner leading to destruction [5]. This leads to the observed double peaked structure in the O− spatial profile. 2.2. Electronegativity In this work, the electronegativity is defined as the density ratio of negative ions and electrons (nO− /ne ). This density ratio is obtained by averaging the corresponding densities in space and time. Figure 2 shows the dependence of the electronegativity on the helium admixture for a constant power (0.1 W/cm2 ) and pressure (100 Pa). Over a long range of He gas fractions the electronegativity increases over-linearly until it reaches its maximum at 0.66 which means that the time and space averaged O− density never exceeds the electron density. Experiments show typically slightly higher electronegativity but this may be explained due to the neglect of other possible negative ion species in the applied model. Furthermore, it is observed that for very high admixtures of helium (> 95%) the electronegativity drops rapidly to an even lower value. Fig. 3: Emission from atomic oxygen line λ = 844 nm for a) pure oxygen and b) 1 % helium admixture at same parameters as figure 2. This is due to the rapid increase in the electron density density with additional helium, whereas the atomic oxygen negative ion does not decrease at the same rate. 2.3. Excitation dynamics The influence of He admixture on the excitation dynamics is shown exemplarily by means of the emission from the atomic oxygen line λ = 844 nm (3 P −3 S) through dissociative detachment of oxygen molecules. Figure 3 illustrates the observed emission features as phase resolved optical emission spectroscopy (PROES) image in grayscale for (a) a pure oxygen discharge and (b) oxygen with 50% helium admixture at same conditions as in figure 2. For a pure oxygen discharge, clearly three excitation features can be observed (figure 3a). These features agree very well with experimental results for a comparable set of parameters [6] and can be identified as sheath expansion (I), sheath collapse (II) and excitation due to secondary electrons (III). As soon as helium is added to the plasma the emission features change drastically (figure 3b). 30th ICPIG, August 28th - September 2nd , 2011, Belfast, UK The additional helium clearly amplifies the emission from the sheath expansion process (I) and at the same time leads to a slightly more pronounced emission from the sheath collapse phase (II). Furthermore, the sheath collapse shows a phase shift of the maximum to later times. The emission from secondary electron collisions (III) decreases and can be explained by means of the higher secondary electron emission coefficient of helium. Moreover, the helium in the discharge promotes a rise of the mean electron energy due to its higher ionisation and excitation energy thresholds. Further investigations need to be conducted with regard to experimental benchmarks and implementations of required modifications to the simulation model to understand and predict better the influence of helium on charged particle dynamics in an electronegative oxygen capacitively coupled plasma. References [1] G.J.M. Hagelaar and L.C. Pitchford, Plasma Sources Sci. Technol. 14 (2005) 722 [2] E. Stoffels, W.W. Stoffels, D. Vender, M. Kando, G.M.W. Kroesen and F.J. de Hoog, Phys. Rev. E 51 (1995) 2425 [3] D. Vender, W.W. Stoffels, E. Stoffels, G.M.W. Kroesen and F.J. de Hoog, Phys. Rev. E 51 (1995) 2436 [4] K. Niemi, S. Reuter, L.M. Graham, J. Waskoenig, N. Knake, V. Schulz-von der Gathen and T. Gans J. Phys. D: Appl. Phys. 43 (2010) 124006 [5] H.M. Katsch, T. Sturm, E. Quandt and H.F. Döbele, Plasma Sources Sci. Technol. 9 (2000) 323 [6] S. Nemschokmichal, K. Dittmann, J. Meichsner, IEEE Trans. Plasma Sci. 36 (2008) 1360 Topic number B5
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