The production and transport dynamics of O2(a 1Δg) and molecules as well as O(3P) atoms has been studied in an O2 flow excited by a 13.56 MHz RF discharge in a quartz tube at pressures of 1–20 Torr. It has been shown that the densities of O2(a 1Δg) and O(3P) are saturated with increasing energy input into the discharge. The maximum yield of singlet oxygen (SO) and the O2 dissociation degree drops with pressure. It is demonstrated that depending on the energy input the RF discharge can exist in three modes: I—in the spatially homogeneous mode or α-mode; III—in the substantially inhomogeneous mode, when plasma jets are present outside the discharge; and II—in the transient mode between modes I and III. In this paper only the homogeneous mode of RF discharge in the O2 flow is considered in detail. A self-consistent model of the α-mode is developed, that allows us to analyse elementary processes responsible for the production and loss of O2(a 1Δg) and molecules as well as O(3P) atoms in detail. To verify both the kinetic scheme of the model and the conclusions, some experiments have been carried out at lower flow velocities and higher pressures (⩾10 Torr), when the stationary densities of O2(a 1Δg), and O(3P) in the discharge area were established not by the escape of particles but by the losses due to the volumetric and surface reactions. The density under these conditions is determined by the balance of production by both direct electron impact and electronic excitation transfer from metastable O(1D) atoms and deactivation by oxygen atoms and tube walls, including quenching by ozone in the afterglow. The O(3P) density is determined by the balance between the production through O2 dissociation by electron impact and heterogeneous loss at the wall recombination. The stationary density of O2(a 1Δg) is provided by the processes of O2(a 1Δg) production by direct electron impact and loss owing to quenching by the tube walls at a low pressure below 4 Torr, as well as by three-body recombination with oxygen atoms with increasing pressure above 7 Torr. The analysis of O2(a 1Δg) three-body quenching by oxygen atoms showed that this process could actually have a high rate constant and be able to provide a fast SO deactivation at high pressures. The approximate value of the rate constant—(1–3) × 10−32 cm3 s−1 has been obtained from the best agreement between the simulated and experimental data on transport dynamics of O2(a 1Δg) molecules and O(3P) atoms. It is shown that the RF discharge α-mode corresponds to a discharge with an effective reduced electrical field in a quasi-neutral plasma of about ∼ 30 Td, which makes possible a rather high efficiency of SO production of ∼3–5%.
O2(a 1Δg) production in a non-self-sustained discharge (ND) in pure oxygen and oxygen mixtures with inert gases (Ar and He) has been studied. A self-consistent model of ND in pure oxygen is developed, allowing us to simulate all the obtained experimental data. Agreement between the experimental and simulated results for pure oxygen over a wide range of reduced electric fields was reached only after taking into account the ion component of the discharge current. It is shown that the correct estimation of the energetic efficiency of O2(a 1Δg) excitation by discharge using the EEDF calculation is possible only with the correct description of the energy deposit into the plasma on the basis of an adequate discharge model. The testing of an O2(a 1Δg) excitation cross-section by direct electron impact, as well as a kinetic scheme of processes involving singlet oxygen, has been carried out by the comparison of experimental and simulated data. The tested model was then used for simulating O2(a 1Δg) production in ND in oxygen mixtures with inert gases. The study of O2(a 1Δg) production in Ar : O2 mixtures with small oxygen content has shown that the ND in these mixtures is spatially non-uniform, which essentially decreases the energetic efficiency of singlet oxygen generation. While simulating the singlet oxygen density dynamics, the process of three-body deactivation of O2(a 1Δg) by O(3P) atoms was for the first time taken into account. The maximal achievable concentration of singlet oxygen in ND can be limited by this quenching. On the basis of the results obtained and the model developed, the influence of hydrogen additives on singlet oxygen kinetics in argon–oxygen–hydrogen mixtures has been analysed. The simulation has shown that fast quenching of O2(a 1Δg) by atomic hydrogen is possible due to significant gas heating in the discharge that can significantly limit the yield of singlet oxygen in hydrogen-containing mixtures.
Microstructure and its effect on field electron emission of grain-size-controlled nanocrystalline diamond films Ultrananocrystalline diamond ͑UNCD͒ films 0.1-2.4 m thick were conformally deposited on sharp single Si microtip emitters, using microwave CH 4 -Ar plasma-enhanced chemical vapor deposition in combination with a dielectrophoretic seeding process. Field-emission studies exhibited stable, extremely high ͑60-100 A/tip͒ emission current, with little variation in threshold fields as a function of film thickness or Si tip radius. The electron emission properties of high aspect ratio Si microtips, coated with diamond using the hot filament chemical vapor deposition ͑HFCVD͒ process were found to be very different from those of the UNCD-coated tips. For the HFCVD process, there is a strong dependence of the emission threshold on both the diamond coating thickness and Si tip radius. Quantum photoyield measurements of the UNCD films revealed that these films have an enhanced density of states within the bulk diamond band gap that is correlated with a reduction in the threshold field for electron emission. In addition, scanning tunneling microscopy studies indicate that the emission sites from UNCD films are related to minima or inflection points in the surface topography, and not to surface asperities. These data, in conjunction with tight binding pseudopotential calculations, indicate that grain boundaries play a critical role in the electron emission properties of UNCD films, such that these boundaries: ͑a͒ provide a conducting path from the substrate to the diamond-vacuum interface, ͑b͒ produce a geometric enhancement in the local electric field via internal structures, rather than surface topography, and ͑c͒ produce an enhancement in the local density of states within the bulk diamond band gap.
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