14,232 research outputs found
Scaling laws for diamond chemical-vapor deposition. I. Diamond surface chemistry
A simplified model of the gas-surface chemistry occurring during chemical-vapor deposition of diamond thin films is presented. The model results in simple scaling relations, useful for process scale-up and optimization, for growth rate and defect density in terms of the local chemical environment at the substrate. A simple two-parameter expression for growth rate is obtained, which with suitable parameter choices reproduces the results of more detailed mechanisms and experiment over two orders of magnitude in growth rate. The defect formation model suggests that the achievable growth rate at specified defect density scales approximately quadratically with the atomic hydrogen concentration at the substrate
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Diamond growth in a novel low pressure flame
Diamond growth using a new low-pressure combustion technique is reported. A large-area hydrogen/oxygen flame is used as the source of atomic hydrogen. Methane diluted in hydrogen is injected into the flame near a heated silicon substrate, on which diamond crystallites nucleate and grow. This technique is potentially capable of large-area film growth, since atomic hydrogen can be generated uniformly over arbitrarily large areas
Numerical Study of Heterogeneous Reactions in an SOFC Anode with Oxygen Addition
Previous experimental studies have shown that addition of small amounts of oxygen to a hydrocarbon fuel stream can control coking in the anode, while relatively large amounts of oxygen are present in the fuel stream in single-chamber solid oxide fuel cells (SOFCs). In order to rationally design an anode for such use, it is important to understand the coupled catalytic oxidation/reforming chemistry and diffusion within the anode under SOFC operating conditions. In this study, the heterogeneous catalytic reactions in the anode of an anode-supported SOFC running on methane fuel with added oxygen are numerically investigated using a model that accounts for catalytic chemistry, porous media transport, and electrochemistry at the anode/electrolyte interface. Using an experimentally validated heterogeneous reaction mechanism for methane partial oxidation and reforming on nickel, we identify three distinct reaction zones at different depths within the anode: a thin outer layer in which oxygen is nearly fully consumed in oxidizing methane and hydrogen, followed by a reforming region, and then a water–gas shift region deep within the anode. Both single-chamber and dual-chamber SOFC anodes are explored
Diamond growth in premixed propylene-oxygen flames
Diamond film growth in low-pressure premixed propylene/oxygen flames is demonstrated. Well-faceted films are grown at a pressure of 180 Torr and a fuel/oxygen ratio of 0.47. Using propylene as the fuel may greatly improve the economics of flame synthesis of diamond, since propylene is an order of magnitude cheaper than acetylene
Temperature dependence of species concentrations near the substrate during diamond chemical vapor deposition
Measurements have been made of the temperature dependence of CH3, CH4, and C2H2 very near the substrate during filament-assisted diamond growth. CH3 was detected using (2+1) resonance-enhanced multiphoton ionization (REMPI), and CH4 and C2H2 concentrations were measured using sampling mass spectrometry. A strong dependence of the CH3 REMPI signal on substrate temperature was observed, which at low temperatures may be characterized as having an activation energy of approximately 4±1 kcal/mole. Methane and acetylene, on the other hand, are relatively independent of substrate temperature. These results are most likely due to recombination of methyl to methane or ethane in the cool gas layer near the substrate or on the surface at low substrate temperatures
Magnetoplasmadynamic (MPD) accelerator assisted synthesis of diamond
The use of a magnetoplasmadynamic (MPD) accelerator for diamond synthesis is investigated. The acceleration process in an MPD device is reviewed and results presented for a test in which a low power (15 kW) MPD accelerator was used as the gas activation source for diamond deposition. A hydrogen–argon mixture was used in the discharge with externally injected methane as the carbon precursor. Results, including SEM images, Raman and x-ray diffraction spectra are presented for a 3.3 µm thick film deposited over a 100 min period. The Raman spectra include a broad background and shift in the diamond peak, indicative of contamination and stresses in the deposited film. Potential scaling benefits of the MPD accelerator as well as some of the drawbacks associated with methane injection and sample contamination underscored by the experiments are identified and discussed
A Two-Dimensional Model of a Single-Chamber SOFC with Hydrocarbon Fuels
The single chamber fuel cell (SCFC) is a novel simplification of the conventional solid oxide fuel cell (SOFC) into which a premixed fuel/air mixture is introduced. It relies on the selectivity of the anode and cathode catalysts to generate a chemical potential gradient across the cell. For SCFC running on hydrocarbon fuels, the anode catalyst promotes in-situ internal reforming of the hydrocarbon and electrochemical oxidation of the syngas, while the cathode catalyst reduces oxygen simultaneously. Laboratory tests of small designs of such fuel cells have demonstrated excellent electrical performance (1, 2)
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