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Content available remote Cyclic voltammetry and impedance studies of undoped diamond films
EN
The undoped, polycrystalline diamond films were deposited on tungsten wire substrates by hot filament chemical vapor deposition (HF CVD), using a precursor gas mixture of methanol with excess of hydrogen. The morphology and quality of the as-deposited films were monitored by scanning electron microscopy (SEM) and Raman spectroscopy. The surface morphology analyzed by SEM resembles a continuous and well faceted diamond film. Raman results showed essential differences in qualities of diamond films grown at different hydrocarbon concentrations. The electrochemical properties of diamond electrodes were examined with cyclic voltammetry (CV) and the electrochemical impedance spectroscopy (EIS). The CV experiments revealed a large chemical window (>~4.3 V) of undoped diamond. Analysis of the ferrocyanide-ferricyanide couple at a diamond electrode suggests some extent of electrochemical quasi-reversibility, but the rates of charge transfer across the diamond substrate interface vary with diamond quality.
EN
Un-doped polycrystalline diamond thin films have been grown on tungsten substrates by hot filament chemical vapor deposition (HF CVD) using a hydrogen and methanol vapor mixture. Diamond films have been analyzed by Raman spectroscopy and scanning electron microscopy (SEM). Cyclic voltammetric behavior of diamond films of different quality and morphology has been studied in acetonitryle with (n-Bu)4NClO4 and in 0.1 M KCl aqueous solutions. Preliminary cyclic voltammetry (CV) measurements showed that our electrodes have a wide potential range over which negligible background response current is observed. The potential windows depend on the type of solvent. In the case of water solution the decomposition of water occurs electrochemically and evolves O2 during positive (anodic) polarization and H2evolution during negative (cathodic) polarization. The electrochemical properties of diamond electrodes have been evaluated by performing cyclic voltammetry measurements in [Fe(CN)6]3-/4- with 0.1 M KCl. The electrode demonstrates reversible kinetics during electrochemical analysis.
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