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Cathodically deposited Ag 2Se, to form a 1-μm-thick film, characterized by energy dispersive X-ray analysis and scanning electron microscopy, showed high electro-catalytic activity for l-ascorbic acid oxidation in alkaline solution. The onset of the process was about 80 mV cathodic of that previously observed on Ag under the same conditions and far superior over glassy carbon and Pt. The values of the exchange current density, standard heterogeneous rate constant, and transfer coefficient of the reaction were 1. 65 × 10 -4 A cm -2, 4. 35 × 10 -7 cm s -1, and 0. 60, respectively. Diffusion coefficient of l-ascorbate di-anion was also measured and was around 7. 00 × 10 -6 cm 2 s -1  

L-Ascorbate anion electro-oxidation on a silver electrode in hydroxide solution in the absence and presence of sodium polysulfide of concentrations from 1 × 10 -5 to 4.5 × 10 -4 mol/L was studied using cyclic voltammetry and electrochemical impedance spectroscopy. Both hydroxide and polysulfide ions inhibited L-ascorbate ion oxidation, with the poisoning effect of polysulfide ion being more pronounced in the potential range of -0.3 to -0.2 V/SCE. The time constants for L-ascorbate ion oxidation in the absence and presence of polysulfide were, 10 -3 to 1 × 10 -2 s and 1 × 10 -4 to 1 × 10 -2 s, respectively depending on the potential used for the impedance analysis. Based on the cyclic... 

Electrochemical oxidation of l-ascorbic acid on polycrystalline silver in alkaline aqueous solutions is studied by cyclic voltammetry (CV), chronoamperometry (CA) and impedance spectroscopy (IS). The anodic electro-oxidation starts at -500 mV versus SCE and shows continued anodic oxidation in the cathodic half cycle in the CV regime signifying slowly oxidizing adsorbates. Diffusion coefficient of ascorbate ion measured under both voltammetric regimes is around 1.4 × 10-5 cm2 s-1. Impedance spectroscopy measures the capacitances associated with double layer and adsorption around 50 μF cm-2 and 4 mF cm-2 as well as the adsorption and decomposition resistances (rates). © 2009 Elsevier B.V. All...