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    Silver selenide as a potential electro-catalyst for l-ascorbic acid electro-oxidation in alkaline solution

    , Article Electrocatalysis ; Volume 2, Issue 4 , December , 2011 , Pages 331-336 ; 18682529 (ISSN) Gobal, F ; Majari Kasmaee, L ; Sharif University of Technology
    Abstract
    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  

    A Study of Ascorbic Acid Electro-Oxidation Process on Silver and Silver Selenide Electrodes

    , Ph.D. Dissertation Sharif University of Technology Majari Kasmaee, Laleh (Author) ; Gobal, Fereydoon (Supervisor)
    Abstract
    Electrocatalytic oxidation of L-ascorbic acid (L-AA) on silver electrode in alkaline solutions was studied employing cyclic voltammetry, chronoamperometry and impedance spectroscopy techniques. In comparison to Pt, the onset potential for L-AA electro-oxidation process on Ag, in a solution containg 0.02 M L-AA and 0.5 M NaOH, was 0.1 V more negative. Also, L-AA oxidation current increased more than 900% at -0.26 V/SCE. According to voltammety and impedance spectropy findings, although hydroxide anion presence was vital for L-AA oxidation to occur, at potentials more positive than -0.2 V/SCE, hydroxide ion tends to inhibit the oxidation process. Studies on the L-AA oxidation process on Ag in...