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Electrocatalytic activity of Chemisorbed Hydroxyl ion towards Oxidation of Hydrogen peroxide anion in Alkaline media

机译:化学吸附的羟离子对碱性介质中过氧化氢阴离子氧化的电催化活性

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In situ chemisorbed hydroxyl ion (OH-) onto clean polycrystalline gold (Au (poly)) electrode showed an extraordinary enhanced electrocatalytic activity towards oxidation of hydrogen peroxide anion (HO2-) in alkaline media. The oxidation of HO2- at the fabricated electrode was found to be a diffusion controlled process. The anodic transfer coefficient of the oxidation reaction was estimated as 0.47. Chloride ion (Cl-) replaced the chemisorbed OH- from the surface of the modified Au (poly) (OH-)Au (poly)) electrode leading to diminishing the observed electrocatalytic activity. The optimized concentration of KOH solution for the highest catalytic activity was found to be ca. 0.1 M. A linear calibration curve for various concentrations of HO2-? in the range of 0.5 to 5 mM was obtained having sensitivity equal to 1.028 A cm-2 M-1.Journal of Bangladesh Academy of Sciences, Vol. 41, No. 1, 29-36, 2017
机译:原位化学吸附的羟基离子(OH-)在干净的多晶金(Au(poly))电极上显示出对碱性介质中过氧化氢阴离子(HO2-)氧化的非凡增强的电催化活性。发现在制造的电极上HO 2-的氧化是扩散控制的过程。氧化反应的阳极转移系数估计为0.47。氯离子(Cl-)取代了修饰的Au(poly)(OH-)Au(poly))电极表面化学吸附的OH-,导致观察到的电催化活性降低。发现具有最高催化活性的KOH溶液的最佳浓度为约。 0.1 M.各种浓度的HO2-?的线性校准曲线获得的灵敏度在0.5至5mM的范围内具有等于1.028A cm-2 M-1的灵敏度。 41,No.1,29-36,2017年

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