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Electrocatalytic reduction of hydrogen peroxide at Prussian blue modified electrodes: a RDE study

机译:在普鲁士蓝修饰电极上电催化还原过氧化氢:RDE研究

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Electrocatalytic reduction of hydrogen peroxide at Prussian blue modified electrode has been studied with rotating disk electrode in pH 5.5 and 7.3 solutions. It has been shown that the electrocatalytic cathodic reduction obeys Koutecky-Levich relationship at electrode potentials ranging from 0.1 to -0.4 V vs. Ag/AgCl for low concentrations of peroxide not exceeding 0.3 mM. Within this potential window, the calculated kinetic cathodic current ranges within the limits of 2.15-6.09 and 1.00-3.60 mA cm(-2) mM(-1) for pH 5.5 and 7.3, respectively. For pH 5.5 and 7.3 solutions, a linear slope of the dependence of kinetic current on electrode potential of -10.8 and -2.89 mA cm(-2) mM(-1) V-1, respectively, has been obtained. At a higher concentration of peroxide, exceeding 0.6 mM, deviations from Koutecky-Levich relationship have been observed. These deviations appear more expressed at higher potentials and higher solution pH. The results obtained have been interpreted within the frame of two-step reaction mechanism, including (1) dissociative adsorption of hydrogen peroxide with the formation of OH radicals and (2) one-electron reduction of these radicals to OH- anions. At a higher concentration of peroxide, and especially at a higher pH, the second process becomes rate limiting.
机译:在pH 5.5和7.3的溶液中,用旋转圆盘电极研究了普鲁士蓝修饰电极上过氧化氢的电催化还原。已经表明,对于不超过0.3mM的低浓度的过氧化物,在相对于Ag / AgCl的电极电势为0.1至-0.4V的范围内,电催化阴极还原遵守Koutecky-Levich关系。在此电位窗口内,对于pH 5.5和7.3,计算出的动力学阴极电流分别在2.15-6.09和1.00-3.60 mA cm(-2)mM(-1)的范围内。对于pH 5.5和7.3溶液,分别获得了动电流对-10.8和-2.89 mA cm(-2)mM(-1)V-1的电极电位的依赖性的线性斜率。在更高的过氧化物浓度下,超过0.6 mM,已经观察到与Koutecky-Levich关系的偏离。这些偏差在较高的电势和较高的溶液pH值下表现得更明显。在两步反应机理的框架内解释了获得的结果,包括(1)过氧化氢的离解吸附和OH自由基的形成,以及(2)这些自由基单电子还原为OH-阴离子。在较高的过氧化物浓度下,尤其是在较高的pH下,第二过程成为速率限制。

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