首页> 外文期刊>Journal of solid state electrochemistry >Electrocatalytic reduction of hydrogen peroxide at Prussian blue modified electrodes: a RDE study
【24h】

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

获取原文
获取原文并翻译 | 示例
           

摘要

Electrocatalytic reduction of hydrogen peroxide at Prussian blue modified electrode has been studied with rotating disk electrode in pH5.5 and 7.3 solutions. It has been shown that the electrocatalytic cathodic reduction obeys Koutecky–Levich relationship at electrode potentials ranging from 0.1 to0.4 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 cm2 mM1 for pH5.5 and 7.3, respectively. For pH5.5 and 7.3 solutions, a linear slope of the dependence of kinetic current on electrode potential of 10.8 and 2.89 mA cm2 mM1 V1, 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:研究了在pH5.5和7.3溶液中用转盘电极在普鲁士蓝修饰电极上电催化还原过氧化氢的方法。研究表明,对于不超过0.3 mM的低浓度过氧化物,在相对于Ag / AgCl的电极电位为0.1至0.4 V的条件下,电催化阴极还原符合Koutecky-Levich关系。在此电位窗口内,对于pH5.5和7.3,计算得出的动力学阴极电流分别在2.15–6.09和1.00–3.60 mA cm2 mM1的范围内。对于pH5.5和7.3溶液,已经获得了动电流对电极电势的依赖性的线性斜率,分别为10.8和2.89 mA cm2 mM1 V1。在较高的过氧化物浓度(超过0.6 mM)下,已观察到与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。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号