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Detection of Hydrogen Peroxide Produced during Electrochemical Oxygen Reduction Using Scanning Electrochemical Microscopy

机译:扫描电化学显微镜检测电化学还原过程中产生的过氧化氢

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The substrate-generation/tip-collection mode of scanning electrochemical microscopy was used to detect hydrogen peroxide formed as an intermediate during oxygen reduction at various electrodes. The experiment is conceptually similar to rotating ring-disk experiments but does not require the production of a ring-disk assembly for the specific electrode material in question. In order to limit the extension of the diffusion layer above the sample, the sample electrode potential is pulsed while the Pt ultra-microelectrode probe (UME) is held at a constant potential for oxidative amperometric detection of hydrogen peroxide. The signal at UME is influenced by the sample region within the diffusion length of hydrogen peroxide during the pulse of 2.5 s. The method is tested with three model electrodes showing different behavior with respect to the oxygen reduction reaction (ORR) in acidic solution. Simple analytical models were used to extract effective rate constants for the most important reaction paths of ORR at gold and palladium-cobalt samples from the chronoamperometric response of the UME to a reduction pulse at the sample electrode.
机译:扫描电化学显微镜的底物生成/尖端收集模式用于检测过氧化氢在各种电极上还原氧过程中作为中间体形成的过氧化氢。该实验在概念上类似于旋转环形盘实验,但不需要为所讨论的特定电极材料生产环形盘组件。为了限制扩散层在样品上方的延伸,在将Pt超微电极探针(UME)保持在恒定电位以对过氧化氢进行氧化安培检测的同时,对样品电极电位施加脉冲。在2.5 s的脉冲期间,UME处的信号受过氧化氢扩散长度内的样本区域影响。用三个模型电极测试了该方法,该电极在酸性溶液中显示出与氧还原反应(ORR)不同的行为。简单的分析模型用于从UME对样品电极上还原脉冲的计时安培响应中提取金和钯-钴样品中ORR最重要反应路径的有效速率常数。

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