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Hydrogen evolution on electrodeposited Ni and Hg ultramicroelectrodes

机译:电沉积的镍和汞超微电极上的析氢

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The hydrogen evolution reaction (her) was studied on two different surfaces obtained by electrodeposition of Ni and Hg on Pt ultramicroelectrodes. This reaction was analyzed in alkaline and acid media by a non-linear regression procedure together with mechanistic considerations. The derivations of the kinetic equations were based on a Volmer-Heyrovsky mechanism with a different rate determining step for each surface. On Pt/Ni electrodes an apparent activation energy of 56 kJ mol(-1) was obtained while on Pt/Hg this value increases up to 204 kJ mol(-1). Such difference was analyzed as a change in the nature of the activated complex formed as intermediate of the reaction. The greater affinity existing between H and Ni facilitates the adsorption step on Ni surfaces, resulting in the Heyrovsky step to be the rate determining one, with an activated complex of the type (Ni-H...H...OH)*. On Hg, the adsorption is more difficult and the Volmer step becomes determining with the species (Hg...H...H2O+)* being the activated complex. The rate constant values for each step were determined by a non-linear regression procedure. In this work, the utilization of ultramicroelectrodes and the special methodology used to conditioning the surface brought important contributions to the interpretation of experimental results by avoiding the influence of ohmic drop and bubbles evolution on the surface, thus increasing the reproducibility of the experiments. (C) 1997 Elsevier Science Ltd. [References: 45]
机译:在通过在Pt超微电极上电沉积Ni和Hg而获得的两个不同表面上研究了析氢反应(她)。通过非线性回归程序以及机理考量,在碱性和酸性介质中分析了该反应。动力学方程式的推导基于Volmer-Heyrovsky机理,每个表面的速率确定步骤不同。在Pt / Ni电极上,表观活化能为56 kJ mol(-1),而在Pt / Hg上,该值增加到204 kJ mol(-1)。分析这种差异,作为在反应中间形成的活化复合物的性质变化。 H和Ni之间存在更大的亲和力,这有利于在Ni表面进行吸附步骤,从而使Heyrovsky步骤成为决定速率的速率,并且活化类型为(Ni-H ... H ... OH)*。在Hg上,吸附更加困难,并且Volmer步骤变得很重要,因为(Hg ... H ... H2O +)*是活化的络合物。通过非线性回归程序确定每个步骤的速率常数值。在这项工作中,超微电极的利用和用于调节表面的特殊方法避免了欧姆滴和气泡在表面上的影响,为解释实验结果做出了重要贡献,从而提高了实验的可重复性。 (C)1997 Elsevier Science Ltd. [参考:45]

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