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The electrochemistry of 'solid/water' interfaces involved in PEM-H2O reactors Part I. The 'Pt/water' interfaces

机译:PEM-H2O反应器中涉及的“固体/水”界面的电化学第一部分。“ Pt /水”界面

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摘要

The nature and properties of Pt surfaces in contact with pure water in PEM-H2O reactors were mimetically studied by employing CV measurements with microelectrode techniques. These "Pt/water" interfaces were found to be electrochemically polarizable, and the local interfacial potential relative to reversible hydrogen electrode (RHE) potential in pure water is numerically the same as the potential value measured against a RHE in contact with PEM as the reference electrode. However, the structural parameters of the electric double layer at the "Pt/water" interfaces can be quite different from those at the "Pt/PEM" interfaces, and the kinetics of electrode processes could be seriously affected by the structure of electric double layer in pure water media. Besides, there is active diffusional flow of intermediates of electrode reactions between the "Pt/water" and the "Pt/PEM" interfaces, thus facilitating the active involvement of the "Pt/water" interfaces in the current-generation mechanism of PEM fuel cells and other types of PEM-H2O reactors.
机译:在PEM-H2O反应器中,与纯水接触的Pt表面的性质和性质通过采用微电极技术的CV测量进行了模拟研究。发现这些“ Pt /水”界面是电化学可极化的,并且相对于纯水中可逆氢电极(RHE)电势的局部界面电势在数值上与针对与PEM接触的RHE测得的电势值相同电极。然而,“ Pt /水”界面处的双电层的结构参数可能与“ Pt / PEM”界面处的双电层的结构参数完全不同,并且双电层的结构可能严重影响电极工艺的动力学。在纯净水介质中。此外,“ Pt /水”和“ Pt / PEM”界面之间存在电极反应中间体的主动扩散流,从而有利于“ Pt /水”界面积极参与PEM燃料的发电机理电池和其他类型的PEM-H2O反应器。

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