铂金
欠电位沉积
吸附
化学
氢
电极
电化学
分析化学(期刊)
电极电位
基质(水族馆)
金属
过渡金属
结晶学
物理化学
无机化学
循环伏安法
催化作用
海洋学
地质学
生物化学
有机化学
色谱法
作者
Roberto Gómez,J.M. Orts,B. Álvarez,Juan Miguel Feliu
摘要
The dependence on temperature of the voltammetric behavior of Pt(111), Pt(100), and Pt(110) electrodes in 0.1 M HClO 4 has been studied. A thermodynamic analysis of the hydrogen underpotential deposition (H UPD ) has been carried out, taking into account that the adsorption process is accompanied by changes in the electrode double layer. The analysis for Pt(100) requires a previous deconvolution of the OH adsorption contribution whereas for Pt(110), the analysis is limited to high H coverages. The Pt−H bond energy values obtained for the Pt( hkl ) electrodes agree with the values obtained in UHV. On Pt(111) and Pt(100), Δ (H UPD ) changes linearly with coverage, with Frumkin repulsive parameters 27 and 9 kJ mol -1, respectively. The values obtained for Δ (H UPD ) (−48 J mol -1 K -1 for Pt(111), − 56 J mol -1 K -1 for Pt(100), and from −55 to − 70 J mol -1 K -1 for Pt(110)) suggest immobile hydrogen adsorption. The fact that Δ (H UPD ) depends significantly on the crystallographic orientation suggests that the symmetry of the platinum substrate strongly influences the degree of order in the water network directly bonded to the metal surface atoms.
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