Preparation and Electrochemical Behavior of PtRu(111) Alloy Single-Crystal Surfaces

被引:16
作者
El-Aziz, Ahmed M. [1 ,2 ]
Hoyer, Ruediger [1 ,3 ]
Kibler, Ludwig A. [1 ]
机构
[1] Univ Ulm, Inst Elektrochem, D-89069 Ulm, Germany
[2] German Univ Cairo, Dept Mat Engn, New Cairo 11835, Egypt
[3] Umicore AG & Co KG, D-63403 Hanau, Germany
关键词
cyclic voltammetry; metal-electrolyte interfaces; platinum; ruthenium; scanning probe microscopy; CO ELECTROOXIDATION; HYDROGEN ADSORPTION; METHANOL OXIDATION; OXYGEN REDUCTION; PTRU ELECTRODES; ZERO CHARGE; RU; PLATINUM; PT(111); DEPOSITION;
D O I
10.1002/cphc.201000261
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The electrochemical behavior of a PtRu(111) single crystal with 1:1 bulk atomic ratio is investigated for the first time by means of cyclic voltammetry and scanning tunneling microscopy (STM). The electrode surfaces are enriched with either Ru or Pt, depending on the cooling conditions after inductive heating. Analysis of the surfaces by STM shows a typical topography with smooth terraces separated by monoatomic high steps. The voltammetric characterization of PtRu(111) in acid media clearly reveals an altered electrochemical behavior of the Pt and Ru surfaces compared to Pt(111) and Ru(0001), respectively. Systematic changes are observed for hydrogen adsorption and underpotential deposition of copper as test reactions. Based on theoretical calculations in the literature, it is experimentally verified that the Pt-rich and the Ru-rich surfaces of the PtRu(111) single-crystal alloy bind adsorbates such as hydrogen significantly weaker and stronger than the pure single-crystal electrode surfaces. Such changes in surface reactivity can be crucial for electrocatalytic reactions.
引用
收藏
页码:2906 / 2911
页数:6
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