An influence of pretreatment conditions on surface structure and reactivity of Pt(100) towards CO oxidation reaction

被引:26
作者
Rudnev, A. V. [1 ,2 ]
Wandlowski, T. [2 ]
机构
[1] Russian Acad Sci, Frumkin Inst Phys Chem & Electrochem, Moscow 119071, Russia
[2] Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
single crystal; platinum; cyclic voltammetry; scanning tunneling microscopy; Pt(100); carbon monoxide; SINGLE-CRYSTAL ELECTRODES; HYDROGEN ADSORPTION STATES; SCANNING-TUNNELING-MICROSCOPY; PLATINUM STEPPED SURFACES; SULFURIC-ACID-SOLUTION; IN-SITU; ELECTROCHEMICAL-BEHAVIOR; UNDERPOTENTIAL DEPOSITION; CARBON-MONOXIDE; OXYGEN REDUCTION;
D O I
10.1134/S1023193512030123
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We present a combined electrochemical and in situ STM study of the surface structure of Pt(100) single crystal electrodes in dependence on the cooling atmosphere after flame annealing. The following cooling conditions were applied: Ar/H-2 and Ar/CO mixtures (reductive atmosphere), argon (inert gas) and air (oxidative atmosphere). Surface characterization by in-situ STM allows deriving direct correlations between surface structure and macroscopic electrochemical behavior of the respective platinum electrodes. We investigated the influence of defect type and density as well as long range surface order on the kinetics of the CO electro-oxidation reaction. The defect-rich Pt(100) electrodes as cooled in air or Ar, and followed by immersion in the hydrogen adsorption region display higher activities as compared to the rather smooth Pt(100)-(1 x 1) electrode cooled in an Ar/H-2-atmosphere.
引用
收藏
页码:259 / 270
页数:12
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