Nitric-oxide adsorption and oxidation on Pt(111) in electrolyte solution under potential control

被引:20
作者
Casero, E
Alonso, C
Martín-Gago, JA
Borgatti, F
Felici, R
Renner, F
Lee, TL
Zegenhagen, J
机构
[1] CSIC, Inst Ciencia Mat, Madrid 28049, Spain
[2] Univ Autonoma Madrid, Fac Ciencias, E-28049 Madrid, Spain
[3] Care Of ESRF, OGG, INFM, Grenoble, France
关键词
nitrogen oxides; platinum; oxidation; chemisorption; surface roughening; X-ray scattering; diffraction; and reflection; X-ray photoelectron spectroscopy;
D O I
10.1016/S0039-6028(02)01337-7
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
We studied the adsorption and oxidation of NO adlayers on Pt(1 1 1) prepared frorn different NO precursors in an electrochemical cell in situ by surface X-ray diffraction and ex Situ by X-ray photoemission spectroscopy. We found that NO adsorbs molecularly, independent of the preparation method. There is no relaxation of the outermost Pt atomic layer induced by the presence of adsorbed NO. We observe a Surface structure of the Pt(1 1 1) very similar to the clean surface prepared under ultra-high vacuum conditions. A surface mediated oxidation process of the NO towards NO2 is initiated at a potential of around 0.95 V vs. normal hydrogen electrode. The in Situ measurements of crystal truncation rods show that this process is accompanied by a significantly roughening of the surface. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:688 / 694
页数:7
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