Tin-oxide overlayer formation by oxidation of Pt-Sn(111) surface alloys

被引:23
作者
Batzill, M [1 ]
Beck, DE [1 ]
Jerdev, D [1 ]
Koel, BE [1 ]
机构
[1] Univ So Calif, Dept Chem, Los Angeles, CA 90089 USA
来源
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A-VACUUM SURFACES AND FILMS | 2001年 / 19卷 / 04期
关键词
D O I
10.1116/1.1345902
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ordered (2X2) and (root3 X root3)R30 degrees Pt-Sn(1 1 1) surface alloys were oxidized by NO2 exposure at 400 K under ultrahigh vacuum conditions. The evolution of the surface morphology with annealing temperature was characterized by using low energy electron diffraction (LEED), scanning tunneling microscopy, Auger electron spectroscopy, and x-ray photoelectron spectroscopy. Both oxidized surface alloys form a SnOx overlayer that wets the substrate. However, the SnOx film does not completely cover the surface for the oxidized (2X2) surface alloy. For the oxidized ( 3 X root3)R30 degrees surface alloy, an ordered (4X4) LEED pattern is formed upon flash annealing above 900 K. The formation of this ordered SnOx adlayer coincides with Sri segregation from the bulk to the interface region. A model for the (4X4) structure is discussed. The SnOx overlayer formed by oxidation of the (2X2) surface alloy is significantly less thermally stable than the oxidized (,3 X root3)R30 degrees surface alloy. Exothermic alloying of Sn with Pt may facilitate the decomposition of the oxide overlayers. Differences in the amount of subsurface tin and its segregation to the surface is proposed to explain the thermal stabilities of the oxide layers. The incompleteness of the SnOx overlayer and less subsurface tin for the oxidized (2X2) surface alloy is proposed to explain its significant lower thermal stability. (C) 2001 American Vacuum Society.
引用
收藏
页码:1953 / 1958
页数:6
相关论文
共 37 条
  • [1] ASBURY DA, 1988, SURF SCI, V199, P552
  • [2] LEED CRYSTALLOGRAPHIC INVESTIGATION OF ULTRATHIN FILMS FORMED BY DEPOSITION OF SN ON THE PT(111) SURFACE
    ATREI, A
    BARDI, U
    WU, JX
    ZANAZZI, E
    ROVIDA, G
    [J]. SURFACE SCIENCE, 1993, 290 (03) : 286 - 294
  • [3] MOSSBAUER-SPECTRA INVESTIGATION OF THE ROLE OF TIN IN PLATINUM-TIN REFORMING CATALYSTS
    BACAUD, R
    BUSSIERE, P
    FIGUERAS, F
    [J]. JOURNAL OF CATALYSIS, 1981, 69 (02) : 399 - 409
  • [4] BATZILL M, 1994, REP PROG PHYS, V57, P939
  • [5] SURFACE-COMPOSITION OF SOME SELECTED GROUP-VIII AU AND GROUP-VIII SN ALLOYS
    BILOEN, P
    BOUWMAN, R
    VANSANTEN, RA
    BRONGERSMA, HH
    [J]. APPLIED SURFACE SCIENCE, 1979, 2 (04) : 532 - 542
  • [6] SURFACE ANALYSIS OF PLATINUM-TIN ALLOYS BY X-RAY PHOTOELECTRON-SPECTROSCOPY
    BOUWMAN, R
    BILOEN, P
    [J]. ANALYTICAL CHEMISTRY, 1974, 46 (01) : 136 - 138
  • [7] SURFACE COMPOSITION AND DEPTH CONCENTRATION PROFILE OF PLATINUM-TIN ALLOYS FROM COMBINED X-RAY PHOTOELECTRON AND AUGER SPECTROSCOPIC DATA
    BOUWMAN, R
    BILOEN, P
    [J]. SURFACE SCIENCE, 1974, 41 (02) : 348 - 358
  • [8] Effects of potassium on silica-supported Pt and Pt/Sn catalysts for isobutane dehydrogenation
    Cortright, RD
    Dumesic, JA
    [J]. JOURNAL OF CATALYSIS, 1995, 157 (02) : 576 - 583
  • [9] XPS INVESTIGATION OF TIN OXIDE SUPPORTED PLATINUM
    COX, DF
    HOFLUND, GB
    LAITINEN, HA
    [J]. LANGMUIR, 1985, 1 (03) : 269 - 273
  • [10] CONVERSION OF N-HEXANE OVER MONO-FUNCTIONAL SUPPORTED AND UNSUPPORTED PTSN CATALYSTS
    DAUTZENBERG, FM
    HELLE, JN
    BILOEN, P
    SACHTLER, WMH
    [J]. JOURNAL OF CATALYSIS, 1980, 63 (01) : 119 - 128