Interactions between Oxygen Atoms on Pt(100): Implications for Ordering during Chemisorption and Catalysis

被引:18
作者
Liu, Da-Jiang [1 ]
Evans, James W. [1 ,2 ,3 ]
机构
[1] Iowa State Univ, Ames Lab, US DOE, Ames, IA 50011 USA
[2] Iowa State Univ, Dept Phys & Astron, Ames, IA 50011 USA
[3] Iowa State Univ, Dept Math & Astron, Ames, IA 50011 USA
关键词
chemisorption; density functional calculations; oxygen; platinum; surface chemistry; TOTAL-ENERGY CALCULATIONS; THIN METAL-FILMS; ADSORBATE-ADSORBATE INTERACTIONS; INITIO MOLECULAR-DYNAMICS; WAVE BASIS-SET; CO OXIDATION; CARBON-MONOXIDE; WORK FUNCTION; TRANSITION; ADSORPTION;
D O I
10.1002/cphc.200900998
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 present a DFT analysis of the interactions between chemisorbed oxygen on the unreconstructed (1 x 1)-Pt(100) surface. These interactions control ordering of O not just for single-species adsorption, but also within O domains during coadsorption and reaction with other species such as CO. The calculations indicate that O prefers bridge sites, as deduced previously. In addition, we find a large difference in the interactions between O at different types of bridge site pairs separated by one lattice constant. There is strong repulsion for pairs separated by a Pt atom, but only a weak interaction for pairs separated by a fourfold hollow site. This finding elucidates the tendency for striped (n x 1)-O ordering often observed in chemisorption and reaction studies.
引用
收藏
页码:2174 / 2181
页数:8
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