Surface oxides on close-packed surfaces of late transition metals

被引:128
作者
Lundgren, Edvin
Mikkelsen, Anders
Andersen, Jesper N.
Kresse, Georg
Schmid, Michael
Varga, Peter
机构
[1] Lund Univ, Dept Synchrotron Radiat Res, S-22100 Lund, Sweden
[2] Univ Vienna, Inst Mat Phys, A-1090 Vienna, Austria
[3] Univ Vienna, Ctr Computat Mat Sci, A-1090 Vienna, Austria
[4] Vienna Univ Technol, Inst Allgemeine Phys, A-1040 Vienna, Austria
关键词
D O I
10.1088/0953-8984/18/30/R01
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
In recent years, the formation of thin, well-ordered but complex surface oxides on late transition metals has been discovered. The driving force for this line of research has been the strong incentive to increase the partial pressure of oxygen from ultra-high vacuum to conditions more relevant for heterogeneous catalysis. Here we review the present status of the research field. Compared to oxygen adatom superstructures, the structure of the surface oxides has proven to be extremely complex, and the investigations have therefore relied on a combination of several experimental and theoretical techniques. The approach to solving the structures formed on close-packed surfaces of Pd and Rh is presented in some detail. Focusing on the structures found, we show that the surface oxides share some general properties with the corresponding bulk oxides. Nevertheless, of all surface oxide structures known today, only the two-dimensional surface oxides on Pd(100) and Pt(110) have the same lattice as the bulk oxides (PdO and PtO, respectively). In addition to two-dimensional oxides, including the O-Rh-O trilayers found on Rh, one-dimensional oxides were observed at ridges or steps of open surfaces such as (110) or vicinal surfaces. Finally, we briefly report on a few studies of the reactivity of surface oxides with well-known structure.
引用
收藏
页码:R481 / R499
页数:19
相关论文
共 76 条
[1]   Structure and reactivity of surface oxides on Pt(110) during catalytic CO oxidation [J].
Ackermann, MD ;
Pedersen, TM ;
Hendriksen, BLM ;
Robach, O ;
Bobaru, SC ;
Popa, I ;
Quiros, C ;
Kim, H ;
Hammer, B ;
Ferrer, S ;
Frenken, JWM .
PHYSICAL REVIEW LETTERS, 2005, 95 (25)
[2]   Two-step reaction on a strained, nanoscale segmented surface [J].
Africh, C ;
Esch, F ;
Li, WX ;
Corso, M ;
Hammer, B ;
Rosei, R ;
Comelli, G .
PHYSICAL REVIEW LETTERS, 2004, 93 (12) :126104-1
[3]   The reconstruction of nickel and rhodium (001) surfaces upon carbon, nitrogen or oxygen adsorptions [J].
Alfè, D ;
de Gironcoli, S ;
Baroni, S .
SURFACE SCIENCE, 1999, 437 (1-2) :18-28
[4]   The reconstruction of Rh(001) upon oxygen adsorption [J].
Alfe, D ;
de Gironcoli, S ;
Baroni, S .
SURFACE SCIENCE, 1998, 410 (2-3) :151-157
[5]   Oxygen induced reconstruction of the Rh(100) surface:: General tendency towards threefold oxygen adsorption site on Rh surfaces [J].
Baraldi, A ;
Cerdá, J ;
Martín-Gago, JA ;
Comelli, G ;
Lizzit, S ;
Paolucci, G ;
Rosei, R .
PHYSICAL REVIEW LETTERS, 1999, 82 (24) :4874-4877
[6]   Order-disorder phase transitions of oxygen on Rh(100) [J].
Baraldi, A ;
Dhanak, VR ;
Comelli, G ;
Prince, KC ;
Rosei, R .
PHYSICAL REVIEW B, 1997, 56 (16) :10511-10517
[7]   XPS identification of the chemical state of subsurface oxygen in the O/Pd(110) system [J].
Bondzie, VA ;
Kleban, P ;
Dwyer, DJ .
SURFACE SCIENCE, 1996, 347 (03) :319-328
[8]   ATOMIC AND MOLECULAR-OXYGEN ADSORPTION ON AG(111) [J].
CAMPBELL, CT .
SURFACE SCIENCE, 1985, 157 (01) :43-60
[9]   Imaging the surface and the interface atoms of an oxide film on Ag{111} by scanning tunneling microscopy:: Experiment and theory [J].
Carlisle, CI ;
King, DA ;
Bocquet, ML ;
Cerdá, J ;
Sautet, P .
PHYSICAL REVIEW LETTERS, 2000, 84 (17) :3899-3902
[10]   OXYGEN-STABILIZED RECONSTRUCTIONS OF PD(100) - PHASE-TRANSITIONS DURING OXYGEN DESORPTION [J].
CHANG, SL ;
THIEL, PA ;
EVANS, JW .
SURFACE SCIENCE, 1988, 205 (1-2) :117-142