From atom-resolved scanning tunneling microscopy (STM) studies to the design of new catalysts

被引:61
作者
Lauritsen, JV
Vang, RT
Besenbacher, F [1 ]
机构
[1] Univ Aarhus, Interdisciplinary Nanosci Ctr, DK-2800 Aarhus C, Denmark
[2] Univ Aarhus, Dept Phys & Astron, DK-2800 Aarhus C, Denmark
关键词
model catalyst; scanning tunneling microscopy; STM; steam reforming; hydrodesulfurization; nanoclustcrs; MoS2;
D O I
10.1016/j.cattod.2005.10.015
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The scanning tunneling microscope (STM) is today established as a unique tool for resolving the atomic-scale structure of surfaces. STM studies of model systems relevant to heterogeneous catalysis have made it possible address and resolve many important, fundamental questions. related to catalytic processes by imaging, in direct space, the atomic-scale structure of catalytically relevant model systems. e.g. adsorbate-covered single crystal surfaces or nanoclusters supported either on metals or oxide surfaces, These studies are normally carried out under well-controlled vacuum or pressure conditions. Here we discuss three recent STM studies of model catalyst systems, all illustrating flow the insight gained from fundamental studies of idealized model systems has been successfully linked to studies oil real catalyst systems operating under realistic conditions, and how this interplay has facilitated the development of new and superior high surface area catalysts. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:34 / 43
页数:10
相关论文
共 69 条
[31]   Chemistry of one-dimensional metallic edge states in MoS2 nanoclusters [J].
Lauritsen, JV ;
Nyberg, M ;
Vang, RT ;
Bollinger, MV ;
Clausen, BS ;
Topsoe, H ;
Jacobsen, KW ;
Lægsgaard, E ;
Norskov, JK ;
Besenbacher, F .
NANOTECHNOLOGY, 2003, 14 (03) :385-389
[32]   Atomic-scale structure of Co-Mo-S nanoclusters in hydrotreating catalysts [J].
Lauritsen, JV ;
Helveg, S ;
Lægsgaard, E ;
Stensgaard, I ;
Clausen, BS ;
Topsoe, H ;
Besenbacher, E .
JOURNAL OF CATALYSIS, 2001, 197 (01) :1-5
[33]   General rules for predicting where a catalytic reaction should occur on metal surfaces: A density functional theory study of C-H and C-O bond breaking/making on flat, stepped, and kinked metal surfaces [J].
Liu, ZP ;
Hu, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (07) :1958-1967
[34]   NI EXAFS STUDIES OF THE NI-MO-S STRUCTURE IN CARBON-SUPPORTED AND ALUMINA-SUPPORTED NI-MO CATALYSTS [J].
LOUWERS, SPA ;
PRINS, R .
JOURNAL OF CATALYSIS, 1992, 133 (01) :94-111
[35]   Atom-resolved noncontact atomic force microscopic and scanning tunneling microscopic observations of the structure and dynamic behavior of CeO2(111) surfaces [J].
Namai, Y ;
Fukui, KI ;
Iwasawa, Y .
CATALYSIS TODAY, 2003, 85 (2-4) :79-91
[36]   INITIAL GROWTH OF AU ON NI(110) - SURFACE ALLOYING OF IMMISCIBLE METALS [J].
NIELSEN, LP ;
BESENBACHER, F ;
STENSGAARD, I ;
LAEGSGAARD, E ;
ENGDAHL, C ;
STOLTZE, P ;
JACOBSEN, KW ;
NORSKOV, JK .
PHYSICAL REVIEW LETTERS, 1993, 71 (05) :754-757
[37]   X-RAY ABSORPTION STUDIES OF THE NI ENVIRONMENT IN NI-MO-S [J].
NIEMANN, W ;
CLAUSEN, BS ;
TOPSOE, H .
CATALYSIS LETTERS, 1990, 4 (4-6) :355-363
[38]   Universality in heterogeneous catalysis [J].
Norskov, JK ;
Bligaard, T ;
Logadottir, A ;
Bahn, S ;
Hansen, LB ;
Bollinger, M ;
Bengaard, H ;
Hammer, B ;
Sljivancanin, Z ;
Mavrikakis, M ;
Xu, Y ;
Dahl, S ;
Jacobsen, CJH .
JOURNAL OF CATALYSIS, 2002, 209 (02) :275-278
[39]   Bridging the pressure gap in surface science at the atomic level:: H/Cu(110) [J].
Österlund, L ;
Rasmussen, PB ;
Thostrup, P ;
Lægsgaard, E ;
Stensgaard, I ;
Besenbacher, F .
PHYSICAL REVIEW LETTERS, 2001, 86 (03) :460-463
[40]   Atomic-scale structure and catalytic reactivity of the RuO2(110) surface [J].
Over, H ;
Kim, YD ;
Seitsonen, AP ;
Wendt, S ;
Lundgren, E ;
Schmid, M ;
Varga, P ;
Morgante, A ;
Ertl, G .
SCIENCE, 2000, 287 (5457) :1474-1476