Chemistry of one-dimensional metallic edge states in MoS2 nanoclusters

被引:178
作者
Lauritsen, JV [1 ]
Nyberg, M
Vang, RT
Bollinger, MV
Clausen, BS
Topsoe, H
Jacobsen, KW
Lægsgaard, E
Norskov, JK
Besenbacher, F
机构
[1] Aarhus Univ, Dept Phys & Astron, CAMP, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ, iNANO, DK-8000 Aarhus C, Denmark
[3] Aarhus Univ, Dept Phys, DK-8000 Aarhus C, Denmark
[4] Haldor Topsoe Res Labs, DK-2800 Lyngby, Denmark
关键词
D O I
10.1088/0957-4484/14/3/306
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nanostructures often have unusual properties that are linked to their small size. We report here on extraordinary chemical properties associated with the edges of two-dimensional MoS2 nanoclusters, which we show to be able to hydrogenate and break up thiophene (C4H4S) molecules. By combining atomically resolved scanning tunnelling microscopy images of single-layer MoS2 nanoclusters and density functional theory calculations of the reaction energetics, we show that the chemistry of the MoS2 nanoclusters can be associated with one-dimensional metallic states located at the perimeter of the otherwise insulating nanoclusters. The new chemistry identified in this work has significant implications for an important catalytic reaction, since MoS2 nanoclusters constitute the basis of hydrotreating catalysts used to clean up sulfur-containing molecules from oil products in the hydrodesulfurization process.
引用
收藏
页码:385 / 389
页数:5
相关论文
共 27 条
[11]   Sulfidation and thiophene hydrodesulfurization activity of nickel tungsten sulfide model catalysts, prepared without and with chelating agents [J].
Kishan, G ;
Coulier, L ;
de Beer, VHJ ;
van Veen, JAR ;
Niemantsverdriet, JW .
JOURNAL OF CATALYSIS, 2000, 196 (01) :180-189
[12]   A FULLY AUTOMATED, THIMBLE-SIZE SCANNING TUNNELLING MICROSCOPE [J].
LAEGSGAARD, E ;
BESENBACHER, F ;
MORTENSEN, K ;
STENSGAARD, I .
JOURNAL OF MICROSCOPY-OXFORD, 1988, 152 :663-669
[13]   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
[14]  
LAURITSEN JV, 2003, UNPUB
[15]   PHOTOCATALYSIS ON TIO2 SURFACES - PRINCIPLES, MECHANISMS, AND SELECTED RESULTS [J].
LINSEBIGLER, AL ;
LU, GQ ;
YATES, JT .
CHEMICAL REVIEWS, 1995, 95 (03) :735-758
[16]   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
[17]   ATOMS, MOLECULES, SOLIDS, AND SURFACES - APPLICATIONS OF THE GENERALIZED GRADIENT APPROXIMATION FOR EXCHANGE AND CORRELATION [J].
PERDEW, JP ;
CHEVARY, JA ;
VOSKO, SH ;
JACKSON, KA ;
PEDERSON, MR ;
SINGH, DJ ;
FIOLHAIS, C .
PHYSICAL REVIEW B, 1992, 46 (11) :6671-6687
[18]  
PRINS R, 1997, HDB HETEROGENEOUS CA, P1908, DOI DOI 10.1002/9783527619474.CHL4B
[19]   Ab initio study of the H2-H2S/MoS2 gas-solid interface:: The nature of the catalytically active sites [J].
Raybaud, P ;
Hafner, J ;
Kresse, G ;
Kasztelan, S ;
Toulhoat, H .
JOURNAL OF CATALYSIS, 2000, 189 (01) :129-146
[20]   Adsorption of thiophene on surfaces of clean and Ni-promoted molybdenum sulfide [J].
Rodriguez, JA ;
Dvorak, J ;
Capitano, AT ;
Gabelnick, AM ;
Gland, JL .
SURFACE SCIENCE, 1999, 429 (1-3) :L462-L468