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Structural Evolution of Gas-Phase Coinage Metal Clusters in Thiolate Self-Assembled Mono layers on Au
被引:7
|作者:
Costelle, Leila
[1
]
Raisanen, Minna T.
[2
]
Joyce, Jennifer T.
[3
,4
]
Silien, Christophe
[3
,4
]
Johansson, Leena-Sisko
[5
]
Campbell, Joseph M.
[5
]
Raisanen, Jyrki
[1
]
机构:
[1] Univ Helsinki, Div Mat Phys, Dept Phys, FI-00014 Helsinki, Finland
[2] Univ Helsinki, Inorgan Chem Lab, Dept Chem, FI-00014 Helsinki, Finland
[3] Univ Limerick, Dept Phys & Energy, Castletroy, Limerick, Ireland
[4] Univ Limerick, Mat & Surface Sci Inst, Castletroy, Limerick, Ireland
[5] Aalto Univ, Sch Chem Technol, Dept Forest Prod Technol, Forest Prod Surface Chem Grp, FI-00076 Aalto, Finland
基金:
芬兰科学院;
关键词:
SCANNING-TUNNELING-MICROSCOPY;
UNDERPOTENTIAL DEPOSITION;
N-ALKANETHIOLS;
MONOLAYERS;
GOLD;
SURFACE;
COPPER;
NANOPARTICLES;
FILMS;
XPS;
D O I:
10.1021/jp307148p
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:
Metallization of organic surfaces is important especially for applications in molecular electronics. It can be realized by different means, one promising albeit less studied method being gas-phase deposition of metal clusters. Here, we report on the interactions of gas-phase Cu, Ag, and Au clusters with n-dodecanethiolate self-assembled monolayers (SAMs) on Au substrate. The morphology and composition of the deposited clusters and their impact on the interface structure of the SAM/Au substrate were investigated using scanning tunneling microscopy. The chemical and physical interactions between the clusters and thiolates were characterized using X-ray photoelectron spectroscopy. The Au clusters are found to penetrate through the monolayer as a whole and partially retain their spherical geometry, whereas atom-by-atom diffusion and/or defect-mediated penetration are proposed for the Cu and Ag clusters.
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页码:22602 / 22607
页数:6
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