Ordering Fullerenes at the Nanometer Scale on Solid Surfaces

被引:106
作者
Sanchez, Luis [2 ]
Otero, Roberto [1 ,3 ]
Maria Gallego, Jose [4 ]
Miranda, Rodolfo [1 ,3 ]
Martin, Nazario [2 ,3 ]
机构
[1] Univ Autonoma Madrid, Dept Fis Mat Condensada, E-28049 Madrid, Spain
[2] Univ Complutense Madrid, Dept Quim Organ, Fac CC Quim, E-28040 Madrid, Spain
[3] IMDEA Nanociencia, Madrid 28049, Spain
[4] Inst Ciencia Mat Madrid, Consejo Super Invest Cient, Madrid 28049, Spain
关键词
SCANNING-TUNNELING-MICROSCOPY; SOLAR-ENERGY CONVERSION; HYDROGEN-BONDS; SUPRAMOLECULAR STRUCTURES; MOLECULAR ELECTRONICS; SELF-ORGANIZATION; AU(111) SURFACE; C-60; TETRATHIAFULVALENE; CHEMISTRY;
D O I
10.1021/cr800441b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Different strategies followed for the incorporation of fullerene molecules onto solid surfaces are reviewed. These strategies include site-selective adsorption of fullerene or fullerene derivatives on a bare metals, generation of a regular network of an organic molecule on the surface, and formation of lateral superlattices at a nanometer scale. The tendency toward faceting of the Au (433) vicinal surface is used with regular 4 nm wide terraces separated by bunches of 1.4 nm terracess to modify the atomic structure of some metal surfaces to fabricate long and narrow fullerene stripes. A 2D supramolecular structure from macrocycle is generated and its codeposition with fullerenes on highly oriented pyrolytic graphite (HOPG) is studied. A coadsorbed system formed by acridine-9-carboxylic acid (ACA) and fullerene C 60 on Ag(111) is used for the formation of the intermixed structures that depend on the balance between C 60-ACA-Ag(111) interactions.
引用
收藏
页码:2081 / 2091
页数:11
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