Archimedean-like tiling on decagonal quasicrystalline surfaces

被引:195
作者
Mikhael, Jules [1 ]
Roth, Johannes [2 ]
Helden, Laurent [1 ]
Bechinger, Clemens [1 ,3 ]
机构
[1] Univ Stuttgart, Inst Phys 2, D-70569 Stuttgart, Germany
[2] Univ Stuttgart, Inst Theoret & Angew Phys, D-70569 Stuttgart, Germany
[3] Max Planck Inst Met Res, D-70569 Stuttgart, Germany
关键词
D O I
10.1038/nature07074
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Monolayers on crystalline surfaces often form complex structures with physical and chemical properties that differ strongly from those of their bulk phases(1). Such hetero-epitactic overlayers are currently used in nanotechnology and understanding their growth mechanism is important for the development of new materials and devices. In comparison with crystals, quasicrystalline surfaces exhibit much larger structural and chemical complexity leading, for example, to unusual frictional(2), catalytical(3) or optical properties(4,5). Deposition of thin films on such substrates can lead to structures that may have typical quasicrystalline properties. Recent experiments have indeed showed 5-fold symmetries in the diffraction pattern of metallic layers adsorbed on quasicrystals(6,7). Here we report a real-space investigation of the phase behaviour of a colloidal monolayer interacting with a quasicrystalline decagonal substrate created by interfering five laser beams. We find a pseudomorphic phase that shows both crystalline and quasicrystalline structural properties. It can be described by an archimedean-like tiling(8,9) consisting of alternating rows of square and triangular tiles. The calculated diffraction pattern of this phase is in agreement with recent observations of copper adsorbed on icosahedral Al(70)Pd(21)Mn(9) surfaces(10). In addition to establishing a link between archimedean tilings and quasicrystals, our experiments allow us to investigate in real space how single-element monolayers can form commensurate structures on quasicrystalline surfaces.
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页码:501 / 504
页数:4
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