Structural and electronic properties of Pt modified Au(100) surface.

Investigations on electronic and geometric structures of platinum adsorbed on monocrystalline gold surfaces are important for understanding the remarkable catalytic properties of bimetallic Pt-Au systems. Herein, the morphology of quasi-hexagonal (hex) Au(100) surface after deposition of platinum for coverage up to 0.5 monolayer (ML) has been investigated by scanning tunneling microscopy (STM).

Self-ordering of chemisorbed PTCDA molecules on Ge(001) driven by repulsive forces.

Realization of future hybrid electronic devices combining organic and inorganic semiconductors requires a well-defined interface between both components. Such an interface can be formed generally by self-ordering of organic molecules on inorganic substrates, which is usually hindered by strong covalent bonds to the semiconductor surface. In this paper, the 3,4,9,10-perylenetetracarboxylic dianhydride (PTCDA) molecules were unexpectedly found to form a locally self-ordered monolayer on a strongly interacting semiconductor surface of the Ge(001).

Local electronic structure of doping defects on Tl/Si(111)1x1.

The Tl/Si(111)1 × 1 surface is a representative of a 2D layer with Rashba-type spin-split electronic bands. To utilize the spin polarization, doping of the system should be understood on atomic level. We present a study of two types of atomic defects predicted to dope the considered electronic system - Si-induced vacancies and defects associated with the presence of extra Tl atoms.

Coexistence of nanowire-like hex and (1 × 1) phases in the topmost layer of Au(100) surface.

Scanning tunneling microscopy and density functional theory calculations were used to study the structure of the Au(100) surface after ion bombardment. The results indicate a development of two phases: the quasi-hexagonal (hex) and the (1 × 1) on the surface. A decrease in the number of surface atoms caused by ion bombardment leads to the development of a coexistence of phases inside the surface layer.

Electric-field-controlled phase transition in a 2D molecular layer.

Self-assembly of organic molecules is a mechanism crucial for design of molecular nanodevices. We demonstrate unprecedented control over the self-assembly, which could allow switching and patterning at scales accessible by lithography techniques. We use the scanning tunneling microscope (STM) to induce a reversible 2D-gas-solid phase transition of copper phthalocyanine molecules on technologically important silicon surface functionalized by a metal monolayer.

Mechanism of a molecular photo-switch adsorbed on Si(100).

We present a very compact molecular photoswitch on the technologically important Si(100) surface. Its adsorption configuration is determined by a combined scanning tunneling microscopy (STM) and density functional theory (DFT) study. The mechanisms of the isomerization reactions are discussed in view of DFT calculations and proven by in situ light irradiation.