0000000000901981
AUTHOR
Bernd Struth
Analysis of the cleaved topaz (001) surface.
We report on the first study of the cleaved (001) topaz surface and the characterization of the chemical composition and atomic arrangement of the surface. We conclude that there is strong evidence for a hydroxyl group termination appropriate for further chemical reactions. The surface itself is easily accessible, atomically flat and suitable for potential technological applications.
Chemical modification of Topaz surfaces
In chemisorption, one is typically faced with the problem that the two-dimensional structure of the organic layer does not match the structure of the inorganic substrate. This work describes the first steps toward an induced epitaxial correlation of organic compounds on an inorganic surface. The idea of this work was to use a single crystal with a two-dimensional surface structure, Topaz (001), that matches an alkyl chain lattice better than existing substrates. X-ray reflectivity and FTIR experiments prove the surface modification of the Topaz, which is probably an etherification of the reactive OH-groups on the Topaz (001) surface.
Self-organization of amphiphilic N-acylated linear polyethyleneimines: investigation of a reversible monolayer collapse
Abstract Poly-N-4-decyloxybenzoylethyleneimine, highly crystalline in bulk, forms a stable monolayer at the air-water interface which undergoes a reversible collapse into a probable bilayer structure at higher surface pressures. We achieved transfer both from the monolayer and “bilayer” region of the polymer film at the water surface onto hydrophilic and hydrophobized quartz supports. Based on X-ray investigations on the deposited Langmuir-Blodgett films, a possible mechanism for the reversible collapse is proposed.