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Constantinos Tsitsilianis

Publications and source records attributed to Constantinos Tsitsilianis.

4 recordsLinked to original sources

Surface morphologies of Langmuir-Blodgett monolayers of PEOnPSn multiarm star copolymers.

Star polymers composed of equal numbers of poly(ethylene oxide) (PEO) and polystyrene (PS) arms with variable lengths and a large (up to 38 total) number of arms, PEO(n)PS(n), have been examined for their ability to form domain nanostructures at the air-water and air-solid interfaces. All PEO(n)PS(n) star polymers formed stable Langmuir-Blodgett (LB) monolayers transferable to a solid substrate. A range of nanoscale surface morphologies have been observed, ranging from cylindrical to circular domains to bicontinuous structures as the weight fraction of the PEO block varied from 19% to 88% and n from 8 to 19. For the PS-rich stars and at elevated surface pressure, a two-dimensional supramolecular netlike nanostructure was formed. In contrast, in the PEO-rich star polymer with the highest PEO content, we observed peculiar dendritic superstructures caused by intramolecular segregation of nonspherical core-shell micellar structures. On the basis of Langmuir isotherms and observed monolayer morphologies, three different models of possible surface behavior of the star polymers at the interfaces were proposed.

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From smart polymer molecules to responsive nanostructured surfaces.

A heteroarm star block copolymer made from seven polystyrene and seven poly(2-vinylpyridine) arms was grafted onto a solid substrate to fabricate a responsive polymer surface consisting of a densely packed monolayer of copolymer molecules. The grafted layer demonstrates a two-level hierarchical response upon external stimuli combining core-shell transitions of single stars with cooperative transitions of the interacting arms between "dimple" and "ripple" morphologies of the monolayer. The response allows for the switching of the surface properties upon changing solvent selectivity or pH of the aqueous environment.

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Chemical contrasting in a single polymer molecule AFM experiment.

We developed a simple contrasting procedure to improve the AFM visualization of single positively charged polymer chains deposited on substrates of a relatively high roughness via the decoration of the molecules with hexacyanoferrate anions or negatively charged clusters of cyanide-bridged complexes.

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