0000000000116812

AUTHOR

Ville Haapasilta

showing 3 related works from this author

Impact of the reaction pathway on the final product in on-surface synthesis

2020

International audience; On-surface synthesis provides a very promising strategy for creating stable functional structures on surfaces. In the past, classical reactions known from solution synthesis have been successfully transferred onto a surface. Due to the presence of the surface, on-surface synthesis provides the potential of directing the reaction pathway in a manner that might not be accessible in classical solution synthesis. In this work, we present evidence for an acetylene polymerization from a terminal alkyne monomer deposited onto calcite (10.4). Strikingly, although the dimer forms on the surface as well, we find no indication for diacetylene polymerization. This is in sharp co…

chemistry.chemical_classificationSurface (mathematics)DiacetyleneDimerFinal productGeneral Physics and AstronomyAlkyne02 engineering and technology540010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundMonomer[CHIM.POLY]Chemical Sciences/PolymersPolymerizationchemistryAcetylene[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Physical and Theoretical Chemistry0210 nano-technology
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Diacetylene polymerization on a bulk insulator surface

2017

| openaire: EC/FP7/610446/EU//PAMS Molecular electronics has great potential to surpass known limitations in conventional silicon-based technologies. The development of molecular electronics devices requires reliable strategies for connecting functional molecules by wire-like structures. To this end, diacetylene polymerization has been discussed as a very promising approach for contacting single molecules with a conductive polymer chain. A major challenge for future device fabrication is transferring this method to bulk insulator surfaces, which are mandatory to decouple the electronic structure of the functional molecules from the support surface. Here, we provide experimental evidence for…

Materials scienceBand gapGeneral Physics and AstronomyNanotechnology02 engineering and technologyElectronic structure010402 general chemistry01 natural sciences530chemistry.chemical_compound[CHIM]Chemical SciencesPhysical and Theoretical Chemistrychemistry.chemical_classificationConductive polymerDiacetyleneta114Molecular electronicsPolymer021001 nanoscience & nanotechnology0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymerschemistryPolymerizationChemical physicsDensity functional theory0210 nano-technology
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Deposition order controls the first stages of a metal-organic coordination network on an insulator surface

2016

| openaire: EC/FP7/610446/EU//PAMS We report on first stages toward the formation of a surface-confined metal-organic coordination network (MOCN) by sequential deposition of biphenyl-4,4′-dicarboxylic acid and iron atoms on the surface of a bulk insulator, calcite (10.4). The influence of the deposition order on the structure formation is studied by noncontact atomic force microscopy operated in ultrahigh vacuum at room temperature. It is found that sequential deposition facilitates MOCN formation when the organic linker molecules are first adsorbed on the surface, followed by iron deposition. This observation is explained by first-principles computations, indicating that the metal-molecule…

CalciteStructure formationta114Atomic force microscopyIron deposition02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistry.chemical_compoundGeneral EnergyAdsorptionchemistryChemical physicsLattice (order)Coordination networkMoleculePhysical and Theoretical Chemistry0210 nano-technologyJournal of Physical Chemistry C
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