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Supramolecular π-Stacked Assemblies of Bis(urea)-Substituted Thiophene Derivatives and Their Electronic Properties Probed with Scanning Tunneling Microscopy and Scanning Tunneling Spectroscopy
76
Citations
38
References
2001
Year
Scanning Tunneling MicroscopySupramolecular AssemblyEngineeringOrganic ElectronicsOligothiophene DerivativesThiophene UnitsOrganic ChemistryChemistryNanoelectronicsBiophysicsOrganic SemiconductorMolecular MaterialThiophene DerivativesSupramolecular ChemistryOrganic Charge-transfer CompoundScanning Tunneling SpectroscopyElectronic MaterialsApplied PhysicsMolecule-based MaterialFunctional MaterialsIsolated Oligothiophene Molecule
In this contribution we investigated the two-dimensional (2D) supramolecular organization and electronic properties of two bis(urea)-substituted oligothiophene derivatives, containing two or three thiophene units (T2 and T3, respectively), at the solution/graphite interface with scanning tunneling microscopy (STM) and scanning tunneling spectroscopy (STS). Because of the π-stacking of the oligomers the observed zero conductance band gap in the I(V) curves of a ribbon is found to be considerably smaller than for an isolated oligothiophene molecule, indicating that there exists an effective conjugation in the π-stacked ribbons on the surface.
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