STM study on the self-assembly of oligothiophene-based organic semiconductors

• Elena Mena-Osteritz,
• Marta Urdanpilleta,
• Erwaa El-Hosseiny,
• Berndt Koslowski,
• Paul Ziemann and
• Peter Bäuerle

Beilstein J. Nanotechnol. 2011, 2, 802–808, doi:10.3762/bjnano.2.88

• ordering on the substrate. Keywords: 2-D crystals; functionalized oligothiophenes; H-bonding; intermolecular interaction; scanning tunneling microscopy; Introduction In the last few decades conjugated organic polymers and oligomers have attracted a broad interest due to their excellent electronic and

• weak intermolecular van der Waals forces and molecule–substrate interactions, as well as intermolecular hydrogen bonding in the case of functionalized oligothiophenes [15][16][17]. The typical flat metallic substrates (HOPG, Au(111), Ag(111), etc.) employed in STM differ from the ITO electrodes used in

• molecular dipole moments. STM and theoretical parameters of 2-D crystals of the investigated carboxylic acid functionalized oligothiophenes HnTCOOH. Acknowledgements The authors gratefully acknowledge the financial support of the Deutsche Forschungsgemeinschaft within the collaborative research unit SFB