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Ultra-high resolution imaging of thin films and single strands of polythiophene using atomic force microscopy

Author

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  • Vladimir V. Korolkov

    (University of Nottingham)

  • Alex Summerfield

    (University of Nottingham)

  • Alanna Murphy

    (University of Nottingham)

  • David B. Amabilino

    (University of Nottingham)

  • Kenji Watanabe

    (National Institute for Materials Science)

  • Takashi Taniguchi

    (National Institute for Materials Science)

  • Peter H. Beton

    (University of Nottingham)

Abstract

Real-space images of polymers with sub-molecular resolution could provide valuable insights into the relationship between morphology and functionality of polymer optoelectronic devices, but their acquisition is problematic due to perceived limitations in atomic force microscopy (AFM). We show that individual thiophene units and the lattice of semicrystalline spin-coated films of polythiophenes (PTs) may be resolved using AFM under ambient conditions through the low-amplitude (≤ 1 nm) excitation of higher eigenmodes of a cantilever. PT strands are adsorbed on hexagonal boron nitride near-parallel to the surface in islands with lateral dimensions ~10 nm. On the surface of a spin-coated PT thin film, in which the thiophene groups are perpendicular to the interface, we resolve terminal CH3-groups in a square arrangement with a lattice constant 0.55 nm from which we can identify abrupt boundaries and also regions with more slowly varying disorder, which allow comparison with proposed models of PT domains.

Suggested Citation

  • Vladimir V. Korolkov & Alex Summerfield & Alanna Murphy & David B. Amabilino & Kenji Watanabe & Takashi Taniguchi & Peter H. Beton, 2019. "Ultra-high resolution imaging of thin films and single strands of polythiophene using atomic force microscopy," Nature Communications, Nature, vol. 10(1), pages 1-8, December.
    • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09571-6
    DOI: 10.1038/s41467-019-09571-6
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