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Metallic nanoparticle contacts for high-yield, ambient-stable molecular-monolayer devices

Author

Listed:
  • Gabriel Puebla-Hellmann

    (IBM Research - Zurich
    University of Basel)

  • Koushik Venkatesan

    (Macquarie University, North Ryde
    University of Zurich)

  • Marcel Mayor

    (University of Basel
    Karlsruhe Institute of Technology, Institute of Nanotechnology
    School of Chemistry, Sun Yat-Sen University)

  • Emanuel Lörtscher

    (IBM Research - Zurich)

Abstract

Accessing the intrinsic functionality of molecules for electronic applications1–3, light emission4 or sensing5 requires reliable electrical contacts to those molecules. A self-assembled monolayer (SAM) sandwich architecture6 is advantageous for technological applications, but requires a non-destructive, top-contact fabrication method. Various approaches ranging from direct metal evaporation6 over poly(3,4-ethylenedioxythiophene) polystyrene sulfonate7 (PEDOT:PSS) or graphene8 interlayers to metal transfer printing9 have been proposed. Nevertheless, it has not yet been possible to fabricate SAM-based devices without compromising film integrity, intrinsic functionality or mass-fabrication compatibility. Here we develop a top-contact approach to SAM-based devices that simultaneously addresses all these issues, by exploiting the fact that a metallic nanoparticle can provide a reliable electrical contact to individual molecules10. Our fabrication route involves first the conformal and non-destructive deposition of a layer of metallic nanoparticles directly onto the SAM (itself laterally constrained within circular pores in a dielectric matrix, with diameters ranging from 60 nanometres to 70 micrometres), and then the reinforcement of this top contact by direct metal evaporation. This approach enables the fabrication of thousands of identical, ambient-stable metal–molecule–metal devices. Systematic variation of the composition of the SAM demonstrates that the intrinsic molecular properties are not affected by the nanoparticle layer and subsequent top metallization. Our concept is generic to densely packed layers of molecules equipped with two anchor groups, and provides a route to the large-scale integration of molecular compounds into solid-state devices that can be scaled down to the single-molecule level.

Suggested Citation

  • Gabriel Puebla-Hellmann & Koushik Venkatesan & Marcel Mayor & Emanuel Lörtscher, 2018. "Metallic nanoparticle contacts for high-yield, ambient-stable molecular-monolayer devices," Nature, Nature, vol. 559(7713), pages 232-235, July.
  • Handle: RePEc:nat:nature:v:559:y:2018:i:7713:d:10.1038_s41586-018-0275-z
    DOI: 10.1038/s41586-018-0275-z
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    Cited by:

    1. Thanh Luan Phan & Sohyeon Seo & Yunhee Cho & Quoc An Vu & Young Hee Lee & Dinh Loc Duong & Hyoyoung Lee & Woo Jong Yu, 2022. "CNT-molecule-CNT (1D-0D-1D) van der Waals integration ferroelectric memory with 1-nm2 junction area," Nature Communications, Nature, vol. 13(1), pages 1-8, December.
    2. Joel M. Fruhman & Hippolyte P.A.G. Astier & Bruno Ehrler & Marcus L. Böhm & Lissa F. L. Eyre & Piran R. Kidambi & Ugo Sassi & Domenico Fazio & Jonathan P. Griffiths & Alexander J. Robson & Benjamin J., 2021. "High-yield parallel fabrication of quantum-dot monolayer single-electron devices displaying Coulomb staircase, contacted by graphene," Nature Communications, Nature, vol. 12(1), pages 1-10, December.
    3. Xinkai Qiu & Ryan C. Chiechi, 2022. "Printable logic circuits comprising self-assembled protein complexes," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
    4. Ping’an Li & Yoram Selzer, 2022. "Molecular ensemble junctions with inter-molecular quantum interference," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    5. Jorge Trasobares & Juan Carlos Martín-Romano & Muhammad Waqas Khaliq & Sandra Ruiz-Gómez & Michael Foerster & Miguel Ángel Niño & Patricia Pedraz & Yannick. J. Dappe & Marina Calero Ory & Julia García, 2023. "Hybrid molecular graphene transistor as an operando and optoelectronic platform," Nature Communications, Nature, vol. 14(1), pages 1-10, December.

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