Curtin University Homepage
  • Library
  • Help
    • Admin

    espace - Curtin’s institutional repository

    JavaScript is disabled for your browser. Some features of this site may not work without it.
    View Item 
    • espace Home
    • espace
    • Curtin Research Publications
    • View Item
    • espace Home
    • espace
    • Curtin Research Publications
    • View Item

    The spontaneous formation of single-molecule junctions via terminal alkynes

    Access Status
    Fulltext not available
    Authors
    Pla-Vilanova, P.
    Aragonès, A.
    Ciampi, S.
    Sanz, F.
    Darwish, Nadim
    Diez-Perez, I.
    Date
    2015
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Pla-Vilanova, P. and Aragonès, A. and Ciampi, S. and Sanz, F. and Darwish, N. and Diez-Perez, I. 2015. The spontaneous formation of single-molecule junctions via terminal alkynes. Nanotechnology. 26 (38).
    Source Title
    Nanotechnology
    DOI
    10.1088/0957-4484/26/38/381001
    ISSN
    0957-4484
    School
    Nanochemistry Research Institute
    URI
    http://hdl.handle.net/20.500.11937/17723
    Collection
    • Curtin Research Publications
    Abstract

    Herein, we report the spontaneous formation of single-molecule junctions via terminal alkyne contact groups. Self-assembled monolayers that form spontaneously from diluted solutions of 1, 4-diethynylbenzene (DEB) were used to build single-molecule contacts and assessed using the scanning tunneling microscopy-break junction technique (STM-BJ). The STM-BJ technique in both its dynamic and static approaches was used to characterize the lifetime (stability) and the conductivity of a single-DEB wire. It is demonstrated that single-molecule junctions form spontaneously with terminal alkynes and require no electrochemical control or chemical deprotonation. The alkyne anchoring group was compared against typical contact groups exploited in single-molecule studies, i.e. amine (benzenediamine) and thiol (benzendithiol) contact groups. The alkyne contact showed a conductance magnitude comparable to that observed with amine and thiol groups. The lifetime of the junctions formed from alkynes were only slightly less than that of thiols and greater than that observed for amines. These findings are important as (a) they extend the repertoire of chemical contacts used in single-molecule measurements to 1-alkynes, which are synthetically accessible and stable and (b) alkynes have a remarkable affinity toward silicon surfaces, hence opening the door for the study of single-molecule transport on a semiconducting electronic platform.

    Related items

    Showing items related by title, author, creator and subject.

    • Metal-Single-Molecule-Semiconductor Junctions Formed by a Radical Reaction Bridging Gold and Silicon Electrodes.
      Peiris, Chandramalika R; Vogel, Yan B; Le Brun, Anton P; Aragonès, Albert C; Coote, Michelle L; Díez-Pérez, Ismael; Ciampi, Simone ; Darwish, Nadim (2019)
      Here we report molecular films terminated with diazonium salts moieties at both ends which enables single-molecule contacts between gold and silicon electrodes at open circuit via a radical reaction. We show that the ...
    • Spontaneous S-Si bonding of alkanethiols to Si(111)-H: Towards Si-molecule-Si circuits
      Peiris, Chandramalika ; Ciampi, Simone ; Dief, Essam ; Zhang, Jinyang ; Canfield, P.J.; Le Brun, A.P.; Kosov, D.S.; Reimers, J.R.; Darwish, Nadim (2020)
      We report the synthesis of covalently linked self-assembled monolayers (SAMs) on silicon surfaces, using mild conditions, in a way that is compatible with silicon-electronics fabrication technologies. In molecular ...
    • Single-molecule electrical contacts on silicon electrodes under ambient conditions
      Aragones, A.; Darwish, Nadim; Ciampi, Simone; Sanz, F.; Gooding, J.; Diez-Perez, I. (2017)
      The ultimate goal in molecular electronics is to use individual molecules as the active electronic component of a real-world sturdy device. For this concept to become reality, it will require the field of single-molecule ...
    Advanced search

    Browse

    Communities & CollectionsIssue DateAuthorTitleSubjectDocument TypeThis CollectionIssue DateAuthorTitleSubjectDocument Type

    My Account

    Admin

    Statistics

    Most Popular ItemsStatistics by CountryMost Popular Authors

    Follow Curtin

    • 
    • 
    • 
    • 
    • 

    CRICOS Provider Code: 00301JABN: 99 143 842 569TEQSA: PRV12158

    Copyright | Disclaimer | Privacy statement | Accessibility

    Curtin would like to pay respect to the Aboriginal and Torres Strait Islander members of our community by acknowledging the traditional owners of the land on which the Perth campus is located, the Whadjuk people of the Nyungar Nation; and on our Kalgoorlie campus, the Wongutha people of the North-Eastern Goldfields.