Mechanical Deformation Distinguishes Tunneling Pathways in Molecular Junctions

Zuoti Xie, Ioan Bâldea, Greg Haugstad, Daniel Frisbie

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Developing a clearer understanding of electron tunneling through molecules is a central challenge in molecular electronics. Here we demonstrate the use of mechanical stretching to distinguish orbital pathways that facilitate tunneling in molecular junctions. Our experiments employ junctions based on self-assembled monolayers (SAMs) of homologous alkanethiols (CnT) and oligophenylene thiols (OPTn), which serve as prototypical examples of σ-bonded and π-bonded backbones, respectively. Surprisingly, molecular conductances (G molecule ) for stretched CnT SAMs have exactly the same length dependence as unstretched CnT SAMs in which molecular length is tuned by the number of CH 2 repeat units, n. In contrast, OPTn SAMs exhibit a 10-fold-greater decrease in G molecule with molecular length for stretched versus unstretched cases. Experiment and theory show that these divergent results are explained by the dependence of the molecule-electrode electronic coupling δ on strain and the spatial extent of the principal orbital facilitating tunneling. In particular, differences in the strain sensitivity of δ versus the repeat-length (n) sensitivity can be used to distinguish tunneling via delocalized orbitals versus localized orbitals. Angstrom-level tuning of interelectrode separation thus provides a strategy for examining the relationship between orbital localization or delocalization and electronic coupling in molecular junctions and therefore for distinguishing tunneling pathways.

Original languageEnglish (US)
Pages (from-to)497-504
Number of pages8
JournalJournal of the American Chemical Society
Volume141
Issue number1
DOIs
StatePublished - Jan 9 2019

Bibliographical note

Funding Information:
C.D.F. acknowledges financial support from the U.S. National Science Foundation (CHE-1708173). I.B acknowledges financial support from the Deutsche Forschungsgemeinschaft (DFG grant BA 1799/3-1) and partial computational support from the State of Baden-Württemberg and the DFG through grant no. INST 40/467-1 FUGG. Parts of this work were carried out in the Characterization Facility, University of Minnesota, which receives partial support from the NSF through the MRSEC program.

Publisher Copyright:
© 2018 American Chemical Society.

How much support was provided by MRSEC?

  • Shared

Reporting period for MRSEC

  • Period 5

PubMed: MeSH publication types

  • Journal Article

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