Mechanical Deformation Distinguishes Tunneling Pathways in Molecular Junctions

Zuoti Xie, Ioan Bâldea, Greg Haugstad, C. Daniel Frisbie*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

7 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
Pages (from-to)497-504
Number of pages8
JournalJournal of the American Chemical Society
Volume141
Issue number1
DOIs
StatePublished - 9 Jan 2019
Externally publishedYes

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