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Issue 2, 2012
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Charge transport in vertically aligned, self-assembled peptide nanotube junctions

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Abstract

The self-assembly propensity of peptides has been extensively utilized in recent years for the formation of supramolecular nanostructures. In particular, the self-assembly of peptides into fibrils and nanotubes makes them promising building blocks for electronic and electro-optic applications. However, the mechanisms of charge transfer in these wire-like structures, especially in ambient conditions, are not yet fully understood. We describe here a layer-by-layer deposition methodology of short self-assembled cyclic peptide nanotubes, which results in vertically oriented nanotubes on gold substrates. Using this novel deposition methodology, we have fabricated molecular junctions with a conductive atomic force microscopy tip as a second electrode. Studies of the junctions' current–voltage characteristics as a function of the nanotube length revealed an efficient charge transfer in these supramolecular structures, with a low current attenuation constant of 0.1 Å−1, which indicate that electron transfer is dominated by hopping. Moreover, the threshold voltage to field-emission dominated transport was found to increase with peptide length in a manner that depends on the nature of the contact with the electrodes. The flexibility in the design of the peptide monomers and the ability to control their sequential order over the nanotube by means of the layer-by-layer assembly process, which is demonstrated in this work, can be used to engineer the electronic properties of self-assembled peptide nanotubes toward device applications.

Graphical abstract: Charge transport in vertically aligned, self-assembled peptide nanotube junctions

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Publication details

The article was received on 10 Aug 2011, accepted on 12 Oct 2011 and first published on 24 Nov 2011


Article type: Paper
DOI: 10.1039/C1NR11068C
Citation: Nanoscale, 2012,4, 518-524
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    Charge transport in vertically aligned, self-assembled peptide nanotube junctions

    M. Mizrahi, A. Zakrassov, J. Lerner-Yardeni and N. Ashkenasy, Nanoscale, 2012, 4, 518
    DOI: 10.1039/C1NR11068C

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