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In situ formation of highly conducting covalent Au–C contacts for single-molecule junctions

Nature Nanotechnology volume 6, pages 353–357 (2011)Cite this article

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Abstract

Charge transport across metal–molecule interfaces has an important role in organic electronics1. Typically, chemical link groups such as thiols2 or amines3 are used to bind organic molecules to metal electrodes in single-molecule circuits, with these groups controlling both the physical structure and the electronic coupling at the interface. Direct metal–carbon coupling has been shown through C60, benzene and π-stacked benzene4,5,6,7, but ideally the carbon backbone of the molecule should be covalently bonded to the electrode without intervening link groups. Here, we demonstrate a method to create junctions with such contacts. Trimethyl tin (SnMe3)-terminated polymethylene chains are used to form single-molecule junctions with a break-junction technique2,3. Gold atoms at the electrode displace the SnMe3 linkers, leading to the formation of direct Au–C bonded single-molecule junctions with a conductance that is ∼100 times larger than analogous alkanes with most other terminations. The conductance of these Au–C bonded alkanes decreases exponentially with molecular length, with a decay constant of 0.97 per methylene, consistent with a non-resonant transport mechanism. Control experiments and ab initio calculations show that high conductances are achieved because a covalent Au–C sigma (σ) bond is formed. This offers a new method for making reproducible and highly conducting metal–organic contacts.

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Figure 1: Conductance data for SnMe3-linked alkanes.
Figure 2: Conductance histogram for SnMe3- and Au-PPh3-terminated compounds.
Figure 3: Calculated geometry and transmission.

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Acknowledgements

This work was supported primarily by the Nanoscale Science and Engineering Initiative of the National Science Foundation (NSF; CHE-0641523), the New York State Office of Science, Technology, and Academic Research (NYSTAR) and an NSF Career Award to L.V. (CHE-07-44185). This work was carried out in part at the Center for Functional Nanomaterials, Brookhaven National Laboratory, which is supported by the Office of Basic Energy Sciences of the US Department of Energy (DOE; DE-AC02-98CH10886). This work was also supported in part by the DOE Energy Frontier Research Centers programme (EFRC; DE-SC0001085).

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Author notes

  1. Z.-L. Cheng and R. Skouta: These authors contributed equally to this work

Authors and Affiliations

  1. Department of Chemistry, Columbia University, 3000 Broadway, New York, New York 10027, USA

    Z.-L. Cheng, R. Skouta, S. Schneebeli, W. Chen & R. Breslow

  2. Center for Electron Transport in Molecular Nanostructures, 530 W 120th Street, New York, New York 10027, USA

    H. Vazquez, R. Breslow & L. Venkataraman

  3. Department of Applied Physics and Applied Mathematics, Columbia University, 530 W 120th Street, New York, New York 10027, USA

    J. R. Widawsky & L. Venkataraman

  4. Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, New York, New York 11973, USA

    M. S. Hybertsen

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  1. Z.-L. Cheng
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Contributions

Z.L.C., R.S., S.S. and W.C. synthesized the compounds. J.R.W. performed the experiments and data analysis. H.V. carried out all calculations. M.S.H., R.B. and L.V. conceived and designed the experiments and calculations, and co-wrote the paper.

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Correspondence to M. S. Hybertsen, R. Breslow or L. Venkataraman.

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The authors declare no competing financial interests.

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Cheng, ZL., Skouta, R., Vazquez, H. et al. In situ formation of highly conducting covalent Au–C contacts for single-molecule junctions. Nature Nanotech 6, 353–357 (2011). https://doi.org/10.1038/nnano.2011.66

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