Unconventional molecule-resolved current rectification in diamondoid-fullerene hybrids
(2014) Nature Communications — Vol. 5, p. 4877 (2014)
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- The unimolecular rectifier is a fundamental building block of molecular electronics. Rectification in single molecules can arise from electron transfer between molecular orbitals displaying asymmetric spatial charge distributions, akin to p-n junction diodes in semiconductors. Here we report a novel all hydrocarbon molecular rectifier consisting of a diamantane-C60 conjugate. By linking both sp3 (diamondoid) and sp2 (fullerene) carbon allotropes, this bybrid molecule opposingly pairs negative and positive electron affinities. The single-molecule conductances of self-assembled domains on Au(111), probed by low-temperature scanning tunneling microscopy and spectroscopy, reveal a large rectifying response of the molecular constructs. This specific electronic behaviour is postulated to originate from the electrostatic repulsion of diamantane-C60 molecules due to positively charged terminal hydrogen atoms on the diamondoid interacting with the top electrode (scanning tip) at various bias voltages. Density functional theory computations scrutinize the electronic and vibrational spectroscopic fingerprints of this unique molecular structure and corroborate the unconventional rectification mechanism.
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Randel, J. C., Niestemski, F. C., Botello Mendez, A. R., Mar, W., Ndabashimiye, G., Melinte, S., Dahl, J. E. P., Carlson, R. M. K., Butova, E. D., Fokin, A. A., Schreiner, P. R., Charlier, J.-C., & Manoharan, H. C. (2014). Unconventional molecule-resolved current rectification in diamondoid-fullerene hybrids. Nature Communications, 5, 4877. https://doi.org/10.1038/ncomms5877 (Original work published 2014)