| Literature DB >> 29875407 |
Marc H Garner1, Haixing Li2,3, Yan Chen4, Timothy A Su3,5, Zhichun Shangguan4,6, Daniel W Paley3,7, Taifeng Liu4, Fay Ng3, Hexing Li4, Shengxiong Xiao8, Colin Nuckolls9,10, Latha Venkataraman11,12, Gemma C Solomon13.
Abstract
The tunnelling of electrons through molecules (and through any nanoscale insulating and dielectric material 1 ) shows exponential attenuation with increasing length 2 , a length dependence that is reflected in the ability of the electrons to carry an electrical current. It was recently demonstrated3-5 that coherent tunnelling through a molecular junction can also be suppressed by destructive quantum interference 6 , a mechanism that is not length-dependent. For the carbon-based molecules studied previously, cancelling all transmission channels would involve the suppression of contributions to the current from both the π-orbital and σ-orbital systems. Previous reports of destructive interference have demonstrated a decrease in transmission only through the π-channel. Here we report a saturated silicon-based molecule with a functionalized bicyclo[2.2.2]octasilane moiety that exhibits destructive quantum interference in its σ-system. Although molecular silicon typically forms conducting wires 7 , we use a combination of conductance measurements and ab initio calculations to show that destructive σ-interference, achieved here by locking the silicon-silicon bonds into eclipsed conformations within a bicyclic molecular framework, can yield extremely insulating molecules less than a nanometre in length. Our molecules also exhibit an unusually high thermopower (0.97 millivolts per kelvin), which is a further experimental signature of the suppression of all tunnelling paths by destructive interference: calculations indicate that the central bicyclo[2.2.2]octasilane unit is rendered less conductive than the empty space it occupies. The molecular design presented here provides a proof-of-concept for a quantum-interference-based approach to single-molecule insulators.Entities:
Year: 2018 PMID: 29875407 DOI: 10.1038/s41586-018-0197-9
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962