| Literature DB >> 27102683 |
Cunlan Guo1, Kun Wang1, Elinor Zerah-Harush2, Joseph Hamill1, Bin Wang1, Yonatan Dubi2,3, Bingqian Xu1.
Abstract
The predictability, diversity and programmability of DNA make it a leading candidate for the design of functional electronic devices that use single molecules, yet its electron transport properties have not been fully elucidated. This is primarily because of a poor understanding of how the structure of DNA determines its electron transport. Here, we demonstrate a DNA-based molecular rectifier constructed by site-specific intercalation of small molecules (coralyne) into a custom-designed 11-base-pair DNA duplex. Measured current-voltage curves of the DNA-coralyne molecular junction show unexpectedly large rectification with a rectification ratio of about 15 at 1.1 V, a counter-intuitive finding considering the seemingly symmetrical molecular structure of the junction. A non-equilibrium Green's function-based model-parameterized by density functional theory calculations-revealed that the coralyne-induced spatial asymmetry in the electron state distribution caused the observed rectification. This inherent asymmetry leads to changes in the coupling of the molecular HOMO-1 level to the electrodes when an external voltage is applied, resulting in an asymmetric change in transmission.Entities:
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Year: 2016 PMID: 27102683 DOI: 10.1038/nchem.2480
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.427