4.8 Article

DNA Base-Specific Modulation of Microampere Transverse Edge Currents through a Metallic Graphene Nanoribbon with a Nanopore

Journal

NANO LETTERS
Volume 12, Issue 1, Pages 50-55

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nl202870y

Keywords

DNA sequencing; graphene nanoribbons; nanopore; first-principles quantum transport; NEGF-DFT

Funding

  1. DOE [DE-FG02-07ER46374]
  2. NIH [R21HG004767, R21HG006313]
  3. NSF [TG-DMR100002, CNS-0958512]
  4. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [R21HG006313, R21HG004767] Funding Source: NIH RePORTER

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We study two-terminal devices for DNA sequencing that consist of a metallic graphene nanoribbon with zigzag edges (ZGNR) and a nanopore in its interior through which the DNA molecule is translocated. Using the nonequilibrium Green functions combined with density functional theory, we demonstrate that each of the four DNA nucleobases inserted into the nanopore, whose edge carbon atoms are passivated by either hydrogen or nitrogen, will lead to a unique change in the device conductance. Unlike other recent biosensors based on transverse electronic transport through translocated DNA, which utilize small (of the order of pA) tunneling current across a nanogap or a nanopore yielding a poor signal-to-noise ratio, our device concept relies on the fact that in ZGNRs local current density is peaked around the edges so that drilling a nanopore away from the edges will not diminish the conductance. Inserting a nucleobase into the nanopore affects the charge density in the surrounding area, thereby modulating edge conduction currents whose magnitude is of the order of microampere at bias voltage 0.1 V. The proposed biosensors are not limited to ZGNRs and they could be realized with other nanowires supporting transverse edge currents, such as chiral GNRs or wires made of two-dimensional topological insulators.

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