Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/8941
Title: Electronic Transport through DNA Nucleotides in Atomically Thin Phosphorene Electrodes for Rapid DNA Sequencing
Authors: Kumawat, Rameshwar L.
Garg, Priyanka
Kumar, Sourabh
Pathak, Biswarup
Keywords: Bias voltage;Density functional theory;DNA;DNA sequences;Nanostructures;Nucleotides;Adenosine monophosphate;Applied bias voltage;black phosphorene;DNA Sequencing;Individual identification;IV characteristics;Non-equilibrium Green's function;Personalized medicines;Gene encoding;DNA;nucleotide;chemistry;DNA sequence;electrode;electron transport;nanopore;procedures;DNA;Electrodes;Electron Transport;Nanopores;Nucleotides;Sequence Analysis, DNA
Issue Date: 2019
Publisher: American Chemical Society
Citation: Kumawat, R. L., Garg, P., Kumar, S., & Pathak, B. (2019). Electronic transport through DNA nucleotides in atomically thin phosphorene electrodes for rapid DNA sequencing. ACS Applied Materials and Interfaces, 11(1), 219-225. doi:10.1021/acsami.8b17239
Abstract: Rapid progresses in developing the fast, low-cost, and reliable methods for DNA sequencing are envisaged for development of personalized medicine. In this respect, nanotechnology has paved the role for the development of advanced DNA sequencing techniques including sequencing with solid-state nanopores or nanogaps. Herein, we have explored the application of a black phosphorene based nanogap-device for DNA sequencing. Using density-functional-theory based non-equilibrium Green's function approach, we have computed transverse transmission and current-voltage (I-V) characteristics of all the four DNA nucleotides (deoxy adenosine monophosphate, deoxy guanidine monophosphate, deoxy thymidine monophosphate, and deoxy cytosine monophosphate) as functions of applied bias voltages. We deduce that it is in principle; possible to differentiate between all the four nucleotides by three sequencing runs at distinct applied bias voltages, i.e., at 0.2, 1.4, and 1.6 V, where individual identification of all the four nucleotides may be possible. Hence, we believe our study might be helpful for experimentalist towards the development of a phosphorene based nanodevice for DNA sequencing to diagnose critical diseases. © 2018 American Chemical Society.
URI: https://doi.org/10.1021/acsami.8b17239
https://dspace.iiti.ac.in/handle/123456789/8941
ISSN: 1944-8244
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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