ﻻ يوجد ملخص باللغة العربية
As a secondary structure of DNA, DNA tetrahedra exhibit intriguing charge transport phenomena and provide a promising platform for wide applications like biosensors, as shown in recent electrochemical experiments. Here, we study charge transport in a multi-terminal DNA tetrahedron, finding that its charge transport properties strongly depend upon the interplay among contact position, on-site energy disorder, and base-pair mismatch. Our results indicate that the charge transport efficiency is nearly independent of contact position in the weak disorder regime, and is dramatically declined by the occurrence of a single base-pair mismatch between the source and the drain, in accordance with experimental results [J. Am. Chem. Soc. {bf 134}, 13148 (2012); Chem. Sci. {bf 9}, 979 (2018)]. By contrast, the charge transport efficiency could be enhanced monotonically by shifting the source toward the drain in the strong disorder regime, and be increased when the base-pair mismatch takes place exactly at the contact position. In particular, when the source moves successively from the top vertex to the drain, the charge transport through the tetrahedral DNA device can be separated into three regimes, ranging from disorder-induced linear decrement of charge transport to disorder-insensitive charge transport, and to disorder-enhanced charge transport. Finally, we predict that the DNA tetrahedron functions as a more efficient spin filter compared to double-stranded DNA and opposite spin polarization could be observed at different drains, which may be used to separate spin-unpolarized electrons into spin-up ones and spin-down ones. These results could be readily checked by electrochemical measurements and may help for designing novel DNA tetrahedron-based molecular nanodevices.
Charge migration along DNA molecules has attracted scientific interest for over half a century. Reports on possible high rates of charge transfer between donor and acceptor through the DNA, obtained in the last decade from solution chemistry experime
First principle calculations of charge transfer in DNA molecules are computationally expensive given that charge carriers migrate in interaction with intra- and inter-molecular atomic motion. Screening sequences, e.g. to identify excellent electrical
We report the results of several nonequilibrium experiments performed on superconducting/normal/superconducting (S/N/S) Josephson junctions containing either one or two extra terminals that connect to normal reservoirs. Currents injected into the jun
We report on charge transport and current fluctuations in a single bacteriorhodpsin protein in a wide range of applied voltages covering direct and injection tunnelling regimes. The satisfactory agreement between theory and available experiments vali
The chirality-induced spin selectivity (CISS), demonstrated in diverse chiral molecules by numerous experimental and theoretical groups, has been attracting extensive and ongoing interest in recent years. As the secondary structure of DNA, the charge