Gate-controlled conductance switching in DNA

被引:105
|
作者
Xiang, Limin [1 ,2 ]
Palma, Julio L. [1 ,2 ,3 ]
Li, Yueqi [1 ,2 ]
Mujica, Vladimiro [2 ]
Ratner, Mark A. [4 ]
Tao, Nongjian [1 ,5 ]
机构
[1] Arizona State Univ, Biodesign Inst, Biodesign Ctr Biosensors & Bioelect, Tempe, AZ 85287 USA
[2] Arizona State Univ, Sch Mol Sci, Tempe, AZ 85287 USA
[3] Penn State Univ, Dept Chem, Eberly Campus,2201 Univ Dr, Lemont Furnace, PA 15456 USA
[4] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[5] Arizona State Univ, Sch Elect Comp & Energy Engn, Tempe, AZ 85287 USA
来源
NATURE COMMUNICATIONS | 2017年 / 8卷
关键词
SINGLE-MOLECULE CONDUCTANCE; SCANNING-TUNNELING-MICROSCOPY; ELECTRON-TRANSFER; QUANTUM INTERFERENCE; CHARGE-TRANSPORT; MEDIATED ELECTROCHEMISTRY; JUNCTION CONDUCTANCE; DENSITY FUNCTIONALS; REDOX MOLECULES; BREAK JUNCTION;
D O I
10.1038/ncomms14471
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Extensive evidence has shown that long-range charge transport can occur along double helical DNA, but active control (switching) of single-DNA conductance with an external field has not yet been demonstrated. Here we demonstrate conductance switching in DNA by replacing a DNA base with a redox group. By applying an electrochemical (EC) gate voltage to the molecule, we switch the redox group between the oxidized and reduced states, leading to reversible switching of the DNA conductance between two discrete levels. We further show that monitoring the individual conductance switching allows the study of redox reaction kinetics and thermodynamics at single molecular level using DNA as a probe. Our theoretical calculations suggest that the switch is due to the change in the energy level alignment of the redox states relative to the Fermi level of the electrodes.
引用
收藏
页数:10
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