In situ measurements of oligoaniline conductance: Linking electrochemistry and molecular electronics

被引:28
作者
Chen, Fan
Nuckolls, Colin
Lindsay, Stuart [1 ]
机构
[1] Arizona State Univ, Dept Phys & Astron, Tempe, AZ 85287 USA
[2] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
[3] Arizona State Univ, Biodesign Inst, Tempe, AZ 85287 USA
[4] Columbia Univ, Dept Chem, New York, NY 10027 USA
基金
美国国家科学基金会;
关键词
single molecule conductance; electrochemical gating; molecular electronics; oligo aniline;
D O I
10.1016/j.chemphys.2005.08.052
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The single-molecule conductance of a dithiolated aniline trimer has been measured under potential control and also under an inert solvent. In each experiment, two sets of currents are found, differing by a factor 4, and these are tentatively assigned to differing connections to the electrodes (e.g., on-top vs. hollow sites). The conductances peak (to 17 +/- 1.6 and 5.8 +/- 0.85 nS) between the first and second oxidations of the molecule and change smoothly with surface potential. There is no evidence for a coexistence of oxidized and reduced molecules. Measurements made at a fixed surface potential as a function of tip to substrate bias show a peak current at 0.1 V followed by a region of negative differential resistance. This is accounted for semi-quantitatively by modification of the local potential by the applied bias altering the oxidation state of the molecule under the probe. Measurements made in toluene are Ohmic, indicating that the tip does not alter the oxidation state of the molecule in the absence of screening ions. We discuss the role of gap geometry and bonding in these processes. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:236 / 243
页数:8
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