Venkataraman Latha, Klare Jennifer E, Tam Iris W, Nuckolls Colin, Hybertsen Mark S, Steigerwald Michael L
Department of Physics, and Center for Electron Transport in Molecular Nanostructures, Columbia University, New York, New York 10027, USA.
Nano Lett. 2006 Mar;6(3):458-62. doi: 10.1021/nl052373+.
We measure the conductance of amine-terminated molecules by breaking Au point contacts in a molecular solution at room temperature. We find that the variability of the observed conductance for the diamine molecule-Au junctions is much less than the variability for diisonitrile- and dithiol-Au junctions. This narrow distribution enables unambiguous conductance measurements of single molecules. For an alkane diamine series with 2-8 carbon atoms in the hydrocarbon chain, our results show a systematic trend in the conductance from which we extract a tunneling decay constant of 0.91 +/- 0.03 per methylene group. We hypothesize that the diamine link binds preferentially to undercoordinated Au atoms in the junction. This is supported by density functional theory-based calculations that show the amine binding to a gold adatom with sufficient angular flexibility for easy junction formation but well-defined electronic coupling of the N lone pair to the Au. Therefore, the amine linkage leads to well-defined conductance measurements of a single molecule junction in a statistical study.
我们通过在室温下于分子溶液中打破金点接触来测量胺端基分子的电导。我们发现,二胺分子 - 金结所观察到的电导变异性远小于二异腈和二硫醇 - 金结的变异性。这种窄分布使得能够对单分子进行明确的电导测量。对于烃链中含有2 - 8个碳原子的烷烃二胺系列,我们的结果显示出电导的系统趋势,从中我们提取出每个亚甲基的隧穿衰减常数为0.91±0.03。我们推测二胺连接优先与结中配位不足的金原子结合。基于密度泛函理论的计算支持了这一点,该计算表明胺与金吸附原子结合时具有足够的角度灵活性,便于形成结,但氮孤对与金之间具有明确的电子耦合。因此,在统计研究中,胺连接导致单分子结的明确电导测量。