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Electron transfer mediating properties of hydrocarbons as a function of chain length: A differential scanning conductive tip atomic force microscopy investigation

机译:碳氢化合物的电子转移介导性质与链长的关系:差示扫描电导尖端原子力显微镜研究

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摘要

The development of novel molecular and biomolecular devices relies on the understanding of charge transport across molecule-substrate interfaces. However, different strategies adopted so far for fabricating and studying transport through metal - molecule - metal junctions yield values for the transport coefficients that differ by up to orders of magnitude even for the same junction. Conductive tip atomic force microscopy (CT-AFM) allows for the simultaneous measurement of transport and morphological properties of molecular assemblies, but absolute transport measurements depend on the nature of the AFM tip - molecule contact. In this work we present a differential approach to the study of metal - molecule - metal junctions based on the combination of AFM-driven nanolithography and CT-AFM. We nanograft patches of alkanethiol molecules in a self-assembled monolayer of alkanethiol molecules of different chain length and measure by CT-AFM the morphology and the transport properties of the nanopatches and of the reference layer. The method allows for the determination of the differential resistance between the two molecular layers and is thus independent of environmental factors. The validity of this approach is demonstrated by measuring the tunneling decay constant of alkanethiols as a function of their length.
机译:新型分子和生物分子装置的开发依赖于对跨分子-底物界面的电荷传输的理解。然而,迄今为止,采用不同的策略来制造和研究通过金属-分子-金属结的传输,即使对于相同的结,其传输系数值也相差最大数量级。导电尖端原子力显微镜(CT-AFM)可以同时测量分子组件的传输和形态特性,但是绝对传输测量取决于AFM尖端-分子接触的性质。在这项工作中,我们提出了一种基于AFM驱动的纳米光刻技术和CT-AFM相结合的金属-分子-金属结研究的差分方法。我们在链长不同的烷硫醇分子的自组装单层中纳米移植了烷硫醇分子的贴剂,并通过CT-AFM测量了纳米贴剂和参考层的形态和传输性能。该方法允许确定两个分子层之间的差分电阻,因此与环境因素无关。通过测量链烷硫醇的隧穿衰减常数作为其长度的函数,证明了该方法的有效性。

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