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Conductance of redox-active single molecular junctions: an electrochemical approach

机译:氧化还原活性单分子结的电导:一种电化学方法

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摘要

The conductance of molecular junctions formed of N, N'-bis(n-thioalkyl)4,4'-bipyridinium bromides or alkanedithiols between a gold (Au) scanning tunnelling microscope tip and a Au(111)-(1x1) electrode has been studied at electrified solid/liquid interfaces. A statistical analysis based on large sets of individual current - distance traces was applied to obtain the electrical conductance of single junctions. The one-electron reduction of the viologen moiety from the dication V2+ to the radical cation state V+. gives rise to a 50% increase of the junction conductance. Increasing the length of the alkyl spacer units leads to a tunnelling decay constant ss(CH2) = 5.9-6.1 nm(-1). This value is significantly lower than ss(CH2) = 8.2 nm(-1) estimated for molecular junctions of alkanedithiols. The difference is attributed to conformational changes within the two junctions. The contact conductance was estimated to 10 mu S.
机译:由金(Au)扫描隧道显微镜尖端和Au(111)-(1x1)电极之间的N,N'-双(n-硫代烷基)4,4'-联吡啶溴化物或烷二硫醇形成的分子结的电导在电气化的固/液界面进行了研究。应用基于大量独立电流-距离轨迹的统计分析来获得单个结的电导率。紫精部分从指示V2 +到自由基阳离子状态V +的单电子还原。导致结电导增加50%。增加烷基间隔基单元的长度会导致隧穿衰减常数ss(CH2)= 5.9-6.1 nm(-1)。该值大大低于估计的链烷二硫醇分子连接的ss(CH2)= 8.2 nm(-1)。差异归因于两个连接点内的构象变化。接触电导估计为10μS。

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