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Azobenzenes as Light-Controlled Molecular Electronic Switches in Nanoscale Metal-Molecule-Metal Junctions

机译:偶氮苯作为纳米级金属-分子-金属连接中的光控分子电子开关

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摘要

The transduction of a conformational change into electrical switching is an attractive approach to performing electronic operations with molecular building blocks. Although there are a few examples in the literature of conductance switching behavior in molecular junctions, the switching mechanisms are controversial and in some cases thought to originate from unexpected sources such as molecule-electrode bond fluctuations or the reversible formation of metallic filaments through the molecular layers. Photochromic molecules such as azobenzenes and di-arylethenes are appealing candidate switches since they undergo well-characterized photoisomerizations. Very recently, electrical switching has been proved with these molecules using large-area contacts. In this report, we consider conductance switching at the single domain level in nanoscale junctions consisting of azobenzene-based molecules which switch from an extended trans to a compact cis form upon UV irradiation.
机译:将构象变化转换为电开关是利用分子构件进行电子操作的一种有吸引力的方法。尽管文献中有几个例子说明了分子结中的电导转换行为,但这种转换机制还是有争议的,在某些情况下被认为是源自意料之外的来源,例如分子电极键的波动或通过分子层可逆形成的金属丝。光致变色分子(如偶氮苯和二芳烃)是吸引人的候选开关,因为它们经历了特征充分的光异构化。最近,已经证明使用大面积接触可以对这些分子进行电开关。在本报告中,我们考虑了由偶氮苯基分子组成的纳米级结在单域水平上的电导转换,该基团在紫外线照射下从扩展的反式转变为紧凑的顺式形式。

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