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Internal Electric Field Modulation in Molecular Electronic Devices by Atmosphere and Mobile Ions

机译:分子电子设备中大气和移动离子对内部电场的调制

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摘要

The internal potential profile and electric field are major factors controlling the electronic behavior of molecular electronic junctions consisting of ∼1–10 nm thick layers of molecules oriented in parallel between conducting contacts. The potential profile is assumed linear in the simplest cases, but can be affected by internal dipoles, charge polarization, and electronic coupling between the contacts and the molecular layer. Electrochemical processes in solutions or the solid state are entirely dependent on modification of the electric field by electrolyte ions, which screen the electrodes and form the ionic double layers that are fundamental to electrode kinetics and widespread applications. The current report investigates the effects of mobile ions on nominally solid-state molecular junctions containing aromatic molecules covalently bonded between flat, conducting carbon surfaces, focusing on changes in device conductance when ions are introduced into an otherwise conventional junction design. Small changes in conductance were observed when a polar molecule, acetonitrile, was present in the junction, and a large decrease of conductance was observed when both acetonitrile (ACN) and lithium ions (Li~(+)) were present. Transient experiments revealed that conductance changes occur on a microsecond–millisecond time scale, and are accompanied by significant alteration of device impedance and temperature dependence. A single molecular junction containing lithium benzoate could be reversibly transformed from symmetric current–voltage behavior to a rectifier by repetitive bias scans. The results are consistent with field-induced reorientation of acetonitrile molecules and Li~(+) ion motion, which screen the electrodes and modify the internal potential profile and provide a potentially useful means to dynamically alter junction electronic behavior.
机译:内部电势分布和电场是控制分子电子结的电子行为的主要因素,该分子电子结由〜1-10 nm厚的平行接触的分子取向的分子层组成。在最简单的情况下,电势分布假定为线性,但可能会受到内部偶极子,电荷极化以及触点与分子层之间的电子耦合的影响。溶液或固态中的电化学过程完全取决于电解质离子对电场的修饰,电解质会屏蔽电极并形成对电极动力学和广泛应用至关重要的离子双层。本报告研究了移动离子对包含共价键合在平坦导电碳表面之间的芳香族分子名义上的固态分子结的影响,重点是将离子引入其他常规结设计中时器件电导的变化。当在连接处存在极性分子乙腈时,观察到电导的微小变化,而在同时存在乙腈(ACN)和锂离子(Li〜(+))时,观察到电导大幅度下降。瞬态实验表明,电导变化发生在微秒至毫秒级,并且伴随着设备阻抗和温度依赖性的显着改变。包含苯甲酸锂的单个分子结可以通过重复偏置扫描可逆地从对称的电流-电压行为转变为整流器。结果与场致乙腈分子的重新定向和Li〜(+)离子运动相一致,后者屏蔽了电极并修改了内部电位分布,并提供了可能有用的手段来动态改变结的电子行为。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2018年第23期|7239-7247|共9页
  • 作者单位

    Department of Chemistry, University of Alberta, Edmonton, Alberta T6G 2G2, Canada;

    Department of Chemistry, University of Alberta, Edmonton, Alberta T6G 2G2, Canada;

    Department of Chemistry, University of Alberta, Edmonton, Alberta T6G 2G2, Canada;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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