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z型压电脉冲调制扫描隧道显微镜断结:迈向具有不同金属电极的单分子整流器

z-Piezo Pulse-Modulated STM Break Junction: Toward Single-Molecule Rectifiers with Dissimilar Metal Electrodes.

作者信息

Li Xiao-Mei, Wang Ya-Hao, Seng Jing-Wen, Zheng Ju-Fang, Cao Rui, Shao Yong, Chen Jing-Zhe, Li Jian-Feng, Zhou Xiao-Shun, Mao Bing-Wei

机构信息

Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Institute of Physical Chemistry, Zhejiang Normal University, Jinhua 321004, China.

Department of Physics, Shanghai University, Shanghai 200444, China.

出版信息

ACS Appl Mater Interfaces. 2021 Feb 24;13(7):8656-8663. doi: 10.1021/acsami.0c21435. Epub 2021 Feb 15.

DOI:10.1021/acsami.0c21435
PMID:33587592
Abstract

Fabricating single-molecule junctions with asymmetric metal electrodes is significant for realizing single-molecule diodes, but it remains a big challenge. Herein, we develop a z-piezo pulse-modulated scanning tunneling microscopy break junction (STM-BJ) technique to construct a robust asymmetric junction with different metal electrodes. The asymmetric Ag/BPY-EE/Au single-molecule junctions exhibit a middle conductance value in between those of the two individual symmetric metal electrode junctions, which is consistent with the order of calculated energy-dependent transmission coefficient () of the asymmetric junctions at . Furthermore, the single-molecule conductance of Ag/BPY-EE/Au decreases by about 70% when reversing the bias voltage from 100 to -100 mV, and a clear asymmetric - feature at the single-molecule level is observed for these junctions. This rectifying behavior could be ascribed to a different interfacial coupling of molecules at the two end electrodes, which is confirmed by the different displacement of () at the two bias voltages. Other asymmetric junctions exhibit similar rectifying behavior. The current work provides a feasible way to fabricate hybrid junctions based on asymmetric metal electrodes and investigate their electron transport toward the design of molecular rectifiers.

摘要

用不对称金属电极制造单分子结对于实现单分子二极管具有重要意义,但仍然是一个巨大的挑战。在此,我们开发了一种z轴压电脉冲调制扫描隧道显微镜断结(STM-BJ)技术,以构建具有不同金属电极的稳健不对称结。不对称的Ag/BPY-EE/Au单分子结在两个单独的对称金属电极结的电导值之间呈现出一个中间电导值,这与不对称结在特定条件下计算出的能量相关传输系数()的顺序一致。此外,当偏置电压从100 mV反转到 -100 mV时,Ag/BPY-EE/Au的单分子电导降低了约70%,并且在这些结的单分子水平上观察到明显的不对称 - 特征。这种整流行为可归因于分子在两个端电极处的不同界面耦合,这通过两个偏置电压下()的不同位移得到证实。其他不对称结也表现出类似的整流行为。当前的工作为基于不对称金属电极制造混合结并研究其电子传输以用于分子整流器的设计提供了一种可行的方法。

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