scholarly journals Large-Amplitude, High-Frequency Single-Molecule Switch

Author(s):  
Nicolò Ferri ◽  
Norah Algethami ◽  
Andrea Vezzoli ◽  
Sara Sangtarash ◽  
Maeve McLaughlin ◽  
...  

We use a scanning tunneling microscope to form and electrically interrogate metal - molecule - metal junctions. To form such junctions, molecules must be functionalised with suitable contact groups (e.g. thiols, thioethers, 4-pyridyls, amines) at each extremity. We show here that 2-(methylthio)thiophene units not only act as contact groups, but can reversibly switch between a monodentate configuration (MeS-only) and a bidentate configuration (MeS- and thienyl S) upon junction compression; as the junction is compressed the electrical conductance increases greatly with the increased molecule-contact interaction. This means that such molecules show a large-amplitude mechanical switching behavior; we also show that this is reversible and that switching can occur at a rate of at least 10 kHz. Control molecules with MeSC6H5 contact groups do not show this behavior. This, together with detailed theoretical and transport calculations on the compressed and extended molecular junctions, supports our contention that it is the thienyl S that is involved in the switching mechanism. <br>

2018 ◽  
Author(s):  
Nicolò Ferri ◽  
Norah Algethami ◽  
Andrea Vezzoli ◽  
Sara Sangtarash ◽  
Maeve McLaughlin ◽  
...  

We use a scanning tunneling microscope to form and electrically interrogate metal - molecule - metal junctions. To form such junctions, molecules must be functionalised with suitable contact groups (e.g. thiols, thioethers, 4-pyridyls, amines) at each extremity. We show here that 2-(methylthio)thiophene units not only act as contact groups, but can reversibly switch between a monodentate configuration (MeS-only) and a bidentate configuration (MeS- and thienyl S) upon junction compression; as the junction is compressed the electrical conductance increases greatly with the increased molecule-contact interaction. This means that such molecules show a large-amplitude mechanical switching behavior; we also show that this is reversible and that switching can occur at a rate of at least 10 kHz. Control molecules with MeSC6H5 contact groups do not show this behavior. This, together with detailed theoretical and transport calculations on the compressed and extended molecular junctions, supports our contention that it is the thienyl S that is involved in the switching mechanism. <br>


2019 ◽  
Vol 10 (43) ◽  
pp. 9998-10002 ◽  
Author(s):  
Tianren Fu ◽  
Shanelle Smith ◽  
María Camarasa-Gómez ◽  
Xiaofang Yu ◽  
Jiayi Xue ◽  
...  

We demonstrate that imidazole based π–π stacked dimers form strong and efficient conductance pathways in single-molecule junctions using the scanning-tunneling microscope-break junction (STM-BJ) technique and density functional theory-based calculations.


Nanoscale ◽  
2020 ◽  
Vol 12 (27) ◽  
pp. 14682-14688 ◽  
Author(s):  
Iain M. Grace ◽  
Gunnar Olsen ◽  
Juan Hurtado-Gallego ◽  
Laura Rincón-García ◽  
Gabino Rubio-Bollinger ◽  
...  

We report measurements on gold|single-molecule|gold junctions, using a modified scanning tunneling microscope-break junction (STM-BJ) technique, of the Seebeck coefficient and electrical conductance of a series of bridged biphenyl molecules.


2011 ◽  
Vol 2 ◽  
pp. 755-759 ◽  
Author(s):  
Shigeto Nakashima ◽  
Yuuta Takahashi ◽  
Manabu Kiguchi

We investigated the effect of the environment on the electrical conductance of a single benzene-1,4-diamine (BDA) molecule bridging Au electrodes, using the scanning tunneling microscope (STM). The conductance of the single BDA molecule junction decreased upon a change in the environment from tetraglyme, to mesitylene, to water, and finally to N2 gas, while the spread in the conductance value increased. The order of the conductance values of the single BDA molecule junction was explained by the strength of the interaction between the solvent molecules and the Au electrodes. The order of the spread in the conductance values was explained by the diversity in the coverage of the BDA molecule at metal electrodes and atomic and molecular motion of the single-molecule junction.


Nano Letters ◽  
2019 ◽  
Vol 19 (5) ◽  
pp. 2803-2811 ◽  
Author(s):  
Kuniyuki Miwa ◽  
Hiroshi Imada ◽  
Miyabi Imai-Imada ◽  
Kensuke Kimura ◽  
Michael Galperin ◽  
...  

2021 ◽  
Author(s):  
Tengyang Gao ◽  
Zhichao Pan ◽  
Zhuanyun Cai ◽  
Jueting Zheng ◽  
Chun Tang ◽  
...  

Here, we report the switching among multiple conductance pathways achieved by sliding the scanning tunneling microscope tip among different binding sites under different electric fields. With the electric field increase,...


NANO ◽  
2006 ◽  
Vol 01 (01) ◽  
pp. 15-33 ◽  
Author(s):  
J. G. HOU ◽  
AIDI ZHAO

Scanning tunneling microscope (STM) is a powerful and unique tool for study single molecules. We review recent advances in single-molecule characterizations including direct STM imaging and I–V spectroscopy, dI/dV spectroscopy and mapping, and d2I/dV2 spectroscopy and mapping. Some recent experiments of STM-excited single-molecule light emission are also introduced. In the final part, recent developments of single-molecule manipulation with the STM as well as the applications are discussed.


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