Evidence map›Paper›PMID 37789027›Full record

ArticleNature communications2023

Controlling piezoresistance in single molecules through the isomerisation of bullvalenes.

Jeffrey R Reimers, Tiexin Li, André P Birvé, Likun Yang, Albert C Aragonès, Thomas Fallon, Daniel S Kosov, Nadim Darwish

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jeffrey R ReimersInternational Centre for Quantum and Molecular Structures and the Department of Physics, Shanghai University, Shanghai, 200444, China. jeffrey.reimers@uts.edu.au.ORCID http://orcid.org/0000-0001-5157-7422
Tiexin LiSchool of Molecular and Life Sciences, Curtin University, Bentley, WA, 6102, Australia.
André P BirvéSchool of Environmental and Life Sciences, University of Newcastle, Callaghan, NSW, 2308, Australia.
Likun YangInternational Centre for Quantum and Molecular Structures and the Department of Physics, Shanghai University, Shanghai, 200444, China.
Albert C AragonèsDepartment of Materials Science and Physical Chemistry, University of Barcelona, Marti i Franquès 1, 08028, Barcelona, Catalonia, Spain.ORCID http://orcid.org/0000-0002-1829-6941
Thomas FallonSchool of Environmental and Life Sciences, University of Newcastle, Callaghan, NSW, 2308, Australia. thomas.fallon@newcastle.edu.au.ORCID http://orcid.org/0000-0002-6495-5282
Daniel S KosovCollege of Science and Engineering, James Cook University, Townsville, QLD, 4811, Australia. daniel.kosov@jcu.edu.au.ORCID http://orcid.org/0000-0002-2881-5477
Nadim DarwishSchool of Molecular and Life Sciences, Curtin University, Bentley, WA, 6102, Australia. nadim.darwish@curtin.edu.au.ORCID http://orcid.org/0000-0002-6565-1723

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoscale electro-mechanical systems (NEMS) displaying piezoresistance offer unique measurement opportunities at the sub-cellular level, in detectors and sensors, and in emerging generations of integrated electronic devices. Here, we show a single-molecule NEMS piezoresistor that operates utilising constitutional and conformational isomerisation of individual diaryl-bullvalene molecules and can be switched at 850 Hz. Observations are made using scanning tunnelling microscopy break junction (STMBJ) techniques to characterise piezoresistance, combined with blinking (current-time) experiments that follow single-molecule reactions in real time. A kinetic Monte Carlo methodology (KMC) is developed to simulate isomerisation on the experimental timescale, parameterised using density-functional theory (DFT) combined with non-equilibrium Green's function (NEGF) calculations. Results indicate that piezoresistance is controlled by both constitutional and conformational isomerisation, occurring at rates that are either fast (equilibrium) or slow (non-equilibrium) compared to the experimental timescale. Two different types of STMBJ traces are observed, one typical of traditional experiments that are interpreted in terms of intramolecular isomerisation occurring on stable tipped-shaped metal-contact junctions, and another attributed to arise from junction‒interface restructuring induced by bullvalene isomerisation.

Identifiers

PMID37789027
PMCPMC10547723

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.