Folding a Single-Molecule Junction
Author(s) -
Chuanli Wu,
Demetris Bates,
Sara Sangtarash,
Nicolò Ferri,
Aidan Thomas,
Simon J. Higgins,
Craig M. Robertson,
Richard J. Nichols,
Hatef Sadeghi,
Andrea Vezzoli
Publication year - 2020
Publication title -
nano letters
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 4.853
H-Index - 488
eISSN - 1530-6992
pISSN - 1530-6984
DOI - 10.1021/acs.nanolett.0c02815
Subject(s) - conductance , molecule , intramolecular force , chemical physics , break junction , quantum tunnelling , moiety , molecular electronics , chemistry , folding (dsp implementation) , density functional theory , nanotechnology , materials science , stereochemistry , computational chemistry , physics , optoelectronics , condensed matter physics , organic chemistry , engineering , electrical engineering
Stimuli-responsive molecular junctions, where the conductance can be altered by an external perturbation, are an important class of nanoelectronic devices. These have recently attracted interest as large effects can be introduced through exploitation of quantum phenomena. We show here that significant changes in conductance can be attained as a molecule is repeatedly compressed and relaxed, resulting in molecular folding along a flexible fragment and cycling between an anti and a syn conformation. Power spectral density analysis and DFT transport calculations show that through-space tunneling between two phenyl fragments is responsible for the conductance increase as the molecule is mechanically folded to the syn conformation. This phenomenon represents a novel class of mechanoresistive molecular devices, where the functional moiety is embedded in the conductive backbone and exploits intramolecular nonbonding interactions, in contrast to most studies where mechanoresistivity arises from changes in the molecule-electrode interface.
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