STM induced manipulation of azulene-based molecules and nanostructures: the role of the dipole moment

Among the different mechanisms that can be used to drive a molecule on a surface by the tip of a scanning tunneling microscope at low temperature, we used voltage pulses to move azulene-based single molecules and nanostructures on Au(111). Upon evaporation, the molecules partially cleave and form me...

Full description

Saved in:
Bibliographic Details
Published inNanoscale Vol. 12; no. 48; pp. 24471 - 24476
Main Authors Kühne, Tim, Au-Yeung, Kwan Ho, Eisenhut, Frank, Aiboudi, Oumaima, Ryndyk, Dmitry A, Cuniberti, Gianaurelio, Lissel, Franziska, Moresco, Francesca
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 23.12.2020
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Among the different mechanisms that can be used to drive a molecule on a surface by the tip of a scanning tunneling microscope at low temperature, we used voltage pulses to move azulene-based single molecules and nanostructures on Au(111). Upon evaporation, the molecules partially cleave and form metallo-organic dimers while single molecules are very scarce, as confirmed by simulations. By applying voltage pulses to the different structures under similar conditions, we observe that only one type of dimer can be controllably driven on the surface, which has the lowest dipole moment of all investigated structures. Experiments under different bias and tip height conditions reveal that the electric field is the main driving force of the directed motion. We discuss the different observed structures and their movement properties with respect to their dipole moment and charge distribution on the surface. The voltage-pulse manipulation of azulene-based single molecules and dimers adsorbed on Au(111) is studied with respect to dipole moment and charge distribution of the structures on the surface.
Bibliography:10.1039/d0nr06809h
Electronic supplementary information (ESI) available. See DOI
ISSN:2040-3364
2040-3372
DOI:10.1039/d0nr06809h