Single-molecular diffusivity and long jumps of large organic molecules: CoPc on Ag(100)

Energy dissipation and the transfer rate of adsorbed molecules do not only determine the rates of chemical reactions but are also a key factor that often dictates the growth of organic thin films. Here, we present a study of the surface dynamical motion of cobalt phthalocyanine (CoPc) on Ag(100) in...

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Main Authors: Agata Sabik, John Ellis, Holly Hedgeland, David J. Ward, Andrew P. Jardine, William Allison, Grażyna Antczak, Anton Tamtögl
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-02-01
Series:Frontiers in Chemistry
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fchem.2024.1355350/full
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author Agata Sabik
Agata Sabik
John Ellis
Holly Hedgeland
David J. Ward
Andrew P. Jardine
William Allison
Grażyna Antczak
Anton Tamtögl
author_facet Agata Sabik
Agata Sabik
John Ellis
Holly Hedgeland
David J. Ward
Andrew P. Jardine
William Allison
Grażyna Antczak
Anton Tamtögl
author_sort Agata Sabik
collection DOAJ
description Energy dissipation and the transfer rate of adsorbed molecules do not only determine the rates of chemical reactions but are also a key factor that often dictates the growth of organic thin films. Here, we present a study of the surface dynamical motion of cobalt phthalocyanine (CoPc) on Ag(100) in reciprocal space based on the helium spin-echo technique in comparison with previous scanning tunnelling microscopy studies. It is found that the activation energy for lateral diffusion changes from 150 meV at 45–50 K to ≈100 meV at 250–350 K, and that the process goes from exclusively single jumps at low temperatures to predominantly long jumps at high temperatures. We thus illustrate that while the general diffusion mechanism remains similar, upon comparing the diffusion process over widely divergent time scales, indeed different jump distributions and a decrease of the effective diffusion barrier are found. Hence a precise molecular-level understanding of dynamical processes and thin film formation requires following the dynamics over the entire temperature scale relevant to the process. Furthermore, we determine the diffusion coefficient and the atomic-scale friction of CoPc and establish that the molecular motion on Ag(100) corresponds to a low friction scenario as a consequence of the additional molecular degrees of freedom.
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spelling doaj.art-7a6a1c7ada034816b8a9285668dcd68f2024-02-06T05:01:37ZengFrontiers Media S.A.Frontiers in Chemistry2296-26462024-02-011210.3389/fchem.2024.13553501355350Single-molecular diffusivity and long jumps of large organic molecules: CoPc on Ag(100)Agata Sabik0Agata Sabik1John Ellis2Holly Hedgeland3David J. Ward4Andrew P. Jardine5William Allison6Grażyna Antczak7Anton Tamtögl8Institute of Experimental Physics, University of Wrocław, Wrocław, PolandDepartment of Semiconductor Materials Engineering, Wrocław University of Science and Technology, Wrocław, PolandCavendish Laboratory, Cambridge, United KingdomCavendish Laboratory, Cambridge, United KingdomCavendish Laboratory, Cambridge, United KingdomCavendish Laboratory, Cambridge, United KingdomCavendish Laboratory, Cambridge, United KingdomInstitute of Experimental Physics, University of Wrocław, Wrocław, PolandInstitute of Experimental Physics, Graz University of Technology, Graz, AustriaEnergy dissipation and the transfer rate of adsorbed molecules do not only determine the rates of chemical reactions but are also a key factor that often dictates the growth of organic thin films. Here, we present a study of the surface dynamical motion of cobalt phthalocyanine (CoPc) on Ag(100) in reciprocal space based on the helium spin-echo technique in comparison with previous scanning tunnelling microscopy studies. It is found that the activation energy for lateral diffusion changes from 150 meV at 45–50 K to ≈100 meV at 250–350 K, and that the process goes from exclusively single jumps at low temperatures to predominantly long jumps at high temperatures. We thus illustrate that while the general diffusion mechanism remains similar, upon comparing the diffusion process over widely divergent time scales, indeed different jump distributions and a decrease of the effective diffusion barrier are found. Hence a precise molecular-level understanding of dynamical processes and thin film formation requires following the dynamics over the entire temperature scale relevant to the process. Furthermore, we determine the diffusion coefficient and the atomic-scale friction of CoPc and establish that the molecular motion on Ag(100) corresponds to a low friction scenario as a consequence of the additional molecular degrees of freedom.https://www.frontiersin.org/articles/10.3389/fchem.2024.1355350/fullsurface diffusionenergy dissipationsingle-molecule studiesorganic thin filmsatom-surface satteringfriction
spellingShingle Agata Sabik
Agata Sabik
John Ellis
Holly Hedgeland
David J. Ward
Andrew P. Jardine
William Allison
Grażyna Antczak
Anton Tamtögl
Single-molecular diffusivity and long jumps of large organic molecules: CoPc on Ag(100)
Frontiers in Chemistry
surface diffusion
energy dissipation
single-molecule studies
organic thin films
atom-surface sattering
friction
title Single-molecular diffusivity and long jumps of large organic molecules: CoPc on Ag(100)
title_full Single-molecular diffusivity and long jumps of large organic molecules: CoPc on Ag(100)
title_fullStr Single-molecular diffusivity and long jumps of large organic molecules: CoPc on Ag(100)
title_full_unstemmed Single-molecular diffusivity and long jumps of large organic molecules: CoPc on Ag(100)
title_short Single-molecular diffusivity and long jumps of large organic molecules: CoPc on Ag(100)
title_sort single molecular diffusivity and long jumps of large organic molecules copc on ag 100
topic surface diffusion
energy dissipation
single-molecule studies
organic thin films
atom-surface sattering
friction
url https://www.frontiersin.org/articles/10.3389/fchem.2024.1355350/full
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