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Going beyond Pentacene: Photoemission Tomography of a Heptacene Monolayer on Ag(110)
[Image: see text] Longer acenes such as heptacene are promising candidates for optoelectronic applications but are unstable in their bulk structure as they tend to dimerize. This makes the growth of well-defined monolayers and films problematic. In this article, we report the successful preparation...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883341/ https://www.ncbi.nlm.nih.gov/pubmed/33603943 http://dx.doi.org/10.1021/acs.jpcc.0c09062 |
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author | Sättele, Marie S. Windischbacher, Andreas Egger, Larissa Haags, Anja Hurdax, Philipp Kirschner, Hans Gottwald, Alexander Richter, Mathias Bocquet, François C. Soubatch, Serguei Tautz, F. Stefan Bettinger, Holger F. Peisert, Heiko Chassé, Thomas Ramsey, Michael G. Puschnig, Peter Koller, Georg |
author_facet | Sättele, Marie S. Windischbacher, Andreas Egger, Larissa Haags, Anja Hurdax, Philipp Kirschner, Hans Gottwald, Alexander Richter, Mathias Bocquet, François C. Soubatch, Serguei Tautz, F. Stefan Bettinger, Holger F. Peisert, Heiko Chassé, Thomas Ramsey, Michael G. Puschnig, Peter Koller, Georg |
author_sort | Sättele, Marie S. |
collection | PubMed |
description | [Image: see text] Longer acenes such as heptacene are promising candidates for optoelectronic applications but are unstable in their bulk structure as they tend to dimerize. This makes the growth of well-defined monolayers and films problematic. In this article, we report the successful preparation of a highly oriented monolayer of heptacene on Ag(110) by thermal cycloreversion of diheptacenes. In a combined effort of angle-resolved photoemission spectroscopy and density functional theory (DFT) calculations, we characterize the electronic and structural properties of the molecule on the surface in detail. Our investigations allow us to unambiguously confirm the successful fabrication of a highly oriented complete monolayer of heptacene and to describe its electronic structure. By comparing experimental momentum maps of photoemission from frontier orbitals of heptacene and pentacene, we shed light on differences between these two acenes regarding their molecular orientation and energy-level alignment on the metal surfaces. |
format | Online Article Text |
id | pubmed-7883341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-78833412021-02-16 Going beyond Pentacene: Photoemission Tomography of a Heptacene Monolayer on Ag(110) Sättele, Marie S. Windischbacher, Andreas Egger, Larissa Haags, Anja Hurdax, Philipp Kirschner, Hans Gottwald, Alexander Richter, Mathias Bocquet, François C. Soubatch, Serguei Tautz, F. Stefan Bettinger, Holger F. Peisert, Heiko Chassé, Thomas Ramsey, Michael G. Puschnig, Peter Koller, Georg J Phys Chem C Nanomater Interfaces [Image: see text] Longer acenes such as heptacene are promising candidates for optoelectronic applications but are unstable in their bulk structure as they tend to dimerize. This makes the growth of well-defined monolayers and films problematic. In this article, we report the successful preparation of a highly oriented monolayer of heptacene on Ag(110) by thermal cycloreversion of diheptacenes. In a combined effort of angle-resolved photoemission spectroscopy and density functional theory (DFT) calculations, we characterize the electronic and structural properties of the molecule on the surface in detail. Our investigations allow us to unambiguously confirm the successful fabrication of a highly oriented complete monolayer of heptacene and to describe its electronic structure. By comparing experimental momentum maps of photoemission from frontier orbitals of heptacene and pentacene, we shed light on differences between these two acenes regarding their molecular orientation and energy-level alignment on the metal surfaces. American Chemical Society 2021-02-03 2021-02-11 /pmc/articles/PMC7883341/ /pubmed/33603943 http://dx.doi.org/10.1021/acs.jpcc.0c09062 Text en © 2021 The Authors. Published by American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Sättele, Marie S. Windischbacher, Andreas Egger, Larissa Haags, Anja Hurdax, Philipp Kirschner, Hans Gottwald, Alexander Richter, Mathias Bocquet, François C. Soubatch, Serguei Tautz, F. Stefan Bettinger, Holger F. Peisert, Heiko Chassé, Thomas Ramsey, Michael G. Puschnig, Peter Koller, Georg Going beyond Pentacene: Photoemission Tomography of a Heptacene Monolayer on Ag(110) |
title | Going beyond Pentacene: Photoemission Tomography of
a Heptacene Monolayer on Ag(110) |
title_full | Going beyond Pentacene: Photoemission Tomography of
a Heptacene Monolayer on Ag(110) |
title_fullStr | Going beyond Pentacene: Photoemission Tomography of
a Heptacene Monolayer on Ag(110) |
title_full_unstemmed | Going beyond Pentacene: Photoemission Tomography of
a Heptacene Monolayer on Ag(110) |
title_short | Going beyond Pentacene: Photoemission Tomography of
a Heptacene Monolayer on Ag(110) |
title_sort | going beyond pentacene: photoemission tomography of
a heptacene monolayer on ag(110) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883341/ https://www.ncbi.nlm.nih.gov/pubmed/33603943 http://dx.doi.org/10.1021/acs.jpcc.0c09062 |
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