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Freestanding non-covalent thin films of the propeller-shaped polycyclic aromatic hydrocarbon decacyclene

Molecularly thin, nanoporous thin films are of paramount importance in material sciences. Their use in a wide range of applications requires control over their chemical functionalities, which is difficult to achieve using current production methods. Here, the small polycyclic aromatic hydrocarbon de...

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Autores principales: van der Ham, Alex, Liu, Xue, Calvani, Dario, Melcrová, Adéla, Kozdra, Melania, Buda, Francesco, Overkleeft, Herman S., Roos, Wouter H., Filippov, Dmitri V., Schneider, Grégory F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993932/
https://www.ncbi.nlm.nih.gov/pubmed/35395820
http://dx.doi.org/10.1038/s41467-022-29429-8
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author van der Ham, Alex
Liu, Xue
Calvani, Dario
Melcrová, Adéla
Kozdra, Melania
Buda, Francesco
Overkleeft, Herman S.
Roos, Wouter H.
Filippov, Dmitri V.
Schneider, Grégory F.
author_facet van der Ham, Alex
Liu, Xue
Calvani, Dario
Melcrová, Adéla
Kozdra, Melania
Buda, Francesco
Overkleeft, Herman S.
Roos, Wouter H.
Filippov, Dmitri V.
Schneider, Grégory F.
author_sort van der Ham, Alex
collection PubMed
description Molecularly thin, nanoporous thin films are of paramount importance in material sciences. Their use in a wide range of applications requires control over their chemical functionalities, which is difficult to achieve using current production methods. Here, the small polycyclic aromatic hydrocarbon decacyclene is used to form molecular thin films, without requiring covalent crosslinking of any kind. The 2.5 nm thin films are mechanically stable, able to be free-standing over micrometer distances, held together solely by supramolecular interactions. Using a combination of computational chemistry and microscopic imaging techniques, thin films are studied on both a molecular and microscopic scale. Their mechanical strength is quantified using AFM nanoindentation, showing their capability of withstanding a point load of 26 ± 9 nN, when freely spanning over a 1 μm aperture, with a corresponding Young’s modulus of 6 ± 4 GPa. Our thin films constitute free-standing, non-covalent thin films based on a small PAH.
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spelling pubmed-89939322022-04-27 Freestanding non-covalent thin films of the propeller-shaped polycyclic aromatic hydrocarbon decacyclene van der Ham, Alex Liu, Xue Calvani, Dario Melcrová, Adéla Kozdra, Melania Buda, Francesco Overkleeft, Herman S. Roos, Wouter H. Filippov, Dmitri V. Schneider, Grégory F. Nat Commun Article Molecularly thin, nanoporous thin films are of paramount importance in material sciences. Their use in a wide range of applications requires control over their chemical functionalities, which is difficult to achieve using current production methods. Here, the small polycyclic aromatic hydrocarbon decacyclene is used to form molecular thin films, without requiring covalent crosslinking of any kind. The 2.5 nm thin films are mechanically stable, able to be free-standing over micrometer distances, held together solely by supramolecular interactions. Using a combination of computational chemistry and microscopic imaging techniques, thin films are studied on both a molecular and microscopic scale. Their mechanical strength is quantified using AFM nanoindentation, showing their capability of withstanding a point load of 26 ± 9 nN, when freely spanning over a 1 μm aperture, with a corresponding Young’s modulus of 6 ± 4 GPa. Our thin films constitute free-standing, non-covalent thin films based on a small PAH. Nature Publishing Group UK 2022-04-08 /pmc/articles/PMC8993932/ /pubmed/35395820 http://dx.doi.org/10.1038/s41467-022-29429-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
van der Ham, Alex
Liu, Xue
Calvani, Dario
Melcrová, Adéla
Kozdra, Melania
Buda, Francesco
Overkleeft, Herman S.
Roos, Wouter H.
Filippov, Dmitri V.
Schneider, Grégory F.
Freestanding non-covalent thin films of the propeller-shaped polycyclic aromatic hydrocarbon decacyclene
title Freestanding non-covalent thin films of the propeller-shaped polycyclic aromatic hydrocarbon decacyclene
title_full Freestanding non-covalent thin films of the propeller-shaped polycyclic aromatic hydrocarbon decacyclene
title_fullStr Freestanding non-covalent thin films of the propeller-shaped polycyclic aromatic hydrocarbon decacyclene
title_full_unstemmed Freestanding non-covalent thin films of the propeller-shaped polycyclic aromatic hydrocarbon decacyclene
title_short Freestanding non-covalent thin films of the propeller-shaped polycyclic aromatic hydrocarbon decacyclene
title_sort freestanding non-covalent thin films of the propeller-shaped polycyclic aromatic hydrocarbon decacyclene
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993932/
https://www.ncbi.nlm.nih.gov/pubmed/35395820
http://dx.doi.org/10.1038/s41467-022-29429-8
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