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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-8993932 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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