Author
Listed:
- Alex Ham
(Leiden University)
- Xue Liu
(Leiden University
Xi’an Jiaotong University)
- Dario Calvani
(Leiden University)
- Adéla Melcrová
(Zernike Institute for Advanced Materials, Rijksuniversiteit Groningen)
- Melania Kozdra
(Leiden University)
- Francesco Buda
(Leiden University)
- Herman S. Overkleeft
(Leiden University)
- Wouter H. Roos
(Zernike Institute for Advanced Materials, Rijksuniversiteit Groningen)
- Dmitri V. Filippov
(Leiden University)
- Grégory F. Schneider
(Leiden University)
Abstract
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.
Suggested Citation
Alex Ham & Xue Liu & Dario Calvani & Adéla Melcrová & Melania Kozdra & Francesco Buda & Herman S. Overkleeft & Wouter H. Roos & Dmitri V. Filippov & Grégory F. Schneider, 2022.
"Freestanding non-covalent thin films of the propeller-shaped polycyclic aromatic hydrocarbon decacyclene,"
Nature Communications, Nature, vol. 13(1), pages 1-8, December.
Handle:
RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-29429-8
DOI: 10.1038/s41467-022-29429-8
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