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Phase Transition toward a Thermodynamically Less Stable Phase: Cross-Nucleation due to Thin Film Growth of a Benzothieno-benzothiophene Derivative

[Image: see text] The molecule 2-decyl-7-phenyl-[1]benzothieno[3,2-b][1]benzothiophene is an organic semiconductor, with outstanding properties in terms of molecular packing and its use in organic electronics. The asymmetric shape of the molecule causes a double layer crystal structure at room tempe...

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Autores principales: Hofer, Sebastian, Hofer, Andreas, Simbrunner, Josef, Ramsey, Michael, Sterrer, Martin, Sanzone, Alessandro, Beverina, Luca, Geerts, Yves, Resel, Roland
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724801/
https://www.ncbi.nlm.nih.gov/pubmed/35003483
http://dx.doi.org/10.1021/acs.jpcc.1c06610
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author Hofer, Sebastian
Hofer, Andreas
Simbrunner, Josef
Ramsey, Michael
Sterrer, Martin
Sanzone, Alessandro
Beverina, Luca
Geerts, Yves
Resel, Roland
author_facet Hofer, Sebastian
Hofer, Andreas
Simbrunner, Josef
Ramsey, Michael
Sterrer, Martin
Sanzone, Alessandro
Beverina, Luca
Geerts, Yves
Resel, Roland
author_sort Hofer, Sebastian
collection PubMed
description [Image: see text] The molecule 2-decyl-7-phenyl-[1]benzothieno[3,2-b][1]benzothiophene is an organic semiconductor, with outstanding properties in terms of molecular packing and its use in organic electronics. The asymmetric shape of the molecule causes a double layer crystal structure at room temperature. In this work we report its thin film growth by physical vapor deposition starting from the monolayer regime up to thick films. The films are studied in terms of their morphology, crystallographic properties, and thermal stability by atomic force microscopy and X-ray diffraction methods. It is found that the bulk molecular packing of the bilayer is formed at the initial thin film growth stage. After a thickness of one double layer, a transition into a new polymorph is observed which is of metastable character. The new phase represents a single layer phase; the crystal structure could be solved by a combination of X-ray diffraction and molecular dynamics simulations. The observed thin film growth is outstanding in terms of surface crystallization: the formation of a metastable phase is not associated with the initial thin film growth, since the first growth stage represents rather the bulk crystal structure of this molecule. Its formation is associated with cross-nucleation of one polymorph by another, which explains why a metastable phase can be formed on top of a thermodynamically more stable phase.
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spelling pubmed-87248012022-01-05 Phase Transition toward a Thermodynamically Less Stable Phase: Cross-Nucleation due to Thin Film Growth of a Benzothieno-benzothiophene Derivative Hofer, Sebastian Hofer, Andreas Simbrunner, Josef Ramsey, Michael Sterrer, Martin Sanzone, Alessandro Beverina, Luca Geerts, Yves Resel, Roland J Phys Chem C Nanomater Interfaces [Image: see text] The molecule 2-decyl-7-phenyl-[1]benzothieno[3,2-b][1]benzothiophene is an organic semiconductor, with outstanding properties in terms of molecular packing and its use in organic electronics. The asymmetric shape of the molecule causes a double layer crystal structure at room temperature. In this work we report its thin film growth by physical vapor deposition starting from the monolayer regime up to thick films. The films are studied in terms of their morphology, crystallographic properties, and thermal stability by atomic force microscopy and X-ray diffraction methods. It is found that the bulk molecular packing of the bilayer is formed at the initial thin film growth stage. After a thickness of one double layer, a transition into a new polymorph is observed which is of metastable character. The new phase represents a single layer phase; the crystal structure could be solved by a combination of X-ray diffraction and molecular dynamics simulations. The observed thin film growth is outstanding in terms of surface crystallization: the formation of a metastable phase is not associated with the initial thin film growth, since the first growth stage represents rather the bulk crystal structure of this molecule. Its formation is associated with cross-nucleation of one polymorph by another, which explains why a metastable phase can be formed on top of a thermodynamically more stable phase. American Chemical Society 2021-12-20 2021-12-30 /pmc/articles/PMC8724801/ /pubmed/35003483 http://dx.doi.org/10.1021/acs.jpcc.1c06610 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Hofer, Sebastian
Hofer, Andreas
Simbrunner, Josef
Ramsey, Michael
Sterrer, Martin
Sanzone, Alessandro
Beverina, Luca
Geerts, Yves
Resel, Roland
Phase Transition toward a Thermodynamically Less Stable Phase: Cross-Nucleation due to Thin Film Growth of a Benzothieno-benzothiophene Derivative
title Phase Transition toward a Thermodynamically Less Stable Phase: Cross-Nucleation due to Thin Film Growth of a Benzothieno-benzothiophene Derivative
title_full Phase Transition toward a Thermodynamically Less Stable Phase: Cross-Nucleation due to Thin Film Growth of a Benzothieno-benzothiophene Derivative
title_fullStr Phase Transition toward a Thermodynamically Less Stable Phase: Cross-Nucleation due to Thin Film Growth of a Benzothieno-benzothiophene Derivative
title_full_unstemmed Phase Transition toward a Thermodynamically Less Stable Phase: Cross-Nucleation due to Thin Film Growth of a Benzothieno-benzothiophene Derivative
title_short Phase Transition toward a Thermodynamically Less Stable Phase: Cross-Nucleation due to Thin Film Growth of a Benzothieno-benzothiophene Derivative
title_sort phase transition toward a thermodynamically less stable phase: cross-nucleation due to thin film growth of a benzothieno-benzothiophene derivative
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8724801/
https://www.ncbi.nlm.nih.gov/pubmed/35003483
http://dx.doi.org/10.1021/acs.jpcc.1c06610
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