TY - JOUR
T1 - Phase Transition toward a Thermodynamically Less Stable Phase
T2 - Cross-Nucleation due to Thin Film Growth of a Benzothieno-benzothiophene Derivative
AU - Hofer, Sebastian
AU - Hofer, Andreas
AU - Simbrunner, Josef
AU - Ramsey, Michael
AU - Sterrer, Martin
AU - Sanzone, Alessandro
AU - Beverina, Luca
AU - Geerts, Yves
AU - Resel, Roland
N1 - Funding Information:
We thank Robert Schwarzl, Graz University of Technology, for calculation of structure factors. The work was supported by the Austrian Science Foundation (FWF) under Grant P30222, by the Belgian National Fund for Scientific Research (FNRS) for financial support through research projects Pi-Fast No. T.0072.18 and 2Dto3D No. 30489208, and by the French Community of Belgium (ARC No. 20061). The authors acknowledge the Elettra Sincrotrone Trieste for allocation of synchrotron radiation and thank Luisa Barba and Nicola Demitri for assistance in using beamline XRD1.
Publisher Copyright:
© 2021 The Authors. Published by American Chemical Society
PY - 2021/12/30
Y1 - 2021/12/30
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85121926878&partnerID=8YFLogxK
U2 - 10.1021/acs.jpcc.1c06610
DO - 10.1021/acs.jpcc.1c06610
M3 - Article
AN - SCOPUS:85121926878
SN - 1932-7447
VL - 125
SP - 28039
EP - 28047
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 51
ER -