a.School of Materials Science and Engineering, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Institute of Green Chemistry and Molecular Engineering, Sun Yat-sen University, Guangzhou 510275, China
b.Deutsches Elektronen-Synchrotron (DESY), Notkestrasse 85, 22607 Hamburg, Germany
c.Department of Fibre and Polymer Technology, KTH Royal Institute of Technology, Teknikringen 56–58, Stockholm SE-100 44, Sweden
d.Technical University of Munich, TUM School of Natural Sciences, Department of Physics, Chair for Functional Materials, James-Franck-Str. 1, Garching 85748, Germany
e.Heinz Maier-Leibnitz-Zentrum (MLZ), Technical University of Munich, Lichtenbergstr. 1, Garching 85748, Germany
f.State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Graduate University of Chinese Academy of Sciences, Chinese Academy of Sciences, Changchun 130022, China
zhangpeng3@mail.sysu.edu.cn
收稿:2024-08-19,
修回:2024-10-19,
录用:2024-11-11,
网络首发:2025-01-18,
纸质出版:2025-02-01
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Zhang, P.; Roth, S. V.; Müller-Buschbaum, P.; He, T. B. Direct observation of early-stage polymer crystallization driven by surface wrinkling and compressive stress in thin films. Chinese J. Polym. Sci. 2025, 43, 360–367
Peng Zhang, Stephan V. Roth, Peter Müller-Buschbaum, et al. Direct Observation of Early-Stage Polymer Crystallization Driven by Surface Wrinkling and Compressive Stress in Thin Films[J]. Chinese Journal of Polymer Science, 2025, 43(2): 360-367.
Zhang, P.; Roth, S. V.; Müller-Buschbaum, P.; He, T. B. Direct observation of early-stage polymer crystallization driven by surface wrinkling and compressive stress in thin films. Chinese J. Polym. Sci. 2025, 43, 360–367 DOI: 10.1007/s10118-025-3264-3.
Peng Zhang, Stephan V. Roth, Peter Müller-Buschbaum, et al. Direct Observation of Early-Stage Polymer Crystallization Driven by Surface Wrinkling and Compressive Stress in Thin Films[J]. Chinese Journal of Polymer Science, 2025, 43(2): 360-367. DOI: 10.1007/s10118-025-3264-3.
Surface wrinkling precedes nucleation and crystal growth in the semicrystalline deblock copolymer thin film
as demonstrated for the first time by in situ atomic force microscopy and synchrotron radiation X-ray scattering data.
The early stages of crystallization and occurrence of surface wrinkling were investigated using poly(butadiene)-block-poly(
ε
-caprolactone) with an ordered lamellar structure. Direct evidence has demonstrated that surface wrinkling precedes nucleation and crystal growth. This study examined the relationship between surface wrinkling
nucleation
and the formation of crystalline supramolecular structures using atomic force microscopy (AFM) and X-ray scattering measurements. Surface wrinkling is attributed to curving induced by accumulated stresses
including residual stress from the sample preparation and thermal stress during cooling. These stresses cause large-scale material flow and corresponding changes in the molecular conformations
potentially reducing the nucleation barrier. This hypothesis is supported by the rapid crystal growth observed following the spread of surface wrinkles. Additionally
the surface curving of the polymer thin film creates local minima of the free energy
facilitating nucleation. The nuclei subsequently grow into crystalline supramolecular structures by incorporating polymer molecules from the melt. This mechanism highlights the role of localized structural inhomogeneity in the early stages of crystallization and provides new insights into structure formation processes.
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