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Direct Observation of Early-Stage Polymer Crystallization Driven by Surface Wrinkling and Compressive Stress in Thin Films
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, 510275, Guangzhou, China.
KTH, Skolan för kemi, bioteknologi och hälsa (CBH), Fiber- och polymerteknologi, Fiberprocesser. Deutsches Elektronen-Synchrotron (DESY), Notkestrasse 85, 22607, Hamburg, Germany.ORCID-id: 0000-0002-6940-6012
Heinz Maier-Leibnitz-Zentrum (MLZ), Technical University of Munich, Lichtenbergstr. 1, 85748, Garching, Germany; TUM School of Natural Sciences, Department of Physics, Chair for Functional Materials, Technical University of Munich, James-Franck-Str. 1, 85748, Garching, Germany.
State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Graduate University of Chinese Academy of Sciences, Chinese Academy of Sciences, 130022, Changchun, China.
2025 (Engelska)Ingår i: Chinese Journal of Polymer Science, ISSN 0256-7679, E-ISSN 1439-6203, Vol. 43, nr 2, s. 360-367Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

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.

Ort, förlag, år, upplaga, sidor
Springer Nature , 2025. Vol. 43, nr 2, s. 360-367
Nyckelord [en]
Nucleation, Polymer crystallization, Stress, Surface wrinkling, Thin film
Nationell ämneskategori
Den kondenserade materiens fysik Materialkemi
Identifikatorer
URN: urn:nbn:se:kth:diva-385756DOI: 10.1007/s10118-025-3264-3ISI: 001401093700001Scopus ID: 2-s2.0-85217163364OAI: oai:DiVA.org:kth-385756DiVA, id: diva2:2087133
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QC 20260717

Tillgänglig från: 2026-07-17 Skapad: 2026-07-17 Senast uppdaterad: 2026-07-17Bibliografiskt granskad

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Roth, Stephan V.
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Fiberprocesser
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Chinese Journal of Polymer Science
Den kondenserade materiens fysikMaterialkemi

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