4.7 Article

Position-Dependent Diffusion Dynamics of Entangled Polymer Melts Nanoconfined by Parallel Immiscible Polymer Films

Journal

ACS MACRO LETTERS
Volume 9, Issue 10, Pages 1483-1488

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsmacrolett.0c00608

Keywords

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Funding

  1. National Research Foundation of Korea [2019R1F1A1059109]
  2. Korea Technology and Information Promotion Agency for SMEs [G21S284165801]
  3. National Research Foundation of Korea [2019R1F1A1059109] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The morphological structure and dynamics of confined polymers adjacent to the polymer-polymer interface have a profound effect on determining the overall physical properties of polymer blends. We measured the diffusion dynamics of poly(methyl methacrylate) (PMMA) melts confined between polystyrene (PS) layers using neutron reflectivity. Combinations of various thicknesses of PMMA and deuterated PMMA (dPMMA allowed us to experimentally reveal the nonmonotonic behavior of polymer mobility near the PS-PMMA interface. From the neutron reflectivity results, we found that the polymers adjacent to the immiscible polymer-polymer interface showed enhanced diffusion dynamics because of the repulsive interaction between PS and PMMA, whereas the polymer at local regions farther from the interface exhibited reduced dynamics. This is probably due to the nonspherical conformation of PMMA and spatial confinement near the PS-PMMA interface.

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