Direct Observations of Segmental Dynamics at the Polymer–Substrate Interface Enabled by Localizing Fluorescent Probes with Polymer Brushes
| Autor: | Myungwoong Kim, Keewook Paeng, Hyangseok Lee, Jieun Nam, Yura Chung, Dongwan Son |
|---|---|
| Rok vydání: | 2021 |
| Předmět: |
chemistry.chemical_classification
Materials science Polymers and Plastics Organic Chemistry Relaxation (NMR) 02 engineering and technology Polymer Substrate (electronics) 010402 general chemistry 021001 nanoscience & nanotechnology Polymer brush 01 natural sciences 0104 chemical sciences Inorganic Chemistry chemistry.chemical_compound chemistry Chemical engineering Materials Chemistry Polymer substrate Wafer Polystyrene Methyl methacrylate 0210 nano-technology |
| Zdroj: | Macromolecules. 54:4546-4556 |
| ISSN: | 1520-5835 0024-9297 |
| Popis: | We employed imaging rotational fluorescence correlation microscopy to directly observe the segmental dynamics of the polymer near the polymer–substrate interface using a probe-tethered polymer brush buried in bulk polymer films. The probe-tethered polymers grafted onto the polymer–substrate interface provide spatial selectivity to probe only the segmental dynamics of polymer near the polymer–substrate interface. The perturbation caused by the grafted polymer chains on the segmental dynamics of the polymer film near the interface was minimized by reducing the molecular weight of the polymer brush compared with the critical entanglement molecular weight of the polymer and grafted with a low grafting density (≈0.1 chains/nm²) using a “grafting-to” method, which allows precisely controlled and fully characterized polymer brush structures. In addition, the molecular weight of the brush polymer was further controlled to ≈10 kg/mol with the root-mean-square end-to-end distance of ≈5 nm to probe dynamics within 10 nm of the polymer–substrate interface. Polystyrene and poly(methyl methacrylate) films carrying rather unfavorable and similar surface energies, respectively, with the silane-modified silicon wafer substrates were investigated. The polymer dynamics near the interface characterized by the degrees of non-Arrhenius temperature dependence and nonexponential relaxation were not altered in both systems compared with those of the bulk, suggesting that the polymer dynamics is not sensitive to moderate differences in enthalpic interaction between the polymer and the substrate. |
| Databáze: | OpenAIRE |
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