Macromolecules · 2015 · 61 citations · 68 references
Natural SciencesMaterials EngineeringMaterials SciencePolymer ChemistryPolymer MaterialsThin FilmsPolymer CharacterizationPolymer PhysicsPolymer Thin FilmsSoft MaterialsThin Film Mechanical PropertiesViscoelastic BehaviorFilm ThicknessGlass TransitionGlass Transition In Thin FilmsGlass Transition TemperatureMechanical Properties Of FilmsPolymer ViscoelasticityUltrathin Polymer FilmsViscoelastic Properties Of Polymers
The mechanical and viscoelastic responses of poly(ethyl methacrylate) (PEMA) ultrathin films over thicknesses ranging from 21 to 112 nm have been studied using a nanobubble inflation method. The stress–strain response of the PEMA thin films shows a rubbery stiffening as the film thickness decreases, and the present results are combined with prior measurements of the rubbery stiffening index S for multiple polymers. We find that S is linearly correlated with the dynamic fragility index m . The results are also consistent with expectation from Ngai et al.’s [ J. Polym. Sci., Part B: Polym. Phys. 2013, 51 (3)] recent proposition based on his coupling model but do not seem to correlate with the molecular composite concept proposed by Page et al. [ Nano Lett. 2014, 14 (5)] as a means to explain the dependence of the rubbery stiffening on chemical structure of the polymer. In addition, we observe a reduction in glass transition temperature of as much as 15.7 K for PEMA films of 21 nm thickness.
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Viscoelastic Properties of Polymers
John D. Ferry, H. S. Myers · Journal of The Electrochemical Society · 1961 · 13.5K citations
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Viscoelastic Properties of Polymers
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Nonexponential relaxations in strong and fragile glass formers
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