Free Surface Relaxations of Star-Shaped Polymer Films

The surface relaxation dynamics of supported star-shaped polymer thin films are shown to be slower than the bulk, persisting up to temperatures at least 50 K above the bulk glass transition temperature T_{g}^{bulk}. This behavior, exhibited by star-shaped polystyrenes with functionality f=8 arms and...

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Published inPhysical review letters Vol. 119; no. 22; p. 227801
Main Authors Glynos, Emmanouil, Johnson, Kyle J, Frieberg, Bradley, Chremos, Alexandros, Narayanan, Suresh, Sakellariou, Georgios, Green, Peter F
Format Journal Article
LanguageEnglish
Published United States 28.11.2017
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Abstract The surface relaxation dynamics of supported star-shaped polymer thin films are shown to be slower than the bulk, persisting up to temperatures at least 50 K above the bulk glass transition temperature T_{g}^{bulk}. This behavior, exhibited by star-shaped polystyrenes with functionality f=8 arms and molecular weights per arm M_{arm}<M_{e} (M_{e} is the entanglement molecular weight), is shown by molecular dynamics simulations to be associated with a preferential localization of these macromolecules at the free surface. This new phenomenon is in notable contrast to that of linear-chain polymer thin film systems, where the surface relaxations are enhanced in relation to the bulk; this enhancement persists only for a limited temperature range above the bulk T_{g}^{bulk}. Evidence of the slow surface dynamics, compared to the bulk, for temperatures well above T_{g} and at length and time scales not associated with the glass transition has not previously been reported for polymers.
AbstractList The surface relaxation dynamics of supported star-shaped polymer thin films are shown to be slower than the bulk, persisting up to temperatures at least 50 K above the bulk glass transition temperature T_{g}^{bulk}. This behavior, exhibited by star-shaped polystyrenes with functionality f=8 arms and molecular weights per arm M_{arm}<M_{e} (M_{e} is the entanglement molecular weight), is shown by molecular dynamics simulations to be associated with a preferential localization of these macromolecules at the free surface. This new phenomenon is in notable contrast to that of linear-chain polymer thin film systems, where the surface relaxations are enhanced in relation to the bulk; this enhancement persists only for a limited temperature range above the bulk T_{g}^{bulk}. Evidence of the slow surface dynamics, compared to the bulk, for temperatures well above T_{g} and at length and time scales not associated with the glass transition has not previously been reported for polymers.
Author Frieberg, Bradley
Chremos, Alexandros
Johnson, Kyle J
Narayanan, Suresh
Green, Peter F
Glynos, Emmanouil
Sakellariou, Georgios
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  givenname: Peter F
  surname: Green
  fullname: Green, Peter F
  organization: National Renewable Energy Laboratory (NREL), Golden, Colorado 80401, USA
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Snippet The surface relaxation dynamics of supported star-shaped polymer thin films are shown to be slower than the bulk, persisting up to temperatures at least 50 K...
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Title Free Surface Relaxations of Star-Shaped Polymer Films
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