Fine-tuning the structure of stimuli-responsive polymer films by hydrostatic pressure and temperature

The response of stimuli-responsive polymer brushes to moderately elevated pressure is investigated by neutron reflectivity and a thermodynamically consistent density functional theory where pressure effects are included by a hydrophobic cavity model. Evidence is provided that temperature and pressur...

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Hauptverfasser: Reinhardt, Matthias (VerfasserIn) , Dzubiella, Joachim (VerfasserIn) , Trapp, Marcus (VerfasserIn) , Gutfreund, Philipp (VerfasserIn) , Kreuzer, Martin (VerfasserIn) , Gröschel, André H. (VerfasserIn) , Müller, Axel H. E. (VerfasserIn) , Ballauff, Matthias (VerfasserIn) , Steitz, Roland (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: August 12, 2013
In: Macromolecules
Year: 2013, Jahrgang: 46, Heft: 16, Pages: 6541-6547
ISSN:1520-5835
DOI:10.1021/ma400962p
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/ma400962p
Verlag, lizenzpflichtig, Volltext: https://pubs.acs.org/doi/10.1021/ma400962p
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Verfasserangaben:Matthias Reinhardt, Joachim Dzubiella, Marcus Trapp, Philipp Gutfreund, Martin Kreuzer, André H. Gröschel, Axel H.E. Müller, Matthias Ballauff, and Roland Steitz
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Zusammenfassung:The response of stimuli-responsive polymer brushes to moderately elevated pressure is investigated by neutron reflectivity and a thermodynamically consistent density functional theory where pressure effects are included by a hydrophobic cavity model. Evidence is provided that temperature and pressure effects on the brush spatial structure are entirely antagonistic. A ∼100 bar/K cancellation effect is found, which we argue is a general feature for hydrophobically associating homopolymers and serves for experimental guidance and fine-control of polymer film structure. Our results also suggest that polymeric interfaces which do not show a marked temperature dependence are also rather insensitive to pressure effects for applied pressures below 1 kbar.
Beschreibung:Gesehen am 10.01.2022
Beschreibung:Online Resource
ISSN:1520-5835
DOI:10.1021/ma400962p