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Journal Article

Molecular dynamics in confining geometries

MPS-Authors
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Ihlein,  Guido
MPI for Polymer Research, Max Planck Society;
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Weiß,  Ö.
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Schüth,  Ferdi
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Citation

Huwe, A., Kremer, F., Hartmann, L., Kratzmüller, T., Braun, H., Kärger, J., et al. (2000). Molecular dynamics in confining geometries. Journal de Physique IV, 10(PR7), PR7-59-PR7-65. doi:10.1051/jp4:2000711.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0024-47BD-7
Abstract
The molecular dynamics of confined (low molecular weight and polymeric) systems is determined by the counterbalance between surface- and confinement-effects : Due to the interaction with the (inner) surfaces (e.g. the formation of H-bonds, grafting, physisorption) the molecular dynamics is slowed down, resulting in an increase in the glass transition temperature of the system. In contrast the confinement may induce an increase in "free volume'' thus making the molecular dynamics faster than in the bulk. This causes a decrease in the glass transition temperature. This counterbalance will be exemplified by employing broadband dielectric spectroscopy (10-2Hz - 109Hz) to study the molecular dynamics of the low molecular weight liquid ethylene glycol being contained in zeolites of different topology.