TY - JOUR A1 - Schönhals, Andreas A1 - Goering, Harald A1 - Schick, Ch. A1 - Frick, b. A1 - Zorn, R. T1 - Polymers in nanoconfinement: What can be learned from relaxation and scattering experiments? JF - Journal of non-crystalline solids N2 - Dielectric spectroscopy in combination with temperature modulated differential scanning calorimetry and quasielastic/inelastic neutron scattering are employed to investigate the molecular (glassy) dynamics of poly(dimethyl siloxane) (PDMS) and poly(methyl phenyl siloxane) (PMPS) confined to random nanoporous glasses with nominal pore sizes between 2.5 nm and 20 nm. Inside the pores PDMS and PMPS have faster molecular dynamics than in the bulk state. Down to a pore size of 7.5 nm the temperature dependence of the relaxation times (or rates) obeys the Vogel/Fulcher/Tammann (VFT) equation where the data obtained from dielectric and thermal spectroscopy agree quantitatively. At a pore size of 5 nm this VFT-like temperature dependence changes to an Arrhenius behavior. At the same confining length scale the increment of the specific heat capacity at Tg normalized to the weight of the confined polymer vanishes. The results indicate that a minimal length scale seems to be relevant for glassy dynamics in both polymers although the estimated length scale of about 5 nm seems to a bit too large in comparison to other experimental results and theoretical approaches. Neutron scattering is employed to investigate methyl group reorientation and the fast segmental dynamics of both polymers in confinement. Although the methyl group rotation is a localized process these experiments show that a part of the methyl groups is immobilized by the confinement whereas the effects for PDMS are much more pronounced than for PMPS. With regard to the segmental dynamics, neutron scattering reveals a big difference in the behavior of both polymers. Whereas the data obtained for PMPS are in accord with a boundary layer formed at the surfaces of the nanopores, for PDMS a considerable amount of elastic scattering is observed. To explain this result it is assumed that some structure formation of PDMS takes place in the nanopores, although the thermal data show no crystallization or melting effects. KW - Glass transition KW - Dielectric loss and relaxation KW - Macromolecular and polymer solutions KW - Polymer melts KW - Swelling PY - 2005 DO - https://doi.org/10.1016/j.jnoncrysol.2005.03.062 SN - 0022-3093 VL - 351 IS - 33-36 SP - 2668 EP - 2677 PB - North-Holland Publ. Co. CY - Amsterdam AN - OPUS4-10856 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -