Glassy Dynamics and Glass Transition in Nanometric Thin Layers of Polystyrene

被引:174
作者
Tress, Martin [1 ]
Erber, Michael [2 ]
Mapesa, Emmanuel U. [1 ]
Huth, Heiko [4 ]
Mueller, Jan [2 ]
Serghei, Anatoli [3 ]
Schick, Christoph [4 ]
Eichhorn, Klaus-Jochen [2 ]
Volt, Brigitte [2 ]
Kremer, Friedrich [1 ]
机构
[1] Univ Leipzig, Inst Expt Phys 1, D-04103 Leipzig, Germany
[2] Leibniz Inst Polymerforsch Dresden eV, D-01069 Dresden, Germany
[3] Univ Massachusetts, Dept Polymer Sci & Engn, Amherst, MA 01003 USA
[4] Univ Rostock, Inst Phys, D-18051 Rostock, Germany
关键词
ULTRATHIN POLYMER-FILMS; AC-CHIP CALORIMETER; MOLECULAR-WEIGHT; TEMPERATURE-DEPENDENCE; SURFACE; RELAXATION; INTERFACE; VISCOSITY; SOLVENT; LIQUID;
D O I
10.1021/ma102031k
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Broadband dielectric spectroscopy (BDS), spectroscopic vis-ellipsometry (SE), X-ray reflectometry (XRR), and alternating current (ACC) as well as differential scanning calorimetry (DSC) are combined to study glassy dynamics and the glass transition in nanometric thin (>= 5 nm) layers of polystyrene (PS) having widely varying molecular weights (27 500-8 090 000 g/mol). For the dielectric measurements two sample geometries are employed, the common technique using evaporated electrodes and a recently developed approach taking advantage of nanostructures as spacers. All applied methods deliver the concurring result that deviations from glassy dynamics and from the glass transition of the bulk do not exceed margins of +/- 3 K independent of the layer thickness and the molecular weight of the polymer under study. Our findings are discussed in the context of the highly controversial literature and prove that an appropriate sample preparation is of paramount importance.
引用
收藏
页码:9937 / 9944
页数:8
相关论文
共 58 条
[1]   ON TEMPERATURE DEPENDENCE OF COOPERATIVE RELAXATION PROPERTIES IN GLASS-FORMING LIQUIDS [J].
ADAM, G ;
GIBBS, JH .
JOURNAL OF CHEMICAL PHYSICS, 1965, 43 (01) :139-&
[2]   SEGMENTAL MOTIONS OF CIS-POLYISOPRENE IN THE BULK STATE - INTERPRETATION OF DIELECTRIC-RELAXATION DATA [J].
BAHAR, I ;
ERMAN, B ;
KREMER, F ;
FISCHER, EW .
MACROMOLECULES, 1992, 25 (02) :816-825
[3]  
CHASON E, 2000, IN SITU REAL TIME CH
[4]   LIQUID-GLASS TRANSITION, A FREE-VOLUME APPROACH [J].
COHEN, MH ;
GREST, GS .
PHYSICAL REVIEW B, 1979, 20 (03) :1077-1098
[5]   Probing glass transition of ultrathin polymer films at a time scale of seconds using fast differential scanning calorimetry [J].
Efremov, MY ;
Olson, EA ;
Zhang, M ;
Zhang, ZS ;
Allen, LH .
MACROMOLECULES, 2004, 37 (12) :4607-4616
[6]   Impacts of polystyrene molecular weight and modification to the repeat unit structure on the glass transition-nanoconfinement effect and the cooperativity length scale [J].
Ellison, CJ ;
Mundra, MK ;
Torkelson, JM .
MACROMOLECULES, 2005, 38 (05) :1767-1778
[7]   Variations in the glass transition temperature of polyester with special architectures confined in thin films [J].
Erber, M. ;
Khalyavina, A. ;
Eichhorn, K. -J. ;
Voit, B. I. .
POLYMER, 2010, 51 (01) :129-135
[8]   Glassy Dynamics and Glass Transition in Thin Polymer Layers of PMMA Deposited on Different Substrates [J].
Erber, Michael ;
Tress, Martin ;
Mapesa, Emmanuel U. ;
Serghei, Anatoli ;
Eichhorn, Klaus-Jochen ;
Voit, Brigitte ;
Kremer, Friedrich .
MACROMOLECULES, 2010, 43 (18) :7729-7733
[9]   Probing slow dynamics in supported thin polymer films [J].
Fakhraai, Z ;
Forrest, JA .
PHYSICAL REVIEW LETTERS, 2005, 95 (02)
[10]   Interface and chain confinement effects on the glass transition temperature of thin polymer films [J].
Forrest, JA ;
DalnokiVeress, K ;
Dutcher, JR .
PHYSICAL REVIEW E, 1997, 56 (05) :5705-5716