Experimental evidence for a new parameter to control the glass transition of confined polymers

被引:62
作者
Srivastava, S. [1 ]
Basu, J. K. [1 ]
机构
[1] Indian Inst Sci, Dept Phys, Bangalore 560012, Karnataka, India
关键词
D O I
10.1103/PhysRevLett.98.165701
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Polymer nanocomposites can be used to study confinement effects on the polymer glass transition temperature (T-g) in a controlled manner by varying interparticle spacing. Using gold nanoparticles in polymethylmethacrylate, we show how the polymer T-g can be tuned by variation of the nanoparticle-polymer interface width (sigma), keeping interparticle spacing fixed. We report the first experimental observation of a crossover in the sign of T-g deviation for confined polymers by variation of sigma and propose a model to explain the dependence of crossover width on the spatial extent of cooperatively rearranging regions.
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页数:4
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共 31 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]   Effects of confinement on material behaviour at the nanometre size scale [J].
Alcoutlabi, M ;
McKenna, GB .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2005, 17 (15) :R461-R524
[3]   Glass-transition temperature behavior of alumina/PMMA nanocomposites [J].
Ash, BJ ;
Siegel, RW ;
Schadler, LS .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2004, 42 (23) :4371-4383
[4]   Nanoparticle polymer composites: Where two small worlds meet [J].
Balazs, Anna C. ;
Emrick, Todd ;
Russell, Thomas P. .
SCIENCE, 2006, 314 (5802) :1107-1110
[5]   Quantitative equivalence between polymer nanocomposites and thin polymer films [J].
Bansal, A ;
Yang, HC ;
Li, CZ ;
Cho, KW ;
Benicewicz, BC ;
Kumar, SK ;
Schadler, LS .
NATURE MATERIALS, 2005, 4 (09) :693-698
[6]   Computer simulations of supercooled polymer melts in the bulk and in-confined geometry [J].
Baschnagel, J ;
Varnik, F .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2005, 17 (32) :R851-R953
[7]   Growing range of correlated motion in a polymer melt on cooling towards the glass transition [J].
Bennemann, C ;
Donati, C ;
Baschnagel, J ;
Glotzer, SC .
NATURE, 1999, 399 (6733) :246-249
[8]   Gradient of glass transition temperature in filled elastomers [J].
Berriot, J ;
Montes, H ;
Lequeux, F ;
Long, D ;
Sotta, P .
EUROPHYSICS LETTERS, 2003, 64 (01) :50-56
[9]   Direct experimental evidence of a growing length scale accompanying the glass transition [J].
Berthier, L ;
Biroli, G ;
Bouchaud, JP ;
Cipelletti, L ;
El Masri, D ;
L'Hôte, D ;
Ladieu, F ;
Pierno, M .
SCIENCE, 2005, 310 (5755) :1797-1800
[10]   Glass transitions in thin polymer films [J].
de Gennes, PG .
EUROPEAN PHYSICAL JOURNAL E, 2000, 2 (03) :201-203