String-like collective motion in the α- and β-relaxation of a coarse-grained polymer melt

被引:65
作者
Betancourt, Beatriz A. Pazmino [1 ,2 ]
Starr, Francis W. [2 ]
Douglas, Jack F. [1 ]
机构
[1] NIST, Mat Sci & Engn Div, Gaithersburg, MD 20899 USA
[2] Wesleyan Univ, Dept Phys, Middletown, CT 06459 USA
关键词
SPATIALLY HETEROGENEOUS DYNAMICS; POTENTIAL-ENERGY LANDSCAPE; STRUCTURAL RELAXATION; COOPERATIVE MOTION; VIBRATIONAL-MODES; GLASS-TRANSITION; EQUILIBRIUM POLYMERIZATION; SUPERCOOLED LIQUIDS; VISCOUS-LIQUIDS; LATTICE MODEL;
D O I
10.1063/1.5009442
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Relaxation in glass-forming liquids occurs as a multi-stage hierarchical process involving cooperative molecular motion. First, there is a "fast" relaxation process dominated by the inertial motion of the molecules whose amplitude grows upon heating, followed by a longer time alpha-relaxation process involving both large-scale diffusive molecular motion and momentum diffusion. Our molecular dynamics simulations of a coarse-grained glass-forming polymer melt indicate that the fast, collective motion becomes progressively suppressed upon cooling, necessitating large-scale collective motion by molecular diffusion for the material to relax approaching the glass-transition. In each relaxation regime, the decay of the collective intermediate scattering function occurs through collective particle exchange motions having a similar geometrical form, and quantitative relationships are derived relating the fast "stringlet" collective motion to the larger scale string-like collective motion at longer times, which governs the temperature-dependent activation energies associated with both thermally activated molecular diffusion and momentum diffusion. Published by AIP Publishing.
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页数:10
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