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

被引:69
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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共 103 条
[51]   SCALING CONCEPTS FOR THE DYNAMICS OF VISCOUS-LIQUIDS NEAR AN IDEAL GLASSY STATE [J].
KIRKPATRICK, TR ;
THIRUMALAI, D ;
WOLYNES, PG .
PHYSICAL REVIEW A, 1989, 40 (02) :1045-1054
[52]   Light scattering of supercooled propylene glycol [J].
Kojima, S ;
Sato, H ;
Yosihara, A .
JOURNAL OF PHYSICS-CONDENSED MATTER, 1997, 9 (46) :10079-10085
[53]   LOCALIZED LOW-FREQUENCY VIBRATIONAL-MODES IN A SIMPLE-MODEL GLASS [J].
LAIRD, BB ;
SCHOBER, HR .
PHYSICAL REVIEW LETTERS, 1991, 66 (05) :636-639
[54]   Universal scaling between structural relaxation and vibrational dynamics in glass-forming liquids and polymers [J].
Larini, L. ;
Ottochian, A. ;
De Michele, C. ;
Leporini, D. .
NATURE PHYSICS, 2008, 4 (01) :42-45
[55]   Does fragility of glass formation determine the strength of Tg-nanoconfinement effects? [J].
Mangalara, Jayachandra Hari ;
Marvin, Michael D. ;
Wiener, Nicholas R. ;
Mackura, Mark E. ;
Simmons, David S. .
JOURNAL OF CHEMICAL PHYSICS, 2017, 146 (10)
[56]   Tuning Polymer Glass Formation Behavior and Mechanical Properties with Oligomeric Diluents of Varying Stiffness [J].
Mangalara, Jayachandra Hari ;
Simmons, David S. .
ACS MACRO LETTERS, 2015, 4 (10) :1134-1138
[57]   Experimental observations of non-Gaussian behavior and stringlike cooperative dynamics in concentrated quasi-two-dimensional colloidal liquids [J].
Marcus, AH ;
Schofield, J ;
Rice, SA .
PHYSICAL REVIEW E, 1999, 60 (05) :5725-5736
[58]   MOLECULAR-DYNAMICS STUDY OF BINARY SOFT-SPHERE MIXTURES - JUMP MOTIONS OF ATOMS IN THE GLASSY STATE [J].
MIYAGAWA, H ;
HIWATARI, Y ;
BERNU, B ;
HANSEN, JP .
JOURNAL OF CHEMICAL PHYSICS, 1988, 88 (06) :3879-3886
[59]   Spatial heterogeneity in supercooled liquids and glasses [J].
Muranaka, T ;
Hiwatari, Y .
JOURNAL OF THE PHYSICAL SOCIETY OF JAPAN, 1998, 67 (06) :1982-1987
[60]   Classification of secondary relaxation in glass-formers based on dynamic properties [J].
Ngai, KL ;
Paluch, M .
JOURNAL OF CHEMICAL PHYSICS, 2004, 120 (02) :857-873