Heterogeneous dynamics during deformation of a polymer glass

被引:90
作者
Riggleman, Robert A. [1 ]
Lee, Hau-Nan [2 ]
Ediger, M. D. [2 ]
de Pablo, Juan J. [3 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[2] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Biol & Chem Engn, Madison, WI 53706 USA
基金
美国国家科学基金会;
关键词
RELAXATION; MOBILITY; LIQUID; FLUID; CREEP;
D O I
10.1039/b912288e
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
The origins of molecular mobility in polymer glasses, particularly under deformation, are not well understood. A concerted experimental and computational approach is adopted to examine the segmental motion of a polymeric glass undergoing creep and constant strain rate deformations. Through a combination of molecular dynamics simulations and optical photobleaching experiments we are able to directly probe how dynamic heterogeneity evolves during deformation. Two distinct regimes emerge from our analysis; early in the deformation, the dynamics of the glass are strongly heterogeneous, as evidenced by the spectrum of relaxation times measured experimentally and the participation ratio of the atomic non-affine displacements measured computationally. After the onset of flow, the dynamics become significantly more homogeneous, and the participation ratio increases considerably.
引用
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页码:287 / 291
页数:5
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