A unifying framework to quantify the effects of substrate interactions, stiffness, and roughness on the dynamics of thin supported polymer films

被引:120
作者
Hanakata, Paul Z. [1 ]
Betancourt, Beatriz A. Pazmino [1 ,2 ]
Douglas, Jack F. [2 ]
Starr, Francis W. [1 ]
机构
[1] Wesleyan Univ, Dept Phys, Middletown, CT 06459 USA
[2] NIST, Mat Sci & Engn, Gaithersburg, MD 20899 USA
关键词
GLASS-TRANSITION TEMPERATURE; COOPERATIVE MOTION; MOLECULAR-WEIGHT; SELF-DIFFUSION; VISCOUS-FLOW; PURE LIQUIDS; RANDOM-WALK; POLYSTYRENE; VISCOSITY; SURFACE;
D O I
10.1063/1.4922481
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
Changes in the dynamics of supported polymer films in comparison to bulk materials involve a complex convolution of effects, such as substrate interactions, roughness, and compliance, in addition to film thickness. We consider molecular dynamics simulations of substrate-supported, coarse-grained polymer films where these parameters are tuned separately to determine how each of these variables influence the molecular dynamics of thin polymer films. We find that all these variables significantly influence the film dynamics, leading to a seemingly intractable degree of complexity in describing these changes. However, by considering how these constraining variables influence string-like collective motion within the film, we show that all our observations can be understood in a unified and quantitative way. More specifically, the string model for glass-forming liquids implies that the changes in the structural relaxation of these films are governed by the changes in the average length of string-like cooperative motions and this model is confirmed under all conditions considered in our simulations. Ultimately, these changes are parameterized in terms of just the activation enthalpy and entropy for molecular organization, which have predictable dependences on substrate properties and film thickness, offering a promising approach for the rational design of film properties. (C) 2015 AIP Publishing LLC.
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页数:18
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