Dynamics near Free Surfaces and the Glass Transition in Thin Polymer Films: A View to the Future

被引:438
作者
Ediger, M. D. [1 ]
Forrest, J. A. [2 ]
机构
[1] Univ Wisconsin, Dept Chem, Madison, WI 53706 USA
[2] Univ Waterloo, Dept Phys & Astron, Waterloo, ON N2L 3G1, Canada
基金
美国国家科学基金会; 加拿大自然科学与工程研究理事会;
关键词
ULTRATHIN POLYSTYRENE FILMS; POLY(METHYL METHACRYLATE); STRUCTURAL RELAXATION; MOLECULAR-MOTION; TEMPERATURE; MOBILITY; BULK; INTERFACE; BEHAVIOR; LIQUIDS;
D O I
10.1021/ma4017696
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The past 20 years have seen a substantial effort to understand dynamics and the glass transition in thin polymer films. In this Perspective, we consider developments in this field and offer a consistent interpretation of some major findings. We discuss recent experiments that directly measure mobility at or near the surface of glassy polymers. These experiments indicate that enhanced mobility near the free surface can exceed bulk mobility by several orders of magnitude and extend for several nanometers into the bulk polymer. Enhanced mobility near the free surface allows a qualitative understanding of many of the observations of a reduced glass transition temperature T-g in thin films. For thin films, knowledge of T-g by itself is less useful than for bulk materials. Because of this, new experimental methods that directly measure important material properties are being developed.
引用
收藏
页码:471 / 478
页数:8
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