Measuring the surface dynamics of glassy polymers

被引:540
作者
Fakhraai, Z.
Forrest, J. A. [1 ]
机构
[1] Univ Waterloo, Dept Phys & Astron, Waterloo, ON N2L 3G1, Canada
关键词
D O I
10.1126/science.1151205
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The motion of polymer chain segments cooled below the glass transition temperature slows markedly; with sufficient cooling, segmental motion becomes completely arrested. There is debate as to whether the chain segments near the free surface, or in thin films, are affected in the same way as the bulk material. By partially embedding and then removing gold nanospheres, we produced a high surface coverage of well- defined nanodeformations on a polystyrene surface; to probe the surface dynamics, we measured the time- dependent relaxation of these surface deformations as a function of temperature from 277 to 369 kelvin. Surface relaxation was observed at all temperatures, providing strong direct evidence for enhanced surface mobility relative to the bulk. The deviation from bulk a relaxation became more pronounced as the temperature was decreased below the bulk glass transition temperature. The temperature dependence of the relaxation time was much weaker than that of the bulk a relaxation of polystyrene, and the process exhibited no discernible temperature dependence between 277 and 307 kelvin.
引用
收藏
页码:600 / 604
页数:5
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