材料科学
埃
结晶
结晶度
无定形固体
聚合物
铸造
薄膜
玻璃化转变
聚合物结晶
硅烷
化学工程
复合材料
结晶学
纳米技术
化学
工程类
作者
C. W. Frank,Veena Rao,M. M. Despotopoulou,R. F. W. Pease,William D. Hinsberg,R. Miller,John F. Rabolt
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1996-08-16
卷期号:273 (5277): 912-915
被引量:469
标识
DOI:10.1126/science.273.5277.912
摘要
The molecular organization in ultrathin polymer films (thicknesses less than 1000 angstroms) and thin polymer films (thicknesses between 1000 and 10,000 angstroms) may differ substantially from that of bulk polymers, which can lead to important differences in resulting thermophysical properties. Such constrained geometry films have been fabricated from amorphous poly(3-methyl-4-hydroxy styrene) (PMHS) and semicrystalline poly(di- n -hexyl silane) (PD6S) by means of spin-casting. The residual solvent content is substantially greater in ultrathin PMHS films, which suggests a higher glass transition temperature that results from a stronger hydrogen-bonded network as compared with that in thicker films. Crystallization of PD6S is substantially hindered in ultrathin films, in which a critical thickness of 150 angstroms is needed for crystalline morphology to exist and in which the rate of crystallization is initially slow but increases rapidly as the film approaches 500 angstroms in thickness.
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