Glass transition in thin supported polystyrene films probed by temperature-modulated ellipsometry in vacuum

被引:35
作者
Efremov, Mikhail Yu. [1 ]
Kiyanova, Anna V.
Last, Julie
Soofi, Shauheen S.
Thode, Christopher
Nealey, Paul F.
机构
[1] Univ Wisconsin, Dept Chem & Biol Engn, Madison, WI 53706 USA
来源
PHYSICAL REVIEW E | 2012年 / 86卷 / 02期
基金
美国国家科学基金会;
关键词
POLYMER-FILMS; T-G; HEAT-CAPACITY; DYNAMICS; MOBILITY; DEPRESSION; INTERFACE; BEHAVIOR;
D O I
10.1103/PhysRevE.86.021501
中图分类号
O35 [流体力学]; O53 [等离子体物理学];
学科分类号
070204 ; 080103 ; 080704 ;
摘要
Glass transition in thin (1-200 nm thick) spin-cast polystyrene films on silicon surfaces is probed by ellipsometry in a controlled vacuum environment. A temperature-modulated modification of the method is used alongside a traditional linear temperature scan. A clear glass transition is detected in films with thicknesses as low as 1-2 nm. The glass transition temperature (T-g) shows no substantial dependence on thickness for coatings greater than 20 nm. Thinner films demonstrate moderate T-g depression achieving 18 K for thicknesses 4-7 nm. Less than 4 nm thick samples are excluded from the T-g comparison due to significant thickness nonuniformity (surface roughness). The transition in 10-20 nm thick films demonstrates excessive broadening. For some samples, the broadened transition is clearly resolved into two separate transitions. The thickness dependence of the glass transition can be well described by a simple 2-layer model. It is also shown that T-g depression in 5 nm thick films is not sensitive to a wide range of experimental factors including molecular weight characteristics of the polymer, specifications of solvent used for spin casting, substrate composition, and pretreatment of the substrate surface.
引用
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页数:11
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