Studying the Adhesion Force and Glass Transition of Thin Polystyrene Films by Atomic Force Microscopy

被引:20
|
作者
Kang, Hua [1 ]
Qian, Xiaoqin [1 ]
Guan, Li [1 ,2 ]
Zhang, Meining [1 ]
Li, Qiang [2 ]
Wu, Aoli [3 ]
Dong, Mingdong [2 ]
机构
[1] Renmin Univ China, Dept Chem, Beijing 100872, Peoples R China
[2] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark
[3] Jiangsu CASRS Pollut Control Engn Co Ltd, Yancheng, Peoples R China
来源
基金
国家重点研发计划; 新加坡国家研究基金会; 中国国家自然科学基金;
关键词
Adhesion Force; Glass Transition Temperature; Polystyrene; Atomic Force Microscope (AFM); Force Distance Curves; ULTRATHIN POLYMER-FILMS; TEMPERATURE; DYNAMICS; SURFACES; RELAXATION; MOBILITY; DEPRESSION; INTERFACE; OXIDATION; GRAPHENE;
D O I
10.1186/s11671-017-2426-9
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The relaxation behaviors of thin polymer films show a strong dependence on temperature and film thickness. Direct quantitative detection of the relaxation behaviors of thin polymer films at nanometer scale by traditional instruments is however challenging. In this study, we employed atomic force microscopy (AFM)-based forcedistance curve to study the relaxation dynamics and the film thickness dependence of glass transition temperature (T-g) for normal thin polystyrene (PS) films supported on silicon substrate. The adhesion force (F-ad) between AFM tip and normal thin PS film surfaces was quantitatively detected in situ under the variation of temperature and film thickness. The T-g of normal thin PS film was successfully obtained by the abrupt variation of Fad under temperature stimulation. Our result showed that the T-g of normal thin PS films decreased with the decreasing film thickness. The study here could be beneficial for understanding the relaxation dynamics of normal thin polymer films.
引用
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页数:8
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