Direct measurement and modeling of viscoelastic-viscoplastic properties of freely standing thin polystyrene films

被引:2
|
作者
Xiao, Yuhan [1 ]
Bai, Pei [1 ]
Zhang, Zhengyang [1 ]
Guo, Yunlong [1 ]
机构
[1] Shanghai Jiao Tong Univ, Univ Michigan Shanghai Jiao Tong Univ Joint Inst, Shanghai 200240, Peoples R China
来源
JOURNAL OF CHEMICAL PHYSICS | 2023年 / 159卷 / 21期
基金
中国国家自然科学基金;
关键词
ULTRATHIN POLYMER-FILMS; AMORPHOUS POLYMERS; GLASS TEMPERATURE; DYNAMICS; MODULUS; ORIENTATION; CONFINEMENT; BEHAVIOR;
D O I
10.1063/5.0176115
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The demand for applications, such as coatings, separation filters, and electronic packaging, has greatly driven the research of polymer films. At nanometer scale, mechanical properties of thin polymer films can significantly deviate from bulk. Despite outstanding progresses, there still lack deep discussions on nonlinear viscoelastic-viscoplastic response and their interactions under nanoconfinement. In this work, by conducting measurements via the bubble inflation method and modelling using Schapery and Perzyna equations, we demonstrate nonlinear viscoelastic-viscoplastic properties of freely standing thin polystyrene (PS) films. The results show the unchanged glassy compliance and the rubbery stiffening phenomenon for thin PS films, where the lower rubbery plateau in rubbery stiffening may originate from the induced molecular orientation by plastic deformation. With decreasing film thickness, viscosity and yield stress in viscoplasticity increase in an exponential and a linear trend, respectively, indicating the significant role of nanoconfinement effect on viscoplastic properties. These findings may reveal that there are many properties from linear viscoelasticity to nonlinear viscoelasticity-viscoplasticity that need to be explored and unveiled for sufficient understanding of the nanoconfinement effect on altering mechanical behavior of polymers.
引用
收藏
页数:9
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