Spatially Distributed Rheological Properties in Confined Polymers by Noncontact Shear

被引:26
作者
Chowdhury, Mithun [1 ]
Guo, Yunlong [1 ,3 ]
Wang, Yucheng [1 ]
Merling, Weston L. [4 ]
Mangalara, Jayachandra H. [4 ]
Simmons, David S. [4 ]
Priestley, Rodney D. [1 ,2 ]
机构
[1] Princeton Univ, Dept Chem & Biol Engn, Princeton, NJ 08544 USA
[2] Princeton Univ, Princeton Inst Sci & Technol Mat, Princeton, NJ 08544 USA
[3] Shanghai Jiao Tong Univ, Univ Michigan Shanghai Jiao Tong Univ Joint Inst, Shanghai 200240, Peoples R China
[4] Univ Akron, Dept Polymer Engn, Akron, OH 44325 USA
基金
美国国家科学基金会;
关键词
GLASS-TRANSITION; FILMS; DYNAMICS; MOBILITY; SURFACES; DEFORMATION; RELAXATION; STIFFNESS; STRESS; FLUIDS;
D O I
10.1021/acs.jpclett.7b00214
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
When geometrically confined to the nanometer length scale, a condition in which a large portion of the material is in the nanoscale vicinity of interfaces, polymers can show astonishing changes in physical properties. In this investigation, we employ a unique noncontact capillary nanoshearing method to directly probe nanoresolved gradients in the rheological response of ultrathin polymer films as a function of temperature and stress. Results show that ultrathin polymer films, in response to an applied shear stress, exhibit a gradient in molecular mobility and viscosity that originates at the interfaces. We demonstrate, via molecular dynamics simulations, that these gradients in molecular mobility reflect gradients in the average segmental relaxation time and the glass-transition temperature.
引用
收藏
页码:1229 / 1234
页数:6
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