In situ Adhesion Measurements Utilizing Layer-by-Layer Functionalized Surfaces

被引:22
|
作者
Nolte, Adam J. [1 ]
Chung, Jun Young [1 ]
Walker, Marlon L. [2 ]
Stafford, Christopher M. [1 ]
机构
[1] Natl Inst Stand & Technol, Div Polymers, Gaithersburg, MD 20899 USA
[2] Natl Inst Stand & Technol, Surface & Microanal Sci Div, Gaithersburg, MD 20899 USA
关键词
JKR; adhesion; layer by layer; polyelectrolyte; responsive; contact mechanics; roughness; POLYELECTROLYTE MULTILAYER FILMS; THIN-FILMS; WEAK POLYELECTROLYTES; FORCE MICROSCOPY; YOUNGS MODULUS; ELASTIC SOLIDS; JKR METHOD; CONTACT; ADSORPTION; POLYMERS;
D O I
10.1021/am8000874
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The adhesion between poly(dimethyisiloxane) (PDMS) hemispheres coated with layer-by-layer (LbL) assemblies of polyelectrolytes and rigid, planar substrates was investigated using Johnson, Kendall, and Roberts (JKR) contact mechanics. Measurements were performed against amine functionalized glass slides both in air aqueous solutions of controlled pH. Despite the increased density of negatively charged carboxylate groups LbL functionalized PDMS exhibited lower adhesion because of the combined effects of increased surface roughness and the high young is modulus of the coating. Measurements of coated PDMS in aqueous solutions revealed tunable adhesion behavior dominated by pH mediated changes in the mechanical properties of the coating Smoothing the surface of the LbL coatings by aqueous salt annealing led to a significant increase in adhesion. Our results suggest that LbL assembly can be an effective means of surface functionalization for in situ adhension measurements, but understanding and predicting the adhesion behavior requires comprehensive knowledge of the chemical mechanical and topological properties of the coating and how such properties change in response to the ambient enviroment.
引用
收藏
页码:373 / 380
页数:8
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