Dual-beam polarization interferometry resolves mechanistic aspects of polyelectrolyte adsorption

被引:38
|
作者
Lane, Thomas J. [1 ]
Fletcher, Will R. [1 ]
Gormally, Michael V. [1 ]
Johal, Malkiat S. [1 ]
机构
[1] Pomona Coll, Dept Chem, Claremont, CA 91711 USA
关键词
D O I
10.1021/la802496h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrostatically driven binding dynamics of a polyelectrolyte multilayer (PEMU) film was investigated in real-time using dual-beam polarization interferometry (DPI) and independently supported by quartz crystal microbalance with dissipation monitoring (QCM-D) studies. Multilayer assemblies of the polyanions poly[1-[4[(3-carboxy-4-hydroxyphenylazo)benzenesulfonamido]-1,2-ethanediyl sodium salt] (PAZO) and poly(styrene sulfonate) (PSS) were respectively constructed with the polycation poly(ethylenimine) (PEI) on anionic functionalized substrates using the layer-by-layer electrostatic self-assembly method. DPI measurements indicate that polyelectrolyte adsorption occurs in three distinct stages. In the first stage, for similar to 5 s, coil-like segments of polyanion partially tether to the surface of the oppositely charged PEI. In the second stage, these Coils unfurl over a period of similar to 10 s to cover the surface resulting in an increase in average density of the film. During the final adsorption step, the surface-bound polyelectrolyte diffuses into the multilayer assembly, exposing the surface to further deposition. This last step occurs over a much longer time period and results in a highly interpenetrated film containing a charge-overcompensated region at the film surface.
引用
收藏
页码:10633 / 10636
页数:4
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