Web Release Date: February 22,
Role of Chain Interpenetration in Layer-by-Layer Deposition of Polyelectrolytes
Hefei National Laboratory for Physical Sciences at Microscale, Department of Chemical Physics, University of Science and Technology of China, Hefei, China
Received: November 5, 2007
In Final Form: December 11, 2007
Abstract:
The effects of temperature, pH, and salt concentration on the layer-by-layer (LBL) deposition of sodium
poly(styrene sulfonate) (PSS)/poly[2-(dimethylamino)ethyl methacrylate] (PDEM) were investigated by use
of a quartz crystal microbalance with dissipation (QCM-D). At pH 4, the frequency change (
f) gradually
decreased to a constant, indicating that the polyelectrolyte complexes of the layer were not dissolved. As the
layer number increased, the -
f oscillatedly increased, indicating that the thickness of the multilayer increased.
At the same time, the dissipation change (
D) oscillatedly increased with the layer number, indicating the
chain interpenetration or complexation that led to the alternative swelling-and-shrinking of the outermost
layer. For the same layer number, as the temperature increased, the amplitude of
D increased, indicating
that the chain interpenetration increased. The thickness also increased with temperature. Further increasing
the pH to 7 led to a thicker layer, reflected in the larger amplitude of
D. At pH 10, the polyelectrolytes no
longer formed multilayers on the surface because of the lack of electrostatic interactions. On the other hand,
the addition of NaCl also led to a thickness increase. The amplitude in
D increased with NaCl concentration,
indicating that the chain interpenetration increased. Our experiments indicated that the LBL deposition of
polyelectrolytes was dominated by the chain interpenetration. Also, the polyelectrolyte complexes in the layer
can redissolve into solution from the surface at a high temperature or a high salt concentration.
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