Lateral mobility of polyelectrolyte chains in multilayers

被引:83
作者
Nazaran, P.
Bosio, V.
Jaeger, W.
Anghel, D. F.
v. Klitzing, R.
机构
[1] Tech Univ Berlin, Stranski Lab Phys & Theoret Chem, D-10623 Berlin, Germany
[2] Max Planck Inst Kolloid, D-14424 Potsdam, Germany
[3] Grenzflachenforsch, D-14424 Potsdam, Germany
[4] Fraunhofer Inst Angew Polymerforsch, D-14476 Potsdam, Germany
[5] Inst Phys Chem, Dept Colloids Ilie Murgulescu, Bucharest 060021, Romania
关键词
D O I
10.1021/jp068768e
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
In this work, the lateral mobility of polyelectrolyte multilayers was investigated by means of the fluorescence recovery after photobleaching (FRAP) technique, with special attention to the effect of relevant parameters during and after preparation. Different polyelectrolytes with respect to charge density, stiffness, and hydrophilicity were compared. From the experimental results emerged that the density of charged sites along the polymer is the most important parameter controlling the formation of polymer complexes. At higher charge density, more complexes are formed, and the diffusion coefficient decreases. It was observed that the intrinsic backbone stiffness reduces the interpenetration of polyelectrolyte layers and the formation of complexes promoting the lateral mobility. In addition, the lateral mobility increases with increasing ionic strength and with decreasing hydration shell of the added anion in the polyelectrolyte solution. The effect of heating or annealing in electrolyte solution after preparation was also investigated along with the embedding of the probing layer at controlled distances to the multilayer surface.
引用
收藏
页码:8572 / 8581
页数:10
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