Early steps in layer-by-layer construction of polyelectrolyte films:: The transition from surface/polymer to polymer/polymer determining interactions

被引:31
作者
Buron, C. C.
Filiatre, C. [1 ]
Membrey, F.
Bainier, C.
Charraut, D.
Foissy, A.
机构
[1] Univ Franche Comte, Inst UTINAM, CNRS 6213, F-25030 Besancon, France
[2] Univ Franche Comte, CNRS, Dept Opt LOPMD, FEMTO ST, F-25030 Besancon, France
关键词
polyelectrolyte multilayers; layer-by-layer adsorption; pH influence; ionic strength influence; poly(acrylic acid); poly(dimethylaminoethyl methacrylate chloride);
D O I
10.1016/j.jcis.2007.05.060
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
The layer-by-layer deposition of two polyelectrolytes, quaternized poly(dimethylaminoethyl methacrylate chloride) (MADQUAT) and poly(acrylic acid) (PAA) on a silica substrate was investigated using optical reflectometry, as a function of pH (pH 4, 5.5 and 9), ionic strength (10(-3) to 10(-1) M) and type of salt. Attention was given to the successive deposited weights and to the corresponding deposited charge densities within the ten first deposited layers. Results show a change of growth regime between an early stage where the substrate had a dominating influence in the build-up and a second stage where the polymer uptake was ruled essentially by poly i ner-pol ymer interactions. The pH was seen to influence the growth via the charge densities of silica (first stage) and PAA (first and second stages). The increase of NaCl concentration induced an increase of the film weight between 10(-3) and 10(-2) M, but the trend was more sophisticated between 10(-2) and 10(-1) NI where the polymer uptake increased in the first stage of the growth and decreased in subsequent layers. The film weight increased in accordance with the rank of ions in the Hofmeister series. AFM images revealed a heterogeneous film morphology with bumps and valleys, which was explained by a growth mechanism made of the successive formation and growth of polymer complexes. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:358 / 366
页数:9
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