Charge regulation in polyelectrolyte brushes studied by FTIR spectroscopy

被引:11
作者
Abe, T
Hayashi, S
Higashi, N
Niwa, M
Kurihara, K [1 ]
机构
[1] Tohoku Univ, Inst Chem React Sci, Aoba Ku, Sendai, Miyagi 9808577, Japan
[2] Doshisha Univ, Fac Engn, Dept Mol Sci & Technol, Kyoto 6100394, Japan
关键词
charge regulation; polyelectrolyte brushes; FTIR spectroscopy;
D O I
10.1016/S0927-7757(00)00470-2
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
Brush layers of a polyelectrolyte, ionized poly(glutamic acid) (polymerization degree n = 48), were studied using FTIR spectroscopy as a function of the polyelectrolyte chain density. The Langmuir-Blodgett (LB) deposition of the mixed monolayers of a poly (glutamic acid) functionalized amphiphile and dioctadecylphospholic acid afforded the preparation of polyelectrolyte brushes at the desired density on various substrates. FTIR spectroscopy on the LB films demonstrated that the ionization degree of the carboxylic acid groups decreased with increasing polyelectrolyte density in order to maintain the charge density below the critical value of 0.8 similar to 1 charge nm(-3). The average distance between the charges at the maximum density was ca. 1.1 +/- 0.1 nm which is close to twice the Bjerrum length, the distance at which the Coulomb interaction between elementary charges is equal to the thermal energy. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:351 / 356
页数:6
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