Moderate the adsorption of cationic surfactant on gold surface by mixing with sparingly soluble anionic surfactant

被引:3
|
作者
Wang, Wei [1 ,2 ,3 ]
Lu, Wensheng [4 ]
Wang, Haifei [4 ]
Xie, Hongtao [1 ]
Wang, Jide [1 ]
机构
[1] Xinjiang Univ, Coll Chem & Chem Engn, Urumqi 830046, Peoples R China
[2] Univ Bergen, Ctr Pharm, N-5007 Bergen, Norway
[3] Univ Bergen, Dept Chem, N-5007 Bergen, Norway
[4] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Key Lab Colloid & Interface, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
C18N3; Arachidic acid; Cationic; Adsorption; Gold surface; Morphology; Aggregation; CYCLIC VOLTAMMETRY; METHYLENE-BLUE; CHAIN; PH; MORPHOLOGY;
D O I
10.1016/j.jcis.2014.10.063
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
Surfactants with amine groups are often used in the nanoparticle synthesis due to the high affinity with Au atoms. The match of charges of a capping reagent with Au has significant influence on structures in nanoparticle synthesis. Thus we studied the adsorption of a catanionic surfactant system on Au surface. The surfactants used in the study are bis[[(amidoethyl)carbamoyl]ethyl]octadecylamine (C18N3) and arachidic acid. Three combinations of the surfactants were studied with regard to the protonation state of the amine groups and the match of charges of the surfactant headgroup. The morphology of the surfactant mixtures changes from high-curvature aggregates to low-curvature with increasing the molar ratio of arachidic acid in the mixtures or the pH of the surfactant solutions. The adsorption of the mixed surfactant systems was studied by means of scanning electron microscopy (SEM), quartz crystal microbalance (QCM) and cyclic voltammetry (CV). The results revealed that the homogeneity and the compactness of the adsorbed layer on a gold surface were increased with the molar ratio of arachidic acid in the complexes. Furthermore, we may obtain the construction of the film of the mixed surfactant on gold surface using the result obtained by QCM. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:16 / 22
页数:7
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