首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >Comparison of permeability of poly(allylamine hydrochloride)/and poly(diallyldimethylammonium chloride)/poly(4-styrenesulfonate) multilayer films: Linear vs. exponential growth
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Comparison of permeability of poly(allylamine hydrochloride)/and poly(diallyldimethylammonium chloride)/poly(4-styrenesulfonate) multilayer films: Linear vs. exponential growth

机译:聚(烯丙胺盐酸盐)/和聚(二烯丙基二甲基氯化铵)/聚(4-苯乙烯磺酸盐)多层膜的渗透性比较:线性与指数增长

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摘要

The ability to form highly tailored polymer thin films with various functional groups or nanoobjects incorporated in the film structure is the main reason of a popularity of the Layer-by-Layer method. In the present paper we concentrated on the formation and permeability of multilayer polyelectrolyte films exhibiting various growth regimes, linear and exponential. Films were formed of two model pairs of polyelectrolytes: poly(allylamine hydrochloride)/poly(4-styrenesulfonate) (PAH/PSS) and poly(diallyl-dimethylammonium chloride)/poly(4-styrenesulfonate) (PDADMAC/PSS) at various ionic strengths of polyelectrolyte solutions. Quartz crystal microbalance with dissipation (QCM-D) was used to determine the films' mass and viscoelastic properties in situ. The results concerning the films growth were compared with the thickness in "dry" state measured by ellipsometry. The Electrochemical Impedance Spectroscopy (EIS) with the redox couple potassium hexacyanoferrate (II) and (III) was used to determine the electrochemical impedance of films deposited at gold rotating disk electrode (ROE). The measurements showed that the obtained ellipsometric thickness, mass and resistance of multilayer films depended on the number of deposited polyelectrolyte layers and the ionic strength of PE solutions. However, PAH/PSS films formed at high ionic strength, exhibiting linear growth had much higher impedance than much thicker PDADMAC/PSS films with the exponential growth. We attributed that effect to the more "spongy" structure of exponentially growing films, containing more water. (C) 2014 Elsevier B.V. All rights reserved.
机译:形成具有各种官能团或掺入薄膜结构中的纳米物体的高度定制的聚合物薄膜的能力是逐层方法普及的主要原因。在本文中,我们集中于多层聚电解质薄膜的形成和渗透性,这些薄膜表现出各种生长方式,线性和指数形式。膜由两对模型的聚电解质形成:聚(烯丙胺盐酸盐)/聚(4-苯乙烯磺酸盐)(PAH / PSS)和聚(二烯丙基-二甲基氯化铵)/聚(4-苯乙烯磺酸盐)(PDADMAC / PSS)电解质溶液的强度。带有耗散的石英晶体微天平(QCM-D)用于原位确定薄膜的质量和粘弹性。将关于膜生长的结果与通过椭圆偏振法测量的“干燥”状态下的厚度进行比较。电化学阻抗谱(EIS)和氧化还原对六氰合铁酸钾(II)和(III)用于确定沉积在金旋转盘电极(ROE)上的薄膜的电化学阻抗。测量表明,获得的多层膜的椭圆偏振厚度,质量和电阻取决于所沉积的聚电解质层的数量和PE溶液的离子强度。但是,具有高离子强度的PAH / PSS膜表现出线性增长,其阻抗要比具有指数增长的厚得多的PDADMAC / PSS膜高得多。我们将这种效果归因于含有更多水的指数增长薄膜的“海绵状”结构。 (C)2014 Elsevier B.V.保留所有权利。

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