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具有抗聚电解质效应的盐响应性聚两性离子刷的结构依赖性

Structural Dependence of Salt-Responsive Polyzwitterionic Brushes with an Anti-Polyelectrolyte Effect.

作者信息

Xiao Shengwei, Zhang Yanxian, Shen Mingxue, Chen Feng, Fan Ping, Zhong Mingqiang, Ren Baiping, Yang Jintao, Zheng Jie

机构信息

Department of Chemical and Biomolecular Engineering, The University of Akron , Akron, Ohio 44325, United States.

出版信息

Langmuir. 2018 Jan 9;34(1):97-105. doi: 10.1021/acs.langmuir.7b03667. Epub 2017 Dec 27.

Abstract

Some polyzwitterionic brushes exhibit a strong "anti-polyelectrolyte effect" and ionic specificity that make them versatile platforms to build smart surfaces for many applications. However, the structure-property relationship of zwitterionic polymer brushes still remains to be elucidated. Herein, we aim to study the structure-dependent relationship between different zwitterionic polymers and the anti-polyelectrolyte effect. To this end, a series of polyzwitterionic brushes with different cationic moieties (e.g., imidazolium, ammonium, and pyridinium) in their monomeric units and with different carbon spacer lengths (e.g., CSL = 1, 3, and 4) between the cation and anion were designed and synthesized to form polymer brushes via the surface-initiated atom transfer radical polymerization. All zwitterionic brushes were carefully characterized for their surface morphologies, compositions, wettability, and film thicknesses by atomic force microscopy, contact angle measurement, and ellipsometry, respectively. The salt-responsiveness of all zwitterionic brushes to surface hydration and friction was further examined and compared both in water and in salt solutions with different salt concentrations and counterion types. The collective data showed that zwitterionic brushes with different cationic moieties and shorter CSLs in salt solution induced higher surface friction and lower surface hydration than those in water, exhibiting strong anti-polyelectrolyte effect salt-responsive behaviors. By tuning the CSLs, cationic moieties, and salt concentrations and types, the surface wettability can be changed from a highly hydrophobic surface (∼60°) to a highly hydrophilic surface (∼9°), while interfacial friction can be changed from ultrahigh friction (μ ≈ 4.5) to superior lubrication (μ ≈ 10). This work provides important structural insights into how subtle structural changes in zwitterionic polymers can yield great changes in the salt-responsive properties at the interface, which could be used for the development of smart surfaces for different applications.

摘要

一些聚两性离子刷表现出强烈的“抗聚电解质效应”和离子特异性,使其成为构建适用于多种应用的智能表面的通用平台。然而,两性离子聚合物刷的结构-性能关系仍有待阐明。在此,我们旨在研究不同两性离子聚合物之间的结构依赖性关系以及抗聚电解质效应。为此,设计并合成了一系列在其单体单元中具有不同阳离子部分(如咪唑鎓、铵和吡啶鎓)且阳离子与阴离子之间具有不同碳间隔长度(如CSL = 1、3和4)的聚两性离子刷,通过表面引发的原子转移自由基聚合形成聚合物刷。分别通过原子力显微镜、接触角测量和椭偏仪对所有两性离子刷的表面形貌、组成、润湿性和膜厚度进行了仔细表征。进一步研究并比较了所有两性离子刷在水和不同盐浓度及抗衡离子类型的盐溶液中对表面水合作用和摩擦的盐响应性。综合数据表明,与在水中相比,盐溶液中具有不同阳离子部分和较短CSL的两性离子刷会引起更高的表面摩擦力和更低的表面水合作用,表现出强烈的抗聚电解质效应盐响应行为。通过调节CSL、阳离子部分、盐浓度和类型,表面润湿性可从高度疏水表面(约60°)变为高度亲水表面(约9°),而界面摩擦力可从超高摩擦力(μ≈4.5)变为优异的润滑性(μ≈10)。这项工作为两性离子聚合物中细微的结构变化如何在界面处产生盐响应特性的巨大变化提供了重要的结构见解,这可用于开发适用于不同应用的智能表面。

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