Quantification of Water-lon Pair Interactions in Polyelectrolyte Multilayers Using a Quartz Crystal Microbalance Method

被引:12
|
作者
Eneh, Chikaodinaka I. [1 ]
Kastinen, Tuuva [2 ,3 ,4 ]
Oka, Suyash [1 ]
Batys, Piotr [5 ]
Sammalkorpi, Maria [6 ,7 ]
Lutkenhaus, Jodie L. [1 ,8 ]
机构
[1] Texas A&M Univ, Artie McFerrin Dept Chem Engn, College Stn, TX 77840 USA
[2] Aalto Univ, Dept Chem & Mat Sci, Aalto 00076, Finland
[3] Aalto Univ, Acad Finland Ctr Excellence Life Inspired Hybrid, Aalto 00076, Finland
[4] Tampere Univ, Fac Engn & Nat Sci Chem & Adv Mat, Tampere 33014, Finland
[5] Polish Acad Sci, Jerzy Haber Inst Catalysis & Surface Chem, PL-30239 Krakow 30239, Poland
[6] Aalto Univ, Dept Chem & Mat Sci, Acad Finland Ctr Excellence Life Inspired Hybrid, Aalto 00076, Finland
[7] Aalto Univ, Dept Bioprod & Biosyst, Aalto 00076, Finland
[8] Texas A&M Univ, Dept Mat Sci & Engn, College Stn, TX 77840 USA
来源
ACS POLYMERS AU | 2022年 / 2卷 / 04期
基金
美国国家科学基金会; 芬兰科学院;
关键词
polyelectrolyte multilayers; swelling; quartz crystal microbalance with dissipation; layer-by-layer assembly; intrinsic ion pairs; salts; doping; EXPONENTIAL-GROWTH; ION DISTRIBUTION; COMPLEXES; LAYER; FILMS; SALT; HYDRATION; BUILDUP; 4-STYRENE-SULFONATE); PLASTICIZATION;
D O I
10.1021/acspolymersau.2c00008
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Water existing within thin polyelectrolyte multilayer (PEM) films has significant influence on their physical, chemical, and thermal properties, having implications for applications including energy storage, smart coatings, and biomedical systems. Ionic strength, salt type, and terminating layer are known to influence PEM swelling. However, knowledge of water's microenvironment within a PEM, whether that water is affiliated with intrinsic or extrinsic ion pairs, remains lacking. Here, we examine the influence of both assembly and post-assembly conditions on the water-ion pair interactions of poly(styrene sulfonate)/poly(diallyldimethylammonium) (PSS/PDADMA) PEMs in NaCl and KBr. This is accomplished by developing a methodology in which quartz crystal microbalance with dissipation monitoring is applied to estimate the number of water molecules affiliated with an ion pair (i), as well as the hydration coefficient, pi(H2O)(salt). PSS/PDADMA PEMs are assembled in varying ionic strengths of either NaCl and KBr and then exposed post-assembly to increasing ionic strengths of matching salt type. A linear relationship between the total amount of water per intrinsic ion pair and the post-assembly salt concentration was obtained at post-assembly salt concentrations >0.5 M, yielding estimates for both i and pi(H2O)(salt). We observe higher values of i and pi(H2O)(salt) in KBr-assembled PEMs due to KBr being more effective in doping the assembly because of KBr's more chaotropic nature as compared to NaCl. Lastly, when PSS is the terminating layer, i decreases in value due to PSS's hydrophobic nature. Classical and ab initio molecular dynamics provide a microstructural view as to how NaCl and KBr interact with individual polyelectrolytes and the involved water shells. Put together, this study provides further insight into the understanding of existing water microenvironments in PEMs and the effects of both assembly and post-assembly conditions.
引用
收藏
页码:287 / 298
页数:12
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