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Cation-Specific Conformational Behavior of Polyelectrolyte Brushes: From Aqueous to Nonaqueous Solvent

Year: 2014

Journal: LANGMUIR, 2014, 30 (43), pp 12850–12859, 20150430

Authors: Wang, Tao; Long, Yunchao; Liu, Lvdan; Wang, Xiaowen; Craig, Vincent S. J.; Zhang, Guangzhao; Liu, Guangming

Organizations: Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Dept Chem Phys, Hefei 230026, Peoples R China; Australian Natl Univ, Res Sch Phys & Engn, Dept Appl Math, Canberra, ACT 0200, Australia; S China Univ Technol, Fac Mat Sci & Engn, Guangzhou 510640, Guangdong, Peoples R China

We have investigated changes in the cation-specific conformational behavior of poly(sodium styrenesulfonate) (PSS) brushes as the solvent changes from water to methanol using a quartz crystal microbalance with dissipation (QCM-D). A solvation to desolvation transition of the grafted chains accompanied by swelling to the collapse transition of the brushes is observed for Na+. In the case of Cs+, the brushes undergo solvation to desolvation to resolvation accompanied by swelling to collapse to reswelling transitions. The resolvation and reswelling transitions for Cs+ are induced by the charge inversion of the brushes via van der Waals interactions between Cs+ and the brushes. All of the transitions for monovalent cations become less obvious as the methanol content increases. For divalent Ca2+ and trivalent La3+, a solvation to desolvation to resolvation transition of the grafted chains accompanied by a swelling to collapse to reswelling transition of the brushes can be observed. The resolvation and reswelling of the brushes for the multivalent cations are induced by the charge inversion of the brushes via charge-image charge interactions. The extent of the transitions for the PSS brushes in the presence of multivalent cations is only slightly influenced by the methanol content.