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    Linear and Star Poly(ionic liquid) Assemblies: Surface Monolayers and Multilayers

    Year: 2017

    Journal: Langmuir, Volume 33, APR 4, page 3187–3199

    Authors: Erwin, Andrew J.; Xu, Weinan; He, Hongkun; Matyjaszewski, Krzysztof; Tsukruk, Vladimir V.

    Organizations: National Science Foundation [DMR 1505234, DMR 1501324]; U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Science and Engineering [DE-FG02-09ER46604]; DoE [ER45998]

    The surface morphology and organization of,poly(ionic liquid)s (PILs), poly[1-(4-vinylbenzyl)-3-butylimida-zolium bis(trifluoromethylsulfonyl)imide] are explored in conjunction with their molecular architecture, adsorption conditions, and postassembly treatments: The formation of stable PIL Langmuir and Langmuir-Blodgett (LB) monolayers at the air-water and air-solid interfaces is demonstrated. The, hydrophobic bis(trifluoromethylsulfonyl)imide (Tf2N- is shown to be a critical agent governing the assembly morphology, as observed in the reversible condensation of LB monolayers into dense nanodroplets. The PIL is then incorporated as an unconventional polyelectrolyte component in,the layer-by-layer (LbL) films of hydrophobic character. We demonstrate that the interplay of capillary forces, macromolecular mobility, and structural relaxation of the polymer chains influence the dewetting mechanisms in the PIL multilayers,, thereby enabling access to a diverse set of highly textured, porous, and interconnected network morphologies for PIL LbL-films that would otherwise be absent in,conventional LbL films. Their compartmentalized internal structure is relevant to molecular separation membranes, ultrathin hydrophobic coatings, targeted cargo delivery, and highly conductive films.
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