Abstract

HypothesisIntegration of ultralow surface energy and surface functionality on one surface coatings is highly desirable in chemical and biomedical applications. However, it is a fundamental challenge to reduce surface energy without cost of surface functionality and vice versa. To address this challenge, the present work made use of the rapid and reversible change of surface orientation conformations of weak polyelectrolyte multilayers to create ionic, perfluorinated surfaces. ExperimentsPoly(allylamine hydrochloride) (PAH) chains and the micelles of sodium perfluorooctanoate (SPFO) were layer-by-layer (LbL) assembled into (SPFO/PAH)n multilayer films, which readily exfoliated to freestanding membranes. The static and dynamic surface wetting behaviors of the resulting membranes were studied by sessile drop technique and their surface charge behaviors in water by electrokinetic analysis. FindingsAs-prepared (SPFO/PAH)n membranes exhibited ultralow surface energy in air; the lowest surface energy is 2.6 ± 0.5 mJ/m2 for PAH-capped surfaces and 7.0 ± 0.9 mJ/m2 for SPFO-capped surfaces. They readily became positively charged in water, which allowed not only effective adsorption of ionic species for further functionalization with subtle change in surface energy, but effective adhesion onto various solid substrates such as glass, stainless steel, and polytetrafluoroethylene to endorse the wide applicability of (SPFO/PAH)n membranes.

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