Abstract
This study explores the effect of salt on the diffusivity of polyelectrolytes of varied molecular architecture in layer-by-layer (LbL) films in directions parallel and perpendicular to the substrate using fluorescence recovery after photobleaching (FRAP) and neutron reflectivity (NR) techniques, respectively. A family of linear, 4-arm, 6-arm, and 8-arm poly(methacrylic acids) (LPMAA, 4PMAA, 6PMAA, and 8PMAA, respectively) of matched molecular weights were synthesized using atom transfer radical polymerization and assembled with a linear polycation, poly[2-(trimethylammonium)ethyl methacrylate chloride] (QPC). NR studies involving deuterated QPC revealed ∼10-fold higher polycation mobility for the 8PMAA/QPC system compared to all-linear LbL films upon exposure to 0.25 M NaCl solutions at pH 6. FRAP experiments showed, however, that lateral diffusion of star PMAAs was lower than LPMAA at NaCl concentrations below ∼0.22 M NaCl, with a crossover to higher mobility of star polymers in more concentrated salt solutions. The stronger response of diffusion of star PMAA to salt is discussed in the context of several theories previously suggested for diffusivity of polyelectrolyte chains in multilayer films and coacervates.
Original language | English |
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Pages (from-to) | 5434-5445 |
Number of pages | 12 |
Journal | Macromolecules |
Volume | 56 |
Issue number | 14 |
DOIs | |
State | Published - Jul 25 2023 |
Externally published | Yes |
Funding
This work was supported by the National Science Foundation under Award DMR-1905535 (S.A.S.). The use of the TAMU Soft Matter Facility is acknowledged. Neutron measurements were performed at the Spallation Neutron Source at the Oak Ridge National Laboratory, managed by UT-Battelle, LLC, for the DOE under contract No. DE-AC05-00OR22725.
Funders | Funder number |
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National Science Foundation | DMR-1905535 |
U.S. Department of Energy | DE-AC05-00OR22725 |
Oak Ridge National Laboratory |