pH-Controlled Electrochemical Deposition of Polyelectrolyte Complex Films.

Langmuir

Department of Materials Science & Engineering, Northwestern University, Evanston, Illinois 60208, United States.

Published: February 2017

AI Article Synopsis

  • Polyelectrolyte complex (PEC) films, made from oppositely charged polymers, have important uses in drug delivery, separation membranes, and biocompatible coatings.
  • Traditional methods for creating these films are slow and complicated, requiring multiple steps to achieve desired thicknesses.
  • This research introduces a fast one-pot electrochemical method to create 1 μm PEC films in just 5 minutes by utilizing hydrogen peroxide reduction, improving the efficiency and potential applications of PEC coatings.

Article Abstract

Polyelectrolyte complex (PEC) films made from oppositely charged polymer chains have applications as drug-delivery vehicles, separation membranes, and biocompatible coatings. Conventional layer-by-layer techniques for polyelectrolyte coatings are low-throughput and multistep processes that are quite slow for building films on the order of micrometers. In this work, PEC films are electrochemically deposited using a rapid one-pot method, yielding thick (1 μm) films within short experimental time scales (5 min). This rapid electrodeposition is achieved by exploiting the reduction of hydrogen peroxide at mild electrode potentials that avoid water electrolysis yet trigger the pH-responsive self-assembly of a PEC film composed of poly(acrylic) acid and poly(allylamine) HCl. In situ rheology using an electrochemical quartz crystal microbalance quantified the shear modulus-density product of the deposited layer to be on the order of 10 Pa g/cm at a frequency of 15 MHz, with a viscoelastic phase angle of approximately 50°. This electrodeposition scheme furthers the development of PEC coatings for more high-throughput applications, where a fast and efficient single-step approach would be desirable for obtaining coatings.

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http://dx.doi.org/10.1021/acs.langmuir.6b04491DOI Listing

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