Self-Supported Polypyrrole/Polyvinylsulfate Films: Electrochemical Synthesis, Characterization, and Sensing Properties of Their Redox Reactions.

Thick films of polypyrrole/polyvinylsulfate (PPy/PVS) blends were electrogenerated on stainless-steel electrodes under potentiostatic conditions from aqueous solution. The best electropolymerization potential window was determined by cyclic voltammetry. After removing the film from the back metal, self-supported electrodes were obtained.

Self-Supported Polypyrrole/Polyvinylsulfate Films: Electrochemical Synthesis, Characterization, and Sensing Properties of Their Redox Reactions.

Invited for this month's cover picture is the group of Professor Toribio F. Otero at the Centre for Electrochemistry, Intelligent Materials and Devices at the Polytechnic University of Cartagena (Spain). The cover picture shows an electrochemical cell as well as three representative cyclic voltammetric responses, displaying the electrolyte potential window, the monomer oxidation-polymerization potential range, and the polymer oxidation-reduction potential window.

Exchanged cations and water during reactions in polypyrrole macroions from artificial muscles.

The movement of the bilayer (polypyrrole-dodecylbenzenesulfonate/tape) during artificial muscle bending under flow of current square waves was studied in aqueous solutions of chloride salts. During current flow, polypyrrole redox reactions result in variations in the volumes of the films and macroscopic bending: swelling by reduction with expulsion of cations and shrinking by oxidation with the insertion of cations. The described angles follow a linear function, different in each of the studied salts, of the consumed charge: they are faradaic polymeric muscles.