Synchronous Cation-Driven and Anion-Driven Polypyrrole-Based Yarns toward In-Air Linear Actuators

Conducting polymers (CP) have shown great features in building textile actuators. To date, most of the yarn-based or CP-yarn actuators have been operated in liquid electrolytes in a three-electrode-cell configuration, comprising an external counter and a reference electrode. For integration in textiles, a two-electrode system is needed, where both electrodes are in a yarn format. This can be achieved by having two CP-yarns, where one acts as the anode and the other as the cathode. For these two CP-yarns to operate synchronically, they both need to expand (or contract) during opposite reactions. This can be achieved by doping one CP-yarn with mobile anions that will expand during oxidation, while the other CP-yarn should be doped with immobile anions expanding during reduction. As a result, the same movement is created upon opposite redox reactions, both collaborating with the actuation in the same direction without the need for an external passive electrode to close the electrical circuit, which could oppose or hinder the movement. Most of the studies on textile actuators are based on cation-driven CP-yarn actuators, while little is known about anion-driven systems in CP-yarn actuators. Here, we first present a study of the effect of the dopants, solvents, and polymer layer combinations on the mechanism and strain of CP-yarns. The CP-yarns are coated with two layers: an inner poly(3,4-ethylenedioxythiophene) (PEDOT) layer and the outer and active polypyrrole (PPy) layer. According to our results, the dopant of the inner PEDOT layer seems to affect the actuation mechanism of the outer PPy layer and, thereby, of the whole CP-yarn actuator, influencing the direction of the movement and enhancing or hindering the total strain of the actuator. We show that a CP-yarn coated with PEDOT(Tos)/PPy(ClO