Simultaneous actuation and sensing properties of a triple layer actuator interchanging cations are presented for the first time. Thick polypyrrole (pPy)/dodecylbenzenesulfonate (DBS) films (36 mm) were electrogenerated on stainless steel electrodes. Sensing characteristics of pPy-DBS/tape/pPy-DBS triple layer artificial muscle were studied as a function of electrolyte concentration, temperature and driving current using lithium perchlorate (LiClO 4 ) aqueous solution as electrolyte. The chronopotentiometric responses were studied by applying consecutive square waves of currents to produce angular movements of AE45 by the free end of the triple layer. The evolution of the muscle potential (anode film versus cathode film) during current flow is a function of the studied chemical and physical variables. The electrical energy consumed to describe a constant angle is a linear function of the working temperature or of the driving electrical current, and a double logarithmic function of the electrolyte concentration. Those are the sensing functions. The cation exchanging bending triple layer actuator senses the working conditions. Similar sensing functions were described in the literature for devices interchanging anions. Irrespective of the reaction mechanism, a single electrochemo-mechanical device comprised of two reactive polymer electrodes (oxidation film and reduction film) works simultaneously as both sensor and actuator (self-sensing actuators). These are the general sensing properties of dense and biomimetic reactive gels of conducting polymers. Thus, any reactive device based on the same type of materials and reactions (batteries, smart windows, actuators, electron-ion transducers) is expected to sense surrounding conditions, as biological organs do.

Free-standing polypyrrole fi lms, being the metal-polymer contact located several millimeters outside the electrolyte, give stationary closed coulovoltammetric (charge/potential) loop responses to consecutive potential sweeps from -2.50 V to 0.65 V in aqueous solutions. The continuous and closed charge evolution corroborates the presence of reversible fi lm reactions (electroactivity), together high electronic and ionic conductivities in the full potential range. The closed charge loop demonstrates that the irreversible hydrogen evolution is fully inhibited from aqueous solutions of different salts up to -2.5 V vs Ag/AgCl. The morphology of the closed charge loops shows abrupt slope changes corresponding to the four basic components of the structural electrochemistry for a 3D electroactive gel: reduction-shrinking, reduction-compaction, oxidation-relaxation, and oxidation-swelling. Freestanding fi lms of conducting polymers behave as 3D gel electrodes (reactors) at the chain level, where reversible electrochemical reactions drive structural conformational and macroscopic (volume variation) changes. Very slow hydrogen evolution is revealed by coulovoltammetric responses at more cathodic potentials than -1.1 V from strong acid solutions, or in neutral salts self-supported blend fi lms of polypyrrole with large organic acids. Conducting polymers overcome graphite, mercury, lead, diamond, or carbon electrodes as hydrogen inhibitors, and can compete with them for some electro-analytical and electrochemical applications in aqueous solutions.

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. The linearity indicates that cations are the only exchanged ions in the studied potential range. By flow of the same specific charge in every electrolyte, different angles were described by the muscle. The charge and the angle allow the number and volume of both the exchanged cations and the water molecules (related to a reference) between the film to be determined, in addition to the electrolyte per unit of charge during the driving reaction. The attained apparent solvation numbers for the exchanged cations were: 0.8, 0.7, 0.6, 0.5, 0.5, 0.4, 0.25, and 0.0 for Na(+), Mg(2+), La(3+), Li(+), Ca(2+), K(+), Rb(+), and Cs(+), respectively.

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Reliable polymeric motors are required for the construction of rising accurate robots for surgeon assistance. Artificial muscles based on the electrochemistry of conducting polymers fulfil most of the required characteristics, except the presence of creeping effects during actuation. To avoid it, or to control it, a deeper knowledge of its physicochemical origin is required. With this aim here bending bilayer tape/PPy-DBSH (Polypyrrole-dodecylbenzylsulphonic acid) full polymeric artificial muscles were cycled between −2.5 and 1 V in aqueous solutions with parallel video recording of the described angular movement. Coulo-voltammetric (charge-potential, QE), dynamo-voltammetric (angle-potential, αE), and coulo-dynamic (charge-angle, Qα) muscular responses corroborate that 10 % of the charge is consumed by irreversible reactions overlapping the polymer reduction at the most cathodic potentials. In parallel, the range of the bending angular movement (145°) shifts by 15°per cycle (creeping effect) pointing to the irreversible charge as possible origin of the irreversible swelling of the PPy-DBS film. Different slopes in the closed loop part of the QE identify the different reaction driven structural processes in the film: oxidation-shrinking, oxidation-compaction, reduction-relaxation, reduction-swelling, and reduction-vesicle's formation. Despite the irreversible charge fraction, the muscle motor keeps a Faradaic behaviour: described angles are linear functions of the consumed charge in the full potential range.

The electrochemical activity of self-supported thick (70 µm) polypyrrole films electrogenerated in a mixed electrolyte of dodecylbenzenesulfonic acid and LiClO 4 was studied in aqueous solutions of LiClO 4 . This material inhibits hydrogen evolution up to cathodic potentials of −3.0 V versus Ag/AgCl. During oxidation or reduction reactions under galvanostatic conditions, the electrical energy consumed for a constant charge is a function of either the working temperature or the flowing current. As a consequence any electrochemical device, moreover artificial muscles, constructed with reactive conducting polymers is expected to work simultaneously as a sensor of the working temperature.

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A bending electro‐chemo‐mechanical monolayer artificial muscle is presented and characterized. A transversal cross‐linking gradient attained during the film electropolymerization is proposed as the origin of the reaction‐driven muscular action. Each unit of charge consumed per unit of polymer weight gives the largest angular displacement described in the literature. This oversimplified polymeric motor for engineering applications saves extra energy required to bend and trail inactive layers from bilayer or multilayer classical structures.