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Response and Driving Mechanism of an EAP Actuator based on an Ion-Gel Electrolyte Satoru Imaizumi, Yuichi Kato, Hisashi Kokubo, Masayoshi Watanabe Department of Chemistry and Biotechnology Yokohama National University 79-5 Tokiwadai, Hodogaya-ku, Yokohama 240-8501, Japan Polymer gels swollen by ionic liquids, named “iongels”, are expected to be applied in several solid electrochemical devices. As one of the applications, we have studied electroactive polymer (EAP) actuators that can change their shapes with the application of electronic stimulus. EAPs have attracted much attention as one of artificial muscles, since their motion is very similar to that of biological systems. Ionic EAP, driven by diffusion or migration of ions, can exhibit relatively large bending deformation by applying a low voltage. However, typical ionic EAP actuators are required to maintain their wetness, therefore, they have a problem in durability under atmospheric condition due to evaporation of a solvent. In contrast, an ion-gel actuator enables to operate in an open atmosphere without evaporation of electrolyte solutions, because of negligible volatility of ionic liquids. A structure of the actuator and chemical structure of the ionic liquid and polymer used in this study are shown in Fig. 1. The actuator has a trilaminar structure, where an ion-gel film was sandwiched between two flexible carbon electrodes consisting of activated carbon and ion-gel. observed after 500 s from the application of voltage, as shown in Fig. 3. By shorting the circuit after 3000 s, the actuator bends toward to the cathodic side and then turns back gradually. Based on these observations, we will propose two driving mechanisms of the ion-gel actuator. 1. Electrostatic repulsive force between ions charged in electric double layer. The cathodic capacitance is larger than the anodic one, determined by constant current charge-discharge measurements using a three-electrode cell. This result suggests that the charge density at the cathode is larger than that of anodic side, because the electric double layer at the cathode becomes thinner, and thus the Coulombic repulsive force at the cathode becomes larger. As a result, the actuator bends toward to the anodic side. However, the back relaxation and the back actuation by the short circuit can not be explained by this electrostatic repulsive mechanism. 2. Asymmetrical volume change with ion transport. In typical ionic liquids, the cationic transference number is larger than 0.5. By applying voltage to the iongel actuator, the cathode and anode electrode layers are swollen and shrunken, respectively, because of the imbalance of the ion transport. After a long-time voltage application, however, back-diffusion of the ionic liquid may occur to offset the concentration gradient. Consequently, the back relaxation takes place because of the reduction in the swelling difference of both electrodes. We have estimated the displacement of the actuator considering the transference number. Carbon electrode Ion-gel electrolyte 0.0 -0.5 Voltage ON CF3 N N C2H5 O O S O N CH3 CF3 S O [C2mim][NTf2] ( CH 2 CF 2 ) 0.88 ( CF 2 CF )0.12 CF 3 P(VDF/HFP) 2 0 -2 50 0 -50 0 20 Fig. 1 A structure of an ion-gel actuator. By applying a voltage between two electrodes, the actuator bends toward to the anodic side with charging the electric double layers. In this study, the response to the potential and the actuation mechanism are presented. In the short time scale (less than 102 s), the displacement of the actuator is increased by charging the electric double layers (Fig. 2). As a result, the displacement decreases by applying voltage with a higher frequency. The resistance of the carbon electrode film toward the tip of the actuator is larger than that of the iongel electrolyte toward thickness direction. Thus, the tip of the actuator is hard to be charged because of a large IRdrop of the electrodes. On the other hand, back relaxation behavior was 40 60 80 Time / s n Fig. 2 Current and displacement responses of an ion-gel actuator with application of 0.5 V rectangular waveform voltage at a cycle of 40 s. Displacement / mm Ionic liquid Displacement / µm Current / mA Ionic liquid Polymer Polymer 0.5 Voltage / V Ionic liquid Carbon materials Polymer 0.2 0.1 0.0 -0.1 0 2000 4000 6000 8000 Time / s Fig. 3 Displacement responses of an ion-gel actuator with application of 0.5 V step voltage for 3000 s, followed by the short circuit.