1. Field of the Invention
The present invention relates to polymer actuator devices that bend when a voltage is applied thereto.
2. Description of the Related Art
Japanese Unexamined Patent Application Publication No. 2008-34268 discloses an invention related to a polymer actuator. This polymer actuator includes an electrolyte layer and a pair of electrode layers disposed on either side of the electrolyte layer in the thickness direction. The polymer actuator bends when a voltage is applied between the pair of electrode layers at a fixed end thereof.
During operation, the voltage (potential difference) is precisely controlled by a potentiostat. After extended operation, however, a potential shift occurs, for example, due to changes near the electrodes or in the electrodes themselves. This potential shift causes the polymer actuator, which is initially driven within the potential window (threshold at which electrolysis occurs) of the ionic liquid contained in the electrode layers and the electrolyte layer, to be driven beyond the potential window of the ionic liquid, thus causing the electrolysis of the ionic liquid. The electrolysis of the ionic liquid results in decreased device reliability, including a deviation from the initial displacement position (displacement) for the same applied voltage, and also results in a shortened device life.
In particular, a configuration including electrode layers containing a nanocarbon material, which has a large specific surface area and various active sites, tends to suffer from the above problems because the potential window of the ionic liquid is narrowed.
The present invention provides a polymer actuator device including a bending device part that can be stably driven and an apparatus and method for driving such a polymer actuator device.
According to an aspect of the present invention, there is provided a polymer actuator device. This device includes a device part including an electrolyte layer, first and second electrode layers disposed on either surface of the electrolyte layer in a thickness direction, and a reference electrode layer disposed between the first and second electrode layers and in contact with the electrolyte layer. The device part bends in response to a voltage applied between the first and second electrode layers.
According to another aspect of the present invention, there is provided an apparatus for driving a polymer actuator device. This apparatus includes the above polymer actuator device and a potentiostat configured to drive the device part. One of the first and second electrode layers serves as a working electrode. The other of the first and second electrode layers serves as a counter electrode. The reference electrode layer has a reference potential.
According to another aspect of the present invention, there is provided a method for driving a polymer actuator device. This method includes driving the device part of the above polymer actuator device using a potentiostat. One of the first and second electrode layers serves as a working electrode. The other of the first and second electrode layers serves as a counter electrode. The reference electrode layer has a reference potential. In this aspect, the device part may be driven at constant potential.
As described above, the polymer actuator device has a three-electrode structure including the reference electrode layer, which has a reference potential. This prevents a potential shift such as occurs in a two-electrode structure in the related art, thus providing stable operating characteristics (e.g., stable displacement position during bending and stable return position).
In the above aspects, the reference electrode layer disposed between the first and second electrode layers preferably has a smaller area than the first and second electrode layers. Such a reference electrode layer does not interfere with the bending motion of the device part and thus allows the polymer actuator device to be properly driven.
In the above aspects, the device part preferably includes a fixed portion at which the device part is fixed and supported at one end thereof and a bending portion at another end thereof. The reference electrode layer disposed between the first and second electrode layers preferably extends in a longitudinal direction being a direction from the fixed portion toward the bending portion. The width of the reference electrode layer in a lateral direction perpendicular to the longitudinal direction is preferably smaller than the width of the first and second electrode layers. This simplifies the structure of the reference electrode layer.
In the above aspects, a portion of the device part preferably has a five-layer structure in which the electrolyte layer is disposed between the reference electrode layer and the first electrode layer and between the reference electrode layer and the second electrode layer.
In the above aspects, the reference electrode layer is preferably made of a flexible material. If such a reference electrode layer is provided in the bending portion, the device part can bend properly while a potential shift is effectively prevented in the bending portion, thus providing more stable operating characteristics.
In the above aspects, the device part preferably includes a fixed portion at which the device part is fixed and supported at one end thereof and a bending portion at another end thereof, and the reference electrode layer preferably extends between the ends of the fixed portion and the bending portion. This allows the reference electrode layer to be easily provided and also effectively prevents a potential shift over the entire device part, thus providing more stable operating characteristics.
In the above aspects, the reference electrode layer preferably extends outward of the fixed portion. A surface of the reference electrode layer at the end of the bending portion is preferably substantially in flush with surfaces of the first and second electrode layers at the end of the bending portion. The electrolyte layer preferably extends outward of the surface of the reference electrode layer at the end of the bending portion and outward of surfaces of the first and second electrode layers at the end of the fixed portion. This prevents a short circuit between the first electrode layer, the second electrode layer, and the reference electrode layer at the ends of the bending portion and the fixed portion.
In the above aspects, the first electrode layer, the second electrode layer, and the reference electrode layer are preferably made of the same material. In this case, the first electrode layer, the second electrode layer, and the reference electrode layer preferably contain carbon nanotubes. This allows the electrode layers to have the same electrode characteristics and thus prevents the reference electrode layer from interfering with ion migration through the electrolyte layer between the first and second electrode layers. In addition, as described above, the reference electrode layer can be made of a flexible material so that the device part can bend properly. Furthermore, improved manufacturing efficiency and reduced manufacturing costs can be achieved.
In the above aspects, the first electrode layer, the second electrode layer, the reference electrode layer, and the electrolyte layer preferably contain the same ionic liquid. That is, the entire device part may contain the same ionic liquid. This allows the driving potential to be set within the potential window of the ionic liquid, thus providing stable operating characteristics.
As shown in
In the polymer actuator device 1 according to this embodiment, the electrolyte layer 2 contains an ionic liquid and a base polymer, and the electrode layers 3 and 4 contain carbon nanotubes, a base polymer, and an ionic liquid.
Examples of base polymers include polyvinylidene fluoride-based polymers and polymethyl methacrylate (PMMA)-based polymers. Particularly preferred are polyvinylidene fluoride-based polymers.
Examples of ionic liquids include ethylmethylimidazolium tetrafluoroborate (EMIBF4) and ethylmethylimidazolium bis(trifluoromethanesulfonyl)imide (EMITFSI).
Examples of ionic liquids that may be used in the present invention include various combinations of cations and anions, which may be used alone or in combination. Examples of ammonium cations that may be used in the present invention include, but not limited to, tetraalkylammonium cations, tetraalkylphosphonium cations, imidazolium cations, pyrazolium cations, pyridinium cations, triazolium cations, pyridazinium cations, thiazolium cations, oxazolium cations, pyrimidinium cations, and pyrazinium cations.
Examples of tetraalkylammonium cations include, but not limited to, tetraethylammonium, tetramethylammonium, tetrapropylammonium, tetrabutylammonium, triethylmethylammonium, trimethylethylammonium, dimethyldiethylammonium, trimethylpropylammonium, trimethylbutylammonium, dimethylethylpropylammonium, methylethylpropylbutylammonium, N,N-dimethylpyrrolidinium, N-ethyl-N-methylpyrrolidinium, N-methyl-N-propylpyrrolidinium, N-ethyl-N-propylpyrrolidinium, N,N-dimethylpiperidinium, N-methyl-N-ethylpiperidinium, N-methyl-N-propylpiperidinium, N-ethyl-N-propylpiperidinium, N,N-dimethylmorpholinium, N-methyl-N-ethylmorpholinium, N-methyl-N-propylmorpholinium, N-ethyl-N-propylmorpholinium, trimethylmethoxymethylammonium, dimethylethylmethoxymethylammonium, dimethylpropylmethoxymethylammonium, dimethylbutylmethoxymethylammonium, diethylmethylmethoxymethylammonium, methylethylpropylmethoxymethylammonium, triethylmethoxymethylammonium, diethylpropylmethoxymethylammonium, diethylbutylmethoxymethylammonium, dipropylmethylmethoxymethylammonium, dipropylethylmethoxymethylammonium, tripropylmethoxymethylammonium, tributylmethoxymethylammonium, trimethylethoxymethylammonium, dimethylethylethoxymethylammonium, dimethylpropylethoxymethylammonium, dimethylbutylethoxymethylammonium, diethylmethylethoxymethylammonium, triethylethoxymethylammonium, diethylpropylethoxymethylammonium, diethylbutylethoxymethylammonium, dipropylmethylethoxymethylammonium, dipropylethylethoxymethylammonium, tripropylethoxymethylammonium, tributylethoxymethylammonium, N-methyl-N-methoxymethylpyrrolidinium, N-ethyl-N-methoxymethylpyrrolidinium, N-propyl-N-methoxymethylpyrrolidinium, N-butyl-N-methoxymethylpyrrolidinium, N-methyl-N-ethoxymethylpyrrolidinium, N-methyl-N-propoxymethylpyrrolidinium, N-methyl-N-butoxymethylpyrrolidinium, N-methyl-N-methoxymethylpiperidinium, N-ethyl-N-methoxymethylpyrrolidinium, N-methyl-N-ethoxymethylpyrrolidinium, N-propyl-N-methoxymethylpyrrolidinium, and N-methyl-N-propoxymethylpyrrolidinium. Examples of tetraalkylphosphonium cations include tetraethylphosphonium, tetramethylphosphonium, tetrapropylphosphonium, tetrabutylphosphonium, triethylmethylphosphonium, trimethylethylphosphonium, dimethyldiethylphosphonium, trimethylpropylphosphonium, trimethylbutylphosphonium, dimethylethylpropylphosphonium, and methylethylpropylbutylphosphonium.
Examples of imidazolium cations include, but not limited to, 1,3-dimethylimidazolium, 1-ethyl-3-methylimidazolium, 1-methyl-3-propylimidazolium, 1-methyl-3-isopropylimidazolium, 1-methyl-3-propylimidazolium, 1-methoxymethyl-3-methylimidazolium, 1-methyl-3-butylimidazolium, 1-methyl-3-pentylimidazolium, 1-methyl-3-hexylimidazolium, 1,3-diethylimidazolium, 1,2-dimethyl-3-ethylimidazolium, 1,2-dimethyl-3-propylimidazolium, 1,2-dimethyl-3-butylimidazolium, and 1,2-dimethyl-3-hexylimidazolium. Examples of pyrazolium cations include, but not limited to, 1,2-dimethylpyrazolium, 1-methyl-2-ethylpyrazolium, 1-propyl-2-methylpyrazolium, and 1-methyl-2-butylpyrazolium. Examples of pyridinium cations include, but not limited to, N-methylpyridinium, N-ethylpyridinium, N-propylpyridinium, N-methoxymethylpyridinium, N-isopropylpyridinium, N-butylpyridinium, N-pentylpyridinium, and N-hexylpyridinium. Examples of triazolium cations include, but not limited to, 1-methyltriazolium, 1-ethyltriazolium, 1-propyltriazolium, 1-isopropyltriazolium, 1-butyltriazolium, 1-pentyltriazolium, and 1-hexyltriazolium. Examples of pyridazinium cations include, but not limited to, 1-methylpyridazinium, 1-ethylpyridazinium, 1-propylpyridazinium, 1-isopropylpyridazinium, 1-methoxymethylpyridazinium, 1-butylpyridazinium, 1-pentylpyridazinium, and 1-hexylpyridazinium. Examples of thiazolium cations include, but not limited to, 1,2-dimethylthiazolium and 1,2-dimethyl-3-propylthiazolium. Examples of oxazolium cations include, but not limited to, 1-ethyl-2-methyloxazolium and 1,3-dimethyloxazolium. Examples of pyrimidinium cations include, but not limited to, 1,2-dimethylpyrimidinium and 1-methyl-3-propylpyrimidinium. Examples of pyrazinium cations include, but not limited to, 1-ethyl-2-methylpyrazinium and 1-butylpyrazinium.
Examples of anions for ammonium salts that may be used in the present invention include BF4-, PF6-, BF3CF3-, BF3C2F5-, BF3(CN)—, B(CN)4-, CF3SO3-, C2F5SO3-, C3F7SO3-, C4F9SO3-, N(SO2F)2-, N(CF3SO2)2-, N(C2F5SO2)2-, N(CF3SO2)(CF3CO)—, N(CF3SO2)(C2F5SO2)-, and N(CF3SO2)(FSO2)-.
The Y1-Y2 and X1-X2 directions shown in
In the embodiment shown in
As shown in
As shown in
Although
In this embodiment, as shown in
The cross-section shown in
As shown in
In this embodiment, as shown in
The reference electrode layer 7 is preferably made of the same material as the first and second electrode layers 3 and 4. In this embodiment, as described above, the first and second electrode layers 3 and 4 contain carbon nanotubes and an ionic liquid, and accordingly, the reference electrode layer 7 contains carbon nanotubes and an ionic liquid. In this embodiment, the first electrode layer 3, the second electrode layer 4, the reference electrode layer 7, and the electrolyte layer 2 preferably contain the same ionic liquid.
The polymer actuator device 1 according to this embodiment is connected to a potentiostat 10 shown in
The potentiostat 10 includes an operational amplifier circuit 11 having a non-inverting input (+), an inverting input (−), and an output. As shown in
In the following description, the first electrode layer 3 is assumed to be the working electrode (WE), and the second electrode layer 4 is assumed to be the counter electrode (CE). The potentiostat 10 shown in
An example of AC driving is illustrated below. For example, a rectangular wave voltage alternating between +1.15 and −1.35 V at a frequency of 5 mHz is applied between the first electrode layer 3, serving as the working electrode (WE), and the reference electrode layer 7. When voltages of +1.15 and −1.35 V are applied between the first electrode layer 3 and the reference electrode layer 7, the potentiostat 10 in
According to this embodiment, the device part 1a can be driven at constant potential because the voltage (potential difference) between the first and second electrode layers 3 and 4 is regulated based on the reference potential of the reference electrode layer 7. In the above example, the device part 1a can be driven at constant potential both when a voltage of +2.5V is applied between the first and second electrode layers 3 and 4 and when a voltage of −2.5V is applied between the first and second electrode layers 3 and 4. This prevents a potential shift such as occurs in a two-electrode structure in the related art. Thus, the displacement position (displacement) H1 reached by the device part 1a when a voltage of +2.5V is periodically applied between the first and second electrode layers 3 and 4 is substantially constant, and the displacement position (displacement) H2 reached by the device part 1a when a voltage of −2.5V is periodically applied between the first and second electrode layers 3 and 4 is substantially constant (see
In the above example, the positive voltage applied between the first electrode layer 3 and the reference electrode layer 7 is +1.15 V, and the negative voltage applied between the first electrode layer 3 and the reference electrode layer 7 is −1.35 V. These voltages are not one half of ±2.5 V, i.e., +1.25 V and −1.25 V, because the reference potential (self-potential) of the reference electrode layer 7 is not 0 V. Even if the reference potential of the reference electrode layer 7 is unknown, the potential of the first electrode layer 3 relative to the reference electrode layer 7 can be controlled, for example, by measuring the current flowing between the first and second electrode layers 3 and 4. It should be noted that no current flows through the reference electrode layer 7.
The absolute values of the displacements (H1) and (−H2) may be varied depending on the input voltage from the input voltage source 12.
In a two-electrode structure in the related art, the potential might not return to the original reference level after the removal of the voltage applied between the first and second electrode layers because of a potential shift. In the three-electrode structure according to this embodiment, the potential can be properly returned to the initial level (reference level). Thus, the device part 1a can be properly returned to the initial position (reference position) indicated by the solid line in
In this embodiment, the electrode layers 3, 4, and 7 and the electrolyte layer 2 that form the device part 1a preferably contain the same ionic liquid. This allows the driving potential for the device part 1a to be properly set within the potential window of the ionic liquid. The potential window of the ionic liquid is known to a certain extent; therefore, in this embodiment, the driving potential can be properly controlled within the potential window of the ionic liquid. In addition, a potential shift can be properly prevented, for example, after extended use because the reference potential of the reference electrode layer 7 is substantially fixed. This inhibits the electrolysis of the ionic liquid and thus allows stable operating characteristics (e.g., stable displacement position during bending and stable return position).
In particular, the potential window of the ionic liquid is narrowed in a configuration including electrode layers containing carbon nanotubes, which have a large specific surface area and various active sites. In this embodiment, the use of a potentiostat including a working electrode, a counter electrode, and a reference electrode allows the driving potential to be properly controlled even within such a narrow potential window. Thus, the polymer actuator device 1 can be stably driven with a large displacement and also has an extended life.
In this embodiment, as shown in
In this embodiment, the reference electrode layer 7 has a smaller area than the first and second electrode layers 3 and 4. The area of the reference electrode layer may be reduced by reducing the width T2, as described above, or may be reduced in other manners. For example, one or more slits or through-holes extending through the reference electrode layer 7 across the thickness may be formed while the width T2 of the reference electrode layer 7 is substantially equal to the width T1 of the first and second electrode layers 3 and 4. This allows the reference electrode layer 7 to have a smaller area than the first and second electrode layers 3 and 4. Nevertheless, the reference electrode layer 7 has a simpler shape if the width T2 is reduced. The width T2 of the reference electrode layer 7 is preferably about 20% to 60% of the width T1 of the first and second electrode layers 3 and 4.
In this embodiment, as shown in
In this embodiment, as shown in
The polymer actuator device 1 according to this embodiment may be DC-driven rather than AD-driven. In either case, a potential shift such as occurs in a two-electrode structure in the related art can be prevented, thus providing stable operating characteristics.
In this experiment, the width T1 of the first and second electrode layers 3 and 4 shown in
The cyclic voltammograms (CV) in
Cyclic Voltammetry (CV) with Varying Lengths of Reference Electrode Layer
An experiment was conducted with varying lengths of the reference electrode layer 7 in the structure shown in
In this experiment, a cyclic voltammogram (CV) substantially identical to those in
Examples of optimum thicknesses were as follows: the optimum thicknesses of the first and second electrode layers 3 and 4 were 112 μm, the optimum thickness of the reference electrode layer 7 was 40 μm, the optimum thickness between the first electrode layer 3 and the reference electrode layer 7 was 21 μm, and the optimum thickness between the second electrode layer 4 and the reference electrode layer 7 was 23 μm (see
In Comparative Example 1, a polymer actuator device having the structure shown in
In Comparative Example 2, a polymer actuator device having the structure shown in
In an inventive example, a polymer actuator device having the three-electrode structure in
The polymer actuator device of the inventive example was AC-driven by applying a rectangular wave voltage (potential difference) alternating between +1.15 and −1.35 V at a frequency of 5 mHz between the reference electrode layer 7 and the first electrode layer 3, serving as the working electrode. Thus, a voltage of ±2.5V was applied between the first and second electrode layers.
The polymer actuator device of the comparative example was AC-driven by applying a rectangular wave voltage of ±2.5V at a frequency of 5 mHz between the first and second electrode layers.
The displacement and the current that flowed between the first and second electrode layers of each polymer actuator device were measured. The experimental results are shown in
As shown in
Number | Date | Country | Kind |
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2012-024690 | Feb 2012 | JP | national |
This application is a Continuation of International Application No. PCT/JP2013/052147 filed on Jan. 31, 2013, which claims benefit of Japanese Patent Application No. 2012-024690 filed on Feb. 8, 2012. The entire contents of each application noted above are hereby incorporated by reference.
Number | Date | Country | |
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Parent | PCT/JP2013/052147 | Jan 2013 | US |
Child | 14447348 | US |