JP5831926B2 - Polymer actuator element and manufacturing method thereof - Google Patents

Description

  The present invention relates to a polymer actuator element including an electrode layer having carbon nanotubes and an ionic liquid, and a method for manufacturing the same.

  Patent Document 1 below discloses a polymer actuator element that includes an ionic liquid and a base polymer in an electrolyte layer, and an ionic liquid, a base polymer, and carbon nanotubes in an electrode layer.

  When a voltage is applied to the electrode layer while one end of the polymer actuator element is fixed, a volume difference occurs between the electrodes due to ion migration, and the polymer actuator element is deformed.

  However, for example, when the polymer actuator element is driven and kept at a certain amount of displacement, there has been a problem of a decrease in durability in which the amount of displacement gradually varies with time.

  As described above, the durability of the conventional polymer actuator element is reduced because moisture absorbed from the atmosphere is electrolyzed by defects in the carbon nanotubes, and promotes ionic liquid deterioration or ionic liquid itself undergoes electrolytic deterioration. It is thought that. For example, a catalyst of hydrogen ions or hydroxide ions that are generated when carbon deficient portions are formed at the end of carbon nanotubes or when various functional groups are present, so that water absorbed from the atmosphere by voltage application is electrolyzed relatively easily. It is considered that the electrolysis is accelerated due to some interaction between the ionic liquid moved between the electrodes and the defects of the carbon nanotubes and certain functional groups.

JP 2010-68675 A

  The present invention solves the above-described conventional problems, and in particular, an object of the present invention is to provide a polymer actuator element having improved durability as compared with the conventional technique and a method for manufacturing the same.

The present invention has an electrolyte layer and electrode layers disposed on both surfaces in the thickness direction of the electrolyte layer, the electrolyte layer and the electrode layer include an ionic liquid and the electrode layer includes a carbon nanotube, In the polymer actuator element that deforms when a voltage is applied between the electrode layers,
The electrode layer includes the carbon nanotube grafted with an oligomer ,
The oligomer is selected from an ethylene glycol oligomer, a dimethylsiloxane oligomer, or an ethylene oxide oligomer . Thereby, durability can be improved compared with the past which has not grafted the oligomer to the carbon nanotube. In particular, in the present invention, when the polymer actuator element is driven and kept at a certain amount of displacement, the variation of the amount of displacement over time can be reduced as compared with the conventional case, and stable actuator characteristics can be obtained.

  In this invention, it is preferable that the average molecular weight of the said oligomer exists in the range of 40-10000. The average molecular weight of the oligomer is more preferably in the range of 400 to 4000. While durability of a polymer actuator element can be improved effectively, an increase in electrode resistance value can be controlled. In addition, castability (film formability) can be improved.

The present invention also includes an electrolyte layer and electrode layers disposed on both sides in the thickness direction of the electrolyte layer. The electrolyte layer and the electrode layer include an ionic liquid, and the electrode layer includes a carbon nanotube. In the method of manufacturing a polymer actuator element that deforms when a voltage is applied between the electrode layers,
A process of grafting an oligomer to a carbon nanotube,
Forming the electrode layer containing the carbon nanotube grafted with the oligomer;
I have a,
The oligomer is selected from an ethylene glycol oligomer, a dimethylsiloxane oligomer, or an ethylene oxide oligomer . This makes it possible to manufacture a polymer actuator element with excellent durability.

  In the present invention, the oligomer is preferably radically polymerized and grafted onto the carbon nanotube. Further, it is preferable that a radical polymerizable oligomer is generated from a polymer azo polymerization initiator, and the radical polymerizable oligomer is radically polymerized and grafted onto the carbon nanotube.

  According to the present invention, it is possible to improve durability as compared with the related art. In particular, in the present invention, when the polymer actuator element is driven and kept at a certain amount of displacement, the variation of the amount of displacement over time can be reduced as compared with the conventional case, and stable actuator characteristics can be obtained.

The fragmentary sectional view of the polymer actuator element in the embodiment of the present invention, Explanatory drawing (image diagram) of the process of grafting oligomer to carbon nanotube, (A) is an analysis result by gas chromatography (GC) -mass (MS) analysis in an untreated carbon nanotube (comparative example), and (b) is a carbon nanotube grafted with an ethylene glycol oligomer having an average molecular weight of about 4000. Analysis results by gas chromatography (GC) -mass (MS) analysis in (Example), (A) is an analysis result by thermogravimetric (TG) analysis of carbon nanotubes (Examples 1 and 2) grafted with an ethylene glycol oligomer having an average molecular weight of about 4000, and (b) is an ethylene having an average molecular weight of about 400. Analysis results by thermogravimetric (TG) analysis on carbon nanotubes grafted with glycol oligomer (Examples 3 and 4), Polymer actuator elements (Examples 1 and 2) having electrode layers formed using carbon nanotubes grafted with ethylene glycol oligomer having an average molecular weight of about 4000, carbon grafted with ethylene glycol oligomer having an average molecular weight of about 400 Polymer actuator elements having electrode layers formed using nanotubes (Examples 3 and 4) and polymer actuator elements having electrode layers formed using untreated carbon nanotubes not grafted with oligomers (Comparative Examples) ), And a graph showing the relationship between the elapsed time and the displacement when each polymer actuator element is deformed by DC driving.

  FIG. 1 shows a partial cross-sectional view of the polymer actuator element of the present embodiment. The structure of the polymer actuator element will be described with reference to FIG.

  As shown in FIG. 1, the polymer actuator element 1 in this embodiment includes an electrolyte layer (ion conductive layer) 2 and electrode layers 3 and 4 formed on both side surfaces in the thickness direction (Z) of the electrolyte layer 2. It is configured with.

  A polymer actuator element 1 according to an embodiment of the present invention includes an electrolyte layer 2 having an ionic liquid and a base polymer, and electrode layers 3 and 4 having an oligomer-grafted carbon nanotube and an ionic liquid. The

  As the base polymer, a polyvinylidene fluoride (PVdF) polymer, a polymethyl methacrylate (PMMA) polymer, or the like can be presented. Among these, it is particularly preferable to use a PVdF-based polymer.

  As the ionic liquid, ethylmethylimidazolium tetrafluoroborate (EMIBF4), ethylmethylimidazolium bis (trifluoromethanesulfonyl) imide (EMITFSI), or the like can be used.

  The base end portion 5 of the polymer actuator element 1 is a fixed end portion, and the base end portion 5 of the polymer actuator element 1 is fixedly supported by the fixing support portions 6 and 6. As shown in FIG. 1, for example, the polymer actuator element 1 is supported in a cantilever manner. When a driving voltage is applied between the electrode layers 3 and 4 on both sides, as shown by the dotted line in FIG. 1, the ion layer 3 moves between the electrode layer 3 and the electrode layer 4 due to ion movement between the electrode layer 3 and the electrode layers 3 and 4. A volume difference is generated and a bending stress is generated, so that the distal end portion 7 which is a free end portion of the polymer actuator element 1 can be bent and deformed. The principle that the difference in volume between electrodes due to ion transfer is generally not unambiguous, but one of the typical principle factors is that the difference in volume occurs due to the difference in ion size between cation and anion. It is known.

  The fixed support portion 6 shown in FIG. 1 is preferably a connection portion (power feeding portion) that is electrically connected to the electrode layers 3 and 4.

  In the present embodiment, oligomers are grafted on the carbon nanotubes (CNT) included in the electrode layers 3 and 4.

  FIG. 2 shows an image of a process for grafting oligomers to carbon nanotubes.

  As shown in FIG. 2, first, the polymer azo polymerization initiator is thermally decomposed to generate a radical polymerizable oligomer. The polymer azo polymerization initiator has a structure in which a polymer segment and an azo group are repeatedly bonded. In FIG. 2, ethylene glycol (EG) is selected as the polymer segment. As a polymer azo polymerization initiator, VPE series, VPS series, etc. of Wako Pure Chemical Industries, Ltd. can be used.

  Next, the radical polymerizable oligomer is grafted onto the carbon nanotube (CNT) by radical polymerization.

  A conductive ink containing a carbon nanotube grafted with an oligomer, an ionic liquid, and a solvent is formed into a predetermined shape by, for example, a casting method, and the solvent is evaporated to form sheet-like electrode layers 3 and 4.

  Then, the polymer actuator element 1 shown in FIG. 1 can be manufactured by superimposing the electrode layers 3 and 4 on both surfaces of the electrolyte layer 2 and bonding the layers by thermocompression bonding or the like.

  Here, the “oligomer” in the present embodiment refers to a monomer polymer having an average molecular weight in the range of 40 to 10,000, preferably 400 to 4000. Moreover, when it is an ethylene glycol oligomer, the polymerization degree may be in the range of 2 to 200, preferably 10 to 100.

  The grafting rate is 1% to 50%, preferably about 5% to 35%. The grafting rate is a weight% value indicating the amount of weight increase after grafting, based on the untreated carbon nanotubes before grafting, as a ratio to the weight of the standard.

  Thereby, the durability of the polymer actuator element can be effectively improved and an increase in the electrode resistance value can be suppressed. Moreover, castability (film forming property) can be improved.

Oh oligomer include ethylene glycol oligomer, dimethylsiloxane oligomers, or Ru is selected Ri by ethylene oxide oligomer chromatography. Any of these can constitute a polymer segment of a polymer azo polymerization initiator. Among these, it is more preferable to select an ethylene glycol oligomer.

  In the present embodiment, there is a characteristic part in that an oligomer is grafted to the carbon nanotubes included in the electrode layers 3 and 4 of the polymer actuator element 1. Since the radical polymerizable oligomer easily reacts with a defect portion of the carbon nanotube, the defect of the carbon nanotube can be effectively repaired. Thereby, it is thought that deterioration of an ionic liquid can be suppressed, and durability can be improved compared with the past (use of the carbon nanotube which is not grafting an oligomer). In particular, as shown in the experiment described later, in this embodiment, when the polymer actuator element 1 is driven and kept at a certain displacement, the variation of the displacement with time can be reduced, and stable actuator characteristics can be obtained. be able to.

(Gas chromatography (GC) -mass (MS) analysis)
In the experiment, untreated carbon nanotubes (comparative examples) and carbon nanotubes (examples) grafted with an ethylene glycol oligomer having an average molecular weight of about 4000 were produced, and the carbon nanotubes of the comparative examples and examples were produced. Gas chromatography (GC) -mass (MS) analysis was performed. HiPco (Unidym) SWCNT was used as the carbon nanotube. Further, the ethylene glycol oligomer was composed of a polymer azo polymerization initiator before grafting, and grafted onto carbon nanotubes by radical polymerization as shown in FIG. VPE-0401 manufactured by Wako Pure Chemical Industries, Ltd. was used as the polymer azo polymerization initiator. Grafting was carried out by dispersing carbon nanotubes and a polymer azo polymerization initiator in a toluene solvent and reacting at 80 ° C. for 6 to 24 hours in an argon atmosphere.

  Moreover, as measurement conditions, a temperature rising rate of 10 ° C./min (40 to 280 ° C.), a holding time of 5 minutes, an ionization method EI, a mass range (m / z) of 30 to 500, a sample amount of about 0.2 mg, and thermal desorption conditions 450 ° C. × 10 minutes, INF temperature was 350 ° C.

3A shows the analysis result of the comparative example, and FIG. 3B shows the analysis result of the example. As shown in FIG. 3B, a spectrum caused by ethylene glycol (—CH ₂ —CH ₂ —O—) was observed.

(Thermogravimetric (TG) analysis and elemental analysis (ESCA))
Next, untreated carbon nanotubes (comparative example), carbon nanotubes (Examples 1 and 2) grafted with an ethylene glycol oligomer having an average molecular weight of about 4000, and ethylene glycol oligomers having an average molecular weight of about 400 are grafted. The carbon nanotubes (Examples 3 and 4) were manufactured, and thermogravimetric (TG) analysis was performed on the carbon nanotubes of the comparative example and Examples 1 to 4. Examples 1 and 2 and Examples 3 and 4 have different reaction times. Examples 1 and 3 have a grafting reaction time of 6 hours, and Examples 2 and 4 have a grafting reaction. The time was 24 hours. HiPco (Unidym) SWCNT was used as the carbon nanotube. Further, the ethylene glycol oligomer was composed of a polymer azo polymerization initiator before grafting, and grafted onto carbon nanotubes by radical polymerization as shown in FIG. As the polymer azo polymerization initiator, VPE-0401 was used as an ethylene glycol oligomer having an average molecular weight of 4000, and an ethylene glycol oligomer having an average molecular weight of 400 synthesized from a monomer was used.

  FIG. 4A shows the thermogravimetric (TG) analysis results in the comparative example and Examples 1 and 2. FIG. 4B shows the thermogravimetric (TG) analysis results in the comparative example and Examples 3 and 4.

The grafting rate was calculated based on the experimental results. The grafting rate is a weight% value indicating the amount of weight increase after grafting, based on the untreated carbon nanotubes before grafting, as a ratio to the weight of the standard.
The experimental results are shown in Table 1 below.

  Then, the elemental analysis of said Examples 1-4 and a comparative example was measured by X-ray photoelectron spectroscopy (ESCA). The experimental results are shown in Table 2 below.

  The grafting rate was calculated based on the oxygen content shown in Table 2. The calculation results are shown in Table 3 below.

  It can be seen that the graphing rate of Table 1 obtained by thermogravimetric analysis and the graphing rate of Table 3 obtained from the oxygen content of elemental analysis by ESCA are almost the same with a maximum deviation of about 3%. It was.

  Examples 1 and 2 were obtained by grafting an ethylene glycol oligomer having an average molecular weight of about 4000, which was twice to five times that of Examples 3 and 4 grafted by an ethylene glycol oligomer having an average molecular weight of about 400. The grafting rate increased to about 6 times.

(Considerations regarding grafting)
From the grafting rate shown in Table 1, the state in which the ethylene glycol oligomer was grafted to the carbon nanotube (CNT) was considered.

  First, the carbon nanotube (HiPco (Unidym) SWCNT) has an average diameter of 1 nm and an average length of 500 nm. The number of carbon elements and the molecular weight occupying an average length of 500 nm were determined by molecular orbital simulation. As a result, the number of carbon elements was 68,000 and the molecular weight was 820000.

  Next, the lengths of the ethylene glycol oligomer having an average molecular weight of 4000 and the ethylene glycol oligomer having an average molecular weight of 400 were determined. First, the length of ethylene glycol (monomer) was simulated. And when the length of the ethylene glycol oligomer (91-mer) having an average molecular weight of 4000 and the ethylene glycol oligomer (9-mer) having an average molecular weight of 400 was determined, the former was 23 nm and the latter was 2.3 nm. .

  Table 4 below shows the grafting rate shown in Table 1, the number of carbon nanotubes and ethylene glycol oligomers in 1 mg, the number ratio of ethylene glycol oligomers to one carbon nanotube, and the length of ethylene glycol oligomers relative to carbon nanotubes. The ratio is shown.

  As shown in Table 4, it is found that about 130 ethylene glycol oligomers having an average molecular weight of about 400 are grafted with respect to one carbon nanotube with a length ratio of about 0.5%. It was. In addition, as shown in Table 4, the ethylene glycol oligomer having an average molecular weight of 4000 is grafted by about 30 to 100 pieces with a length ratio of about 5% with respect to one carbon nanotube. I understood it.

(Measurement of electrode resistance and range of average molecular weight)
Then, the electrode layer was formed using each sample of said Examples 1-4 and a comparative example. Conductive ink containing each carbon nanotube (about 15 mg), ionic liquid (EMIBF; about 40 mg) and solvent (DMAc) is formed into a predetermined shape by a casting method, and the solvent is evaporated to obtain a sheet-like electrode layer. It was.

  It has been found that the cast film formability is slightly improved by applying Examples, 1 and 2 having a larger average molecular weight to the electrode layer than the Comparative Examples.

  However, as shown in Table 5, it was found that the electrode resistance value was increased to about 2 to 10 times in the example compared to the comparative example. In order to obtain good actuator characteristics and responsiveness, it is preferable that the resistance value is low. Therefore, it is necessary to regulate the range of the average molecular weight of the ethylene glycol oligomer. Although the electrode resistance value can be put to practical use even if it is a little larger than the results listed in Table 5, if the molecular weight exceeds 10,000, the grafted ethylene glycol oligomer becomes longer and it becomes easier to wrap around the carbon nanotube, resulting in a rapid resistance. The upper limit of the average molecular weight was 10,000, preferably 4000.

  Moreover, if the lower limit of the average molecular weight of the oligomer is too small, the effect of repairing the defects of the carbon nanotubes is small and the durability cannot be sufficiently improved. In this example, the lower limit of the average molecular weight of the oligomer was set to 40, preferably 400.

(Durability experiment)
Next, the polymer actuator element shown in FIG. 1 was manufactured and a durability experiment was conducted. The polymer actuator element of the example shown in FIG. 5 has an electrode layer formed using carbon nanotubes of Examples 1 and 2 (ethylene glycol oligomer having an average molecular weight of about 4000 grafted to CNT). These are four types having electrode layers formed using carbon nanotubes of Examples 3 and 4 (ethylene glycol oligomer having an average molecular weight of about 400 grafted to CNT).

  Further, the polymer actuator element of the comparative example has an electrode layer formed using untreated carbon nanotubes according to the comparative example (one in which ethylene glycol oligomer is not grafted to CNT).

  In the experiment, the state in which 2.5 V was applied to each polymer actuator element was maintained in the atmosphere (23 ° C., 45 RH%) (DC drive), and the relationship between the elapsed time and the change in displacement was measured.

  The time on the horizontal axis in FIG. 5 is an arbitrary unit, and time “1” is the start of driving. At this time, each polymer actuator element is deformed from the reference state (displacement amount 0) to a predetermined displacement amount. Since it is DC drive, maintaining the amount of displacement over time will provide excellent durability, but as shown in FIG. 5, in the polymer actuator element of the comparative example as time passes, It was found that the displacement amount fluctuated greatly. On the other hand, when PEG having an average molecular weight of 4000 is grafted (Examples 1 and 2) and when PEG having an average molecular weight of 400 is grafted (Examples 3 and 4), both of the polymer actuator elements are displaced. It turned out that the fluctuation | variation of quantity can be suppressed rather than a comparative example. In particular, in Examples 1 and 2 in which an oligomer having an average molecular weight of about 4000 was grafted to carbon nanotubes, it was found that durability superior to Examples 3 and 4 could be obtained.

  The reason why the durability could be improved in Examples 1 and 2 and Examples 3 and 4 is that the defects of the carbon nanotubes could be repaired by the grafting of the oligomer and the deterioration of the ionic liquid could be suppressed.

1 Polymer Actuator Element 2 Electrolyte Layer 3 and 4 Electrode Layer

Claims (8)

An electrolyte layer, and electrode layers disposed on both sides in the thickness direction of the electrolyte layer, the electrolyte layer and the electrode layer include an ionic liquid, the electrode layer includes a carbon nanotube, and the electrode layer includes In a polymer actuator element that deforms when a voltage is applied,
The electrode layer includes the carbon nanotube grafted with an oligomer ,
The polymer actuator element , wherein the oligomer is selected from an ethylene glycol oligomer, a dimethylsiloxane oligomer, or an ethylene oxide oligomer .   The polymer actuator element according to claim 1, wherein an average molecular weight of the oligomer is in a range of 40 to 10,000.   The polymer actuator element according to claim 2, wherein an average molecular weight of the oligomer is in a range of 400 to 4000. An electrolyte layer, and electrode layers disposed on both sides in the thickness direction of the electrolyte layer, the electrolyte layer and the electrode layer include an ionic liquid, the electrode layer includes a carbon nanotube, and the electrode layer includes In the method of manufacturing a polymer actuator element that deforms when a voltage is applied,
A process of grafting an oligomer to a carbon nanotube,
Forming the electrode layer containing the carbon nanotube grafted with the oligomer;
I have a,
A method for producing a polymer actuator element, wherein the oligomer is selected from an ethylene glycol oligomer, a dimethylsiloxane oligomer, or an ethylene oxide oligomer . The method for producing a polymer actuator element according to claim 4, wherein the oligomer is radically polymerized and grafted onto the carbon nanotube. 6. The method for producing a polymer actuator element according to claim 5 , wherein a radical polymerizable oligomer is produced from a polymer azo polymerization initiator, and the radical polymerizable oligomer is radically polymerized and grafted onto the carbon nanotube. The method for producing a polymer actuator element according to any one of claims 4 to 6 , wherein the average molecular weight of the oligomer is in the range of 40 to 10,000. The method for producing a polymer actuator element according to claim 7 , wherein the average molecular weight of the oligomer is in the range of 400 to 4000.

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