Electroactive polymer
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(b) A voltage is applied and the EAP fingers deform in order to release the ball.
(c) When the voltage is removed, the EAP fingers return to their original shape and grip the ball
An electroactive polymer (EAP) is a polymer that exhibits a change in size or shape when stimulated by an electric field. The most common applications of this type of material are in actuators<ref name=ArtificialMuscles>"Bar-Cohen, Yoseph: "Artificial Muscles using Electroactive Polymers (EAP): Capabilities, Challenges and Potential" (PDF).</ref> and sensors.<ref name=EAPsensing>Wang, T.; Farajollahi, M.; Choi, Y. S.; Lin, I. T.; Marshall, J. E.; Thompson, N. M.; Kar-Narayan, S.; Madden, J. D. W.; Smoukov, S. K. (2016). "Electroactive polymers for sensing". Interface Focus. 6 (4): 1–19. doi:10.1098/rsfs.2016.0026. PMC 4918837. PMID 27499846.</ref><ref>Ionic Polymer Metal Composites (IPMCs) Set, Editor: Mohsen Shahinpoor, Royal Society of Chemistry, Cambridge 2016, https://pubs.rsc.org/en/content/ebook/978-1-78262-720-3 Archived 2020-08-01 at the Wayback Machine</ref> A typical characteristic property of an EAP is that they will undergo a large amount of deformation while sustaining large forces.
The majority of historic actuators are made of ceramic piezoelectric materials. While these materials are able to withstand large forces, they commonly will only deform a fraction of a percent. In the late 1990s, it has been demonstrated that some EAPs can exhibit up to a 380% strain, which is much more than any ceramic actuator.<ref name=ArtificialMuscles/> One of the most common applications for EAPs is in the field of robotics in the development of artificial muscles; thus, an electroactive polymer is often referred to as an artificial muscle.
History
The field of EAPs emerged back in 1880, when Wilhelm Röntgen designed an experiment in which he tested the effect of an electrostatic field on the mechanical properties of a stripe of natural rubber.<ref>Keplinger, Christoph; Kaltenbrunner, Martin; Arnold, Nikita; Bauer, Siegfried (2010-03-09). "Röntgen's electrode-free elastomer actuators without electromechanical pull-in instability". Proceedings of the National Academy of Sciences. 107 (10): 4505–4510. Bibcode:2010PNAS..107.4505K. doi:10.1073/pnas.0913461107. ISSN 0027-8424. PMC 2825178. PMID 20173097.</ref> The rubber stripe was fixed at one end and was attached to a mass at the other. Electric charges were then sprayed onto the rubber, and it was observed that the length changed. It was in 1925 that the first piezoelectric polymer was discovered (Electret). Electret was formed by combining carnauba wax, rosin and beeswax, and then cooling the solution while it is subject to an applied DC electrical bias. The mixture would then solidify into a polymeric material that exhibited a piezoelectric effect.
Polymers that respond to environmental conditions, other than an applied electric current, have also been a large part of this area of study. In 1949 Katchalsky et al. demonstrated that when collagen filaments are dipped in acid or alkali solutions, they would respond with a change in volume.<ref name="ElectrochemistryEncyclopedia">"Electrochemistry Encyclopedia: Electroactive Polymers (EAP)". Archived from the original on 2012-12-12.</ref> The collagen filaments were found to expand in an acidic solution and contract in an alkali solution. Although other stimuli (such as pH) have been investigated, due to its ease and practicality most research has been devoted to developing polymers that respond to electrical stimuli in order to mimic biological systems.
The next major breakthrough in EAPs took place in the late 1960s. In 1969 Kawai demonstrated that polyvinylidene fluoride (PVDF) exhibits a large piezoelectric effect.<ref name=ElectrochemistryEncyclopedia /> This sparked research interest in developing other polymers systems that would show a similar effect. In 1977 the first electrically conducting polymers were discovered by Hideki Shirakawa et al.<ref name=EAPHistory>Finkenstadt, Victoria L. (2005). "Natural polysaccharides as electroactive polymers". Appl Microbiol Biotechnol. 67 (6): 735–745. doi:10.1007/s00253-005-1931-4. PMID 15724215. S2CID 22935320.</ref> Shirakawa, along with Alan MacDiarmid and Alan Heeger, demonstrated that polyacetylene was electrically conductive, and that by doping it with iodine vapor, they could enhance its conductivity by 8 orders of magnitude. Thus the conductance was close to that of a metal. By the late 1980s a number of other polymers had been shown to exhibit a piezoelectric effect or were demonstrated to be conductive.
In the early 1990s, ionic polymer-metal composites (IPMCs) were developed and shown to exhibit electroactive properties far superior to previous EAPs. The major advantage of IPMCs was that they were able to show activation (deformation) at voltages as low as 1 or 2 volts.<ref name=ElectrochemistryEncyclopedia /> This is orders of magnitude less than any previous EAP. Not only was the activation energy for these materials much lower, but they could also undergo much larger deformations. IPMCs were shown to exhibit anywhere up to 380% strain, orders of magnitude larger than previously developed EAPs.<ref name=ArtificialMuscles />
In 1999, Yoseph Bar-Cohen proposed the Armwrestling Match of EAP Robotic Arm Against Human Challenge.<ref name=ElectrochemistryEncyclopedia /> This was a challenge in which research groups around the world competed to design a robotic arm consisting of EAP muscles that could defeat a human in an arm wrestling match. The first challenge was held at the Electroactive Polymer Actuators and Devices Conference in 2005.<ref name=ElectrochemistryEncyclopedia /> Another major milestone of the field is that the first commercially developed device including EAPs as an artificial muscle was produced in 2002 by Eamex in Japan.<ref name=ArtificialMuscles /> This device was a fish that was able to swim on its own, moving its tail using an EAP muscle. But the progress in practical development has not been satisfactory.<ref name=Mistakes>Eftekhari, Ali (2010). "Comment on "A Linear Actuation of Polymeric Nanofibrous Bundle for Artificial Muscles"". Chemistry of Materials. 22 (8): 2689–2690. doi:10.1021/cm903343t.</ref>
DARPA-funded research in the 1990s at SRI International and led by Ron Pelrine developed an electroactive polymer using silicone and acrylic polymers; the technology was spun off into the company Artificial Muscle in 2003, with industrial production beginning in 2008.<ref>Feldman, Randy (2008-02-20). "Electroactive Polymer Artificial Muscle - A Polymer Based Generator?" (PDF). Thin Film Users Group. Northern California Chapter of the American Vacuum Society. Archived from the original (PDF) on 2016-12-06. Retrieved 2012-07-16.</ref> In 2010, Artificial Muscle became a subsidiary of Bayer MaterialScience.<ref>"Electroactive Polymer "Artificial Muscle"". SRI International. Retrieved 2012-07-16.</ref>
Types
EAP can have several configurations, but are generally divided in two principal classes: Dielectric and Ionic.
Dielectric
Dielectric EAPs are materials in which actuation is caused by electrostatic forces between two electrodes which squeeze the polymer. Dielectric elastomers are capable of very high strains and are fundamentally a capacitor that changes its capacitance when a voltage is applied by allowing the polymer to compress in thickness and expand in area due to the electric field. This type of EAP typically requires a large actuation voltage to produce high electric fields (hundreds to thousands of volts), but very low electrical power consumption. Dielectric EAPs require no power to keep the actuator at a given position. Examples are electrostrictive polymers and dielectric elastomers.
Ferroelectric polymers
Ferroelectric polymers are a group of crystalline polar polymers that are also ferroelectric, meaning that they maintain a permanent electric polarization that can be reversed, or switched, in an external electric field.<ref>"Ferroelectric Properties of Vinylidene Fluoride Copolymers," by T. Furukawa, in Phase Transitions, Vol. 18, pp. 143-211 (1989).</ref><ref name ="Polymers">Nalwa, H. (1995). Ferroelectric Polymers (First ed.). New York: Marcel Dekker, INC. ISBN 978-0-8247-9468-2.</ref> Ferroelectric polymers, such as polyvinylidene fluoride (PVDF), are used in acoustic transducers and electromechanical actuators because of their inherent piezoelectric response, and as heat sensors because of their inherent pyroelectric response.<ref name=lovinger>Lovinger, A. J. (1983). "Ferroelectric polymers". Science. 220 (4602): 1115–1121. Bibcode:1983Sci...220.1115L. doi:10.1126/science.220.4602.1115. PMID 17818472. S2CID 45870679.</ref>
Electrostrictive graft polymers
Electrostrictive graft polymers consist of flexible backbone chains with branching side chains. The side chains on neighboring backbone polymers cross link and form crystal units. The backbone and side chain crystal units can then form polarized monomers, which contain atoms with partial charges and generate dipole moments, shown in Figure 2.<ref name="Electrostrictive Graft">Wang, Youqi; Changjie Sun; Eric Zhou; Ji Su (2004). "Deformation Mechanisms of Electrostrictive Graft Elastomers". Smart Materials and Structures. Institute of Physics Publishing. 13 (6): 1407–1413. Bibcode:2004SMaS...13.1407W. doi:10.1088/0964-1726/13/6/011. ISSN 0964-1726. S2CID 250859649.</ref> When an electrical field is applied, a force is applied to each partial charge and causes rotation of the whole polymer unit. This rotation causes electrostrictive strain and deformation of the polymer.
Liquid crystalline polymers
Main-chain liquid crystalline polymers have mesogenic groups linked to each other by a flexible spacer. The mesogens within a backbone form the mesophase structure causing the polymer itself to adopt a conformation compatible with the structure of the mesophase. The direct coupling of the liquid crystalline order with the polymer conformation has given main-chain liquid crystalline elastomers a large amount of interest.<ref name="LCpol">Ishige, Ryohei; Masatoshi Tokita; Yu Naito; Chun Ying Zhang; Junji Watanabe (January 22, 2008). "Unusual Formation of Smectic A Structure in Cross-Linked Monodomain Elastomer of Main-Chain LC Polyester with 3-Methylpentane Spacer". Macromolecules. American Chemical Society. 41 (7): 2671–2676. Bibcode:2008MaMol..41.2671I. doi:10.1021/ma702686c.</ref> The synthesis of highly oriented elastomers leads to have a large strain thermal actuation along the polymer chain direction with temperature variation resulting in unique mechanical properties and potential applications as mechanical actuators.
Ionic
Ionic EAPs are polymers in which actuation is caused by the displacement of ions inside the polymer. Only a few volts are needed for actuation, but the ionic flow implies a higher electrical power needed for actuation, and energy is needed to keep the actuator at a given position. Examples of ionic EAPS are conductive polymers, ionic polymer-metal composites (IPMCs), and responsive gels. Yet another example is a Bucky gel actuator, which is a polymer-supported layer of polyelectrolyte material consisting of an ionic liquid sandwiched between two electrode layers consisting of a gel of ionic liquid containing single-wall carbon nanotubes.<ref>Qu, L.; Peng, Q.; Dai, L.; Spinks, G. M.; Wallace, G. G.; Baughman, R. H. (2008). "Carbon Nanotube Electroactive Polymer Materials: Opportunities and Challenges". MRS Bulletin. 33 (3): 215–224. doi:10.1557/mrs2008.47. S2CID 138644259.ISSN 0883-7694</ref> The name comes from the similarity of the gel to the paper that can be made by filtering carbon nanotubes, the so-called buckypaper.<ref>Fukushima, Takanori; Kinji Asaka, Atsuko Kosaka, Takuzo Aida (2005). "Fully Plastic Actuator through Layer-by-Layer Casting with Ionic-Liquid-Based Bucky Gel". Angewandte Chemie International, Edition Volume 44, Issue 16 2410.</ref>
Electrorheological fluid
Electrorheological fluids change the viscosity of a solution with the application of an electric field. The fluid is a suspension of polymers in a low dielectric-constant liquid.<ref name="Polymer Rheology">Glass, J. Edward; Schulz, Donald N.; Zukosi, C.F (May 13, 1991). "1". Polymers as Rheology Modifiers. ACS Symposium Series. Vol. 462. American Chemical Society. pp. 2–17. ISBN 9780841220096.</ref> With the application of a large electric field the viscosity of the suspension increases. Potential applications of these fluids include shock absorbers, engine mounts and acoustic dampers.<ref name="Polymer Rheology" />
Ionic polymer-metal composite
Ionic polymer-metal composites consist of a thin ionomeric membrane with noble metal electrodes plated on its surface. It also has cations to balance the charge of the anions fixed to the polymer backbone.<ref name="IPM composites">Nemat-Nasser, S.; Thomas, C. (2001). "6". In Yoseph Bar-Cohen (ed.). Electroactive Polymer (EAP) Actuators as Artificial Muscles-Reality, Potential and Challenges. SPIE Press. pp. 139–191.</ref> They are very active actuators that show very high deformation at low applied voltage and show low impedance. Ionic polymer-metal composites work through electrostatic attraction between the cationic counter ions and the cathode of the applied electric field, a schematic representation is shown in Figure 3. These types of polymers show the greatest promise for bio-mimetic uses as collagen fibers are essentially composed of natural charged ionic polymers.<ref name="IPMC">Shahinpoor, M.; Y. Bar-Cohen; T. Xue; J. O. Simpson; J. Smith (5 March 1996). "Ionic Polymer-Metal Composties (IPMC) As Biomimetic Sensors and Actuators" (PDF). SPIE. p. 17. Archived from the original (PDF) on 28 May 2010. Retrieved 6 April 2010.</ref> Nafion and Flemion are commonly used ionic polymer metal composites.<ref>Park, I. S.; Jung, K.; Kim, D.; Kim, S. M.; Kim, K. J. (2008). "Physical Principles of Ionic Polymer–Metal Composites as Electroactive Actuators and Sensors". MRS Bulletin. 33 (3): 190–195. doi:10.1557/mrs2008.44. S2CID 135613424.ISSN 0883-7694</ref>
Stimuli-responsive gels
Stimuli-responsive gels (hydrogels, when the swelling agent is an aqueous solution) are a special kind of swellable polymer networks with volume phase transition behaviour. These materials change reversibly their volume, optical, mechanical and other properties by very small alterations of certain physical (e.g. electric field, light, temperature) or chemical (concentrations) stimuli.<ref>Schneider, Hans-Jörg (ed.), 2015. Chemoresponsive Materials. Royal Society of Chemistry, Cambridge.</ref> The volume change of these materials occurs by swelling/shrinking and is diffusion-based. Gels provide the biggest change in volume of solid-state materials.<ref name ="Hydrogel Sensors and Actuators">Gerlach, G.; Arndt, K.-F. (2009). Hydrogel Sensors and Actuators (First ed.). Berlin: Springer. ISBN 978-3-540-75644-6.</ref> Combined with an excellent compatibility with micro-fabrication technologies, especially stimuli-responsive hydrogels are of strong increasing interest for microsystems with sensors and actuators. Current fields of research and application are chemical sensor systems, microfluidics and multimodal imaging systems.
Comparison of dielectric and ionic EAPs
Dielectric polymers are able to hold their induced displacement while activated under a DC voltage.<ref name="Editorial">Bar-Cohen, Yoseph; Kwang J. Kim; Hyouk Ryeol Choi; John D. W. Madden (2007). "Electroactive Polymer Materials". Smart Materials and Structures. Institute of Physics Publishing. 16 (2). doi:10.1088/0964-1726/16/2/E01. S2CID 61500961.</ref> This allows dielectric polymers to be considered for robotic applications. These types of materials also have high mechanical energy density and can be operated in air without a major decrease in performance. However, dielectric polymers require very high activation fields (>10 V/µm) that are close to the breakdown level.
The activation of ionic polymers, on the other hand, requires only 1-2 volts. They however need to maintain wetness, though some polymers have been developed as self-contained encapsulated activators which allows their use in dry environments.<ref name=IPMC /> Ionic polymers also have a low electromechanical coupling. They are however ideal for bio-mimetic devices.
Characterization
While there are many different ways electroactive polymers can be characterized, only three will be addressed here: stress–strain curve, dynamic mechanical thermal analysis, and dielectric thermal analysis.
Stress–strain curve
Stress strain curves provide information about the polymer's mechanical properties such as the brittleness, elasticity and yield strength of the polymer. This is done by providing a force to the polymer at a uniform rate and measuring the deformation that results.<ref name="Textbook">Cowie, J. M. G.; Valerai Arrighi (2008). "13". Polymers: Chemistry and Physics of Modern Material (Third ed.). Florida: CRC Press. pp. 363–373. ISBN 978-0-8493-9813-1.</ref> An example of this deformation is shown in Figure 4. This technique is useful for determining the type of material (brittle, tough, etc.), but it is a destructive technique as the stress is increased until the polymer fractures.
Dynamic mechanical thermal analysis (DMTA)
Both dynamic mechanical analysis is a non destructive technique that is useful in understanding the mechanism of deformation at a molecular level. In DMTA a sinusoidal stress is applied to the polymer, and based on the polymer's deformation the elastic modulus and damping characteristics are obtained (assuming the polymer is a damped harmonic oscillator).<ref name=Textbook /> Elastic materials take the mechanical energy of the stress and convert it into potential energy which can later be recovered. An ideal spring will use all the potential energy to regain its original shape (no damping), while a liquid will use all the potential energy to flow, never returning to its original position or shape (high damping). A viscoeleastic polymer will exhibit a combination of both types of behavior.<ref name=Textbook />
Dielectric thermal analysis (DETA)
DETA is similar to DMTA, but instead of an alternating mechanical force an alternating electric field is applied. The applied field can lead to polarization of the sample, and if the polymer contains groups that have permanent dipoles (as in Figure 2), they will align with the electrical field.<ref name= Textbook /> The permittivity can be measured from the change in amplitude and resolved into dielectric storage and loss components. The electric displacement field can also be measured by following the current.<ref name=Textbook /> Once the field is removed, the dipoles will relax back into a random orientation.
Applications
EAP materials can be easily manufactured into various shapes due to the ease in processing many polymeric materials, making them very versatile materials. One potential application for EAPs is that they can potentially be integrated into microelectromechanical systems (MEMS) to produce smart actuators.
Artificial muscles
As the most prospective practical research direction, EAPs have been used in artificial muscles.<ref name=":0">Kim, K.J.; Tadokoro, S. (2007). Electroactive Polymers for Robotic Applications, Artificial Muscles and Sensors. London: Springer. ISBN 978-1-84628-371-0.</ref> Their ability to emulate the operation of biological muscles with high fracture toughness, large actuation strain and inherent vibration damping draw the attention of scientists in this field.<ref name="ElectrochemistryEncyclopedia"/> EAPs have even successfully been used to make a type of hand.<ref name=":0" />
Tactile displays
In recent years, "electro active polymers for refreshable Braille displays"<ref name="Electroactive polymers for refreshable Braille displays">Bar-Cohen, Yoseph (11 September 2009). "Electroactive polymers for refreshable Braille displays". SPIE.</ref> has emerged to aid the visually impaired in fast reading and computer assisted communication. This concept is based on using an EAP actuator configured in an array form. Rows of electrodes on one side of an EAP film and columns on the other activate individual elements in the array. Each element is mounted with a Braille dot and is lowered by applying a voltage across the thickness of the selected element, causing local thickness reduction. Under computer control, dots would be activated to create tactile patterns of highs and lows representing the information to be read.
Visual and tactile impressions of a virtual surface are displayed by a high resolution tactile display, a so-called "artificial skin" (Fig. 6).<ref>Richter, A.; Paschew, G. (2009). "Optoelectrothermic Control of Highly Integrated Polymer-Based MEMS Applied in an Artificial Skin". Advanced Materials. 21 (9): 979–983. Bibcode:2009AdM....21..979R. doi:10.1002/adma.200802737. S2CID 137163635.</ref> These monolithic devices consist of an array of thousands of multimodal modulators (actuator pixels) based on stimuli-responsive hydrogels. Each modulator is able to change individually their transmission, height and softness. Besides their possible use as graphic displays for visually impaired such displays are interesting as free programmable keys of touchpads and consoles.
Microfluidics
EAP materials have huge potential for microfluidics e.g. as drug delivery systems, microfluidic devices and lab-on-a-chip. A first microfluidic platform technology reported in literature is based on stimuli-responsive gels. To avoid the electrolysis of water hydrogel-based microfluidic devices are mainly based on temperature-responsive polymers with lower critical solution temperature (LCST) characteristics, which are controlled by an electrothermic interface. Two types of micropumps are known, a diffusion micropump and a displacement micropump.<ref>Richter, A.; Klatt, S.; Paschew, G.; Klenke, C. (2009). "Micropumps operated by swelling and shrinking of temperature-sensitive hydrogels". Lab on a Chip. 9 (4): 613–618. doi:10.1039/B810256B. PMID 19190798. S2CID 28050680.</ref> Microvalves based on stimuli-responsive hydrogels show some advantageous properties such as particle tolerance, no leakage and outstanding pressure resistance.<ref>Richter, A.; Kuckling, D.; Howitz, S.; Gehring, T; Arndt, K.-F. (2003). "Electronically controllable microvalves based on smart hydrogels: magnitudes and potential applications". Journal of Microelectromechanical Systems. 12 (5): 748–753. doi:10.1109/JMEMS.2003.817898.</ref><ref>Yu, C., Mutlu, S., Selvaganapathy, P. Mastrangelo, C. H., Svec, F., Fréchet, J. M. J. (2003). "Flow control valves for analytical microfluidic chips without mechanical parts based on thermally responsive monolithic polymers". Analytical Chemistry. 75 (8): 1958–1961. doi:10.1021/ac026455j. PMID 12713057. S2CID 23726246.{{cite journal}}: CS1 maint: multiple names: authors list (link)</ref><ref name="Hydrogel Micro Valve">"Hydrogel Micro Valves". GeSiM mbH. 2009. Archived from the original on 2015-10-09. Retrieved 2013-09-13.</ref> Besides these microfluidic standard components the hydrogel platform provides also chemical sensors<ref>Richter, A.; Paschew, G.; Klatt, S.; Lienig, J.; Arndt, K.-F.; Adler, H.-J. (2008). "Review on Hydrogel-based pH Sensors and Microsensors". Sensors. 8 (1): 561–581. Bibcode:2008Senso...8..561R. doi:10.3390/s8010561. PMC 3668326. PMID 27879722.</ref> and a novel class of microfluidic components, the chemical transistors (also referred as chemostat valves).<ref>Richter, A.; Türke, A.; Pich, A. (2007). "Controlled Double-Sensitivity of Microgels Applied to Electronically Adjustable Chemostats". Advanced Materials. 19 (8): 1109–1112. Bibcode:2007AdM....19.1109R. doi:10.1002/adma.200601989. S2CID 95750078.</ref> These devices regulate a liquid flow if a threshold concentration of certain chemical is reached. Chemical transistors form the basis of microchemomechanical fluidic integrated circuits. "Chemical ICs" process exclusively chemical information, are energy-self-powered, operate automatically and are able for large-scale integration.<ref>Greiner, R., Allerdißen, M., Voigt, A., Richter A. (2012). "Fluidic microchemomechanical integrated circuits processing chemical information". Lab on a Chip. 12 (23): 5034–5044. doi:10.1039/C2LC40617A. PMID 23038405.{{cite journal}}: CS1 maint: multiple names: authors list (link)</ref>
Another microfluidic platform is based on ionomeric materials. Pumps made from that material could offer low voltage (battery) operation, extremely low noise signature, high system efficiency, and highly accurate control of flow rate.<ref name="Electroactive Polymer Pumps">"Electroactive Polymer Pumps". Discover technologies Inc. 7 June 2009. Archived from the original on 26 January 2010. Retrieved 9 April 2010.</ref>
Another technology that can benefit from the unique properties of EAP actuators is optical membranes. Due to their low modulus, the mechanical impedance of the actuators, they are well-matched to common optical membrane materials. Also, a single EAP actuator is capable of generating displacements that range from micrometers to centimeters. For this reason, these materials can be used for static shape correction and jitter suppression. These actuators could also be used to correct for optical aberrations due to atmospheric interference.<ref name="Adaptive Membrane Optics">"Adaptive Membrane Optics". Discover technologies Inc. 7 June 2009. Archived from the original on 26 January 2010. Retrieved 9 April 2010.</ref>
Since these materials exhibit excellent electroactive character, EAP materials show potential in biomimetic-robot research, stress sensors and acoustics field, which will make EAPs become a more attractive study topic in the near future. They have been used for various actuators such as face muscles and arm muscles in humanoid robots.<ref>http://eap.jpl.nasa.gov/ NASA WorldWide Electroactive Polymer Actuators Webhub</ref>
Future directions
The field of EAPs is far from mature, which leaves several issues that still need to be worked on.<ref name="ElectrochemistryEncyclopedia"/> The performance and long-term stability of the EAP should be improved by designing a water impermeable surface. This will prevent the evaporation of water contained in the EAP, and also reduce the potential loss of the positive counter ions when the EAP is operating submerged in an aqueous environment. Improved surface conductivity should be explored using methods to produce a defect-free conductive surface. This could possibly be done using metal vapor deposition or other doping methods. It may also be possible to utilize conductive polymers to form a thick conductive layer. Heat resistant EAP would be desirable to allow operation at higher voltages without damaging the internal structure of the EAP due to the generation of heat in the EAP composite. Development of EAPs in different configurations (e.g., fibers and fiber bundles), would also be beneficial, in order to increase the range of possible modes of motion.
