Soft actuators based on liquid-crystalline elastomers.
Soft actuators based on liquid-crystalline elastomers.
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DOI:
10.1002/anie.200601760
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发表时间:
2006-08
影响因子:
--
通讯作者:
Yanlei Yu;T. Ikeda
中科院分区:
文献类型:
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作者:
Yanlei Yu;T. Ikeda
There is a growing interest in the development of artificial muscle-like actuators, which are ideal for the realization of biomimetic movements as they change their shapes and dimensions when a potential is applied. Polymer actuators play a leading role in this field because they provide such advantages as flexibility, light weight, low costs, and quiet operation compliance.[1] Various materials are under current investigation in this field, such as polymer gels,[1] conjugated polymers,[2] carbon nanotubes,[3] and dielectric elastomers,[4] and various chemical and physical stimuli have been applied to induce the responses of these materials, including pH, solvent composition, temperature, electric field, magnetic field, and light. Among these polymer soft actuation materials, gels and conducting polymers are most promising for applications in the field of biomimetic actuation. However, the low elastic modulus and low yield strength of gels provide important limitations for actuator performance, whereas for battery-like conducting polymers faradaic processes involving solid-state dopant diffusion and structural changes limit the rate, cycle life, and energy conversion efficiencies.Recently, there has been a growing focus on the study of soft actuation materials based on liquid-crystalline elastomers (LCEs) as a result of their unique combination of the anisotropic features of liquid crystal (LC) phases and the rubber elasticity of polymer networks. In 1997, deGennes etal. reported theoretical studies on the possibility of using LCEs as artificial muscles.[5] They proposed that a slight drop in the temperature across the isotropic (I)-to-LC transition is able to cause a strong uniaxial deformation of LCEs at nearly constant volume owing to a change in the LC order. Finkelmann and Kundler later reported that nematic LCE (NLCE) films containing polysiloxanes exhibited a spontaneous contraction along the director axis when heated toward the N-to-I phase-transition temperature (Figure 1).[6a] By synthesizing NLCE films through a hydrosilylation reaction of a monofunctional LC compound and a bifunctional LC polyether with poly (methylhydrogensiloxane), a shape change over 300% was obtained.[6b, c] This thermomechanical effect was also observed in side-on NLCE films and fibers that contained poly-