How does the initial alignment of mesogens affect the photoinduced bending behavior of liquid-crystalline elastomers?

How does the initial alignment of mesogens affect the photoinduced bending behavior of liquid-crystalline elastomers?
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DOI:
10.1002/anie.200503684
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发表时间:
2006-01-01
影响因子:
16.6
通讯作者:
Ikeda, T
Ikeda, T
中科院分区:
化学1区
文献类型:
--
作者:
Kondo, M;Yu, YL;Ikeda, T

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The development of actuators that show bending movement is of increasing interest. The bending movement is usually induced by an asymmetric contraction or expansion in the materials.[1–4] This type of actuator has more advantages than the actuators that show only two-dimensional movements, such as expansion and contraction, from the viewpoint of precise three-dimensional actuation and long lifetime owing to small deformation for the bending action. Because of these unique properties, the bending actuators are expected to be used for cantilevers, micropumps, and many other micromechanical applications.Various materials have been reported as the bending actuators, such as piezoelectric transducers,[5] shape-memory alloys,[6] and polymers.[2] In comparison with other materials, the polymer actuators are much softer, lighter, and highly processible, which makes them easily made into various shapes; consequently, studies have been performed on the actuation of polymer materials and many applications have been proposed.[7] In addition, the bending of most polymer actuators, such as conducting polymers is driven by electrical energy; thus, these materials require wires to acquire electrical power.[3] On the other hand, elastomeric polymers, including gels and shape-memory polymers, can undergo mechanical actuation in response to various physical stimuli, such as pH,[8] solvent composition,[9] heat,[10–12] and light.[13, 14] Light can be controlled remotely and rapidly as an external stimulus, so it is of great importance in developing simple, efficient, and compact elastomeric polymer actuators that can be driven by light. It is known that liquid-crystalline elastomers (LCEs) exhibit a spontaneous contraction along the director axis when heated above their nematic (N)–isotropic (I) phase-transition temperatures.[15–17] On the other hand, when azobenzene chromophores are incorporated into LCEs, they can undergo the contraction isothermally because of the change in alignment order by light.[18–20] Furthermore, as the extinction coefficient of the azobenzene moieties at