اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدMonolithic shape-programmable dielectric liquid crystal elastomer actuators
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Macroscale robotic systems have demonstrated great capabilities of high speed, precise, and agile functions. However, the ability of soft robots to perform complex tasks, especially in centimeter and millimeter scale, remains limited due to the unavailability of fast, energy-efficient soft actuators that can programmably change shape. Here, we combine desirable characteristics from two distinct active materials: fast and efficient actuation from dielectric elastomers and facile shape programmability from liquid crystal elastomers into a single shape changing electrical actuator. Uniaxially aligned monoliths achieve strain rates over 120%/s with energy conversion efficiency of 20% while moving loads over 700 times the actuator weight. The combined actuator technology offers unprecedented opportunities towards miniaturization with precision, efficiency, and more degrees of freedom for applications in soft robotics and beyond.
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Instabilities in thin elastic sheets, such as wrinkles, are of broad interest both from a fundamental viewpoint and also because of their potential for engineering applications. Nematic liquid crystal elastomers offer a new form of control of these i
nstabilities through direct coupling between microscopic degrees of freedom, resulting from orientational ordering of rod-like molecules, and macroscopic strain. By a standard method of dimensional reduction, we construct a plate theory for thin sheets of nematic elastomer. We then apply this theory to the study of the formation of wrinkles due to compression of a thin sheet of nematic liquid crystal elastomer atop an elastic or fluid substrate. We find the scaling of the wrinkle wavelength in terms of material parameters and the applied compression. The wavelength of the wrinkles is found to be non-monotonic in the compressive strain owing to the presence of the nematic. Finally, due to soft modes, the critical stress for the appearance of wrinkles can be much higher than in an isotropic elastomer and depends nontrivially on the manner in which the elastomer was prepared.
Auxetic materials have the counter-intuitive property of expanding rather than contracting perpendicular to an applied stretch, formally they have negative Poissons Ratios (PRs).[1,2] This results in properties such as enhanced energy absorption and
indentation resistance, which means that auxetics have potential for applications in areas from aerospace to biomedical industries.[3,4] Existing synthetic auxetics are all created by carefully structuring porous geometries from positive PR materials. Crucially, their geometry causes the auxeticity.[3,4] The necessary porosity weakens the material compared to the bulk and the structure must be engineered, for example, by using resource-intensive additive manufacturing processes.[1,5] A longstanding goal for researchers has been the development of a synthetic material that has intrinsic auxetic behaviour. Such molecular auxetics would avoid porosity-weakening and their very existence implies chemical tuneability.[1,4-9] However molecular auxeticity has never previously been proven for a synthetic material.[6,7] Here we present a synthetic molecular auxetic based on a monodomain liquid crystal elastomer (LCE). When stressed perpendicular to the alignment direction, the LCE becomes auxetic at strains greater than approximately 0.8 with a minimum PR of -0.8. The critical strain for auxeticity coincides with the occurrence of a negative liquid crystal order parameter (LCOP). We show the auxeticity agrees with theoretical predictions derived from the Warner and Terentjev theory of LCEs.[10] This demonstration of a synthetic molecular auxetic represents the origin of a new approach to producing molecular auxetics with a range of physical properties and functional behaviours. Further, it demonstrates a novel feature of LCEs and a route for realisation of the molecular auxetic technologies that have been proposed over the years.
In this paper, the two-dimensional pure bending of a hyperelastic substrate coated by a nematic liquid crystal elastomer (abbreviated as NLCE) is studied within the framework of nonlinear elasticity. The governing system, arising from the deformation
al momentum balance, the orientational momentum balance and the mechanical constraint, is formulated, and the corresponding exact solution is derived for a given constitutive model. It is found that there exist two different bending solutions. In order to determine which the preferred one is, we compare the total potential energy for both solutions and find that the two energy curves may have an intersection point at a critical value of the bending angle $alpha_c$ for some material parameters. In particular, the director $bm n$ abruptly rotates $dfrac{pi}{2}$ from one solution to another at $alpha_c$, which indicates a director reorientation (or jump). Furthermore, the effects of different material and geometric parameters on the bending deformation and the transition angle $alpha_c$ can be revealed using the obtained bending solutions. Meanwhile, the exact solution can offer a benchmark problem for validating the accuracy of approximated plate models for liquid crystal elastomers.
We present a generalized approach to compute the shape and internal structure of two-dimensional nematic domains. By using conformal mappings, we are able to compute the director field for a given domain shape that we choose from a rich class, which
includes drops with large and small aspect ratios, and sharp domain tips as well as smooth ones. Results are assembled in a phase diagram that for given domain size, surface tension, anchoring strength, and elastic constant shows the transitions from a homogeneous to a bipolar director field, from circular to elongated droplets, and from sharp to smooth domain tips. We find a previously unaccounted regime, where the drop is nearly circular, the director field bipolar and the tip rounded. We also find that bicircular director fields, with foci that lie outside the domain, provide a remarkably accurate description of the optimal director field for a large range of values of the various shape parameters.
Topological photonics harnesses the physics of topological insulators to control the behavior of light. Photonic modes robust against material imperfections are an example of such control. In this work, we propose a soft-matter platform based on nema
tic liquid crystals that supports photonic topological insulators. The orientation of liquid crystal molecules introduces an extra geometric degree of freedom which in conjunction with suitably designed structural properties, leads to the creation of topologically protected states of light. The use of soft building blocks potentially allows for reconfigurable systems that exploit the interplay between light and the soft responsive medium.
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