ترغب بنشر مسار تعليمي؟ اضغط هنا

Coincident Molecular Auxeticity and Negative Order Parameter in a Liquid Crystal Elastomer

79   0   0.0 ( 0 )
 نشر من قبل Devesh Mistry
 تاريخ النشر 2018
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

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.

قيم البحث

اقرأ أيضاً

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 unava ilability 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.
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.
143 - Yang Liu , Wendi Ma , Hui-Hui Dai 2020
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.
Using computer simulations, we establish that the structure of a supercooled binary atomic liquid mixture consists of common neighbour structures similar to those found in the equilibrium crystal phase, a Laves structure. Despite the large accumulati on of crystal-like structure, we establish that the supercooled liquid represents a true metastable liquid and that liquid can borrow crystal structure without being destabilized. We consider whether this feature might be the origin of all instances of liquids of a strongly favoured local structure.
Measurements of the surface x-ray scattering from several pure liquid metals (Hg, Ga, and In) and from three alloys (Ga-Bi, Bi-In, and K-Na) with different heteroatomic chemical interactions in the bulk phase are reviewed. Surface-induced layering is found for each elemental liquid metal. The surface structure of the K-Na alloy resembles that of an elemental liquid metal. Bi-In displays pair formation at the surface. Surface segregation and a wetting film are found for Ga-Bi.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا