No Arabic abstract
Liquid crystal elastomers/glasses are active materials that can have significant metric change upon stimulation. The local metric change is determined by its director pattern that describes the ordering direction and hence the direction of contraction. We study logarithmic spiral patterns on flat sheets that evolve into cones on deformation, with Gaussian curvature localized at tips. Such surfaces, Gaussian flat except at their tips, can be combined to give compound surfaces with GC concentrated in lines. We characterize all possible metric-compatible interfaces between two spiral patterns, specifically where the same metric change occurs on each side. They are classified as hyperbolic-type, elliptic-type, concentric spiral, and continuous-director interfaces. Upon the cone deformations and additional isometries, the actuated interfaces form creases bearing non-vanishing concentrated Gaussian curvature, which is formulated analytically for all cases and simulated numerically for some examples. Analytical calculations and the simulations agree qualitatively well. Furthermore, the relaxation of Gaussian-curved creases is discussed and cantilevers with Gaussian curvature-enhanced strength are proposed. Taken together, our results provide new insights in the study of curved creases, lines bearing Gaussian curvature, and their mechanics arising in actuated liquid crystal elastomers/glasses, and other related active systems.
The Gaussian (saddle splay) rigidity of fluid membranes controls their equilibrium topology but is notoriously difficult to measure. In lipid mixtures, typical of living cells, linear interfaces separate liquid ordered (LO) from liquid disordered (LD) bilayer phases at subcritical temperatures. Here we consider such membranes supported by curved supports that thereby control the membrane curvatures. We show how spectral analysis of the fluctuations of the LO-LD interface provides a novel way of measuring the difference in Gaussian rigidity between the two phases. We provide a number of conditions for such interface fluctuations to be both experimentally measurable and sufficiently sensitive to the value of the Gaussian rigidity, whilst remaining in the perturbative regime of our analysis.
The relation between elasticity and yielding is investigated in a model polymer solid by Molecular-Dynamics simulations. By changing the bending stiffness of the chain and the bond length, semicrystalline and disordered glassy polymers - both with bond disorder - as well as nematic glassy polymers with bond ordering are obtained. It is found that in systems with bond disorder the ratio Ty/G between the shear yield strength Ty and the shear modulus G is close to the universal value of the atomic metallic glasses. The increase of the local nematic order in glasses leads to the increase of the shear modulus and the decrease of the shear yield strength, as observed in experiments on nematic thermosets. A tentative explanation of the subsequent reduction of the ratio Ty/G in terms of the distributions of the per-monomer stress is offered.
Within the framework of continuum theory, we draw a parallel between ferromagnetic materials and nematic liquid crystals confined on curved surfaces, which are both characterized by local interaction and anchoring potentials. We show that the extrinsic curvature of the shell combined with the out-of-plane component of the director field gives rise to chirality effects. This interplay produces an effective energy term reminiscent of the chiral term in cholesteric liquid crystals, with the curvature tensor acting as a sort of anisotropic helicity. We discuss also how the different nature of the order parameter, a vector in ferromagnets and a tensor in nematics, yields different textures on surfaces with the same topology as the sphere. In particular, we show that the extrinsic curvature governs the ground state configuration on a nematic spherical shell, favouring two antipodal disclinations of charge +1 on small particles and four $+1/2$ disclinations of charge located at the vertices of a square inscribed in a great circle on larger particles.
The surfaces of growing biological tissues, swelling gels, and compressed rubbers do not remain smooth, but frequently exhibit highly localized inward folds. We reveal the morphology of this surface folding in a novel experimental setup, which permits to deform the surface of a soft gel in a controlled fashion. The interface first forms a sharp furrow, whose tip size decreases rapidly with deformation. Above a critical deformation, the furrow bifurcates to an inward folded crease of vanishing tip size. We show experimentally and numerically that both creases and furrows exhibit a universal cusp-shape, whose width scales like $y^{3/2}$ at a distance $y$ from the tip. We provide a similarity theory that captures the singular profiles before and after the self-folding bifurcation, and derive the length of the fold from large deformation elasticity.
We describe a general family of curved-crease folding tessellations consisting of a repeating lens motif formed by two convex curved arcs. The third author invented the first such design in 1992, when he made both a sketch of the crease pattern and a vinyl model (pictured below). Curve fitting suggests that this initial design used circular arcs. We show that in fact the curve can be chosen to be any smooth convex curve without inflection point. We identify the ruling configuration through qualitative properties that a curved folding satisfies, and prove that the folded form exists with no additional creases, through the use of differential geometry.