Search for: All records

When a ribbon or tube is twisted far enough it forms buckles and wrinkles. Its new geometry can be strikingly ordered or hopelessly disordered. Here we study this process in a tube with hybrid boundary conditions: one end a cylinder and the other end crimped flat like a ribbon, so that the sample resembles a toothpaste tube. The resulting irregular structures and mechanical responses can be dramatically different from those of a ribbon. However, when we form two creases in the tube prior to twisting, we obtain an ordered structure composed of repeating triangular facets oriented at varying angles and a more elastic torque response, reminiscent of the creased helicoid structure of a twisted ribbon. We measure how the torque and structural evolution depend on parameters such as material thickness and the twist angle. When only part of the tube is precreased, the ordered structures are confined to this segment. Surprisingly, in some tubes made from thicker sheets, an ordered structure forms without precreasing. This study provides insights into controlling the buckling of thin shells, offering a potential pathway for designing ordered structures in soft materials. 

A buckled sheet offers a reservoir of material that can be unfurled at a later time. For sufficiently thin yet stiff materials, this geometric process has a striking mechanical feature: when the slack runs out, the material locks to further extension. Here, we establish a simple route to a tunable locking material: a system with an interval where it is freely deformable under a given deformation mode, and where the endpoints of this interval can be changed continuously over a wide range. We demonstrate this type of mechanical response in a thin sheet formed into a cylindrical shell and subjected to axial twist and compression, and we rationalize our results with a simple geometric model. 

When an amorphous solid is deformed cyclically, it may reach a steady state in which the paths of constituent particles trace out closed loops that repeat in each driving cycle. A remarkable variant has been noticed in simulations where the period of particle motions is a multiple of the period of driving, but the reasons for this behavior have remained unclear. Motivated by mesoscopic features of displacement fields in experiments on jammed solids, we propose and analyze a simple model of interacting soft spots—locations where particles rearrange under stress and that resemble two-level systems with hysteresis. We show that multiperiodic behavior can arise among just three or more soft spots that interact with each other, but in all cases it requires frustrated interactions, illuminating this otherwise elusive type of interaction. We suggest directions for seeking this signature of frustration in experiments and for achieving it in designed systems. 

When stressed sufficiently, solid materials yield and deform plastically via reorganization of microscopic constituents. Indeed, it is possible to alter the microstructure of materials by judicious application of stress, an empirical process utilized in practice to enhance the mechanical properties of metals. Understanding the interdependence of plastic flow and microscopic structure in these nonequilibrium states, however, remains a major challenge. Here, we experimentally investigate this relationship, between the relaxation dynamics and microscopic structure of disordered colloidal solids during plastic deformation. We apply oscillatory shear to solid colloidal monolayers and study their particle trajectories as a function of shear rate in the plastic regime. Under these circumstances, the strain rate, the relaxation rate associated with plastic flow, and the sample microscopic structure oscillate together, but with different phases. Interestingly, the experiments reveal that the relaxation rate associated with plastic flow at time t is correlated with the strain rate and sample microscopic structure measured at earlier and later times, respectively. The relaxation rate, in this nonstationary condition, exhibits power-law, shear-thinning behavior and scales exponentially with sample excess entropy. Thus, measurement of sample static structure (excess entropy) provides insight about both strain rate and constituent rearrangement dynamics in the sample at earlier times.