Arthur A. Evans
University of Massachusetts Amherst
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Featured researches published by Arthur A. Evans.
Science | 2014
Jesse L. Silverberg; Arthur A. Evans; Lauren McLeod; Ryan C. Hayward; Thomas C. Hull; Christian D. Santangelo; Itai Cohen
Folding robots and metamaterials The same principles used to make origami art can make self-assembling robots and tunable metamaterials—artificial materials engineered to have properties that may not be found in nature (see the Perspective by You). Felton et al. made complex self-folding robots from flat templates. Such robots could potentially be sent through a collapsed building or tunnels and then assemble themselves autonomously into their final functional form. Silverberg et al. created a mechanical metamaterial that was folded into a tessellated pattern of unit cells. These cells reversibly switched between soft and stiff states, causing large, controllable changes to the way the material responded to being squashed. Science, this issue p. 644, p. 647; see also p. 623 Origami folded sheets can be structurally altered by adding defects to control the mechanical properties. [Also see Perspective by You] Although broadly admired for its aesthetic qualities, the art of origami is now being recognized also as a framework for mechanical metamaterial design. Working with the Miura-ori tessellation, we find that each unit cell of this crease pattern is mechanically bistable, and by switching between states, the compressive modulus of the overall structure can be rationally and reversibly tuned. By virtue of their interactions, these mechanically stable lattice defects also lead to emergent crystallographic structures such as vacancies, dislocations, and grain boundaries. Each of these structures comes from an arrangement of reversible folds, highlighting a connection between mechanical metamaterials and programmable matter. Given origami’s scale-free geometric character, this framework for metamaterial design can be directly transferred to milli-, micro-, and nanometer-size systems.
Advanced Materials | 2015
Jun-Hee Na; Arthur A. Evans; Jinhye Bae; Maria Chiappelli; Christian D. Santangelo; Robert J. Lang; Thomas C. Hull; Ryan C. Hayward
Self-folding microscale origami patterns are demonstrated in polymer films with control over mountain/valley assignments and fold angles using trilayers of photo-crosslinkable copolymers with a temperature-sensitive hydrogel as the middle layer. The characteristic size scale of the folds W = 30 μm and figure of merit A/ W (2) ≈ 5000, demonstrated here represent substantial advances in the fabrication of self-folding origami.
Nature Materials | 2015
Jesse L. Silverberg; Jun-Hee Na; Arthur A. Evans; Bin Liu; Thomas C. Hull; Christian D. Santangelo; Robert J. Lang; Ryan C. Hayward; Itai Cohen
Origami is used beyond purely aesthetic pursuits to design responsive and customizable mechanical metamaterials. However, a generalized physical understanding of origami remains elusive, owing to the challenge of determining whether local kinematic constraints are globally compatible and to an incomplete understanding of how the folded sheets material properties contribute to the overall mechanical response. Here, we show that the traditional square twist, whose crease pattern has zero degrees of freedom (DOF) and therefore should not be foldable, can nevertheless be folded by accessing bending deformations that are not explicit in the crease pattern. These hidden bending DOF are separated from the crease DOF by an energy gap that gives rise to a geometrically driven critical bifurcation between mono- and bistability. Noting its potential utility for fabricating mechanical switches, we use a temperature-responsive polymer-gel version of the square twist to demonstrate hysteretic folding dynamics at the sub-millimetre scale.
Angewandte Chemie | 2015
Adam W. Hauser; Arthur A. Evans; Jun-Hee Na; Ryan C. Hayward
Patterning deformation within the plane of thin elastic sheets represents a powerful tool for the definition of complex and stimuli-responsive 3D buckled shapes. Previous experimental methods, however, have focused on sheets that access a limited number of shapes pre-programmed into the sheet, restricting the degree of dynamic control. Here, we demonstrate on-demand reconfigurable buckling of poly(N-isopropylacrylamide-co-acrylic acid) (PNIPAM) hydrogel network films containing gold nanoparticles (AuNPs) by patterned photothermal deswelling. Predictable, easily controllable, and reversible transformations from a single flat gel sheet to numerous different three-dimensional forms are shown. Importantly, the response time is limited by poroelastic mass transport, rather than photochemical switching kinetics, enabling reconfiguration of shape on timescales of several seconds, with further increases in speed possible by reducing film thickness.
Physics of Fluids | 2011
Arthur A. Evans; Takuji Ishikawa; Takami Yamaguchi; Eric Lauga
We use numerical simulations to probe the dynamics of concentrated suspensions of spherical microswimmers interacting hydrodynamically. Previous work in the dilute limit predicted orientational instabilities of aligned suspensions for both pusher and puller swimmers, which we confirm computationally. Unlike previous work, we show that isotropic suspensions of spherical swimmers are also always unstable. Both types of initial conditions develop long-time polar order of a nature which depends on the hydrodynamic signature of the swimmer but very weakly on the volume fraction up to very high volume fractions.
Physical Review Letters | 2016
Bryan Gin-ge Chen; Bin Liu; Arthur A. Evans; Jayson Paulose; Itai Cohen; Vincenzo Vitelli; Christian D. Santangelo
Origami and kirigami have emerged as potential tools for the design of mechanical metamaterials whose properties such as curvature, Poisson ratio, and existence of metastable states can be tuned using purely geometric criteria. A major obstacle to exploiting this property is the scarcity of tools to identify and program the flexibility of fold patterns. We exploit a recent connection between spring networks and quantum topological states to design origami with localized folding motions at boundaries and study them both experimentally and theoretically. These folding motions exist due to an underlying topological invariant rather than a local imbalance between constraints and degrees of freedom. We give a simple example of a quasi-1D folding pattern that realizes such topological states. We also demonstrate how to generalize these topological design principles to two dimensions. A striking consequence is that a domain wall between two topologically distinct, mechanically rigid structures is deformable even when constraints locally match the degrees of freedom.
Proceedings of the National Academy of Sciences of the United States of America | 2015
Nakul Bende; Arthur A. Evans; Sarah Innes-Gold; Luis Marín; Itai Cohen; Ryan C. Hayward; Christian D. Santangelo
Significance Shape-programmable structures have recently used origami to reconfigure using a smooth folding motion, but are hampered by slow speeds and complicated material assembly. Inspired by natural systems like the leaves of Venus flytraps and hummingbird beaks, we use curved creases to imbue elastic shells with programmable fast “snapping” motion. This deformation between preprogrammed states can be tuned to be either continuously foldable or snap discontinuously. Our results provide a purely geometrical mechanism for designing multistable structures, thus circumventing the need for complex materials or fabrication methods in creating structures with fast dynamics. This technique will find application in designing structures over a wide range of length scales, including self-folding materials, tunable optics, and switchable frictional surfaces for microfluidics. Curvature and mechanics are intimately connected for thin materials, and this coupling between geometry and physical properties is readily seen in folded structures from intestinal villi and pollen grains to wrinkled membranes and programmable metamaterials. While the well-known rules and mechanisms behind folding a flat surface have been used to create deployable structures and shape transformable materials, folding of curved shells is still not fundamentally understood. Shells naturally deform by simultaneously bending and stretching, and while this coupling gives them great stability for engineering applications, it makes folding a surface of arbitrary curvature a nontrivial task. Here we discuss the geometry of folding a creased shell, and demonstrate theoretically the conditions under which it may fold smoothly. When these conditions are violated we show, using experiments and simulations, that shells undergo rapid snapping motion to fold from one stable configuration to another. Although material asymmetry is a proven mechanism for creating this bifurcation of stability, for the case of a creased shell, the inherent geometry itself serves as a barrier to folding. We discuss here how two fundamental geometric concepts, creases and curvature, combine to allow rapid transitions from one stable state to another. Independent of material system and length scale, the design rule that we introduce here explains how to generate snapping transitions in arbitrary surfaces, thus facilitating the creation of programmable multistable materials with fast actuation capabilities.
Physical Review E | 2010
Arthur A. Evans; Eric Lauga
Confinement and wall effects are known to affect the kinematics and propulsive characteristics of swimming microorganisms. When a solid body is dragged through a viscous fluid at constant velocity, the presence of a wall increases fluid drag, and thus the net force required to maintain speed has to increase. In contrast, recent optical trapping experiments have revealed that the propulsive force generated by human spermatozoa is decreased by the presence of boundaries. Here, we use a series of simple models to analytically elucidate the propulsive effects of a solid boundary on passively actuated filaments and model flagella. For passive flexible filaments actuated periodically at one end, the presence of the wall is shown to increase the propulsive forces generated by the filaments in the case of displacement-driven actuation, while it decreases the force in the case of force-driven actuation. In the case of active filaments as models for eukaryotic flagella, we demonstrate that the manner in which a solid wall affects propulsion cannot be known a priori, but is instead a nontrivial function of the flagellum frequency, wavelength, its material characteristics, the manner in which the molecular motors self-organize to produce oscillations (prescribed activity model or self-organized axonemal beating model), and the boundary conditions applied experimentally to the tethered flagellum. In particular, we show that in some cases, the increase in fluid friction induced by the wall can lead to a change in the waveform expressed by the flagella, which results in a decrease in their propulsive force.
Physical Review E | 2015
Arthur A. Evans; Jesse L. Silverberg; Christian D. Santangelo
Origami-based design holds promise for developing materials whose mechanical properties are tuned by crease patterns introduced to thin sheets. Although there have been heuristic developments in constructing patterns with desirable qualities, the bridge between origami and physics has yet to be fully developed. To truly consider origami structures as a class of materials, methods akin to solid mechanics need to be developed to understand their long-wavelength behavior. We introduce here a lattice theory for examining the mechanics of origami tessellations in terms of the topology of their crease pattern and the relationship between the folds at each vertex. This formulation provides a general method for associating mechanical properties with periodic folded structures and allows for a concrete connection between more conventional materials and the mechanical metamaterials constructed using origami-based design.
Soft Matter | 2013
Arthur A. Evans; Saverio E. Spagnolie; Denis Bartolo; Eric Lauga
When a flexible filament is confined to a fluid interface, the balance between capillary attraction, bending resistance, and tension from an external source can lead to a self-buckling instability. We perform an analysis of this instability and provide analytical formulae that compare favorably with the results of detailed numerical computations. The stability and long-time dynamics of the filament are governed by a single dimensionless elastocapillary number quantifying the ratio between capillary to bending stresses. Complex, folded filament configurations such as loops, needles, and racquet shapes may be reached at longer times, and long filaments can undergo a cascade of self-folding events.