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A new paradigm for generating adaptive functionality in materials. 

The viscous fingering instability, which forms when a less-viscous fluid invades a more-viscous one within a confined geometry, is an iconic system for studying pattern formation. For both miscible and immiscible fluid pairs the growth dynamics change after the initial instability onset and the global structures, typical of late-time growth, are governed by the viscosity ratio. Here we introduce an experimental technique to measure flow throughout the inner and outer fluids. This probes the existence of a new length scale associated with the local pressure gradients around the interface and allows us to compare our results to the predictions of a previously proposed model for late-time finger growth. Published by the American Physical Society2024 

A particle raft floating on an expanding liquid substrate provides a macroscopic analog for studying material failure. The time scales in this system allow both particle-relaxation dynamics and rift formation to be resolved. In our experiments, a raft, an aggregate of particles, is stretched uniaxially by the expansion of the air–liquid interface on which it floats. Its failure morphology changes continuously with pulling velocity. This can be understood as a competition between two velocity scales: the speed of re-aggregation, in which particles relax towards a low-energy configuration determined by viscous and capillary forces, and the difference of velocity between neighboring particles caused by the expanding liquid surface area. This competition selects the cluster length, i.e. , the distance between adjacent rifts. A model based on this competition is consistent with the experimental failure patterns. 

Evolution in time-varying environments naturally leads to adaptable biological systems that can easily switch functionalities. Advances in the synthesis of environmentally responsive materials therefore open up the possibility of creating a wide range of synthetic materials which can also be trained for adaptability. We consider high-dimensional inverse problems for materials where any particular functionality can be realized by numerous equivalent choices of design parameters. By periodically switching targets in a given design algorithm, we can teach a material to perform incompatible functionalities with minimal changes in design parameters. We exhibit this learning strategy for adaptability in two simulated settings: elastic networks that are designed to switch deformation modes with minimal bond changes and heteropolymers whose folding pathway selections are controlled by a minimal set of monomer affinities. The resulting designs can reveal physical principles, such as nucleation-controlled folding, that enable such adaptability. 

The introduction of transient degrees of freedom into a system can lead to novel material design and training protocols that guide a system into a desired metastable state. In this approach, some degrees of freedom, which were not initially included in the system dynamics, are first introduced and subsequently removed from the energy minimization process once the desired state is reached. Using this conceptual framework, we create stable jammed packings that exist in exceptionally deep energy minima marked by the absence of low-frequency quasilocalized modes; this added stability persists in the thermodynamic limit. The inclusion of particle radii as transient degrees of freedom leads to deeper and much more stable minima than does the inclusion of particle stiffnesses. This is because particle radii couple to the jamming transition, whereas stiffnesses do not. Thus, different choices for the added degrees of freedom can lead to very different training outcomes.