Search arXivSearch

arXiv · 2606.22795

Hierarchical Granular Metamaterials

Abstract

Granular materials dissipate energy efficiently through intergranular interactions, yet their disordered, dense nature precludes precise control and integration into lightweight systems. Architected materials offer tunable mechanical responses at low densities but tend to localize stress, limiting dissipation efficiency. Here, we introduce hierarchical granular metamaterials that reconcile these trade-offs through three levels of design: lightweight architected grains engineered with hollow elliptical inclusions, crystal-inspired grain packings, and functional gradients and defects within grain tessellations. These metamaterials exhibit simultaneous increases in impact energy absorption per unit mass and reductions in transmitted peak force at low densities, outperforming conventional architected materials. In situ nanomechanical experiments and nonlinear computational models reveal that enhanced lateral grain expansion drives recruitment of neighboring grains, amplifying plastic and frictional dissipation. Multiscale impact experiments confirm that these mechanisms persist across length scales, constituent materials, and dimensionalities. Beyond mechanical performance, we demonstrate that spatially programmable inter-grain contact networks enable deterministic routing of deformation, which extends to electrical transport pathways independently of packing geometry. By combining granular principles with architected material design, this work establishes a paradigm for multifunctional metamaterials whose contact topology, mechanical response, and transport properties can be programmed independently.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

James Utama Surjadi, Bastien F. G. Aymon, Ayan Kumar, Lei Wu, Jet Lem, Ken N. Kamrin, Carlos M. Portela. 2026-06-22. Hierarchical Granular Metamaterials. https://arxiv.org/abs/2606.22795

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Deformation and organization of droplet-encapsulated soft beads

Many biological, culinary, and engineering processes lead to the co-encapsulation of several soft particles within a liquid interface. In these situations the particles are bound together by the capillary forces that deform them and influence their biological or rheological properties. Here, we introduce an experimental approach to encapsulate a controlled number of soft beads within aqueous droplets in oil. These droplet-encapsulated gels are manipulated in a deformable microfluidic device to merge them and modify the liquid fraction. In the dry limit the contact surface between the hydrogels is found to be determined by the elastocapillary number $E_c$, with the contact radius following a $E_c^{1/3}$ dependence, indicating that the deformation increases for soft or small particles. When multiple beads are co-encapsulated within a single droplet they can be arranged into linear or three-dimensional aggregates that remain at a local energy minimum.

cond-mat.soft

Flexoelectricity-driven softening of bend elasticity leads to spontaneous chiral symmetry breaking in a polar fluid

The origin of the recently observed spontaneous chiral symmetry breaking in polar fluids composed of achiral molecules is an unsolved problem, raising fundamental questions about how heliconical structures emerge in such systems. Here, we investigate the pretransitional fluctuations leading to the formation of the spontaneously chiral twist-bend ferroelectric nematic phase using dielectric spectroscopy, light scattering, and small-angle X-ray scattering. We observe simultaneous softening of the bend elastic constant and the emergence of a collective dielectric mode on approaching the transition. By developing a theoretical model, we show that these phenomena are signatures of a flexoelectricity-driven transition arising from the coupling between electric polarization and bend deformation.

cond-mat.soft

Taylor dispersion in a soft tube

Diffusion of a solute along a tube is enhanced by hydrodynamic flow, a phenomenon known as Taylor dispersion. In microfluidic applications, the compliance of the tube boundaries modifies the hydrodynamic flow and thus solutal transport. Here, we develop the theory of solutal dispersion in a soft, axisymmetric tube where the tube walls respond to the hydrodynamic pressure through a Winkler response. By deriving the modified macro-transport equation for the solutal concentration dynamics based on multiple-time-scale analysis, we explore the influence of softness on solutal transport for steady and pulsatile configurations. Our main finding is that softness enhances the effective advection velocity and dispersion coefficient, which might have practical implication in biology and microfluidic technology.

cond-mat.soft