Search arXivSearch

arXiv · 2604.07080

Phase coherence and disorder-induced wave propagation in micromotor arrays

Abstract

Machines are designed, assembled, and programmed to convert power into predetermined dynamics and functions. In contrast, living systems such as interacting cells and animal groups self-organize, synchronize, and perform complex tasks without predefined patterns. Inspired by these decentralized architectures, experiments have shown that small assemblies of elastically coupled self-propelled robots can achieve two fundamental functionalities observed in nature: collective motion and oscillatory deformations. However, biological inspiration has steered research toward translational self-propulsion, while active rotation remains an underexplored route to designing broader animate materials. Here, we study the self-organization of microscopic metamachines composed of thousands of 3D-printed rotary motors. We first demonstrate and explain how motors precessing in unspecified directions collectively arrange their dynamics into a pristine antiferromagnetic phase. Next, we elucidate the emergence of spatiotemporal order in the form of phase coherence in the rotors' precession. Finally, we show how quenched disorder initiates the free propagation of phase waves across self-organized regions with mismatched rotation speeds. Our results suggest that spinner-based metamachines could illuminate metachronal-wave formation in living systems, and signal propagation in synthetic animate materials.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Romane Braun, Alexis Poncet, Alexandre Morin, Denis Bartolo. 2026-04-08. Phase coherence and disorder-induced wave propagation in micromotor arrays. https://arxiv.org/abs/2604.07080

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

KEEP EXPLORING

Related papers

Transient Elasticity -- A Unifying Framework for Thixotropy, Polymers, and Granular Media

Thixotropic yield stress fluids, such as paint or ketchup, are traditionally viewed as elastic structures that, under shear rates, break into viscous liquids with lumps, and reconnect at rest. An alternative framework is presented here: Upon shear, structural destruction is incomplete, leaving sufficient connections. As a result, elasticity fundamentally underlies their non-Newtonian behavior, though they do appear purely viscous under a steady shear, displaying little direct evidence of elastic rebound---same as granular media and polymers. Consequently, all three are described by the same set of evolution equations, differing only in their parameters. These equations are set up by starting from solid dynamics and allowing the elastic strain $\varepsilon^e$ to relax, which in effect interpolates between solid and fluid behavior, appropriate for systems that display both types of behavior. Incorporating in addition a two-temperature framework, tracking how energy is dissipated in two consecutive stages, yields the nonlinear model of Transient Elasticity (TE). It describes an elasticity that is transient in time yet persistent under shear. Previously validated for polymers and granular media, TE is here applied to thixotropic yield-stress fluids. As shown, it successfully accounts for a wide range of characteristic phenomena, including over- and undershoot, viscosity bifurcation, shear banding, and oscillatory rheography. Given its appropriateness across structurally diverse systems, TE offers a unified, surprisingly general account of non-Newtonian phenomena.

cond-mat.soft

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