Achieving adjustable elasticity with non-affine to affine transition.

For various engineering and industrial applications it is desirable to realize mechanical systems with broadly adjustable elasticity to respond flexibly to the external environment. Here we discover a topology-correlated transition between affine and non-affine regimes in elasticity in both two- and three-dimensional packing-derived networks. Based on this transition, we numerically design and experimentally realize multifunctional systems with adjustable elasticity. Within one system, we achieve solid-like affine response, liquid-like non-affine response and a continuous tunability in between. Moreover, the system also exhibits a broadly tunable Poisson's ratio from positive to negative values, which is of practical interest for energy absorption and for fracture-resistant materials. Our study reveals a fundamental connection between elasticity and network topology, and demonstrates its practical potential for designing mechanical systems and metamaterials.

A universal state and its relaxation mechanisms of long-range interacting polygons.

Using polygonal magnetic particles, we conduct experiments to explore the space-filling properties of anisotropic blocks with long-range interactions. In contrast to previous studies, we obtain the surprising finding that our systems' structures do not depend on the shape of building blocks: a single state, the hexagonal plastic crystal, appears as a universal attractor for a wide range of different polygons. This robust particle-shape independency appears as the interactions go beyond nearest neighbors. Particle shape plays an essential role in system relaxation, and determines the basic relaxation dynamics through a microscopic control parameter, internal roughness, produced by particle vertices. Thus our study reveals a new pattern-forming paradigm, in which particle shape plays little role in the static structure but determines the essential relaxation dynamics. Due to the ubiquity of long-range interactions and anisotropic building blocks, our discovery may shed new light on diverse problems involving structure formation, self-assembly, and packing.

Probing the Role of Mobility in the Collective Motion of Nonequilibrium Systems.

By systematically varying the mobility of self-propelled particles in a 2D lattice, we experimentally study the influence of particle mobility on system's collective motion. Our system is intrinsically nonequilibrium due to the lack of energy equipartition. By constructing the covariance matrix of spatial fluctuations and solving for its eigenmodes, we obtain the collective motions of the system with various magnitudes. Interestingly, our structurally ordered nonequilibrium system exhibits properties almost identical to disordered glassy systems under thermal equilibrium: the modes with large overall motions are spatially correlated and quasilocalized while the modes with small collective motions are highly localized, resembling the low- and high-frequency modes in glass. More surprisingly, a peak similar to the boson peak forms in our nonequilibrium system as the number of mobile particles increases, revealing the possible origin of the boson peak from a dynamic aspect. We further illustrate that the spatially correlated large-movement modes can be produced by the cooperation of highly active particles above a threshold fraction, while the localized small-movement modes can be created by adding individual inactive particles. Our study clarifies the role of mobility in collective motions, and further suggests a promising possibility of extending the powerful mode analysis approach to nonequilibrium systems.