Nuno A. M. Araújo – Soft Matter Lab

Environmental Memory Boosts Group Formation of Clueless Individuals published in Nature Communications

Non-monotonic size dependence of group formation on environmental crowding. *(Excerpt from Fig. 2 of the manuscript.)*

Environmental Memory Boosts Group Formation of Clueless Individuals
Cristóvão S. Dias, Manish Trivedi, Giovanni Volpe, Nuno A. M. Araújo, Giorgio Volpe
Nature Communications, 14, 7324 (2023)
doi: 10.1038/s41467-023-43099-0
arXiv: 2306.00516

The formation of groups of interacting individuals improves performance and fitness in many decentralised systems, from micro-organisms to social insects, from robotic swarms to artificial intelligence algorithms. Often, group formation and high-level coordination in these systems emerge from individuals with limited information-processing capabilities implementing low-level rules of communication to signal to each other. Here, we show that, even in a community of clueless individuals incapable of processing information and communicating, a dynamic environment can coordinate group formation by transiently storing memory of the earlier passage of individuals. Our results identify a new mechanism of indirect coordination via shared memory that is primarily promoted and reinforced by dynamic environmental factors, thus overshadowing the need for any form of explicit signalling between individuals. We expect this pathway to group formation to be relevant for understanding and controlling self-organisation and collective decision making in both living and artificial active matter in real-life environments.

Ordering of Binary Colloidal Crystals by Random Potentials published on Soft Matter

Ordering of Binary Colloidal Crystals by Random Potentials
André S. Nunes, Sabareesh K. P. Velu, Iryna Kasianiuk, Denys Kasyanyuk, Agnese Callegari, Giorgio Volpe, Margarida M. Telo da Gama, Giovanni Volpe & Nuno A. M. Araújo
Soft Matter 16, 4267-4273 (2020)
doi: https://doi.org/10.1039/D0SM00208A
arXiv: 1903.01579

Structural defects are ubiquitous in condensed matter, and not always a nuisance. For example, they underlie phenomena such as Anderson localization and hyperuniformity, and they are now being exploited to engineer novel materials. Here, we show experimentally that the density of structural defects in a 2D binary colloidal crystal can be engineered with a random potential. We generate the random potential using an optical speckle pattern, whose induced forces act strongly on one species of particles (strong particles) and weakly on the other (weak particles). Thus, the strong particles are more attracted to the randomly distributed local minima of the optical potential, leaving a trail of defects in the crystalline structure of the colloidal crystal. While, as expected, the crystalline ordering initially decreases with an increasing fraction of strong particles, the crystalline order is surprisingly recovered for sufficiently large fractions. We confirm our experimental results with particle-based simulations, which permit us to elucidate how this non-monotonic behavior results from the competition between the particle-potential and particle-particle interactions.

Ordering of binary colloidal crystals by random potentials on ArXiv

Ordering of binary colloidal crystals by random potentials
André S. Nunes, Sabareesh K. P. Velu, Iryna Kasianiuk, Denys Kasyanyuk, Agnese Callegari, Giorgio Volpe, Margarida M. Telo da Gama, Giovanni Volpe & Nuno A. M. Araújo
arXiv: 1903.01579

Structural defects are ubiquitous in condensed matter, and not always a nuisance. For example, they underlie phenomena such as Anderson localization and hyperuniformity, and they are now being exploited to engineer novel materials. Here, we show experimentally that the density of structural defects in a 2D binary colloidal crystal can be engineered with a random potential. We generate the random potential using an optical speckle pattern, whose induced forces act strongly on one species of particles (strong particles) and weakly on the other (weak particles). Thus, the strong particles are more attracted to the randomly distributed local minima of the optical potential, leaving a trail of defects in the crystalline structure of the colloidal crystal. While, as expected, the crystalline ordering initially decreases with increasing fraction of strong particles, the crystalline order is surprisingly recovered for sufficiently large fractions. We confirm our experimental results with particle-based simulations, which permit us to elucidate how this non-monotonic behavior results from the competition between the particle-potential and particle-particle interactions.