Breaking action-reaction with active apolar colloids: emergent transport and velocity inversion.

Artificial active particles are autonomous agents able to convert energy from the environment into net propulsion, breaking detailed balance and the action-reaction law, clear signatures of their out-of-equilibrium nature. Here we investigate the emergence of directed motion in clusters composed of passive and catalytically active apolar colloids. We use a light-induced chemophoretic flow to rapidly assemble hybrid self-propelling clusters composed of hematite particles and passive silica spheres. By increasing the size of the passive cargo, we observe a reversal in the transport direction of the pair. We explain this complex yet rich phenomenon using a theoretical model which accounts for the generated chemical field and its coupling with the surrounding medium. We exploit further our technique to build up more complex, chemically driven, architectures capable of carrying several passive or active species, that quickly assemble and disassemble under light control.

Rectification and confinement of photokinetic bacteria in an optical feedback loop.

Active particles can self-propel by exploiting locally available energy resources. When powered by light, these resources can be distributed with high resolution allowing spatio-temporal modulation of motility. Here we show that the random walks of light-driven bacteria are rectified when they swim in a structured light field that is obtained by a simple geometric transformation of a previous system snapshot. The obtained currents achieve an optimal value that we establish by general theoretical arguments. This optical feedback is used to gather and confine bacteria in high-density and high-activity regions that can be dynamically relocated and reconfigured. Moving away from the boundaries of these optically confined states, the density decays to zero in a few tens of micrometers, exhibiting steep exponential tails that suppress cell escape and ensure long-term stability. Our method is general and scalable, providing a versatile tool to produce localized and tunable active baths for microengineering applications and systematic studies of non-equilibrium phenomena in active systems.

Emergent collective colloidal currents generated via exchange dynamics in a broken dimer state.

Controlling the flow of matter down to micrometer-scale confinement is of central importance in material and environmental sciences, with direct applications in nano and microfluidics, drug delivery, and biotechnology. Currents of microparticles are usually generated with external field gradients of different nature (e.g., electric, magnetic, optical, thermal, or chemical ones), which are difficult to control over spatially extended regions and samples. Here, we demonstrate a general strategy to assemble and transport polarizable microparticles in fluid media through combination of confinement and magnetic dipolar interactions. We use a homogeneous magnetic modulation to assemble dispersed particles into rotating dimeric state and frustrated binary lattices, and generate collective currents that arise from a novel, field-synchronized particle exchange process. These dynamic states are similar to cyclotron and skipping orbits in electronic and molecular systems, thus paving the way toward understanding and engineering similar processes at different length scales across condensed matter.

Tunable self-healing of magnetically propelling colloidal carpets.

The process of crystallization is difficult to observe for transported, out-of-equilibrium systems, as the continuous energy injection increases activity and competes with ordering. In emerging fields such as microfluidics and active matter, the formation of long-range order is often frustrated by the presence of hydrodynamics. Here we show that a population of colloidal rollers assembled by magnetic fields into large-scale propelling carpets can form perfect crystalline materials upon suitable balance between magnetism and hydrodynamics. We demonstrate a field-tunable annealing protocol based on a controlled colloidal flow above the carpet that enables complete crystallization after a few seconds of propulsion. The structural transition from a disordered to a crystalline carpet phase is captured via spatial and temporal correlation functions. Our findings unveil a novel pathway to magnetically anneal clusters of propelling particles, bridging driven systems with crystallization and freezing in material science.

Leap-frog transport of magnetically driven anisotropic colloidal rotors.

In this article, we combine experiments and theory to investigate the transport properties of anisotropic hematite colloidal rotors that dynamically assemble into translating clusters upon application of a rotating magnetic field. The applied field exerts a torque to the particles forcing rotation close to a surface and thus a net translational motion at a frequency tunable speed. When approaching, pairs of particles are observed to assemble into stable three-dimensional clusters that perform a periodic leap-frog type dynamics and propel at a faster speed. We analyze the cluster formation and its lifetime and investigate the role of particle shape in the propulsion speed and stability. We show that the dynamics of the system results from a delicate balance between magnetic dipolar interactions and hydrodynamics, and we introduce a theoretical model that qualitatively explains the observed phenomena.

Edge transport at the boundary between topologically equivalent lattices.

Edge currents of paramagnetic colloidal particles propagate at the edge between two topologically equivalent magnetic lattices of different lattice constant when the system is driven with periodic modulation loops of an external magnetic field. The number of topologically protected particle edge transport modes is not determined by a bulk-boundary correspondence. Instead, we find a rich variety of edge transport modes that depend on the symmetry of both the edge and the modulation loop. The edge transport can be ratchet-like or adiabatic, time or non-time reversal symmetric. The topological nature of the edge transport is classified by a set of winding numbers around bulk fence points extended by winding numbers around edge specific bifurcation points that cannot be deduced from the two bulk lattices.

Active apolar doping determines routes to colloidal clusters and gels.

Collections of interacting active particles, self-propelling or not, have shown remarkable phenomena including the emergence of dynamic patterns across different length scales, from animal groups to vibrated grains, microtubules, bacteria, and chemical- or field-driven colloids. Burgeoning experimental and simulation activities are now exploring the possibility of realizing solid and stable structures from passive elements that are assembled by a few active dopants. Here we show that such an elusive task may be accomplished by using a small amount of apolar dopants, namely synthetic active but not self-propelling units. We use blue light to rapidly assemble 2D colloidal clusters and gels via nonequilibrium diffusiophoresis, where microscopic hematite dockers form long-living interstitial bonds that strongly glue passive silica microspheres. By varying the relative fraction of doping, we uncover a rich phase diagram including ordered and disordered clusters, space-filling gels, and bicontinuous structures formed by filamentary dockers percolating through a solid network of silica spheres. We characterize the slow relaxation and dynamic arrest of the different phases via correlation and scattering functions. Our findings provide a pathway toward the rapid engineering of mesoscopic gels and clusters via active colloidal doping.

Assembly and Transport of Microscopic Cargos via Reconfigurable Photoactivated Magnetic Microdockers.

The realization of micromotors able to dock and transport microscopic objects in a fluid medium has direct applications toward the delivery of drugs and chemicals in small channels and pores, and the realization of functional wireless microrobots in lab-on-a-chip technology. A simple and general method to tow microscopic particles in water by using remotely controllable light-activated hematite microdockers is demonstrated. These anisotropic ferromagnetic particles can be synthesized in bulk and present the remarkable ability to be activated by light while independently manipulated via external fields. The photoactivation process induces a phoretic flow capable to attract cargos toward the surface of the propellers, while a rotating magnetic field is used to transport the composite particles to any location of the experimental platform. The method allows the assembling of small colloidal clusters of various sizes, composed by a skeleton of mobile magnetic dockers, which cooperatively keep, transport, and release the microscopic cargos. The possibility to easily reconfigure in situ the location of the docker above the cargo is demonstrated, which enables optimize transport and cargo release operations.

Orientational dynamics of fluctuating dipolar particles assembled in a mesoscopic colloidal ribbon.

We combine experiments and theory to investigate the dynamics and orientational fluctuations of ferromagnetic microellipsoids that form a ribbonlike structure due to attractive dipolar forces. When assembled in the ribbon, the ellipsoids display orientational thermal fluctuations with an amplitude that can be controlled via application of an in-plane magnetic field. We use video microscopy to investigate the orientational dynamics in real time and space. Theoretical arguments are used to derive an analytical expression that describes how the distribution of the different angular configurations depends on the strength of the applied field. The experimental data are in good agreement with the developed model for all the range of field parameters explored. Understanding the role of fluctuations in chains composed of dipolar particles is important not only from a fundamental point of view, but it may also help understanding the stability of such structures against thermal noise, which is relevant in microfluidics and laboratory-on-a-chip applications.

Bidirectional particle transport and size selective sorting of Brownian particles in a flashing spatially periodic energy landscape.

We demonstrate a size sensitive experimental scheme which enables bidirectional transport and fractionation of paramagnetic colloids in a fluid medium. It is shown that two types of magnetic colloidal particles with different sizes can be simultaneously transported in opposite directions, when deposited above a stripe-patterned ferrite garnet film subjected to a square-wave magnetic modulation. Due to their different sizes, the particles are located at distinct elevations above the surface, and they experience two different energy landscapes, generated by the modulated magnetic substrate. By combining theoretical arguments and numerical simulations, we reveal such energy landscapes, which fully explain the bidirectional transport mechanism. The proposed technique does not require pre-imposed channel geometries such as in conventional microfluidics or lab-on-a-chip systems, and permits remote control over the particle motion, speed and trajectory, by using relatively low intense magnetic fields.