The past two decades have seen a remarkable progress in the development of synthetic colloidal agents which are capable of creating directed motion in an unbiased environment at the microscale. These self-propelling particles are often praised for their enormous potential to self-organize into dynamic nonequilibrium structures such as living clusters, synchronized super-rotor structures or self-propelling molecules featuring a complexity which is rarely found outside of the living world. However, the precise mechanisms underlying the formation and dynamics of many of these structures are still barely understood, which is likely to hinge on the gaps in our understanding of how active colloids interact. In particular, besides showing comparatively short-ranged interactions which are well known from passive colloids (Van der Waals, electrostatic etc), active colloids show novel hydrodynamic interactions as well as phoretic and substrate-mediated ‘osmotic’ cross-interactions which hinge on the action of the phoretic field gradients which are induced by the colloids on other colloids in the system. The present article discusses the complexity and the intriguing properties of these interactions which in general are long-ranged, non-instantaneous, non-pairwise and non-reciprocal and which may serve as key ingredients for the design of future nonequilibrium colloidal materials. Besides providing a brief overview on the state of the art of our understanding of these interactions a key aim of this review is to emphasize open key questions and corresponding open challenges.

Most synthetic microswimmers do not reach the autonomy of their biological counterparts in terms of energy supply and diversity of motions. Here, this work reports the first all‐aqueous droplet swimmer powered by self‐generated polyelectrolyte gradients, which shows memory‐induced chirality while self‐solidifying. An aqueous solution of surface tension–lowering polyelectrolytes self‐solidifies on the surface of acidic water, during which polyelectrolytes are gradually emitted into the surrounding water and induce linear self‐propulsion via spontaneous symmetry breaking. The low diffusion coefficient of the polyelectrolytes leads to long‐lived chemical trails which cause memory effects that drive a transition from linear to chiral motion without requiring any imposed symmetry breaking. The droplet swimmer is capable of highly efficient removal (up to 85%) of uranium from aqueous solutions within 90 min, benefiting from self‐propulsion and flow‐induced mixing. These results provide a route to fueling self‐propelled agents which can autonomously perform chiral motion and collect toxins.

We provide a generic scheme to separate the particles of a mixture by their physical properties like mass, friction, or size. The scheme employs a periodically shaken two-dimensional dissipative lattice and hinges on a simultaneous transport of particles in species-specific directions. This selective transport is achieved by controlling the late-time nonlinear particle dynamics, via the attractors embedded in the phase space and their bifurcations. To illustrate the spectrum of possible applications of the scheme, we exemplarily demonstrate the separation of polydisperse colloids and mixtures of cold thermal alkali atoms in optical lattices.

We show that the direction of directed particle transport in a two-dimensional ac-driven lattice can be dynamically reversed by changing the structure of the lattice in the direction perpendicular to the applied driving force. These structural changes introduce dimensional coupling effects, the strength of which governs the timescale of the current reversals. The underlying mechanism is based on the fact that dimensional coupling allows the particles to explore regions of phase space which are inaccessible otherwise. The experimental realization for cold atoms in ac-driven optical lattices is discussed.

We provide a generic scheme offering real-time control of directed particle transport using superimposed driven lattices. This scheme allows one to accelerate, slow, and freeze the transport on demand by switching one of the lattices subsequently on and off. The underlying physical mechanism hinges on a systematic opening and closing of channels between transporting and nontransporting phase space structures upon switching and exploits cantori structures which generate memory effects in the population of these structures. Our results should allow for real-time control of cold thermal atomic ensembles in optical lattices but might also be useful as a design principle for targeted delivery of molecules or colloids in optical devices.