Interaction between dipolar forces, such as permanent magnets, generally leads to the formation of one-dimensional chains and rings. We investigated whether it was possible to let dipoles self-assemble into three-dimensional structures by encapsulating them in a shell with a specific shape. We found that the condition for self-assembly of a three-dimensional crystal is satisfied when the energies of dipoles in the parallel and antiparallel states are equal. Our experiments show that the most regular structures are formed using cylinders and cuboids and not by
spheroids. This simple design rule will help the self-assembly community to realize three-dimensional crystals from objects in the micrometer range, which opens up the way toward previously unknown metamaterials.@en

The extent to which one can use a thermodynamic description of turbulent flow as a source of stochastic kinetic energy for 3D self‐assembly of magnetically interacting macroscopic particles is investigated. It is confirmed that the speed of the objects in the flow field generated in this system obeys the Maxwell–Boltzmann distribution, and their random walk can be defined by a diffusion coefficient following from the Einstein relation. However, it is discovered that the analogy with Brownian dynamics breaks down when considering the directional components of the velocity. For the vectorial components, neither the equipartition theorem nor the Einstein relation is obeyed. Moreover, the kinetic energy estimated from the random walk of individual objects is one order of magnitude higher than the value estimated from Boltzmann statistics on the interaction between two spheres with embedded magnets. These results show that introducing stochastic kinetic energy into a self‐assembly process by means of turbulent flow can to a great extent be described by standard thermodynamic theory, but anisotropies and the specific nature of the interactions need to be taken into account.@en

We present an experimental study of the kinetics of orbitally-shaken, sliding macroscopic particles confined to a two-dimensional space bounded by walls. Discounting the forcing action of the external periodic actuation, the particles undergo a qualitative transition from a ballistic to a diffusive motion regime with time. Despite the deterministic input of kinetic energy provided by the shaker, the particles show translational velocities and diffusivity consistent with a confined random walk model. Such experimental system may therefore represent a suitable macroscopic analog to investigate aspects of molecular dynamics and self-assembly.

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A 3-DoF micro-electromechanical (MEMS) stage has been designed with an innovative integrated feedback system based on thermal sensors. The stage is integrated in the device layer of a silicon-oninsulator-wafer, which means that no assembly is required and the stage can be fabricated using only a single mask. The range of motion is over 160 μm in two directions and 325 mrad of rotation, which exceeds the range of motion of existing MEMS stages by far.@en