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A methodology of 3D self-assembly is presented, pairing neighboring electromechanical system (MEMS) elements to create Yin or Yang-shaped structures. After sacrificial layer removal and during the sequential drying process, (i) surface tension forces bring the neighboring MEMS shutter blades very close to each other, and (ii) Casimir forces and van der Waals forces keep the blades attached tightly. Various experimental trials to reopen the tight attachments are reported. The relative significance of fundamental forces during 1D and 3D scaling of the system is presented. [ABSTRACT FROM AUTHOR]

Cloaking is a method of making obstacles undetectable. Here we cloak unit cells of a magnetic pattern squeezed into an otherwise periodic pattern from a magnetically driven colloidal flow. We apply a time-periodic external magnetic field loop to an ensemble of paramagnetic colloidal particles on the deformed periodic magnetic pattern. There exist topological loops where the particles avoid to trespass the cloaked regions by robustly traveling around the cloak. Afterwards the ensemble of particles continues with a motion identical to the motion as if the distorted region were nonexistent and the ensemble would have trespassed the undeformed region. We construct the cloak by continuously squeezing new conformally mapped unit cells between those of the originally undeformed and periodic pattern. We find a cloaking/decloaking transition as a function of the size and shape of the newly squeezed-in region. A cloak is scalable to arbitrary size if the biholomorphic map from the undistorted periodic lattice to the region outside the cloak locally rotates by less than an angle of forty five degrees. The work generalizes cloaking from waves toward particles., Competing Interests: Competing interests: The authors declare no competing interests., (© 2025. The Author(s).)

We measure the dynamical behavior of colloidal singlets and dumbbells on an inclined magnetic moiré pattern, subject to a precessing external homogeneous magnetic field. At low external field strength single colloidal particles and dumbbells move everywhere on the pattern: at stronger external field strengths colloidal singlets and dumbbells are localized in generic locations. There are however nongeneric locations of flat channels that cross the moiré Wigner Seitz cell. In the flat channels we find gravitational driven translational and non-translational dynamic phase behavior of the colloidal singlets and dumbbells depending on the external field strength and the precession angle of the external homogeneous magnetic field.

Topological growth control allows to produce a narrow distribution of outgrown colloidal rods with defined and adjustable length. We use an external magnetic field to assemble paramagnetic colloidal spheres into colloidal rods of a chosen length. The rods reside above a metamorphic hexagonal magnetic pattern. The periodic repetition of specific loops of the orientation of an applied external field renders paramagnetic colloidal particles and their assemblies into active bipeds that walk on the pattern. The metamorphic patterns allow the robust and controlled polymerization of single colloids to bipeds of a desired length. The colloids are exposed to this fixed external control loop that causes multiple simultaneous responses: Small bipeds and single colloidal particles interpret the external magnetic loop as an order to walk toward the active zone, where they assemble and polymerize. Outgrown bipeds interpret the same loop as an order to walk away from the active zone. The topological transition occurs solely for the growing biped and nothing is changed in the environment nor in the magnetic control loop. As in many biological systems the decision of a biped that reached its outgrown length to walk away from the reaction site is made internally, not externally., (© 2024. The Author(s).)

Nitrogen-vacancy (NV) color centers in diamond are excellent quantum sensors possessing high sensitivity and nano-scale spatial resolution. Their integration in photonic structures is often desired, since it leads to an increased photon emission and also allows the realization of solid-state quantum technology architectures. Here, we report the fabrication of diamond nano-pillars with diameters up to 1000 nm by electron beam lithography and inductively coupled plasma reactive ion etching in nitrogen-rich diamonds (type Ib) with [100] and [111] crystal orientations. The NV centers were created by keV-He ion bombardment and subsequent annealing, and we estimate an average number of NVs per pillar to be 4300 ± 300 and 520 ± 120 for the [100] and [111] samples, respectively. Lifetime measurements of the NVs' excited state showed two time constants with average values of τ 1 ≈ 2 ns and τ 2 ≈ 8 ns, which are shorter as compared to a single color center in a bulk crystal (τ ≈ 10 ns). This is probably due to a coupling between the NVs as well as due to interaction with bombardment-induced defects and substitutional nitrogen (P1 centers). Optically detected magnetic resonance measurements revealed a contrast of about 5% and average coherence and relaxation times of T 2 [100] = 420 ± 40 ns, T 2 [111] = 560 ± 50 ns, and T 1 [100] = 162 ± 11 μs, T 1 [111] = 174 ± 24 μs. These pillars could find an application for scanning probe magnetic field imaging.