No Arabic abstract
Additive manufacturing strives to combine any combination of materials into three dimensional functional structures and devices, ultimately opening up the possibility of 3D printed machines. It remains difficult to actuate such devices, thus limiting the scope of 3D printed machines to passive devices or necessitating the incorporation of external actuators that are manufactured differently. Here we explore 3D printed hybrid thermoplast/conducter bilayers, that can be actuated by differential heating caused by externally controllable currents flowing through their conducting faces. We uncover the functionality of such actuators and show that they allow to 3D print, in one pass, simple flexible robotic structures that propel forward under step-wise applied voltages. Moreover, exploiting the thermoplasticity of the non-conducting plastic parts at elevated temperatures, we show how strong driving leads to irreversible deformations - a form of 4D printing - which also enlarges the range of linear response of the actuators. Finally, we show how to leverage such thermoplastic relaxations to accumulate plastic deformations and obtain very large deformations by alternatively driving both layers of a bilayer; we call this ratcheting. Our strategy is scalable and widely applicable, and opens up a new approach to reversible actuation and irreversible 4D printing of arbitrary structures and machines.
Optical metasurfaces have been heralded as the platform to integrate multiple functionalities in a compact form-factor, potentially replacing bulky components. A central stepping stone towards realizing this promise is the demonstration of multifunctionality under several constraints (e.g. at multiple incident wavelengths and/or angles) in a single device -- an achievement being hampered by design limitations inherent to single-layer planar geometries. Here, we propose a general framework for the inverse design of volumetric 3D metaoptics via topology optimization, showing that even few-wavelength thick devices can achieve high-efficiency multifunctionality. We embody our framework in multiple closely-spaced patterned layers of a low-index polymer. We experimentally demonstrate our approach with an inverse-designed 3d-printed light concentrator working at five different non-paraxial angles of incidence. Our framework paves the way towards realizing multifunctional ultra-compact 3D nanophotonic devices.
Ultrashort photoemitted electron bunches can provide high electron currents within sub-picosecond timeframes, enabling time-resolved investigations of ultrafast physical processes with nanoscale resolution. Non-resonant conductive nanotips are typically employed to realize nanoscale photoelectron sources with high brightness. However, such emitters require complex non-scalable fabrication procedures featuring poor reproducibility. Planar resonant antennas fabricated via photolithography have been recently investigated, also because of their superior field enhancement properties. Nevertheless, the electron emission from these structures is parallel to the substrate plane, which limits their practical use as electron sources. In this work, we present an innovative out-of-plane, resonant nanoantenna design for field-driven photoemission enabled by high-resolution 3D printing. Numerical and experimental evidences demonstrate that gold-coated, terahertz resonant nanocones provide large local electric fields at their apex, automatically ensuring out-of-plane coherent electron emission and acceleration. We show that the resonant structures can be conveniently arranged in an array form, for a further significant electron extraction enhancement via a collective terahertz response. Remarkably, such collective behaviour can also be harvested to boost photoemission from an individual nano-source. Our approach opens the path for a new generation of photocathodes that can be reproducibly fabricated and designed at will, significantly relaxing the requirement for intense terahertz drivers.
Numerical simulations of assemblies of grains under cyclic loading exhibit ``granular ratcheting: a small net deformation occurs with each cycle, leading to a linear accumulation of deformation with cycle number. We show that this is due to a curious property of the most frequently used models of the particle-particle interaction: namely, that the potential energy stored in contacts is path-dependent. There exist closed paths that change the stored energy, even if the particles remain in contact and do not slide. An alternative method for calculating the tangential force removes granular ratcheting.
To enable robust rheological measurements of the properties of yield stress fluids, we introduce a class of modified vane fixtures with fractal-like cross-sectional structures. A greater number of outer contact edges leads to increased kinematic homogeneity at the point of yielding and beyond. The vanes are 3D printed using a desktop stereolithography machine, making them inexpensive (disposable), chemically-compatible with a wide range of solvents, and readily adaptable as a base for further design innovations. To complete the tooling set, we introduce a textured 3D printed cup, which attaches to a standard rheometer base. We discuss general design criteria for 3D printed rheometer vanes, including consideration of sample volume displaced by the vanes, stress homogeneity, and secondary flows that constrain the parameter space of potential designs. We also develop a conversion from machine torque to material shear stress for vanes with an arbitrary number of arms. We compare a family of vane designs by measuring the viscosity of Newtonian calibration oils with error <5% relative to reference measurements made with a cone-and-plate geometry. We measure the flow curve of a simple Carbopol yield stress fluid, and show that a 24-arm 3D printed fractal vane agrees within 1% of reference measurements made with a roughened cone-and-plate geometry. Last, we demonstrate use of the 24-arm fractal vane to probe the thixo-elasto-visco-plastic (TEVP) response of a Carbopol-based hair gel, a jammed emulsion (mayonnaise), and a strongly alkaline carbon black-based battery slurry.
We demonstrate and characterize a source of Li atoms made from direct metal laser sintered titanium. The sources outgassing rate is measured to be $5 ,(2)cdot 10^{-7}$,$rm{Pa}~ rm{L}~ rm{s}^{-1}$ at a temperature $T=330,^circ$C, which optimizes the number of atoms loaded into a magneto-optical trap. The source loads $approx 10^7$ $^7$Li atoms in the trap in $approx 1$,s. The loaded source weighs 700,mg and is suitable for a number of deployable sensors based on cold atoms.