Particle-stabilized oscillating diver: a self-assembled responsive capsule

We report the experimental discovery of a self-assembled capsule, with density set by interfacial glass beads and an internal bubble, that automatically performs regular oscillations up and down a vial in response to a temperature gradient. Similar composites featuring interfacial particles and multiple internal compartments could be the solution to a variety of application challenges.Comment: 7 pages, 3 figure

Assembly Modulated by Particle Position and Shape: A New Concept in Self-Assembly

In this communication we outline how the bespoke arrangements and design of micron-sized superparamagnetic shapes provide levers to modulate their assembly under homogeneous magnetic fields. We label this new approach, ‘assembly modulated by particle position and shape’ (APPS). Specifically, using rectangular lattices of superparamagnetic micron-sized cuboids, we construct distinct microstructures by adjusting lattice pitch and angle of array with respect to a magnetic field. Broadly, we find two modes of assembly: (1) immediate 2D jamming of the cuboids as they rotate to align with the applied field (rotation-induced jamming) and (2) aggregation via translation after their full alignment (dipole-dipole assembly). The boundary between these two assembly pathways is independent on field strength being solely a function of the cuboid’s dimensions, lattice pitch, and array angle with respect to field—a relationship which we capture, along with other features of the assembly process, in a ‘phase diagram’. In doing so, we set out initial design rules to build custom made assemblies. Moreover, these assemblies can be made flexible thanks to the hinged contacts of their particle building blocks. This flexibility, combined with the superparamagnetic nature of the architectures, renders our assembly method particularly appropriate for the construction of complex actuators at a scale hitherto not possible

Propulsion of Magnetic Beads Asymmetrically Covered with DNA Origami Appendages

Eukaryotic cells that swim by the beating of nanoscale elastic filaments (flagella) present a promising locomotion paradigm for man-made analogues essential for next-generation in-vivo treatments and for the study of collective phenomena at the low Reynolds number limit. However, artificial analogues have been limited to many microns in size due to the engineering challenges of fabricating actable flexible filaments at the nanoscale-thereby narrowing the application scope. Here, made-to-order nanoscale filaments designed on the molecular level are fabricated using the DNA-origami technique. It is found that magnetic beads anisotropically covered with such bundles move in a ballistic fashion when wagged back and forth under an external magnetic field. Furthermore, by comparing bead dynamics at a range of bundle coverages and driving frequencies, compelling evidence is amassed to suggest that this ballistic motion is imparted by the beating of the DNA origami filaments as synthetic flagella. This proof-of-concept work opens up avenues for further made-for-purpose appendages designed using DNA self-assembly and with it ever more complex locomotion on the nano and microscale

Direct transformation of bijels into bicontinuous composite electrolytes using a pre-mix containing lithium salt

We report a general strategy for making bicontinuous conducting composite materials in a controllable fashion. Our approach begins with a bicontinuous interfacially jammed emulsion gel (bijel) fabricated from a pre-mix containing a salt, here bis(trifluoromethane)sulfonimide lithium salt (LiTFSI). The resulting structure has interpenetrating ionic conducting and non-conducting domains comprised of an ethylene carbonate (EC)-rich phase and a p-xylene (xylene)-rich phase of roughly equal volumes. This is the first time that bijel fabrication has been carried out with the underlying two-fluid phase diagram modified by a salt. Diffusing polystyrene (PS) into the xylene-rich phase enables the facile formation of a PS-filled bijel in place of a multi-step polymerization of added monomers. Drying the bijel results in the selective removal of xylene, reducing the total sample volume without compromising the morphology of the EC domain. Electrochemical impedance spectroscopy of the composite electrolytes confirms the existence of ion conducting pathways

{N,N′-[2,2′-(Ethane-1,2-diyldisulfanediyl)di-o-phenyl­ene]bis­(quinoline-2-carboxamidato)}copper(II)

In the title compound, [Cu(C34H24N4O2S2)] or [Cu(bqdapte)], where H2bqdapte is 1,2-{bis­[2-(quinoline-2-carboxamido)­phen­yl]sulfan­yl}ethane, the CuII ion is coordinated to the dianionic hexa­dentate bqdapte2− ligand by two amide and two quinoline N atoms and two thio­ether S atoms. In the observed conformation of the hexa­dentate ligand, the quinoline rings attain positions related by a twofold axis. The Cu atom displays a Jahn–Teller-distorted octa­hedral CuN4S2 geometry axially compressed along the two trans-configured Cu—Namidate bonds

Constructing 3D crystal templates for photonic band gap materials using holographic optical tweezers

A simple and robust method is presented for the construction of 3-dimensional crystals from silica and polystyrene microspheres. The crystals are suitable for use as templates in the production of three-dimensional photonic band gap (PBG) materials. Manipulation of the microspheres was achieved using a dynamic holographic assembler (DHA) consisting of computer controlled holographic optical tweezers. Attachment of the microspheres was achieved by adjusting their colloidal interactions during assembly. The method is demonstrated by constructing a variety of 3-dimensional crystals using spheres ranging in size from 3 µm down to 800 nm. A major advantage of the technique is that it may be used to build structures that cannot be made using self-assembly. This is illustrated through the construction of crystals in which line defects have been deliberately included, and by building simple cubic structures

Surface Pressure of Liquid Interfaces Laden with Micron-Sized Particles

We consider the surface pressure of a colloid-laden liquid interface. As micron-sized particles of suitable wettability can be irreversibly bound to the liquid interface on experimental timescales, we use the canonical ensemble to derive an expression for the surface pressure of a colloid-laden interface. We use this expression to show that adsorption of particles with only hard-core interactions has a negligible effect on surface pressures from typical Langmuir-trough measurements. Moreover, we show that Langmuir-trough measurements cannot be used to extract typical interparticle potentials. Finally, we argue that the dependence of measured surface pressure on surface fraction can be explained by particle coordination number at low to intermediate particle surface fractions. At high surface fractions, where the particles are jammed and cannot easily rearrange, contact-line sliding and/or deformations of the liquid interface at the length scale of the particles play a pivotal role.Comment: 13 pages, 5 figure

Long-Lived Foams Stabilized by a Hydrophobic Dipeptide Hydrogel

A hydrogel of hydrophobic dipeptides can be used to create a wet foam with long-term stability. The dipeptide molecules self-assemble into fiber-like networks (due to the presence of metal ions) both at air–water interfaces and in the continuous phase. The former creates an interfacial film stabilizing the air bubbles while the latter forms a bulk gel, which prevents bubble movement and retards growth. If the storage modulus (G′) of the bulk hydrogel is sufficiently high it can stop the coarsening of the air bubbles and thus dramatically improve the stability of the foam. Cryogenic scanning electron microscopy and Raman spectra reveals the width of the fibers (200 nm) and that they are held together by hydrogen bonds. In the absence of bubbles, phase separation is observed between a hydrogel and a water-rich phase; in the foam this can be suppressed provided that the concentration of dipeptides and metal ions are sufficiently high. It is speculated that the resistance of the bubble arrangement to compaction and hence further drainage arrests the process of phase separation. This foam system has the advantages of long stability, low cost, as well as easy preparation; therefore, it has potential applications in food manufacturing, drug delivery, and personal care industries