Adsorption and assembly of colloidal particles at the surface of liquid droplets are at the base of particle-stabilized emulsions and templating. Here we report that electrohydrodynamic and electro-rheological effects in leaky-dielectric liquid drops can be used to structure and dynamically control colloidal particle assemblies at drop surfaces, including electric-field-assisted convective assembly of jammed colloidal 'ribbons', electro-rheological colloidal chains confined to a two-dimensional surface and spinning colloidal domains on that surface. In addition, we demonstrate the size control of 'pupil'-like openings in colloidal shells. We anticipate that electric field manipulation of colloids in leaky dielectrics can lead to new routes of colloidosome assembly and design for 'smart armoured' droplets.

Cetyltrimethylammonium bromide (CTAB) modified synthetic laponite is synthesized by an ion exchange method and characterized by simultaneous small-angle X-ray scattering (SAXS) and wide angle X-ray scattering (WAXS), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), energy dispersive spectrometry (EDS), atomic force microscopy (AFM), thermal analysis and rheometry. Through the formation of the organoclay, the properties of clay change from hydrophilic to hydrophobic. Morphology results show that the hydrophilic particles are aggregating easily, whereas the suitable CTAB modified laponite can get near monodispersed nanoparticles due to its hydrophobic properties. It is proposed that CTAB is intercalated and adsorbed onto the laponite partially depending on the substituted concentration of the surfactant cation exchange capacity (CEC) (0.5CEC to 6CEC). The electrorheological (ER) effect is investigated for suspensions of CTAB modified laponite dispersed in silicone oil. The two-dimensional SAXS images from ER bundles of CTAB modified laponite exhibit markedly anisotropic SAXS patterns, giving a measure for laponite particle alignment within the ER structure. An optimum electrorheological effect can be attained at a particular CEC substituted concentration. On the basis of the structure analysis and dielectric measurements, we attribute the enhancement of ER activity to the improvement in the dielectric properties that showed an increase in the dielectric constant and the dielectric loss at low frequency and their regular optimum change with CTAB modification.

We describe a rapid environmentally friendly wet-chemical approach to synthesize extremely stable non-toxic, biocompatible, water-soluble monodispersed gold nanoparticles (AuNPs) in one step at room temperature. The particles have been successfully achieved in just a few minutes by merely adding sodium hydroxide (NaOH) acting as an initiator for the reduction of HAuCl₄ in aqueous solution in the presence of polyvinylpyrrolidone (PVP) without the use of any reducing agent. It is also proved to be highly efficient for the preparation of AuNPs with controllable sizes. The AuNPs show remarkable stability in water media with high concentrations of salt, various buffer solutions and physiological conditions in biotechnology and biomedicine. Moreover, the AuNPs are also non-toxic at high concentration (100 µM). Therefore, it provides great opportunities to use these AuNPs for biotechnology and biomedicine. This new approach also involved several green chemistry concepts, such as the selection of environmentally benign reagents and solvents, without energy consumption, and less reaction time.

A good material for CO₂ capture should possess some specific properties: (i) a large effective surface area with good adsorption capacity, (ii) selectivity for CO₂, (iii) regeneration capacity with minimum energy input, allowing reutilization of the material for CO₂ adsorption and (iv) low cost and high environmental friendliness. Smectite clays are layered nanoporous materials that may be good candidates in this context. Here we report experiments which show that gaseous CO₂ intercalates into the interlayer nano-space of smectite clay (synthetic fluorohectorite) at conditions close to ambient. The rate of intercalation, as well as the retention ability of CO₂ was found to be strongly dependent on the type of the interlayer cation, which in the present case is Li⁺, Na⁺ or Ni²⁺. Interestingly, we observe that the smectite Li-fluorohectorite is able to retain CO₂ up to a temperature of 35°C at ambient pressure and that the captured CO₂ can be released by heating above this temperature. Our estimates indicate that smectite clays, even with the standard cations analyzed here, can capture an amount of CO₂ comparable to other materials studied in this context.

Janus and patchy particles have designed heterogeneous surfaces that consist of two or several patches with different materials properties. These particles are emerging as building blocks for a new class of soft matter and functional materials. Here we introduce a route for forming heterogeneous capsules by producing highly ordered jammed colloidal shells of various shapes with domains of controlled size and composition. These structures combine the functionalities offered by Janus or patchy particles, and those given by permeable shells such as colloidosomes. The simple assembly route involves the synergetic action of electro-hydrodynamic flow and electro-coalescence. We demonstrate that the method is robust and straightforwardly extendable to production of multi-patchy capsules. This forms a starting point for producing patchy colloidosomes with domains of anisotropic chemical surface properties, permeability or mixed liquid-solid phase domains, which could be exploited to produce functional emulsions, light and hollow supra-colloidosome structures, or scaffolds.

Droplets covered by adsorbed particles are used in a wide range of research studies and applications, including stabilising emulsions used in the food or cosmetic industries, and fabricating new materials, such as microcapsules or multi-cavity structures. Pickering emulsions are commonly prepared by bulk emulsification techniques, for instance, by ultrasonic homogenisation or mechanical stirring, by membrane emulsification, or with the use of microfluidics. The latter two methods typically allow for more precise control of the droplet size distribution, whereas the bulk techniques guarantee high throughput. Here we propose a new bulk approach to fabricating Pickering emulsions by utilising electric fields. We prepare oil-in-oil emulsions stabilised by microparticles and control the mean size of the Pickering droplets. In our approach we take advantage of total surface area reduction of emulsion droplets by electrocoalescence. This leads to an increase in particle coverage, and eventually to formation of densely packed particle shells on Pickering droplets. First, we prepare an unstable pre-emulsion with droplets having small sizes and low particle coverages, from which the final Pickering emulsion is formed via consecutive coalescence events speeded up by application of electric fields. We monitor the development of the emulsions with optical microscopy imaging. The results demonstrate that the utilisation of electric fields goes beyond the mere role of enhancing coalescence; it plays an important role in surface particle manipulation and droplet rotation that further promote formation of stable particle-covered drops.