scholarly journals Chains of cubic colloids at fluid–fluid interfaces

Soft Matter ◽  
2021 ◽  
Author(s):  
Carmine Anzivino ◽  
Giuseppe Soligno ◽  
René van Roij ◽  
Marjolein Dijkstra

Inspired by recent experimental observations of spontaneous chain formation of cubic particles adsorbed at a fluid–fluid interface, we theoretically investigate whether capillary interactions can be responsible for this self-assembly process.

Author(s):  
M. Janjua ◽  
S. Nudurupati ◽  
I. Fischer ◽  
P. Singh ◽  
N. Aubry

It was recently shown by us that spherical particles floating on a fluid-fluid interface can be self-assembled, and the lattice between them can be controlled, using an electric field. In this paper we show that the technique can also be used to self assemble rod-like particles on fluid-fluid interfaces. The method consists of sprinkling particles at a liquid interface and applying an electric field normal to the interface, thus resulting in a combination of hydrodynamic (capillary) and electrostatic forces acting on the particles. A rod floating on the fluid interface experiences both a lateral force and a torque normal to the interface due to capillarity, and in the presence of an electric field, it is also subjected to an electric force and torque. The electric force affects the rods’ approach velocity and the torque aligns the rods parallel to each other. In the absence of an electric field, two rods that are initially more than one rod length away from each other come in contact so that they are either perpendicular or parallel to the line joining their centers, depending on their initial orientations. In the latter case, their ends are touching. Our experiments show that in an electric field of sufficiently large strength, only the latter arrangement is stable. Experiments also show that in this case the electric field causes the rods of the monolayer to align parallel to one another and that the lattice spacing of a self-assembled monolayer of rods increases.


Soft Matter ◽  
2019 ◽  
Vol 15 (12) ◽  
pp. 2638-2647 ◽  
Author(s):  
Carmine Anzivino ◽  
Fuqiang Chang ◽  
Giuseppe Soligno ◽  
René van Roij ◽  
Willem K. Kegel ◽  
...  

We numerically investigate the adsorption of a variety of Janus particles (dumbbells, elongated dumbbells and spherocylinders) at a fluid–fluid interface by using a numerical method that takes into account the interfacial deformations. We also experimentally synthesize micrometer–sized charged Janus dumbbells and let them adsorb at a water–decane interface. We find a good agreement between numerical and experimental results.


Soft Matter ◽  
2018 ◽  
Vol 14 (1) ◽  
pp. 42-60 ◽  
Author(s):  
Giuseppe Soligno ◽  
Marjolein Dijkstra ◽  
René van Roij

Colloidal particles adsorbed at fluid–fluid interfaces can self-assemble, thanks to capillary interactions, into 2D ordered structures.


Author(s):  
N. Aubry ◽  
S. Nudurupati ◽  
M. Janjua ◽  
P. Singh

It was recently shown in [1–3] that spherical particles floating on a fluid-fluid interface can be self-assembled, and the lattice between them can be controlled, using an electric field. The technique works for a broad range of fluids and particles, including electrically neutral (i.e., uncharged) particles and small particles (micro- and nano-sized particles). In this paper we show that the technique also works for rod-like and cubical particles floating on fluid-fluid interfaces. The method consists of sprinkling particles at a liquid interface and applying an electric field normal to the interface, thus resulting in a combination of hydrodynamic (capillary) and electrostatic forces acting on the particles. It is shown that the relative orientation of two rod-like particles can be controlled by applying an electric field normal to the interface. The lattice spacing of the self-assembled monolayer of rods can be increased by increasing the electric field strength. Furthermore, experiments show that there is a tendency for the rods to align so that they are parallel to each other. The alignment however is not complete. Similarly, the spacing between two cubes, as well as the spacing of a monolayer of cubes, can be adjusted by controlling the electric field strength.


Soft Matter ◽  
2015 ◽  
Vol 11 (40) ◽  
pp. 7969-7976 ◽  
Author(s):  
Gary B. Davies ◽  
Lorenzo Botto

Capillary interactions have emerged as a tool for the directed self-assembly of particles adsorbed at fluid interfaces. Recent observations of anisotropic particle monolayers interacting via induced dipolar capillary interactions showed very interesting phenomenology. Our investigations explain many of the observed monolayer properties.


Author(s):  
Krishna Sailaja A ◽  
Amareshwar P

In order to see the functionality and toxicity of nanoparticles in various food and drug applications, it is important to establish procedures to prepare nanoparticles of a controlled size. Desolvation is a thermodynamically driven self-assembly process for polymeric materials. In this study, we prepared BSA nanoparticles using the desolvation technique using acetone as desolvating agent. Acetone was added intermittently into 1% BSA solution at different pH under stirring at 700 rpm. Amount of acetone added, intermittent timeline of acetone addition, and pH of solution were considered as process parameters to be optimized. The effect of the process parameters on size of the nanoparticles was studied. The results indicated that the size control of BSA nanoparticles was achieved by adding acetone intermittently. The standard deviation of average size of BSA nanoparticles at each preparation condition was minimized by adding acetone intermittently. The intermittent addition in polymeric aqueous solution can be useful for size control for food or drug applications.  


Materials ◽  
2021 ◽  
Vol 14 (15) ◽  
pp. 4239
Author(s):  
Pezhman Mohammadi ◽  
Fabian Zemke ◽  
Wolfgang Wagermaier ◽  
Markus B. Linder

Macromolecular assembly into complex morphologies and architectural shapes is an area of fundamental research and technological innovation. In this work, we investigate the self-assembly process of recombinantly produced protein inspired by spider silk (spidroin). To elucidate the first steps of the assembly process, we examined highly concentrated and viscous pendant droplets of this protein in air. We show how the protein self-assembles and crystallizes at the water–air interface into a relatively thick and highly elastic skin. Using time-resolved in situ synchrotron X-ray scattering measurements during the drying process, we showed that the skin evolved to contain a high β-sheet amount over time. We also found that β-sheet formation strongly depended on protein concentration and relative humidity. These had a strong influence not only on the amount, but also on the ordering of these structures during the β-sheet formation process. We also showed how the skin around pendant droplets can serve as a reservoir for attaining liquid–liquid phase separation and coacervation from the dilute protein solution. Essentially, this study shows a new assembly route which could be optimized for the synthesis of new materials from a dilute protein solution and determine the properties of the final products.


Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3598
Author(s):  
Nirmal K. Shee ◽  
Hee-Joon Kim

A series of porphyrin triads (1–6), based on the reaction of trans-dihydroxo-[5,15-bis(3-pyridyl)-10,20-bis(phenyl)porphyrinato]tin(IV) (SnP) with six different phenoxy Zn(II)-porphyrins (ZnLn), was synthesized. The cooperative metal–ligand coordination of 3-pyridyl nitrogens in the SnP with the phenoxy Zn(II)-porphyrins, followed by the self-assembly process, leads to the formation of nanostructures. The red-shifts and remarkable broadening of the absorption bands in the UV–vis spectra for the triads in CHCl3 indicate that nanoaggregates may be produced in the self-assembly process of these triads. The emission intensities of the triads were also significantly reduced due to the aggregation. Microscopic analyses of the nanostructures of the triads reveal differences due to the different substituents on the axial Zn(II)-porphyrin moieties. All these nanomaterials exhibited efficient photocatalytic performances in the degradation of rhodamine B (RhB) dye under visible light irradiation, and the degradation efficiencies of RhB in aqueous solution were observed to be 72~95% within 4 h. In addition, the efficiency of the catalyst was not impaired, showing excellent recyclability even after being applied for the degradation of RhB in up to five cycles.


Nanomaterials ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 1686
Author(s):  
Ruohong Sui ◽  
Paul A. Charpentier ◽  
Robert A. Marriott

In the past two decades, we have learned a great deal about self-assembly of dendritic metal oxide structures, partially inspired by the nanostructures mimicking the aesthetic hierarchical structures of ferns and corals. The self-assembly process involves either anisotropic polycondensation or molecular recognition mechanisms. The major driving force for research in this field is due to the wide variety of applications in addition to the unique structures and properties of these dendritic nanostructures. Our purpose of this minireview is twofold: (1) to showcase what we have learned so far about how the self-assembly process occurs; and (2) to encourage people to use this type of material for drug delivery, renewable energy conversion and storage, biomaterials, and electronic noses.


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