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Register a new userSelf-Assembly of Nanoparticles from Evaporating Sessile Droplets: Fresh Look into the Role of Particle/Substrate Interaction
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We studied the dependence of solid deposit shape obtained by free drying of sessile drops on the particles concentration and Derjaguin-Landau-Verwey-Overbeek (DLVO) particle/substrate interaction. In contrast to previous contributions using pH as a control parameter of interactions, we investigated an unprecedentedly wide range of concentrations and particle/substrate DLVO forces by modifying the nature of the substrate and particles as well as their size and surface chemistry whereas long-distance repulsive interactions between particles were maintained for most of the drying time. Our main result is that the different shapes of deposits obtained by modifying the particle concentration are the same in the different regimes of concentration regardless of particle/substrate interaction in the studied range of DLVO forces and particle concentrations. The second result is that, contrary to expectations, the dominant morphology of dry patterns at low particle concentration always shows a dot-like pattern for all the studied systems.
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Building structures with hierarchical order through the self-assembly of smaller blocks is not only a prerogative of nature, but also a strategy to design artificial materials with tailored functions. We explore in simulation the spontaneous assembly of colloidal particles into extended structures, using spheres and size-asymmetric dimers as solute particles, while treating the solvent implicitly. Besides rigid cores for all particles, we assume an effective short-range attraction between spheres and small monomers to promote, through elementary rules, dimer-mediated aggregation of spheres. Starting from a completely disordered configuration, we follow the evolution of the system at low temperature and density, as a function of the relative concentration of the two species. When spheres and large monomers are of same size, we observe the onset of elongated aggregates of spheres, either disconnected or cross-linked, and a crystalline bilayer. As spheres grow bigger, the self-assembling scenario changes, getting richer overall, with the addition of flexible membrane sheets with crystalline order and monolayer vesicles. With this wide assortment of structures, our model can serve as a viable template to achieve a better control of self-assembly in dilute suspensions of microsized particles.
The elastic scattering between dark matter particles and radiation represents an attractive possibility to solve a number of discrepancies between observations and standard cold dark matter predictions, as the induced collisional damping would imply a suppression of small-scale structures. We consider this scenario and confront it with measurements of the ionization history of the Universe at several redshifts and with recent estimates of the counts of Milky Way satellite galaxies. We derive a conservative upper bound on the dark matter-photon elastic scattering cross section of $sigma_{gamma rm{DM}} < 8 times 10^{-10} , sigma_T , left(m_{rm DM}/{rm GeV}right)$ at $95%$~CL, about one order of magnitude tighter than previous {constraints from satellite number counts}. Due to the strong degeneracies with astrophysical parameters, the bound on the dark matter-photon scattering cross section derived here is driven by the estimate of the number of Milky Way satellite galaxies. Finally, we also argue that future 21~cm probes could help in disentangling among possible non-cold dark matter candidates, such as interacting and warm dark matter scenarios. Let us emphasize that bounds of similar magnitude to the ones obtained here could be also derived for models with dark matter-neutrino interactions and would be as constraining as the tightest limits on such scenarios.
We report on self-assembled iron oxide nanoparticle films on silicon substrates. In addition to homogeneously assembled layers, we fabricated patterned trenches of 40-1000 nm width using electron beam lithography for the investigation of assisted self-assembly. The nanoparticles with a diameter of 20 nm +/- 7% were synthesized by thermal decomposition of iron oleate complexes in trioctylamine in presence of oleic acid. Samples with different track widths and nanoparticle concentration were characterized by scanning electron microscopy and by superconducting quantum interference device magnetometry.
This article explores the governing role of the internal hydrodynamics and advective transport within sessile colloidal droplets on the self assembly of nanostructures to form floral patterns. Water acetone binary fluid and Bi2O3 nanoflakes based complex fluids are experimented with. Microliter sessile droplets are allowed to vaporize and the dry out patterns are examined using scanning electron microscopy. The presence of distributed self assembled rose like structures is observed. The population density, structure and shape of the floral structures are noted to be dependent on the binary fluid composition and nanomaterial concentration. Detailed microscopic particle image velocimetry analysis is undertaken to qualitatively and quantitatively describe the solutal Marangoni advection within the evaporating droplets. It has been shown that the kinetics, regime and location of the internal advection are responsible factors towards the hydrodynamics influenced clustering, aggregation and self-assembly of the nanoflakes. In addition, the size of the nanostructures and the complex fluids.
When two sessile drops of the same liquid touch, they merge into one drop, driven by capillarity. However, the coalescence can be delayed, or even completely stalled for a substantial period of time, when the two drops have different surface tensions, despite being perfectly miscible. A temporary state of non-coalescence arises, during which the drops move on their substrate, only connected by a thin neck between them. Existing literature covers pure liquids and mixtures with low surface activities. In this paper, we focus on the case of large surface activities, using aqueous surfactant solutions with varying concentrations. It is shown that the coalescence behavior can be classified into three regimes that occur for different surface tensions and contact angles of the droplets at initial contact. However, not all phenomenology can be predicted from surface tension contrast or contact angles alone, but strongly depends on the surfactant concentrations as well. This reveals that the merging process is not solely governed by hydrodynamics and geometry, but also depends on the molecular physics of surface adsorption.
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