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When polyelectrolyte-neutral block copolymers are mixed in solutions to oppositely charged species (e.g. surfactant micelles, macromolecules, proteins etc), there is the formation of stable supermicellar aggregates combining both components. The resulting colloidal complexes exhibit a core-shell structure and the mechanism yielding to their formation is electrostatic self-assembly. In this contribution, we report on the structural properties of supermicellar aggregates made from yttrium-based inorganic nanoparticles (radius 2 nm) and polyelectrolyte-neutral block copolymers in aqueous solutions. The yttrium hydroxyacetate particles were chosen as a model system for inorganic colloids, and also for their use in industrial applications as precursors for ceramic and opto-electronic materials. The copolymers placed under scrutiny are the water soluble and asymmetric poly(sodium acrylate)poly(acrylamide) diblocks. Using static and dynamical light scattering experiments, we demonstrate the analogy between surfactant micelles and nanoparticles in the complexation phenomenon with oppositely charged polymers. We also determine the sizes and the aggregation numbers of the hybrid organic-inorganic complexes. Several additional properties are discussed, such as the remarkable stability of the hybrid aggregates and the dependence of their sizes on the mixing conditions.
Using monomer-resolved Molecular Dynamics simulations and theoretical arguments based on the radial dependence of the osmotic pressure in the interior of a star, we systematically investigate the effective interactions between hard, colloidal particl
Aggregation of like-charged polymers is widely observed in biological and soft matter systems. In many systems, bundles are formed when a short-range attraction of diverse physical origin like charge-bridging, hydrogen-bonding or hydrophobic interact
The thermodynamic and elastic properties of a flexible polymer in the presence of dipole interactions are studied via Monte Carlo simulations. The structural coil-globular, solid-globular, and solid-solid transitions are mapped in the hyperphase diag
Thin films of azopolymer-nanoparticles hybrid materials were fabricated with poly[1-[4-(3-carboxy-4-hydroxyphenylazo) benzenesulfonamido]-1,2-ethanediyl] (PAZO) and different concentrations of Ag and AgAu nanoparticles (NPs). By illuminating the film
We report the results of molecular dynamics simulations of the properties of a pseudo-atom model of dodecane thiol ligated 5-nm diameter gold nanoparticles (AuNP) in vacuum as a function of ligand coverage and particle separation in three state of ag