Y-shaped polymer brushes represent a special class of binary mixed polymer brushes, in which a combination of different homopolymers leads to unique phase behavior. While most theoretical and simulation studies use monodisperse models, experimental systems are always polydisperse. This discrepancy hampers linking theoretical and experimental results. In this theoretical study, we employed dissipative particle dynamics to study the influence of polydispersity on the phase behavior of Y-shaped brushes grafted to flat surfaces under good solvent conditions. Polydispersity was kept within experimentally achievable values and was modeled via Schulz-Zimm distribution. In total, 10 systems were considered, thus covering the phase behavior of monodisperse, partially polydisperse and fully polydisperse systems. Using such generic representation of real polymers, we observed a rippled structure and aggregates in monodisperse systems. In addition, polydisperse brushes formed a stable perforated layer not observed previously in monodisperse studies, and influenced the stability of the remaining phases. Although the perforated layer was experimentally observed under good solvent conditions and in the melt state, further confirmation of its presence in systems under good solvent conditions required mapping real polymers onto mesoscale models that reflected, for example, different polymer rigidity, and excluded volume effects or direct influence of the surface, just to mention a few parameters. Finally, in this work, we show that mesoscale modeling successfully describes polydisperse models, which opens the way for rapid exploring of complex systems such as polydisperse Y-shaped brushes in selective or bad solvents or under non-equilibrium conditions.

• Keywords
• Y-shaped brush, dissipative particle dynamics, ripple phase, self-assembly, surface,
• Publication type
• Journal Article MeSH

Although the behavior of the confined semi-dilute solutions of self-assembling copolymers represents an important topic of basic and applied research, it has eluded the interest of scientists. Extensive series of dissipative particle dynamics simulations have been performed on semi-dilute solutions of A5B5 chains in a selective solvent for A in slits using a DL-MESO simulation package. Simulations of corresponding bulk systems were performed for comparison. This study shows that the associates in the semi-dilute bulk solutions are partly structurally organized. Mild steric constraints in slits with non-attractive walls hardly affect the size of the associates, but they promote their structural arrangement in layers parallel to the slit walls. Attractive walls noticeably affect the association process. In slits with mildly attractive walls, the adsorption competes with the association process. At elevated concentrations, the associates start to form in wide slits when the walls are sparsely covered by separated associates, and the association process prevents the full coverage of the surface. In slits with strongly attractive walls, adsorption is the dominant behavior. The associates form in wide slits at elevated concentrations only after the walls are completely and continuously covered by the adsorbed chains.

• Keywords
• confined copolymer, dissipative particle dynamics, polymer–wall interaction, selective solvent, self-assembly, slit,
• Publication type
• Journal Article MeSH

Design and preparation of functional nanomaterials with specific properties requires precise control over their microscopic structure. A prototypical example is the self-assembly of diblock copolymers, which generate highly ordered structures controlled by three parameters: the chemical incompatibility between blocks, block size ratio and chain length. Recent advances in polymer synthesis have allowed for the preparation of gradient copolymers with controlled sequence chemistry, thus providing additional parameters to tailor their assembly. These are polydisperse monomer sequence, block size distribution and gradient strength. Here, we employ dissipative particle dynamics to describe the self-assembly of gradient copolymer melts with strong, intermediate, and weak gradient strength and compare their phase behavior to that of corresponding diblock copolymers. Gradient melts behave similarly when copolymers with a strong gradient are considered. Decreasing the gradient strength leads to the widening of the gyroid phase window, at the expense of cylindrical domains, and a remarkable extension of the lamellar phase. Finally, we show that weak gradient strength enhances chain packing in gyroid structures much more than in lamellar and cylindrical morphologies. Importantly, this work also provides a link between gradient copolymers morphology and parameters such as chemical incompatibility, chain length and monomer sequence as support for the rational design of these nanomaterials.

• Keywords
• block copolymers, dissipative particle dynamics, gradient copolymers, gradient strength, microphase separation, nanomaterials, self-assembly,
• Publication type
• Journal Article MeSH

Nanogels are chemically crosslinked polymeric nanoparticles endowed with high encapsulation ability, tunable size, ease of preparation, and responsiveness to external stimuli. The presence of specific functional groups on their surfaces provides an opportunity to tune their surface properties and direct their behavior. In this work, we used mesoscale modeling to describe conformational and mechanical properties of nanogel surfaces formed by crosslinked polyethylene glycol and polyethyleneimine, and grafted by charged alkylamine brushes of different lengths. Simulations show that both number of chains per area and chain length can be used to tune the properties of the coating. Properly selecting these two parameters allows switching from a hydrated, responsive coating to a dried, highly charged layer. The results also suggest that the scaling behavior of alkylamine brushes, e.g., the transition from a mushroom to semi-dilute brush, is only weakly coupled with the shielding ability of the coating and much more with its compressibility.

• Keywords
• adsorption, charged brushes, dissipative particle dynamics, nanogels, responsive surfaces, smart surfaces,
• Publication type
• Journal Article MeSH