Hierarchical superstructures assembled by binary mixed homopolymer-grafted nanoparticles are investigated by using a self-consistent field theory (SCFT). Our results demonstrate that grafting mixed homopolymer brushes provides an effective way to program the spatial lattice arrangement of the nanoparticles. For the polymer-grafted nanoparticles with specific interaction parameter and total grafting density, the unusual non-close-packed simple cubic (SC) crystal lattice is obtained at small spherical core/polymer size ratios (R/( N b) < 1). As the size ratio increases to R N b /() > 1, the nanoparticle arrangement transforms into a body-centered cubic (BCC) crystal lattice. Meanwhile, some unconventional microphases are formed in the polymer matrix, such as the tetragonal cylinder and simple cubic sphere phases. Furthermore, the two-dimensional (2D) model calculations reveal that the binary hairy nanoparticles prefer to arrange into the lattice in a way they can maintain the free energy-minimizing morphology as an isolated particle. Our findings suggest a possible strategy to design hierarchical nanomaterials composed of unique inorganic/organic hybrid superstructures.

Binary polymer brushes, including mixed homopolymer brushes and diblock copolymer brushes, are an attractive class of environmentally responsive nanostructured materials. Owing to microphase separation of the two chemically distinct components in the brush, multifaceted nanomaterials with functionalized and patterned surfaces can be obtained. This review summarizes recent progress on the theory and simulations related to binary polymer brushes grafted to flat, spherical, and cylindrical substrates, with a focus on patterned morphologies of multifaceted hairy nanoparticles, an intriguing class of hybrid nanostructured particles (e.g., nanospheres and nanorods). In particular, powerful field theory and particlebased simulations suitable for revealing novel structures on these patterned surfaces, including self-consistent field theory and dissipative particle dynamics simulations, are emphasized.The unsolved yet critical issues in this research field, such as dynamic response of binary polymer brushes to environmental stimuli and the hierarchical self-assembly of binary hairy nanoparticles, are briefly discussed.

A classical density functional theory (DFT) is applied to investigate the behavior of compressed polymer brushes composed of hard-sphere chains. The excluded volume interactions among the chain segments are explicitly treated. Two compression systems are used to study the behavior of brush-wall and brush-brush interactions. For the brush-brush systems, an obvious interpenetration zone has been observed. The extent of the interpenetration depends strongly on the grafting density. Furthermore, the repulsive force between the brush and wall or between the two brushes has been obtained as a function of the compression distance. Compared to the prediction of the analytic self-consistent field theory, such force increases more rapidly in the brush-wall compression with high polymer grafting densities or at higher compressions. In the brush-brush compression system, the interpenetration between the two compressed brushes creates a "softer" interaction. The influence of hard-sphere solvents on the behavior of compressed brushes is also discussed.

The conformation of homodendrimers and amphiphilic dendrimers in various solvents is studied using classical density functional theory (DFT), in which the excluded-volume effects are treated explicitly. For homodendrimers in an athermal solvent, DFT results predict a remarkable fold-back behavior for the outer generation of segments, supporting the dense-core model. A coil-to-globule transition is observed for homodendrimers in a poor solvent. The size of the dendrimers, characterized by the radius of gyration, ⟨Rg⟩, is found to follow the scaling relationship, ⟨Rg⟩ ∼ N(ν), where N is the total number of segments of the dendrimers. For amphiphilic dendrimers, DFT results show that chemical modification in the outermost generation is an effective method to drive the ends toward the periphery of the dendrimers. In particular, a conformation with a hollow interior structure could be formed for amphiphilic dendrimers with longer end spacers in a selective solvent. The resulting unimolecular micelles with a hollow core and dense shell could serve as a unique candidate for encapsulation applications, such as sustained-drug-release nanocontainers.

We report on microphase separation behaviors of mixed polymer brushes grafted onto an infinitely long cylindrical rod by performing polymer self-consistent field theory (SCFT) calculation with "masking" technique. The "masking" technique is especially suitable to deal with systems of confined polymers grafted onto curved surfaces. We have developed a method to solve the morphology of block copolymers confined into complicated topographic surfaces with SCFT. In this paper, this unique technique is extended to solve the SCFT for nanorod grafted by mixed polymer brushes. Furthermore, the use of simple Cartesian grids in a cubic computational cell with periodic boundary conditions makes it possible to solve diffusion equations in SCFT by utilizing an efficient and highly accurate pseudo-spectral method involving fast Fourier transform. Both parallel rippled phase and ring-shaped phase are predicted. We have investigated the influences of the cylinder radius, grafting density and interaction between the two incompatible grafting polymers on the stability of the two typical phases. Our results show that the system prefers the ring-shaped phase with the increase of the cylinder radius, grafting density and interaction between the two grafting polymers. Phase diagrams involving these parameters are constructed, and we explain the reason of the transition between the parallel rippled phase and ring-shaped phase in terms of the degree of phase segregation. Again, the degree of phase segregation is higher with larger cylinder radius, grafting density and interaction between the two grafting polymers. By comparing the degree of phase segregation and free energy of the parallel rippled and ring-shaped phases at the same condition, we found that the ring-shaped phase favors the entropic part of the free energy while the parallel rippled phase significantly reduces the enthalpy. Therefore, when the degree of phase segregation is low, the free energy of the system is dominated by the enthalpy, leading to the parallel rippled phase; when the degree of phase segregation is high, the free energy of the system is dominated by the entropic part and the ring-shaped phase is stable. We also found that the domain numbers of parallel rippled phase and the period of alternating ring-shaped phase vary with the radius of cylinder. These predictions are expected to be helpful in rational design and fabrication of such novel polymer brushes.