Since many advanced applications require specific assemblies of nanoparticles (NPs), considerable efforts have been made to fabricate nanoassemblies with specific geometries. Although nanoassemblies can be fabricated through top-down approaches, recent...

The adhesion modes and endocytosis pathway of spherocylindrical nanoparticles (NPs) are investigated numerically using molecular dynamics simulations of a coarse-grained implicit-solvent model. The investigations is performed systematically with respect to the adhesion energy density ξ, NP's diameter D, and NP's aspect ratio α. At weak ξ, the NP adheres to the membrane through a parallel mode, i.e. such that its principal axis is parallel to the membrane. However, for relatively large ξ, the NP adheres through a perpendicular mode, i.e. the NP is invaginated such as its principal axis is nearly perpendicular to the membrane. The value of ξ at the transition from the parallel to the perpendicular mode decreases with increasing the D or α, in agreement with theoretical arguments based on the Helfrich Hamiltonian. As ξ is further increased, the NP undergoes endocytosis, with the value of ξ at the endocytosis threshold that is independent of the aspect ratio but decreases with increasing D. The kinetics of endocytosis depends strongly on ξ and D. While for low values of D, the NP first rotates to a parallel orientation then to a perpendicular orientation. At high values of ξ or D, the NP endocytoses while in the parallel orientation.

Using molecular dynamics simulations of a coarse-grained model, in conjunction with the weighted histogram analysis method, the adhesion modes of two spherical Janus nanoparticles (NPs) on the outer or inner side of lipid vesicles are explored in detail.

We present a numerical investigation of the modes of adhesion and endocytosis of two spherocylindrical nanoparticles (SCNPs) on planar and tensionless lipid membranes, using systematic molecular dynamics simulations of an...

The present work focuses on the development of a relatively simple phase field crystal model for materials with nanoscale porous inclusions. We found that the pore's main effect is to act as a nucleation agent, promoting crystallization of material at the pore’s interface, followed by micro-structural evolution of the solid in the supercooled liquid. Details of the crystal around the pore are investigated in terms of the pore radius and density of material outside the pore. Moreover, details of the pore-material interface is investigated through the interfacial tension and pressure. Finally, the model is extended to investigate the effect of multiple pores on the kinetics of crystallization.