Diffusion of Nanorods with Various Lengths and Rigidities in Cross-Linked Networks.

We investigated diffusion of thin and thick nanorods with varying lengths and rigidities in cross-linked polymer networks using coarse-grained molecular dynamics (CGMD) simulations. Our results show that the translational diffusion of nanorods slows down with power scaling laws as their length increases, exhibiting a non-monotonic dependence on rigidity of thin nanorods, and decreases with the rigidity of thick nanorods. The sub-diffusion of nanorods is observed at short time scales, which becomes more pronounced for rigid nanorods. The nanorods show anisotropic diffusion behavior with favoring motion along their major axes in cross-linked networks, and the anisotropy enhances by increasing either rigidity or length of nanorods, especially for thick nanorods. The sub-diffusion behavior of nanorods is primarily due to the strong heterogeneity of motions perpendicular to major axes of nanorods, and the time scales of this heterogeneous diffusion increase with the length and rigidity of nanorods. In rotational dynamics, nanorods with higher rigidity rotate more slowly, and the effect is more evident in longer nanorods. The rotational diffusion coefficient follows a power scaling law with the rigidity of nanorods, when the effective length of a nanorod exceeds the mesh size of cross-linked network. The rotations of nanorods also display heterogeneous dynamics, in which the time scale of heterogeneous rotation increase with rigidity, and such heterogeneity is more pronounced in softer nanorods. Overall, our work elucidates the microscopic mechanisms governing both translational and rotational diffusion of nanorods in cross-linked networks.