A nano rotation–translation convertor with a deformable rotor is presented, and the dynamic responses of the system are investigated considering the coupling among the van der Waals (vdW), centrifugal and frictional forces. When an input rotational frequency (ω) is applied at one end of the rotor, the other end exhibits a translational motion, which is an output of the system and depends on both the geometry of the system and the forces applied on the deformable part (DP) of the rotor. When centrifugal force is stronger than vdW force, the DP deforms by accompanying the translation of the rotor. It is found that the translational displacement is stable and controllable on the condition that ω is in an interval. If ω exceeds an allowable value, the rotor exhibits unstable eccentric rotation. The system may collapse with the rotor escaping from the stators due to the strong centrifugal force in eccentric rotation. In a practical design, the interval of ω can be found for a system with controllable output translation.

It is difficult to obtain a nanotube from phosphorus with a 3sp² electron configuration by chemical synthesis. However, a physical fabrication approach, such as self-assembly, is worth trying. In an experiment, when using a carbon nanotube (CNT) to trigger self-assembly of a black phosphorus (BP) ribbon, the final configuration of the BP component may be sensitive to the initial relative position of the CNT to the BP ribbon. For instance, using the same CNT with different initial relative positions to the BP ribbon, the BP ribbon may finally become a nanotube, or a scroll, or just wind upon the CNT, or escape from the CNT, etc. In this study, the sensitivity is investigated using molecular dynamics simulations. Numerical results illustrate some essentials for potential fabrication of a BP nanotube from ribbon.

A method is proposed for designing tunable chiral nano-networks using partly hydrogenated graphene ribbons and carbon nanotubes (CNTs). In the network, the hydrogenated graphene ribbons (HGRs) act as basic components, which connect each other via CNT joints. Each component contains two HGR segments and an internal graphene joint (G-J2) or CNT joint (CNT-J2). Since the two HGR segments are hydrogenated at opposite surfaces, they may wind in chiral about the internal joint to form a scroll (G-J2-scroll or CNT-J2-scroll) or about the two end joints to form CNT-J4-scrolls. In general, a G-J2-scroll is formed more easily than both a CNT-J4-scroll and a CNT-J2-scroll. Because of scrolling, the surface energy is reduced. This reduction is converted to and stored as deformation potential energy. By means of molecular-dynamics simulations, we studied the final configurations of two types of networks from the same components, the maximum shrinkage, and their capacity of energy storage for potential application of energy storage or as large-deformable components in a nano-device. The results indicate that the network reaches a stable state when the shrinkage reaches 70% of the two in-plane dimensions.