Dynamic behavior of nickel atoms in graphitic networks

The dynamic behavior of nickel atoms in graphitic carbon onions, observed by in situ atomic-resolution electron microscopy, shows the formation of stable new C-Ni phases. Nickel is observed to take substitutional in-plane positions in graphene layers, forming a planar graphitelike C-Ni lattice. Evidence is furthermore seen for the formation of a cubic C-Ni phase, suggesting a possible phase transformation in C-Ni from a graphitelike to a diamondlike structure. The stability of the planar phases is shown by first-principles calculations which also indicate that the C-Ni planes are metallic.

New metallic allotropes of planar and tubular carbon

We propose a new family of layered sp(2)-like carbon crystals, incorporating five-, six-, and seven-membered rings in 2D Bravais lattices. These periodic sheets can be rolled so as to generate nanotubes of different diameter and chirality. We demonstrate that these sheets and tubes are metastable and more favorable than C60, and it is also shown that their mechanical properties are similar to those of graphene. Density of states calculations of all structures revealed an intrinsic metallic behavior, independent of orientation, tube diameter, and chirality.

Synthesis of high coercivity core-shell nanorods based on nickel and cobalt and their magnetic properties.

Hybrid magnetic nanostructures with high coercivity have immense application potential in various fields. Nickel (Ni) electrodeposited inside Cobalt (Co) nanotubes (a new system named Ni @ Co nanorods) were fabricated using a two-step potentiostatic electrodeposition method. Ni @ Co nanorods were crystalline, and they have an average diameter of 150 nm and length of ~15 µm. The X-ray diffraction studies revealed the existence of two separate phases corresponding to Ni and Co. Ni @ Co nanorods exhibited a very high longitudinal coercivity. The general mobility-assisted growth mechanism proposed for the growth of one-dimensional nanostructures inside nano porous alumina during potentiostatic electrodeposition is found to be valid in this case too.

Coalescence of single-walled carbon nanotubes

The coalescence of single-walled nanotubes is studied in situ under electron irradiation at high temperature in a transmission electron microscope. The merging process is investigated at the atomic level, using tight-binding molecular dynamics and Monte Carlo simulations. Vacancies induce coalescence via a zipper-like mechanism, imposing a continuous reorganization of atoms on individual tube lattices along adjacent tubes. Other topological defects induce the polymerization of tubes. Coalescence seems to be restricted to tubes with the same chirality, explaining the low frequency of occurrence of this event.