RESUMO
The 2D naphthylene-ß structure is a theoretically proposed sp2 nanocarbon allotrope based on the assembly of naphthalene-based molecular building blocks, which features metallic properties. We report that 2D naphthylene-ß structures host a spin-polarized configuration which turns the system into a semiconductor. We analyze this electronic state in terms of the bipartition of the lattice. In addition, we study the electronic properties of nanotubes obtained from the rolling up of 2D naphthylene-ß. We show that they inherit the properties of the parent 2D nanostructure, such as the emergence of spin-polarized configurations. We further rationalize the results in terms of a zone-folding scheme. We also show that the electronic properties can be modulated using an external transverse electric field, including a semiconducting-to-metallic transition for sufficiently large field strength.
RESUMO
Several bottom-up chemical routes have been developed in the last few years to find ways to grow new forms of nanocarbon by devising a strategical selection of molecular precursors. Here, theoretical calculations are performed on 2D nanocarbon allotropes obtained from the fusion of triphenylene-like units through tetragonal rings. This 2D triphenylene structure has a metallic character in a closed shell configuration, but it also features a spin-polarized semiconducting state. The behavior of the electronic properties of the system is investigated when the structure is cast into nanoribbon forms. It is found that to be metallic in the nonpolarized case, the ribbons must be sufficiently wide while narrow 1D systems are semiconducting. A lower threshold width is also needed for the emergence of a spin-polarized semiconducting configuration in these nanoribbons. These behaviors are robust as they do not depend on edge geometry and chirality, thus offering opportunities for their possible applications in nanoscale devices.