Straining to make a transistor: The use of carbon nanotubes (CNTs) as short-channel-length transistors will require control of their chirality, which determines whether they are semiconducting or metallic and if they form strong, low-resistance contacts. Tang et al . fabricated CNT intramolecular transistors by progressive heating and straining of individual CNTs within a transmission electron microscope. Changes to chirality along sections of the nanotube created metallic-to-semiconducting transitions. A semiconducting nanotube channel was covalently bonded to the metallic nanotube source and drain regions. The resulting CNT intramolecular transistors had channel lengths as short as 2.8 nanometers. —PDS

Band gap control by an external field is useful in various optical, infrared and THz applications. However, widely tunable band gaps are still not practical due to a variety of reasons. Using the orthogonal tight-binding method for π -electrons, we have investigated the effect of the external electric field on a subclass of monolayer chevron-type graphene nanoribbons that can be referred to as jagged graphene nanoribbons. A classification of these ribbons was proposed and band gaps for applied fields up to the SiO ₂ breakdown strength (1 V nm ⁻¹ ) were calculated. According to the tight-binding model, band gap opening (or closing) takes place for some types of jagged graphene nanoribbons in the external electric field that lies on the plane of the structure and perpendicular to its longitudinal axis. Tunability of the band gap up to 0.6 eV is attainable for narrow ribbons. In the case of jagged ribbons with armchair edges larger jags forming a chevron pattern of the ribbon enhance the controllability of the band gap. For jagged ribbons with zigzag and armchair edges regions of linear and quadratic dependence of the band gap on the external electric field can be found that are useful in devices with controllable modulation of the band gap.

Diamanes are 2D diamond-like films that are nanometers in thickness. Diamanes can exist as bilayer or multilayer graphene with various modes of stacking and interlayer covalent sp³ bonds. The term “diamane” is used broadly for a variety of diamond-like materials at the nanoscale, from individual diamond clusters to nanocrystal films. A short overview of recent progress in the investigation of diamanes, starting from the first theoretical predictions to practical realization, is presented. The results of both theoretical and experimental studies on diamanes with various atomic structures and types of functionalization are considered. It is shown that diamanes are stronger than graphene and graphane and have wide bandgaps ranging from 3.1 to 4.5 eV depending on the structure. Diamane-like structures have been obtained using different experimental techniques, and their structures have been determined by Raman spectroscopy. The potential applications of these carbon nanostructures are briefly reviewed.

Using a combination of the density functional theory and tight-binding calculations, we study electronic and optical properties of asymmetric chevron-type graphene nanoribbons recently...

The stability and the electronic properties of new AB-stacking and moiré bilayer graphene superlattices with closed edge nanoholes are studied using DFT calculations.