The fabrication of graphene nanoribbons from carbon nanotubes (CNTs) treated with potassium permanganate in a concentrated sulfuric acid solution has been reported by Kosynkin et al. [Nature (London) 458, 872 (2009)]. Here we report ab initio density functional theory calculations of such unzipping process. We find that the unzipping starts with the potassium permanganate attacking one of the internal C–C bonds of the CNT, stretching and breaking it. The created defect weakens neighboring bonds along the length of the CNT, making them energetically prone to be attacked too.

Using ab initio density functional theory methods, the optimized structure of the single-, double-, and triple-layered graphene nanoribbons with different stacking orders and edges is calculated along with their Raman spectrums. For each case studied, graphene is found to be a potential source of vibrational signals in the terahertz region of the spectrum when molecules or another layer are adsorbed in the surface; this effect is independent of the hydrogen presence at the edges, and the stacking order. The visible low-frequency modes increase with the addition of graphene layers, and the number of modes may be influenced by the type of edges. The monolayer shows better performance due to the lower number of vibrational modes. The nanoribbon with fewer modes at the terahertz range is used to show a potential application of graphene acting as a sensor of single molecules.

A high sensitivity and selectivity sensor is proposed using graphene ribbons which are able to read molecular vibrations and molecular electrostatic potentials, acting as an amplifier and as a transducer converting molecular signals into current-voltage quantities of standard electronics. Two sensing mechanisms are used to demonstrate the concept using ab initio density functional methods. By using the terahertz region of the spectrum, we can characterize modes when single molecules are adsorbed on the ribbon surface. Characteristic modes can be obtained and used as fingerprints, which can be transduced into current by applying a voltage along the ribbons. On the other hand, the fully delocalized frontier molecular orbitals of graphene ribbons, commonly denominated plasmons in larger solid state structures, are extremely sensitive to any moiety approach; once plasmons are in contact with an "agent" (actually its molecular potential), the transport through the ribbons acting as electrodes catching the signals is strongly affected.

We demonstrate the switchability of the molecular conductivity of a citrate. This was made possible through mechanical stretching of two conformers of such citrate capped on and linked between gold nanoparticles (AuNPs) self-assembled as a film. On the basis of experimental results, theoretical analysis was conducted using the density function theory and Green's function to study the electron flux in the backbone. We found that the molecular conductivity depended on the pathways of electrons that were controlled by the applied mechanical stress. Under stress, we could tune the conductivity up and down for as much as 10-fold. The mechanochemistry behind this phenomenon is an alternative branch of chemistry.

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