Thanks to their highly tunable band gaps, graphene nanoribbons (GNRs) with atomically precise edges are emerging as mechanically and chemically robust candidates for nanoscale light emitting devices of modulable emission color. While their optical properties have been addressed theoretically in depth, only few experimental studies exist, limited to ensemble measurements and without any attempt to integrate them in an electronic-like circuit. Here we report on the electroluminescence of individual GNRs suspended between the tip of a scanning tunneling microscope (STM) and a Au(111) substrate, constituting thus a realistic optoelectronic circuit. Emission spectra of such GNR junctions reveal a bright and narrow band emission of red light, whose energy can be tuned with the bias voltage applied to the junction, but always lying below the gap of infinite GNRs. Comparison with ab initio calculations indicates that the emission involves electronic states localized at the GNR termini. Our results shed light on unpredicted optical transitions in GNRs and provide a promising route for the realization of bright, robust, and controllable graphene-based light-emitting devices.

We report a comparative study involving the formation of self-assembled molecular films by two types of alkanethiols (1-octadecanethiol and 1-dodecanethiol) on graphene grown via chemical vapor deposition, for heavy metal sensing applications. Scanning tunneling microscopy measurements confirm that the alkanethiol molecules can form localized, ordered molecular films on single-layer graphene despite the presence of structural and chemical irregularities. To test and compare the sensory characteristics associated with graphene functionalized by 1-octadecanethiol and 1-dodecanethiol, graphene-based field effect transistors are fabricated via photolithography on silicon dioxide substrates. Devices based on graphene functionalized with 1octadecanethiol are successfully employed to demonstrate the detection of mercury and lead ions at the 10 ppm level via Dirac point shifts, with a notable difference in response associated with the use of different heavy metal ions. On the other hand, devices based on graphene functionalized with 1-dodecanethiol exhibit p-type character, before and/or after exposure to heavy metal ions, complicating their use in heavy metal sensing in a straightforward fashion via Dirac point shifts.

In the present work, nanostructured graphene nanosheets were added to hybrid silica sols and deposited on aluminium alloy A2024-T3 to study the effect on the corrosion behaviour. Sols were prepared using tetraethyl-orthosilicate (TEOS), 3-glycidoxypropyl-trimethoxysilane (GPTMS) and a colloidal silica suspension (LUDOX) as silica precursors with adding chemically modified graphene nanosheets (GN-chem). The graphene nanosheets were modified through a straightforward and simple hydrothermal approach and then, dispersed into a silica sol (SiO2/GN-chem). ATR-FTIR was used to optimize the silica sol–gel synthesis and to confirm the cross-linking of the silica network. The corrosion behaviour of the SiO2/GN-chem coatings was also analysed by electrochemical measurement (potentiodynamic polarization) in 0.05 M NaCl solution. The results showed that the incorporation of modified graphene nanosheets into hybrid silica sol–gel coatings affected the corrosion properties of the substrates. An improvement in the corrosion resistance was observed likely due to the enhanced barrier property and hydrophobic behaviour obtained by incorporation of GN-chem and colloidal silica nanoparticles.