Graphene nano-sieves by femtosecond laser irradiation.

The formation of nano-pores in graphene crystal structure is alternative way to engineer its electronic properties, chemical reactivity, and surface interactions, enabling applications in technological fields such as sensing, energy and separation. The past few years, nano-perforation of graphene sheets has been accomplished by a variety of different methods suffering mainly from poor scalability and cost efficiency issues. In this work, we introduce an experimental protocol to engineer nanometer scale pores in CVD graphene membranes under ambient conditions, using low power ultra-short laser pulses and overcoming the drawbacks of other perforation techniques. Using Atomic Force Microscopy (AFM) and Scanning Electron Microscopy (SEM) we visualized and quantified the nanopore network while Raman spectroscopy is utilized to correlate the nano-perforated area with the nanotopographic imaging. We suggest that Raman imaging provides the identification of nanoporous area and, in combination with AFM, we provide solid evidence for the reproducibility of the method, since under these experimental conditions, nanopores of a certain size distribution are formed.

Compressive response and buckling of graphene nanoribbons.

We examine the mechanical response of single layer graphene nanoribbons (GNR) under constant compressive loads through molecular dynamics simulations. Compressive stress-strain curves are presented for GNRs of various lengths and widths. The dependence of GNR's buckling resistance on its size, aspect ratio, and chiral angle is discussed and approximate corresponding relations are provided. A single master curve describing the dependence of the critical buckling stress of GNRs on their aspect ratio is presented. Our findings were compared to the continuum elasticity theories for wide plates and wide columns. In the large width limit, the response of the GNRs agrees with the predictions of the wide plates theory and thus, with that of wide graphenes. In the small width limit, the behavior of graphene nanoribbons deviates from that of periodic graphenes due to various edge related effects which govern the stiffness and the stability of the graphene membranes, but it qualitatively agrees with the theory of wide columns. In order to assess the effect of thermal fluctuations on the critical buckling stress a wide range of temperatures is examined. The findings of the current study could provide important insights regarding the feasibility and the evaluation of the performance of graphene-based devices.

Transforming graphene nanoribbons into nanotubes by use of point defects.

Using molecular dynamics simulations with semi-empirical potentials, we demonstrate a method to fabricate carbon nanotubes (CNTs) from graphene nanoribbons (GNRs), by periodically inserting appropriate structural defects into the GNR crystal structure. We have found that various defect types initiate the bending of GNRs and eventually lead to the formation of CNTs. All kinds of carbon nanotubes (armchair, zigzag, chiral) can be produced with this method. The structural characteristics of the resulting CNTs, and the dependence on the different type and distribution of the defects, were examined. The smallest (largest) CNT obtained had a diameter of ∼ 5 Å (∼ 39 Å). Proper manipulation of ribbon edges controls the chirality of the CNTs formed. Finally, the effect of randomly distributed defects on the ability of GNRs to transform into CNTs is considered.

Raman spectroscopic study of the rare-earth fullerides Eu6-xSrxC60.

We present Raman spectroscopic studies of the isostructural and isoelectronic Eu(6-x)Sr(x)C(60) (x = 0, 3, 5, 6) and Ba(6)C(60) compounds. The Raman spectra of the Eu-based fullerides show dramatic changes compared to the pure alkaline-earth systems, including significant broadening, splitting and frequency shifts of the fivefold degenerate H(g) intramolecular modes of C(60). Moreover, the A(g)(2) mode exhibits an even larger downshift and a remarkable broadening. These findings are consistent with distortions of the C(60) molecular cages and a considerable electron-phonon coupling strength-strongly enhanced in the Eu containing systems-originating from the strong orbital hybridization between the metal atom and the C(60) molecule.

Single-walled carbon nanotubes decorated with a pyrene-fluorenevinylene conjugate.

Single-walled carbon nanotubes are noncovalently functionalized using a pyrene-fluorenevinylene dye and the resulting nanohybrids are isolated from the free molecules. The tubes modified by means of this noncovalent approach show enhanced solubility in organic media. The structure and morphology of this hybrid material are fully characterized using absorption, infrared and Raman spectroscopies as well as atomic force and scanning electron microscopies. Steady state fluorescence measurements reveal that significant quenching of the pyrene derivative excited state takes place through an energy transfer mechanism.