Graphene exfoliation in organic solvents and switching solubility in aqueous media with the aid of amphiphilic block copolymers.

The successful exfoliation of graphite to graphene sheets in liquid phase via tip sonication was achieved. A number of solvents were examined for several time periods and it was found that o-dichlorobenzene (o-DCB) and N-methyl-1,2-pyrolidone (NMP) are ideal solvents to exfoliate graphite and produce stable 10 dispersions of graphene. The exfoliated graphene dispersions were characterized by complementary techniques including AFM, DLS, TGA and Raman. Furthermore, treatment of stable dispersions of exfoliated graphene sheets in NMP with poly[styrene-b-(2-vinylpyridine)] block copolymer, under acidic conditions, resulted on aqueous solubilization of graphene. Similar results were obtained, i.e. transfer of graphene from the organic to the aqueous phase, when poly(isoprene-b-acrylic acid) block copolymer was 15 added on exfoliated graphene in NMP

In situ growth of redox-active iron-centered nanoparticles on graphene sheets for specific capacitance enhancement

AbstractA fast and facile approach is proposed to enhance the specific capacitance of N-Methyl-2-pyrrolidone (NMP)-exfoliated graphene. Redox-active nickel ferricyanide (NiFeCN) nanoparticles were grown on the surface of graphene sheets using a simple co-precipitation method. Apart from the synergetic effect of graphene as double layer capacitance and NiFeCN as pseudocapacitance in specific capacitance enhancement, the NiFeCN nanoparticles served as the spacer to prevent the graphene sheets agglomeration. The NiFeCN/graphene exhibited specific capacitance of 113.5Fg−1, which was 2 times higher than the NMP-exfoliated graphene (52Fg−1) and 6times higher than the pure NiFeCN (18Fg−1). The findings suggested the NiFeCN/graphene could be the potential candidate for supercapacitor electrode

Elastic properties of graphene suspended on a polymer substrate by e-beam exposure

A method for fabricating multiple free-standing structures on the same sheet of graphene is demonstrated. Mechanically exfoliated mono- and bilayer graphene sheets were sandwiched between two layers of polymethyl-methacrylate. Suspended areas were defined by e-beam exposure allowing precise control over their shape and position. Mechanical characterization of suspended graphene sheets was performed by nanoindentation with an atomic force microscopy tip. The obtained built-in tensions of 12 nN are significantly lower than those in suspended graphene exfoliated on an SiO2 substrate, and therefore permit access to the intrinsic properties of this material system

Spectro-microscopy of single and multi-layer graphene supported by a weakly interacting substrate

We report measurements of the electronic structure and surface morphology of exfoliated graphene on an insulating substrate using angle-resolved photoemission and low energy electron diffraction. Our results show that although exfoliated graphene is microscopically corrugated, the valence band retains a massless fermionic dispersion, with a Fermi velocity of ~10^6 m/s. We observe a close relationship between the morphology and electronic structure, which suggests that controlling the interaction between graphene and the supporting substrate is essential for graphene device applications.Comment: 10 pages of text, 4 JPEG figure

Utilization of multiple graphene layers in fuel cells. 1. An improved technique for the exfoliation of graphene-based nanosheets from graphite

An improved, safer and mild method was proposed for the exfoliation of graphene like sheets from graphite to be used in fuel cells. The major aim in the proposed method is to reduce the number of layers in the graphite material and to produce large quantities of graphene bundles to be used as catalyst support in polymer electrolyte membrane fuel cells. Graphite oxide was prepared using potassium dichromate/sulfuric acid as oxidant and acetic anhydride as intercalating agent. The oxidation process seemed to create expanded and leafy structures of graphite oxide layers. Heat treatment of samples led to the thermal decomposition of acetic anhydride into carbondioxide and water vapor which further swelled the layered graphitic structure. Sonication of graphite oxide samples created more separated structures. Morphology of the sonicated graphite oxide samples exhibited expanded the layer structures and formed some tullelike translucent and crumpled graphite oxide sheets. The mild procedure applied was capable of reducing the average number of graphene sheets from 86 in the raw graphite to nine in graphene-based nanosheets. Raman spectroscopy analysis showed the significant reduction in size of the in-plane sp2 domains of graphene nanosheets obtained after the reduction of graphite oxide