RESUMO
Low-cost, high-yield production of graphene nanosheets (GNs) is essential for practical applications. We have achieved high yield of edge-selectively carboxylated graphite (ECG) by a simple ball milling of pristine graphite in the presence of dry ice. The resultant ECG is highly dispersable in various solvents to self-exfoliate into single- and few-layer (≤ 5 layers) GNs. These stable ECG (or GN) dispersions have been used for solution processing, coupled with thermal decarboxylation, to produce large-area GN films for many potential applications ranging from electronic materials to chemical catalysts. The electrical conductivity of a thermally decarboxylated ECG film was found to be as high as 1214 S/cm, which is superior to its GO counterparts. Ball milling can thus provide simple, but efficient and versatile, and eco-friendly (CO(2)-capturing) approaches to low-cost mass production of high-quality GNs for applications where GOs have been exploited and beyond.
RESUMO
The development of a versatile method for nitrogen-doping of graphitic structure is an important challenge for many applications, such as energy conversions and storages and electronic devices. Here, we report a simple but efficient method for preparing nitrogen-doped graphene nanoplatelets via wet-chemical reactions. The reaction between monoketone (CâO) in graphene oxide (GO) and monoamine-containing compound produces imine (Shiff base) functionalized GO (iGO). The reaction between α-diketone in GO and 1,2-diamine (ortho-diamine)-containing compound gives stable pyrazine ring functionalized GO (pGO). Subsequent heat-treatments of iGO and pGO result in high-quality, nitrogen-doped graphene nanoplatelets to be designated as hiGO and hpGO, respectively. Of particular interest, hpGO was found to display the n-type field-effect transistor behavior with a charge neutral point (Dirac point) located at around -16 V. Furthermore, hpGO showed hole and electron mobilities as high as 11.5 and 12.4 cm(2)V(-1)s(-1), respectively.
RESUMO
To endorse sufficient water affinity to multiwalled carbon nanotubes (MWCNTs), dendritic hyperbranched poly(ether-ketone) (HPEK) was first covalently grafted to the surface of a MWCNT via a Friedel-Crafts acylation reaction. The resultant HPEK-grafted MWCNT (HPEK-g-MWCNT) was subsequently sulfonated in chlorosulfonic acid to produce sulfonated HPEK-g-MWCNT (SHPEK-g-MWCNT), which is dispersible well in water showing a zeta potential value of -57.8 mV. The SHPEK-g-MWCNT paper simply formed by filtration of aqueous dispersion has a sheet resistance as low as 63 Ω/sq. Its thin film shows a high electrocatalytic activity for oxygen reduction reaction (ORR). Thus, the newly produced water-dispersible MWCNT is a new class of high performance cathode material for ORR.
RESUMO
We report an effective route to prepare highly conducting and flexible few-walled carbon nanotube (FWNT) thin films. The free-standing thin films were fabricated by functionalizing FWNTs with 4-ethoxybenzoic acid (EBA) via a direct Friedel-Crafts acylation reaction in a nondestructive polyphosphoric acid/phosphorus pentoxide medium. The resulting ethoxybenzoyl-functionalized FWNT (EBA-f-FWNT) was readily dispersible in water. EBA-f-FWNT thin films were formed by a simple suction filtration of the dispersed solution. Electron microscopic studies were employed to characterize the morphologies of the resulting thin films. The obtained results indicate that the structure of FWNTs was not perturbed by the incorporation of EBA moieties, which were uniformly grafted onto FWNTs forming the FWNT networks. Room temperature electrical conductivity of the thin films was obtained using standard four-probe measurements, which revealed a value as high as 29 400 S m(-1), while the tensile strength and modulus of the film were found to be about 80 MPa and 15 GPa, respectively. Cyclic voltammograms revealed a rectangular shape, with superior capacitive behaviors nearing 133 F/g for the thin films, which is very attractive for capacitor applications.