Michael Shtein

Critical parameters in exfoliating graphite into graphene

Dispersing graphite into few-layers graphene sheets (GS) in water is very appealing as an environmental-friendly, low-cost, low-energy method of obtaining graphene. Very high GS concentrations in water (0.7 mg mL(-1)) were obtained by optimizing the nature of dispersant and the type of ultra-sonic generator. We find that a multi-step sonication procedure involving both tip and bath sources considerably enhances the yield of exfoliated GS. Raman and transmission electron microscopy indicate few-layers graphene patches with typical size of ∼0.65 μm in one dimension and ∼0.35 μm in the other. These were further employed in combination with water-dispersed CNTs to fabricate conductive transparent electrodes for a molecularly-controlled solar-cell with an open-circuit voltage of 0.53 V.

Graphene-Based Hybrid Composites for Efficient Thermal Management of Electronic Devices

Thermal management has become a critical aspect in next-generation miniaturized electronic devices. Efficient heat dissipation reduces their operating temperatures and insures optimal performance, service life, and efficacy. Shielding against shocks, vibrations, and moisture is also imperative when the electronic circuits are located outdoors. Potting (or encapsulating) them in polymer-based composites with enhanced thermal conductivity (TC) may provide a solution for both thermal management and shielding challenges. In the current study, graphene is employed as a filler to fabricate composites with isotropic ultrahigh TC (>12 W m(-1) K(-1)) and good mechanical properties (>30 MPa flexural and compressive strength). To avoid short-circuiting the electronic assemblies, a dispersion of secondary ceramic-based filler reduces the electrical conductivity and synergistically enhances the TC of composites. When utilized as potting materials, these novel hybrid composites effectively dissipate the heat from electronic devices; their operating temperatures decrease from 110 to 37 °C, and their effective thermal resistances are drastically reduced, by up to 90%. The simple filler dispersion method and the precise manipulation of the composite transport properties via hybrid filling offer a universal approach to the large-scale production of novel materials for thermal management and other applications.

Polymer binding to carbon nanotubes in aqueous dispersions: residence time on the nanotube surface as obtained by NMR diffusometry.

The binding of block copolymer Pluronic F-127 in aqueous dispersions of single- (SWCNT) and multiwalled (MWCNT) carbon nanotubes has been studied by pulsed-field-gradient (PFG) (1)H NMR spectroscopy. We show that a major fraction of polymers exist as a free species while a minor fraction is bound to the carbon nanotubes (CNT). The polymers exchange between these two states with residence times on the nanotube surface of 24 ± 5 ms for SWCNT and of 54 ± 11 ms for MWCNT. The CNT concentration in the solution was determined by improved thermal gravimetric analysis (TGA) indicating that the concentration of SWCNT dispersed by F-127 was significantly higher than that for MWCNT. For SWCNT, the area per adsorbed Pluronic F-127 molecule is estimated to be about 40 nm(2).

A simple solution for the determination of pristine carbon nanotube concentration

Upon dispersant-assisted exfoliation, pristine carbon nanotubes (CNTs) are divided between the supernatant and precipitate, which makes the determination of dispersant concentration a challenging task. We have developed a thermogravimetric-spectroscopy-based approach to accurately determine the dispersant-assisted CNT (or nanoparticles, in general) concentration in dispersion. A thermogravimetric analysis of the filtered and washed precipitate, that is usually discarded after centrifugation, is used here to accurately calculate the CNT mass in the precipitate and (through mass-balance) its mass in the supernatant. Once the true CNT concentration has been determined, a conventional spectroscopy-based concentration calibration plot is constructed for simple and swift use in further concentration measurements. Such true concentration analysis is crucial for studying the concentration-property relationship.

Optimal nanomaterial concentration: harnessing percolation theory to enhance polymer nanocomposite performance

A major challenge in nanocomposite research is to predict the optimal nanomaterial concentration (ONC) yielding a maximal reinforcement in a given property. We present a simple approach to identify the ONC based on our finding that it is typically located in close proximity to an abrupt increase in polymer matrix viscosity, termed the rheological percolation threshold, and thus may be used as an indicator of the ONC. This premise was validated by rheological and fractography studies of composites loaded by nanomaterials including graphene nanoribbons or carbon or tungsten disulfide nanotubes. The correlation between in situ viscosity, the rheological percolation threshold concentration and the nanocomposite fractography demonstrates the utility of the method.

Cement Reinforcement by Nanotubes

Loading a matrix with nano-sized particles such as nanotubes (carbon or tungsten di-sulfide) is expected to improve the mechanical properties of composite materials better than traditional (macroscopic) fillers due to extra-ordinary mechanical properties accompanied by high surface area. One of the major challenges towards achieving this goal is an effective dispersion of the as-produced aggregated nanotubes. In this work we demonstrate a novel dispersion method, facilitating the integration of individual nanotubes in cement paste matrix. We demonstrate the effectiveness of our nanotubes dispersion method by enhancing both flexural strength and compressive strength of cement paste using carbon and tungsten di-sulfide nanotubes. Finally, a comprehensive fractography study indicates that both types of nanotubes fail via pull-out mechanism with an intermediate state of bridging mechanism.