Graphene flakes, one of the most popular form of graphene, can be used for many applications. Their synthesis is in the path to reach the large-scale production if the cost of production is further improved.

Of these different surfactants, the tri-chain aromatic surfactant TC3Ph3 (sodium 1,5-dioxo-1,5-bis(3-phenylpropoxy)-3-((3phenylpropoxy)carbonyl) pentane-2-sulfonate) was shown to be highly graphene-compatible (nanocomposite electrical conductivity = 2.22 × 10 S cm), demonstrating enhanced electrical conductivity over nine orders of magnitude higher than neat natural rubber-latex matrix (1.51 × 10 S cm). Varying the number of aromatic moieties in the surfactants appears to cause significant differences to the final properties of the nanocomposites.

Here is presented a systematic study of the dispersibility of multiwall carbon nanotubes (MWCNTs) in natural rubber latex (NR-latex) assisted by a series of single-, double-, and triple-sulfosuccinate anionic surfactants containing phenyl ring moieties. Optical polarising microscopy, field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and Raman spectroscopy have been performed to obtain the dispersion-level profiles of the MWCNTs in the nanocomposites. Interestingly, a triple-chain, phenyl-containing surfactant, namely sodium 1,5-dioxo-1,5-bis(3-phenylpropoxy)-3-((3-phenylpropoxy)carbonyl) pentane-2-sulfonate (TCPh), has a greater capacity the stabilisation of MWCNTs than a commercially available single-chain sodium dodecylbenzenesulfonate (SDBS) surfactant. TCPh provides significant enhancements in the electrical conductivity of nanocomposites, up to ∼10(-2) S cm(-1), as measured by a four-point probe instrument. These results have allowed compilation of a road map for the design of surfactant architectures capable of providing the homogeneous dispersion of MWCNTs required for the next generation of polymer-carbon-nanotube materials, specifically those used in aerospace technology.

Graphene is the newest member of the carbon family, and has revolutionized materials science especially in the field of polymer nanocomposites. However, agglomeration and uniform dispersion remains an Achilles" heel (even an elephant in the room), hampering the optimization of this material for practical applications. Chemical functionalization of graphene can overcome these hurdles but is often rather disruptive to the extended piconjugation, altering the desired physical and electronic properties. Employing surfactants as stabilizing agents in latex technology circumvents the need for chemical modification allowing for the formation of nanocomposites with retained graphene properties. This article reviews the recent progress in the use of surfactants and polymers to prepare graphene/polymer nanocomposites via latex technology. Of special interest here are surfactant structure-performance relationships, as well as background on the roles surfactantgraphene interactions for promoting stabilization.

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Aluminium (Al)-doped zinc-oxide (ZnO) nanorod arrays have been successfully prepared using a novel and low-temperature sonicated sol–gel immersion method. The photoluminescence (PL) spectrum reveals the appearance of two emission peaks from the nanorod that are centred at 381 and 590 nm. The nanorod has a hexagonal structure with a flat-end facet, as observed using field-emission electron microscopy (FESEM). Interestingly, all samples have similar surface morphologies and diameter sizes of 40 to 150 nm after immersion in different precursor-solution volumes. The thickness-measurement results show that the thicknesses of the samples increase after immersion in higher precursor-solution volumes. We show for the first time that the growth of nanorod arrays along the c-axis can be controlled using different precursor volumes, and its growth mechanism is discussed. X-ray diffraction (XRD) spectra indicate that the prepared nanorods are ZnO with a hexagonal wurtzite structure that grows preferentially along the c-axis.

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