Multiwalled carbon nanotubes (MWCNTs) were oxidized in air and acids while varying the treatment time and/or temperature. The goal of this approach was to create the highest density of carboxyl groups with moderate sample loss, which is necessary for nanocomposite applications. In situ Raman experiments allowed real-time observation of the structural changes in MWCNTs upon oxidation. The ratio of the Raman intensities of the D and G bands was used to estimate the concentration of defects. It was found that while an oxidation for 6 h in H 2 SO 4 /HNO 3 provided the strongest effect, a 'flash oxidation' in air (15 min at 550°C) also leads to an efficient functionalization in a cost-effective and environmentally friendly way. Transmission electron microscopy, Fourier-transform infrared (FTIR) spectroscopy, thermogravimetric analysis and electrophoretic mobility analysis were used to study the oxidized nanotubes.

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In this work, we experimentally investigated the surface-enhanced Raman spectroscopy (SERS) activity of faceted gold nanoparticles, which have been theoretically predicted to yield giant enhancements. Glycine was used to determine the SERS activity as a function of pH and ionic strength and to estimate the corresponding enhancement factor (EF). By optimizing the synthesis conditions of the flat prismatic nanoparticles, it was possible to control their size and shape. We demonstrate that the maximum SERS intensity increases with the edge length of the triangle, reaching a maximum EF of ∼10 13 for 1.9 µm triangles (the largest tested). The corresponding glycine detection limit was as low as 10 −12 M, close to the single-molecule threshold.

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Silicon carbide fibers of different generation/processing routes (NLM-Nicalon and Tyranno SA3) were thermally treated to trigger the growth of nanocrystals, which were analyzed using Raman spectroscopy and transmission electron microscopy (TEM). The nanocrystals were also aged in molten sodium nitrate to investigate their reactivity. The spatial correlation model has been used to model the Raman spectra and extract accurate and statistical information on the nanocrystallites' structure and dimension. For the NLM fibers, an average size of 2.5 to 7.0 nm was calculated, which was in good agreement with TEM observations. For the Tyranno SA3 fiber, despite the heavily faulted stacking sequence, the Raman peaks remained sharp, indicating that the crystallite dimension calculated from the Raman spectra is only dependent on the actual size of the nanocrystals and is not affected by the sequence of the stacking faults.

Electrospun polyamide 11 (PA11) nanofiber films are used as a guide for the deposition of two‐dimensional networks of multi‐walled carbon nanotubes (MWNTs). This method allows for the manufacturing of transparent and electrically conductive thin films. It is demonstrated that the sheet resistance (Rs) and transmittance (T) decrease, as the films become thicker due to longer electrospinning times or larger fibers. The transmittance could be improved by fusing (melting) the fibers at moderate temperatures or impregnating the film with a resin, showing that light scattering rather than absorption by the MWNTs or the polymer was responsible for a low transmittance. As the number of MWNT deposition cycles increases, the Rs decreases with a constant transmittance. A fused 100 nm film obtained after 10 min of electrospinning of the 2 wt % PA11 solution shows Rs = 154 kΩ sq−1 and T = 83% after ten MWNT deposition cycles. A 95% transmittance was achieved after removing the polymer fibers by heating the glass plate in air (Rs = 440 kΩ sq−1 after five MWNT deposition cycles).