Discrimination of B–C–N nanotubes through energy-filtering electron microscopy

Various multi-walled nanotubes in the B–C–N system are thoroughly investigated using a JEOL-3100FEF high-resolution field emission transmission electron microscope operating at 300 kV and equipped with an in-column built Omega filter. Spatially-resolved B, C and N elemental maps of the nanotubes are constructed. It is realized that a wide variety of tubular arrays composed of B, C and N atoms may exist in the system. Sandwich-like BN-rich and C-rich alternating tubular shells, graphitic C layers inside and outside of pure BN shells induced either by surface contamination, or electron beam irradiation, separation of C-rich and BN-rich tubes and/or BN particles within tubular bunches may take place. One should carefully take these effects into account while analyzing nanotube physical properties, e.g., electrical or optical, rather than simply rely on electron energy loss spectra typically collected from B, C and N containing nanostructures as a whole. Striking dependence of an individual nanotube electrical conductivity on tubular shell chemistry is demonstrated using I–V curve recording in an atomic force microscope.     

Nanoweb Formation: 2D Self‐Assembly of Semiconductor Gallium Oxide Nanowires/Nanotubes

This paper reports a method to produce networks of crystalline gallium oxide comprised of one‐dimensional (1D) nanostructures. Because of the unique arrangement of wires, these crystalline networks are termed as ‘nanowebs’. Nanowebs are of great technological interest since they contain wire densities of the order of 10⁹ cm^–2. A possible mechanism for the fast self‐assembly of crystalline metal oxide nanowires involves multiple nucleation and coalescence via oxidation–reduction reactions at the molecular level. The preferential growth of nanowires parallel to the substrate enabled them to coalesce into regular polygonal networks. The individual segments of the polygonal network consist of both nanowires and nanotubules of β‐gallium oxide. Individual wire properties contribute to a nanoweb’s overall capacity and the implications for devices based on nanowebs are expected to be enormous.     

Modifizierung des ABSE‐Polycarbosilazans mit Multi‐Walled Carbon Nanotubes zur Herstellung spinnfähiger Massen

Modification of the ABSE polycarbosilazane with multi‐walled carbon nanotubes for the creation of spinable masses An inexpensive method has been found to produce ceramic SiCN‐fibres via the precursor route consisting of five processing steps: synthesis of the polymer, preparation of the spinning mass, melt‐spinning, curing via electron beam and subsequent pyrolysis at 1100 °C in a nitrogen atmosphere. A special solid and meltable fibre polymer, the so‐called polycarbosilazane ABSE, has been developed in the last decade for this purpose. Due to its low molecular weight, an adequate catalytic and thermal aftertreatment was necessary to guarantee a stable melt‐spinning process. This article discusses an alternative way to prepare a qualified spinning mass, i.e. the addition of Multi‐Walled Carbon Nanotubes (MWCNTs) to the ABSE melt. For this purpose a homogeneous dispergation of the MWCNTs in the ABSE matrix is necessary. In this study, spinning masses were fabricated in different ways. By optical analysis and comparison of the level of dispergation in these spinning masses an optimized process for integration of the MWCNTs was identified. The influence of the addition of a dispersing agent is investigated as well. In using a dispersing agent, the level of homogeneous dispersion of the MWCNTs increases whereas the interactions between the particles and the precursor melt decrease. In first spinning experiments a good spinability of the masses were noticed. Thus the addition of MWCNTs represents a new way to modify the ABSE precursor for the melt‐spinning process.