Single-wall fullerene nanotubes were converted from nearly endless, highly tangled ropes into short, open-ended pipes that behave as individual macromolecules. Raw nanotube material was purified in large batches, and the ropes were cut into 100- to 300-nanometer lengths. The resulting pieces formed a stable colloidal suspension in water with the help of surfactants. These suspensions permit a variety of manipulations, such as sorting by length, derivatization, and tethering to gold surfaces.

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We report a general chemical strategy for producing reduced-symmetry metallodielectric nanoparticles, nanocups, and nanocaps that combines nanoscale masking techniques and nanoparticle-seeded electroless plating. Using this approach, silica nanoparticles with a gold cup-shaped shell and, alternatively, a gold cap, are obtained. The plasmon response of both nanostructures is a sensitive function of orientation of the nanostructure with respect to the direction and polarization of incident light. This orientation dependence is examined experimentally by studying the extinction spectra of oriented nanocups and nanocaps on transparent substrates, and is also evaluated theoretically using a three-dimensional finite difference time domain (FDTD) method. † Part of the special issue "Arnim Henglein Festschrift".

Characterisation and quantification of tissue structures is limited by sectioning-induced artefacts and by the difficulties of visualising and segmenting 3D volumes. Here we demonstrate that, even in the absence of X-ray contrast agents, X-ray computed microtomography (microCT) and nanotomography (nanoCT) can circumvent these problems by rapidly resolving compositionally discrete 3D tissue regions (such as the collagen-rich adventitia and elastin-rich lamellae in intact rat arteries) which in turn can be segmented due to their different X-ray opacities and morphologies. We then establish, using X-ray tomograms of both unpressurised and pressurised arteries that intra-luminal pressure not only increases lumen cross-sectional area and straightens medial elastic lamellae but also induces profound remodelling of the adventitial layer. Finally we apply microCT to another human organ (skin) to visualise the cell-rich epidermis and extracellular matrix-rich dermis and to show that conventional histological and immunohistochemical staining protocols are compatible with prior X-ray exposure. As a consequence we suggest that microCT could be combined with optical microscopy to characterise the 3D structure and composition of archival paraffin embedded biological materials and of mechanically stressed dynamic tissues such as the heart, lungs and tendons.

Here we present detailed microstructural investigations of a commercially available Li-ion battery cathode. Without a priori knowledge of the cathode material, we have conducted a thorough multi-modal analysis of the battery electrode using XRD, multi-length scale X-ray microscopy (XRM) and electron microscopy. Multiple length scale X-ray microscopy experiments reveal a wealth of microstructural information in three dimensions including phase fractions, volume specific surface area and tortuosity. At the highest resolution, XRM also reveals internal defects in the solid structure. The resolution requirement for three-dimensional microstructural characterization is found to be specific to the physical parameter under investigation, demonstrating the need for a multi-length scale approach. This is especially true for surface area which increases with increasing resolution in a fractal-like way.

Fluorescence intensity measurements have the potential to facilitate the diagnoses of many pathological conditions. However, accurate interpretation of the measurements is complicated by the distorting effects of tissue scattering and absorption. Consequently, different techniques have been developed to attempt to compensate for these effects. This paper reviews currently available correction techniques with emphasis on clinical application and consideration given to the intrinsic accuracy and limitations of each technique.

A gas-phase purification method for raw nanotube material has been developed which incorporates a chlorine, water, and hydrogen chloride gas mixture to remove unwanted carbon. The evolved gases can be easily monitored by infrared spectroscopy to follow the cleaning process. The quality of the final material was verified by SEM (scanning electron microscopy), TGA (thermogravimetric analysis), and UV−vis (ultraviolet and visible absorption spectroscopy). The yield of ∼15 wt % indicates a uniquely selective carbon surface chemistry that prevents etching of the nanotubes, which are generally more reactive due to their larger curvature. Although the technique's usefulness for large-scale purification was not determined, the ability to purify single-wall nanotubes by a gas-phase method has been demonstrated, and a mechanism proposed.

Inorganic sol-gel solutions were electrospun to produce the first bioactive three-dimensional (3-D) scaffolds for bone tissue regeneration with a structure like cotton-wool (or cotton candy). This flexible 3-D fibrous structure is ideal for packing into complex defects. It also has large inter-fiber spaces to promote vascularization, penetration of cells and transport of nutrients throughout the scaffold. The 3-D fibrous structure was obtained by electrospinning, where the applied electric field and the instabilities exert tremendous force on the spinning jet, which is required to be viscoelastic to prevent jet break up. Previously, polymer binding agents were used with inorganic solutions to produce electrospun composite two-dimensional fibermats, requiring calcination to remove the polymer. This study presents novel reaction and processing conditions for producing a viscoelastic inorganic sol-gel solution that results in fibers by the entanglement of the intermolecularly overlapped nanosilica species in the solution, eliminating the need for a binder. Three-dimensional cotton-wool-like structures were only produced when solutions containing calcium nitrate were used, suggesting that the charge of the Ca(2+) ions had a significant effect. The resulting bioactive silica fibers had a narrow diameter range of 0.5-2μm and were nanoporous. A hydroxycarbonate apatite layer was formed on the fibers within the first 12h of soaking in simulated body fluid. MC3T3-E1 preosteoblast cells cultured on the fibers showed no adverse cytotoxic effect and they were observed to attach to and spread in the material.