The synthesis of nanocrystalline ZnO by thermal decomposition of zinc hydroxyacetate, Zn(5)(OH)(8)(CH(3)CO(2))(2)·nH(2)O, was investigated. The decomposition process was examined using X-ray diffraction, thermogravimetric analysis, mass spectrometry, electron microscopy, Brunauer-Emmett-Teller surface area analysis, and solid-state NMR spectroscopy. Intermediate Zn(5)(OH)(8)(CH(3)CO(2))(2)·nH(2)O phases form at temperatures up to 110 °C from the starting compound Zn(5)(OH)(8)(CH(3)CO(2))(2)·2H(2)O by partial dehydration. At ∼110 °C, 4 equiv of ZnO and 1 equiv of Zn(CH(3)CO(2))(2) are formed. Further heating causes Zn(CH(3)CO(2))(2) to decompose to acetone, acetic acid, acetic anhydride, and ZnO. Notably, a portion of Zn(CH(3)CO(2))(2) sublimes during the process. Overall, the product of the calcination is equiaxed ZnO nanocrystals of 20-100 nm diameter.

We examine the optical properties of nanostructures comprised of titanium nitride, TiN, an electrically conducting intermetallic-like compound. This material can be deposited in the form of durable films by physical vapor deposition. Use of nanosphere templating techniques extends the range of nanostructures that can be produced to include the versatile semi-shell motif. The dielectric properties of TiN(1-x) depend upon stoichiometry and are favorable for plasmon resonance phenomena in the mid-visible to near-infrared range of the spectrum and for x approximately 0. We analyze the optical phenomena operating in such structures using a combination of experiment and simulation and show that semi-shells of TiN exhibit a tunable localized plasmon resonance with light. The material is, however, unsuitable for applications in which a long-distance surface plasmon polariton is desired.

Peptides based on unnatural β3-amino acids offer a versatile platform for the design of self-assembling nanostructures due to the folding stability of the 14-helix and the high symmetry of the side chains inherent in this geometry. We have previously described that N-terminal acetylation (Ac-) forms a supramolecular self-assembly motif that allows β3-peptides to assemble head-to-tail into a helical nanorod which then further bundles into hierarchical superstructures. Here we investigate the effect of the topography of the 14-helical nanorod on lateral self-assembly. Specifically, we report on the variations in the superstructure of three isomeric peptides comprising the same three β3-amino acid residues: β3-leucine (L), β3-isoleucine (I) β3-alanine (A) to give peptides Ac-β3[LIA], Ac-β3[IAL] and Ac-β3[ALI]. AFM imaging shows markedly different superstructures for the three peptides. Well defined synchrotron far-infrared spectra reveal uniform geometries with a high degree of similarity between the isomeric peptides in the amide modes of the 400–650 wavenumber range. Far-IR also confirms that the C-terminal carboxyl group is free in the assemblies, thus it is solvated in the dispersant. Hence, the differences in the superstructures formed by the fibers are defined primarily by van der Waals energy minimization between the varied cross sectional morphologies of the core nanorods.

The combination of metal and semiconductor components in nanoscale to form a hybrid nanocrystal provides an important approach for achieving advanced functional materials with special optical, magnetic and photocatalytic functionalities. Here, a facile solution method is reported for the synthesis of Au-Ni-ZnO metal-semiconductor hybrid nanocrystals with a flower-like morphology and multifunctional properties. This synthetic strategy uses noble and magnetic metal Au@Ni nanocrystal seeds formed in situ to induce the heteroepitaxial growth of semiconducting ZnO nanopyramids onto the surface of metal cores. Evidence of epitaxial growth of ZnO{0001} facets on Ni {111} facets is observed on the heterojunction, even though there is a large lattice mismatch between the semiconducting and magnetic components. Adjustment of the amount of Au and Ni precursors can control the size and composition of the metal core, and consequently modify the surface plasmon resonance (SPR) and magnetic properties. Room-temperature superparamagnetic properties can be achieved by tuning the size of Ni core. The as-prepared Au-Ni-ZnO nanocrystals are strongly photocatalytic and can be separated and re-cycled by virtue of their magnetic properties. The simultaneous combination of plasmonic, semiconducting and magnetic components within a single hybrid nanocrystal furnishes it multifunctionalities that may find wide potential applications.

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A compact, high-power emitter of half-cycle terahertz (THz) radiation is demonstrated. The device consists of an epitaxial InAs emitter upon a GaAs prism and produces THz pulses that are 20 times more powerful than those from conventional planar InAs emitters. This improvement is a direct result of reorienting the transient THz dipole such that its axis is not perpendicular to the emitting surface.

The resolution of laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) elemental bioimaging is usually constrained by the diameter of the laser spot size and is often not adequate to explore in situ sub-cellular distributions of elements and / or proteins in biological tissue sections. Super-resolution reconstruction is a method typically used for many imaging modalities and combines multiple lower resolution images to create a higher resolution image. Here, we present a super-resolution reconstruction method for LA-ICP-MS imaging by ablating consecutive layers of a biological specimen with offset orthogonal scans, resulting in a 10x improvement in resolution for quantitative measurement of dystrophin in murine muscle fibres. Layer-by-layer image reconstruction was also extended to the third dimension without the requirement of image registration across multiple thin section specimens. Quantitative super-resolution reconstruction, combined with Gaussian filtering and application of the Richardson-Lucy total variation algorithm, provided superior image clarity and fidelity in two-and three-dimensions.

An acoustic impedance spectrometer was used to measure the frequencies R1 and R2 of the first two resonances of the vocal tract. The measurement was made just outside the mouth, in parallel with the free field, using a new technique that provides precise information about the acoustic response of the vocal tract in real time. Values measured for native speakers for a particular vowel were used as target parameters for subjects who used a visual display of an impedance spectrum of their own vocal tracts as real-time feedback to realise the vocal tract configuration required to pronounce the target vowel. We report the values (R1,R2) for eleven non-nasalised vowels of French. These values are similar to the formant frequencies measured previously for these vowels, and their relative positions in the (R2,R1) plane are similar to those of the same vowels in the (F2,F1) formant plane. The confusion and correct identification of these vowels are shown to be strongly related to their separation in the (R2,R1) plane. We report the results of attempts to imitate six of these vowels by monolingual anglophone subjects. One group used a traditional method of learning pronunciation: they heard the vowel sounds and then attempted to imitate them. Another group also heard the sounds, but were assisted by the vocal tract feedback described above when imitating the target sounds. The acoustic properties and recognizability of the vowels were significantly superior when the subjects used vocal-tract feedback.