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Heterostructures built from 2D, atomically thin crystals are bound by the van der Waals force and exhibit unique optoelectronic properties. Here, we report the structure, composition and optoelectronic properties of 1D van der Waals heterostructures comprising carbon nanotubes wrapped by atomically thin nanotubes of boron nitride and molybdenum disulfide (MoS2). The high quality of the composite was directly made evident on the atomic scale by transmission electron microscopy, and on the macroscopic scale by a study of the heterostructure’s equilibrium and ultrafast optoelectronics. Ultrafast pump−probe spectroscopy across the visible and terahertz frequency ranges identified that, in the MoS 2 nanotubes, excitons coexisted with a prominent population of free charges. The electron mobility was comparable to that found in high-quality atomically thin crystals. The high mobility of the MoS2 nanotubes highlights the potential of 1D van der Waals heterostructures for nanoscale optoelectronic devices.

We report the observation of four unprecedented new crystalline forms of SnSe, obtained as a result of encapsulation in narrow to medium diameter single-walled carbon nanotubes. Aberration-corrected scanning transmission electron microscopy at 80 kV revealed linear, zigzag, helical (i.e., 2 × 1) atomic chains and a new form of encapsulated SnSe. This new form is apparently isostructural to free-standing MoS, MoSe, and WSe extreme nanowires etched from the corresponding monolayer dichalcogenides and also recently observed encapsulated MoTe. A structural model has been attained from annular dark-field (ADF) images. The experimental imaging agrees well with image simulations produced from models anticipated for the new structural forms.

One-dimensional (1D) atomic chains of CsI were previously reported in double-walled carbon nanotubes with ∼0.8 nm inner diameter. Here, we demonstrate that, while 1D CsI chains form within narrow ∼0.73 nm diameter single-walled carbon nanotubes (SWCNTs), wider SWCNT tubules (∼0.8-1.1 nm) promote the formation of helical chains of CsI 2 × 1 atoms in cross-section. These CsI helices create complementary oval distortions in encapsulating SWCNTs with highly strained helices formed from strained Cs2I2 parallelogram units in narrow tubes to lower strain Cs2I2 units in wider tubes. The observed structural changes and charge distribution were analyzed by density-functional theory and Bader analysis. CsI chains also produce conformation-selective changes to the electronic structure and optical properties of the encapsulating tubules. The observed defects are an interesting variation from defects commonly observed in alkali halides as these are normally associated with the Schottky and Frenkel type. The energetics of CsI 2 × 1 helix formation in SWCNTs suggests how these could be controllably formed.

The development of THz technology and communication systems is creating demand for devices that can modulate THz beams rapidly. Here we report the design and characterisation of high-performance, broadband THz modulators based on the photo-induced transparency of carbon nanotube films. Rather than operating in the standard modulation mode, where optical excitation lowers transmission, this new class of modulators exhibits an inverted modulation mode with an enhanced transmission. Under femtosecond pulsed illumination, modulation depths reaching + 80 % were obtained simultaneously with modulation speeds of 340 GHz. The influence of the film thickness on the insertion loss, modulation speed and modulation depth was explored over a frequency range from 400 GHz to 2.6 THz. The excellent modulation depth and high modulation speed demonstrated the significant potential of carbon nanotube thin films for ultrafast THz modulators.

A strong negative photoconductivity was identified in thin film networks of single-walled carbon nanotubes using optical pump, THz probe spectroscopy. The films were controllably doped, using eithe...

Heterostructures built from 2D, atomically thin crystals are bound by the van der Waals force and exhibit unique optoelectronic properties. Here, we report the structure, composition and optoelectronic properties of 1D van der Waals heterostructures comprising carbon nanotubes wrapped by atomically thin nanotubes of boron nitride and molybdenum disulfide (MoS

Stem cells are one of the foundational evolutionary novelties that allowed the independent emergence of multicellularity in the plant and animal lineages. In plants, the homeodomain (HD) transcription factor WUSCHEL (WUS) is essential for the maintenance of stem cells in the shoot apical meristem. WUS has been reported to bind to diverse DNA motifs and to act as transcriptional activator and repressor. However, the mechanisms underlying this remarkable behavior have remained unclear. Here, we quantitatively delineate WUS binding to three divergent DNA motifs and resolve the relevant structural underpinnings. We show that WUS exhibits a strong binding preference for TGAA repeat sequences, while retaining the ability to weakly bind to TAAT elements. This behavior is attributable to the formation of dimers through interactions of specific residues in the HD that stabilize WUS DNA interaction. Our results provide a mechanistic basis for dissecting WUS dependent regulatory networks in plant stem cell control., WUSCHEL is a homeodomain transcription factor that is essential for stem cell maintenance in the plant shoot apical meristem. Here, via structural and biochemical approaches, Sloan et al. show that strong WUSCHEL binding to preferential target motifs can be attributed to dimer formation that stabilizes DNA binding.

Large diameter single-walled carbon nanotubes films are shown to have a doping level and THz conductivity that can be readily controlled using adsorption doping or electrostatic gating. The giant negative photoconductivity observed upon optical excitation is due to a rapid reduction in mobile carrier density, synchronously to a lowering of the momentum scattering rate. The large modulation depth and tunable recovery time open prospects for carbon nanotube films in ultrafast and THz devices.

We have investigated the structure of atomic defects within monolayer NbSe2 encapsulated in graphene by combining atomic resolution transmission electron microscope imaging, density functional theory (DFT) calculations, and strain mapping using geometric phase analysis. We demonstrate the presence of stable Nb and Se monovacancies in monolayer material and reveal that Se monovacancies are the most frequently observed defects, consistent with DFT calculations of their formation energy. We reveal that adventitious impurities of C, N, and O can substitute into the NbSe2 lattice stabilizing Se divacancies. We further observe evidence of Pt substitution into both Se and Nb vacancy sites. This knowledge of the character and relative frequency of different atomic defects provides the potential to better understand and control the unusual electronic and magnetic properties of this exciting two-dimensional material.

The structural organization of compounds in a confined space of nanometer-scale cavities is of fundamental importance for understanding the basic principles for atomic structure design at the nanolevel. Here, we explore size-dependent structure relations between one-dimensional PbTe nanocrystals and carbon nanotube containers in the diameter range of 2.0-1.25 nm using high-resolution transmission electron microscopy and ab initio calculations. Upon decrease of the confining volume, one-dimensional crystals reveal gradual thinning, with the structure being cut from the bulk in either a110or a100growth direction until a certain limit of ∼1.3 nm. This corresponds to the situation when a stoichiometric (uncharged) crystal does not fit into the cavity dimensions. As a result of the in-tube charge compensation, one-dimensional superstructures with nanometer-scale atomic density modulations are formed by a periodic addition of peripheral extra atoms to the main motif. Structural changes in the crystallographic configuration of the composites entail the redistribution of charge density on single-walled carbon nanotube walls and the possible appearance of the electron density wave. The variation of the potential attains 0.4 eV, corresponding to charge density fluctuations of 0.14 e/atom.

Graphite nanoplatelets (GNP) were prepared by a high-pressure homogenisation process (HPHP) via exfoliation of bulk graphite, yielding GNP in the form of square shaped platelets with lateral dimensions on the micrometre (μm) scale and thicknesses on the nanometre (nm) scale (

2D Boron Nitride Nano-sheets (BNNS) were prepared using a high-pressure homogenisation process to exfoliate bulk hexagonal boron nitride (h-BN). The effectiveness of this process was studied by characterising bulk h-BN and BNNS post-processing using numerous techniques. The BNNS produced was composed of a mixture of sheets having lengths on the nanometre (nm) scale, but lateral thicknesses on the micron (μm) length scale. The product was a macro-porous material containing slit-like pores with a surface area of 170 m2 g−1. It had a polycrystalline structure with d002 = 0.335 nm and L002 = 2 nm. From the sharp E2g peak in the Raman spectrum at 1360 cm−1 (FWHM = 12.5 cm−1), the sheets had a low defect density and were highly exfoliated. X-Ray photoelectron spectroscopy (XPS) studies detected B–OH and N–H groups on the BNNS surface and the presence of residual surfactant. Contact angle measurements (60° ± 3° (0 s); 40° ± 2° (10 s)) confirmed a hydrophilic surface. The BNNS was thermally stable under oxidative conditions up to 323 °C.

We study the normal vibrations of $2\ifmmode\times\else\texttimes\fi{}2$ and $3\ifmmode\times\else\texttimes\fi{}3$ potassium iodide (KI) crystalline nanowires embedded in single-walled carbon nanotubes (SWCNTs) by density functional theory calculations, accompanied by Raman spectroscopy measurements on SCWNTs infiltrated with KI. The calculated stand-alone KI nanowires are found to be fully stable, while their vibrational energies are very close to the additional low-frequency Raman lines experimentally detected in the KI@SCWNT systems and ascribed to the encapsulated KI crystals. The difference between the relaxed and observed geometries of the KI nanowires evidences an electron transfer from these nanowires to the surrounding SWCNTs. Calculated radial and tangential vibrational frequencies of KI nanowires compared to those of supplementary discovered Raman lines suggest that the nanowire-SWCNT interaction is of a van der Waals origin and exclude the possibility of functionalization between the KI nanocrystals and the nanotube walls.

Nanostructuring, e. g., reduction of dimensionality in materials, offers a viable route toward regulation of materials electronic and hence functional properties. Here, we present the extreme case of nanostructuring, exploiting the capillarity of single-walled carbon nanotubes (SWCNTs) for the synthesis of the smallest possible SnTe nanowires with cross sections as thin as a single atom column. We demonstrate that by choosing the appropriate diameter of a template SWCNT, we can manipulate the structure of the quasi-one-dimensional (1D) SnTe to design electronic behavior. From first principles, we predict the structural re-formations that SnTe undergoes in varying encapsulations and confront the prediction with TEM imagery. To further illustrate the control of physical properties by nanostructuring, we study the evolution of transport properties in a homologous series of models of synthesized and isolated SnTe nanowires varying only in morphology and atomic layer thickness. This extreme scaling is predicted to significantly enhance thermoelectric performance of SnTe, offering a prospect for further experimental studies and future applications.

Monosubstituted lacunary Keggin [CoSiW11O39](6-) ions on graphene oxide (GO) were used in a comparative imaging study using aberration corrected transmission electron microscopy at two different acceleration voltages, 80 and 200 kV. By performing a set of static and dynamical studies, together with image simulations, we show how the use of lower voltages results in better stability and resolution of the underlying GO support while the use of higher voltages permits better resolution of the individual tungsten atoms and leads to less kinetic motion of the cluster, thus leading to a more accurate identification of cluster orientation and better stability under dynamical imaging conditions. Applying different voltages also influences the visibility of both GO and the lighter Co at lower or higher voltages, respectively.

This paper presents the results of measurements of the temperature dependence of resonance Raman scattering from 2 atom diameter HgTe nanowires embedded in the central pore of single walled carbon nanotubes, over the temperature range 4–295 K and excitation photon energies in the range 1.65 to 1.90 eV. The spectra are analysed to extract the temperature dependence of the phonon energies and linewidths and the central energy, linewidth and peak scattering strength of the optical resonances. The temperature dependence of the peak scattering strength is explained by a model in which the resonance broadening is dominated by coherence lifetime broadening, allowing us to determine the coherence lifetime of the underlying optical transition: 9 fs at 295 K and 18 fs at 50 K. The results are comparable with similar results on carbon nanotubes which suggests that the optical transitions responsible for the Raman resonances are excitonic.

A new barium ruthenium oxyhydroxide Ba4Ru3O10.2(OH)1.8 crystallises under hydrothermal conditions at 200 °C: powder neutron diffraction data show it adopts an 8H hexagonal perovskite structure with a new stacking sequence, while high resolution electron microscopy reveals regions of ordered layers of vacant Ru sites, and magnetometry shows antiferromagnetism with TN = 200(5) K.

HRTEM and HAADF STEM of 1DTbBrx@SWCNT meta-nanotubes reveal three structural modifications of 1D nanocrystals within single wall carbon nanotube channels attributed to a different stoichiometry of the guest crystal. For SWCNTs with diameters Dm > 1.4 nm a most complete tetragonal unit cell is observed. When crystallization occurs inside SWCNT with Dm < 1.4 nm 1D TbBrx crystal deforms a nanotube to elliptical shape in cross section. In this case the 1D crystal unit cell becomes monoclinic, with possible loss of a part of bromine atoms. Two modifications of a monoclinic unit cell appear. One of them is characterized by single or pair vacancies in the structure of the 1D crystal. Another structure is explained by peripheral and central bromine atoms loss. An appearance of such modifications can be stimulated by electron irradiation. The loss of bromine atoms is in agreement with chemical analysis data. Electronic properties of obtained meta-nanotubes are investigated using optical absorption and Raman spectroscopy. It is shown that intercalation of terbium bromide into SWCNTs leads to acceptor doping of SWCNTs. According to local EDX analysis and elemental mapping this doping can arise from significant stoichiometry change in 1D nanocrystal indicating an average Tb:Br atomic ratio of 1:2.8 ± 0.1.

Electrodeposition of Sn from supercritical difluoromethane has been performed into anodic alumina templates with pores down to 3 nm in diameter and into mesoporous silica templates with pores of diameter 1.5 nm. Optimized deposits have been characterized using X-ray diffraction, scanning electron microscopy, and scanning transmission electron microscopy (bright field, high-angle annular dark field, and energy-dispersive X-ray elemental mapping). Crystalline 13 nm diameter Sn nanowires have been electrodeposited in symmetric pore anodic alumina. Direct transmission electron microscopy evidence of sub 7 nm Sn nanowires in asymmetric anodic alumina has been obtained. These same measurements present indirect evidence for electrodeposition through 3 nm constrictions in the same templates. A detailed transmission electron microscopy study of mesoporous silica films after Sn deposition is presented. These indicate that it is possible to deposit Sn through the 1.5 nm pores in the mesoporous films, but that the nanowires formed are not stable. Suggestions of why this is the case and how such extreme nanowires could be stabilized are presented.

Despite email playing a central role in university business, little is known about the strategies used by staff to manage email and the factors contributing to email overload.In a mixed method study undertaken in one Australian university comparing academic(n = 193) and professional (n = 278) staff, we found that while email volume was higher in academics they used fewer email management strategies. For both groups,thematic analyses of commentary responses revealed that the unnecessary use of emails by staff and students, the expectation of a quick turnaround and an escalation in email traffic were associated with email overload and, as a consequence, increased work-related stress. In conclusion, we suggest that email overload typifies the working environment of academic and professional staff in modern universities, pointing to the importance of training staff in email management strategies for improving productivity and well-being. Refereed/Peer-reviewed

International audience; The production of thin mesoporous silica films with small (similar to 2-3 nm) pores oriented perpendicular to a titanium nitride growth surface is demonstrated using two methods. These are the growth from a Stober silica solution with surfactant ordering at the surface of the electrode, and electrochemically assisted growth from an acidic sol achieved by polarisation of the electrode surface. The thickness, pore order and pore size that can be achieved with these two methods is contrasted. A number of methods to vary the pore size by using different surfactants and swelling agents are explored. The advantage of applying these growth methods on titanium nitride surfaces is that it provides access to a wider electrochemical window for nanowire growth and sensor applications with non-aqueous electrolytes whilst retaining good film growth and adhesion properties.

Solvothermal synthesis at 240 °C in ethanol from titanium(IV) isopropoxide and cerium(III) nitrate hexahydrate produces nanocrystalline powders of anatase-structured TiO2. At low Ce content (0.5 mol% Ti replaced by Ce) the materials contain mixtures of Ce3+ and Ce4+, seen from Ce LIII-edge X-ray absorption near-edge structure (XANES) spectroscopy, which are well dispersed in the anatase structure as evidenced from nanometre-scale electron energy loss spectroscopy maps and powder X-ray diffraction (XRD). The addition of lactic acid to the solvothermal reaction produces less crystalline samples, proved by powder XRD and Raman spectroscopy, with higher surface areas from nitrogen adsorption, and that contain a higher proportion of Ce3+. This leads to material with high activity for photocatalytic hydrogen production from water under UV irradiation in the presence of sacrificial methanol and Pt catalyst. Further in situ XANES experiments at the Ce LIII-edge recorded on heating the materials in air above 300 °C shows that oxidation to Ce4+ occurs. This process, typical of the conditions usually used in the synthesis of Ce-doped titania materials, yields materials with lower photocatalytic activity.

Germanium telluride has attracted great research interest, primarily because of its phase-change properties. We have developed a general scheme, based on the ab initio random structure searching (AIRSS) method, for predicting the structures of encapsulated nanowires, and using this we predict a number of thermodynamically stable structures of GeTe nanowires encapsulated inside carbon nanotubes of radii under $9\phantom{\rule{0.16em}{0ex}}\AA{}$. We construct the phase diagram of encapsulated GeTe, which provides quantitative predictions about the energetic favorability of different filling structures as a function of the nanotube radius, such as the formation of a quasi-one-dimensional rock-salt-like phase inside nanotubes of radii between 5.4 and $7.9\phantom{\rule{0.16em}{0ex}}\AA{}$. Simulated TEM images of our structures show excellent agreement between our results and experimental TEM imagery. We show that, for some nanotubes, the nanowires undergo temperature-induced phase transitions from one crystalline structure to another due to vibrational contributions to the free energy, which is a first step toward nano-phase-change memory devices.

International audience; A variety of iodine-based one-dimensional (1-D) nanocrystals were introduced into double-wall carbon nanotubes (DWCNTs) using the molten phase method, as an intermediate step for ultimately obtaining encapsulated metal nanowires. Based on high-resolution transmission electron microscopy (HRTEM) observations using different imaging modes (bright field, dark field, and scanningTEM)and associated analytical tools (electron energy loss spectroscopy), it is revealed that the reality of nanotube filling is much more complex than expected. For some iodides (typically NiI2 ), earlier decomposition during the filling step was observed, which could not be anticipated from the known data on the bulk material. Other filling materials (e.g., iodine) show a variety of atomic structuration inside and outside the CNTs, which is driven by the available space being filled. Most of the encapsulated structures were confirmed by modeling

Extreme nanowires (ENs) represent the ultimate class of crystals: They are the smallest possible periodic materials. With atom-wide motifs repeated in one dimension (1D), they offer a privileged perspective into the physics and chemistry of low-dimensional systems. Single-walled carbon nanotubes (SWCNTs) provide ideal environments for the creation of such materials. Here we present a comprehensive study of Te ENs encapsulated inside ultranarrow SWCNTs with diameters between 0.7 nm and 1.1 nm. We combine state-of-the-art imaging techniques and 1D-adapted ab initio structure prediction to treat both confinement and periodicity effects. The studied Te ENs adopt a variety of structures, exhibiting a true 1D realization of a Peierls structural distortion and transition from metallic to insulating behavior as a function of encapsulating diameter. We analyze the mechanical stability of the encapsulated ENs and show that nanoconfinement is not only a useful means to produce ENs but also may actually be necessary, in some cases, to prevent them from disintegrating. The ability to control functional properties of these ENs with confinement has numerous applications in future device technologies, and we anticipate that our study will set the basic paradigm to be adopted in the characterization and understanding of such systems.

The pyrochlore solid solution (Na0.33Ce0.67)(2)-(Ir1-xRux)(2)O-7 (0

We present a study of two new solvothermal synthesis approaches to mixed-metal oxide materials and structural characterisation of the products formed. The solvothermal oxidation of metallic gallium by a diethanolamine solution of iron(II) chloride at 240 °C produces a crystalline sample of a spinel-structured material, made up of nano-scale particles typically 20 nm in dimension. XANES spectroscopy at the K-edge shows that the material contains predominantly Fe2+ in an octahedral environment, but that a small amount of Fe3+ is also present. Careful analysis using transmission electron microscopy and powder neutron diffraction shows that the sample is actually a mixture of two spinel materials: predominantly (>97%) an Fe2+ phase Ga1.8Fe1.2O3.9, but with a minor impurity phase that is iron-rich. In contrast, the hydrothermal reaction of titanium bis(ammonium lactato)dihydroxide in water with increasing amounts of Sn(IV) acetate allows nanocrystalline samples of the SnO2–TiO2 solid solution to be prepared directly, as proved by powder XRD and Raman spectroscopy.

Cyclic voltammetry of silver coordination complexes in acetonitrile and in a single-phase supercritical carbon dioxide/acetonitrile (scCO2/CH3CN) system is reported. Five silver precursors are investigated: (1,5-cyclooctadiene)(hexafluoroacetylacetonato) silver(I) [Ag(hfac)(COD)], (hexafluoroacetylacetonato)(triphenylphosphine) silver(I) [Ag(hfac)(PPh3)], (perfluorooctanoato)bis(triphenylphosphine) silver(I) [Ag(CF3(CF2)6CO2)(PPh3)2], tetrakis(triphenylphosphine) silver(I) tetrafluoroborate [Ag(PPh3)4][BF4] and tetrakis(acetonitrile) silver(I) tetrafluoroborate [Ag(CH3CN)4][BF4]. Of these, [Ag(CH3CN)4][BF4] is found to be the most suitable for electrodeposition of silver from scCO2/CH3CN.

A new mixed rare-earth orthochromite series, LaxSm1-xCrO3, prepared through single-step hydrothermal synthesis is reported. Solid solutions (x = 0, 0.25, 0.5, 0.625, 0.75, 0.875, and 1.0) were prepared by the hydrothermal treatment of amorphous mixed-metal hydroxides at 370 °C for 48 h. Transmission electron microscopy (TEM) reveals the formation of highly crystalline particles with dendritic-like morphologies. Rietveld refinements against high-resolution powder X-ray diffraction (PXRD) data show that the distorted perovskite structures are described by the orthorhombic space group Pnma over the full composition range. Unit cell volumes and Cr-O-Cr bond angles decrease monotonically with increasing samarium content, consistent with the presence of the smaller lanthanide in the structure. Raman spectroscopy confirms the formation of solid solutions, the degree of their structural distortion. With the aid of shell-model calculations the complex mixing of Raman modes below 250 cm(-1) is clarified. Magnetometry as a function of temperature reveals the onset of low-temperature antiferromagnetic ordering of Cr(3+) spins with weak ferromagnetic component at Néel temperatures (TN) that scale linearly with unit cell volume and structural distortion. Coupling effects between Cr(3+) and Sm(3+) ions are examined with enhanced susceptibilities below TN due to polarization of Sm(3+) moments. At low temperatures the Cr(3+) sublattice is shown to undergo a second-order spin reorientation observed as a rapid decrease of susceptibility.

We have investigated the structure of atomic defects within monolayer NbSe

Cation size effects were examined in the mixed A-site perovskites La0.5 Sm0.5 CrO3 and La0.5 Tb0.5 CrO3 prepared through both hydrothermal and solid-state methods. Atomically resolved electron energy loss spectroscopy (EELS) in the transmission electron microscope shows that while the La and Sm cations are randomly distributed, increased cation-radius variance in La0.5 Tb0.5 CrO3 results in regions of localised La and Tb layers, an atomic arrangement exclusive to the hydrothermally prepared material. Solid-state preparation gives lower homogeneity resulting in separate nanoscale regions rich in La3+ and Tb3+ . The A-site layering in hydrothermal La0.5 Tb0.5 CrO3 is randomised upon annealing at high temperature, resulting in magnetic behaviour that is dependent on synthesis route.

International audience; Filling double-walled carbon nanotubes with iodine and various metal iodides (metals, alkali metals and transition metals) by the molten phase method was performed and the influence of possibly relevant chemical and physical properties of the filling materials on the filling rate was investigated. It was found, within the metal iodides series, that the filling rate can be mainly related to the redox potential (E MIx/M) of the filling material. Other parameters such as the possible formation of dimers, surface tension, or the early release of iodine may also play an additional role in the filling process.

In organic synthesis, the composition and structure of products are predetermined by the reaction conditions; however, the synthesis of well-defined inorganic nanostructures often presents a significant challenge yielding nonstoichiometric or polymorphic products. In this study, confinement in the nanoscale cavities of single-walled carbon nanotubes (SWNTs) provides a new approach for multistep inorganic synthesis where sequential chemical transformations take place within the same nanotube. In the first step, SWNTs donate electrons to reactant iodine molecules (I2), transforming them to iodide anions (I–). These then react with metal hexacarbonyls (M(CO)6, M = Mo or W) in the next step, yielding anionic nanoclusters [M6I14]2–, the size and composition of which are strictly dictated by the nanotube cavity, as demonstrated by aberration-corrected high resolution transmission electron microscopy, scanning transmission electron microscopy, and energy dispersive X-ray spectroscopy. Atoms in the nanoclusters [...

The magnetic structures of Ca3LiRuO6 and Ca3NaRuO6 have been deduced from powder neutron diffraction data. In each case successive Ru5+ cations in the [001] chains of the Sr4PtO6-like structure are antiferromagnetically coupled, and nearest-neighbour Ru5+ cations in adjacent chains are also antiferromagnetically coupled.

The structure of Nd5Ti5O17 has been refined from a reconstruction of the specimen exit-plane wave restored from a series of incrementally defocused high-resolution transmission electron microscope (HRTEM) images. The phase of the exit-plane wave shows contrast attributable to the oxygen anion sublattice and coupled with simulations provides confirmation of the composition of the cation sites as a function of sample thickness. The enhanced resolution in the exit-plane wave additionally allows a direct measurement of the `skewing' of the perovskite slabs.

The synthesis and characterization of a polycrystalline sample of the n = 2 Ruddlesden-Popper phase Nd 2BaLiRuO 7 are reported. X-ray and neutron diffraction show that the 6-coordinate sites are occupied by a 1:1 ordered arrangement of Li and Ru, that the 12-coordinate sites within the perovskite-like blocks are occupied by Ba, and that the cation sites on the block edges are occupied by Nd. Transmission electron microscopy shows that this compound is less susceptible to stacking faults then many other n = 2 phases, and 7Li MAS NMR spectroscopy shows that the environment of the single Li site in the structure is well-defined. The compound is an antiferromagnet below 32 K, with ordered magnetic moments of 2.2(2) μ B and 2.53(8) μ B on the Ru and Nd cations respectively at 2 K. © 2005 American Chemical Society.

The capability of sodium hydride as a reducing agent in oxide deintercalation reactions is explored. The Ni(III) perovskite LaNiO3 can be reduced topotactically to LaNiO2, isostructural with the 'infinite layer' cuprates, using solid sodium hydride in a sealed evacuated tube at 190 ≤ T/°C ≤ 210, and a similar infinite-layer phase is prepared by reduction of NdNiO3. Structural characterization indicates the coexistence of incompletely reduced regions, with five-coordinate Ni centers due to the introduction of oxide anions between the NiO23- sheets, giving samples with a refined stoichiometry of LaNiO(2.025(3)). Neutron powder diffraction and magnetization measurements indicate that the lamellar Ni(I) phase does not show the long-range antiferromagnetic ordering characteristic of isoelectronic Cu(II) oxides. This may be due either to the influence of the interlamellar oxide defect regions or to the reduced covalent mixing of Ni 3d and O 2p levels.

We describe here the high yield filling (i.e. > 50%) of single walled nanotubes (SWNTs) with a variety of halides, achieved according to various modified filling procedures. Both bundles and discrete SWNTs can be filled continuously up to lengths of several hundred nm, often with filling yields approaching 60-70% or better. In addition some high yield filled SWNTs were subjected to long-term washing in either boiling or room temperature, aqueous media, which does not remove the filling from the tubules, but enables effective removal of water-soluble extraneous materials.

The comparative crystallisation and HRTEM imaging properties of simple binary halides formed by the alkali iodides MI (M = Li, K, Na, Rb and Cs) within single walled carbon nanotubes (SWNTs) are described. The most common structure type observed within SWNTs is the rocksalt archetype, although CsI was observed to form both bcc and rocksalt structure types. In SWNTs forming in the 1.2-1.6 nm diameter range, all of the incorporated halides showed preferred orientation, with the (100) growth direction predominating for rocksalt-type packing and (112) so far observed exclusively for bcc packing. Crystals with dimensions spanning 2-6 atomic layers thickness in projection invariably exhibited lattice expansions that were attributed predominantly to a net reduction in coordination at the crystal-carbon interface. The crystallisation behaviour of UCl4-KCl and AgI-AgCl eutectic melts was compared in carbon nanotubes of different diameters and a pronounced ordering influence over the normally glassy melts was observed in narrower capillaries. HgI2 crystallised within nanotubes with ultra-narrow (i.e., 0.8 nm) capillaries were observed to form helical 2 × 1 layer crystals. © 2003 Académie des sciences. Published by Elsevier SAS. All rights reserved.

Using high resolution electron microscopy and first principles quantum mechanical calculations we have explored the fundamental physics and chemistry of the semiconductor, HgTe grown inside single wall carbon nanotubes. This material forms a low-dimensional structure based on a repeating Hg2Te2 motif in which both atom species adopt new coordination geometries not seen in the bulk. Density-functional theory calculations confirm the stability of this structure and demonstrate conclusively that it arises solely as a consequence of constrained low dimensionality. This change is directly correlated with a modified electronic structure in which the low-dimensional form of HgTe is transformed from a bulk semimetal to a semiconductor.