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Novel rattling of K atoms in aluminium-doped defect pyrochlore tungstate
No full textRattling dynamics have been identified as fundamental to superconductivity in defect pyrochlore osmates and aluminium vanadium intermetallics, as well as low thermal conductivity in clathrates and filled skutterudites. Combining inelastic neutron scattering (INS) measurements and ab initio molecular dynamics (MD) simulations, we use a new approach to investigate rattling in the Al-doped defect pyrochlore tungstates: AAl0.33W1.67O6 (A = K, Rb, Cs). We find that although all the alkali metals rattle, the rattling of the K atoms is unique, not only among the tungstates but also among the analogous defect osmates, KOs2O6 and RbOs2O6. Detailed analysis of the MD trajectories reveals that two unique features set the K dynamics apart from the rest, namely, (1) quasi one-dimensional local diffusion within a cage, and (2) vibration at a range of frequencies. The local diffusion is driven by strongly anharmonic local potentials around the K atoms exhibiting a double-well structure in the direction of maximum displacement, which is also the direction of local diffusion. On the other hand, vibration at a range of frequencies is a consequence of the strong anisotropy in the local potentials around the K atoms as revealed by directional magnitude spectra. We present evidence to show that it is the smaller size rather than the smaller mass of the K rattler which leads to the unusual dynamics. Finally, we suggest that the occurrence of local diffusion and vibration at a range of frequencies in the dynamics of a single rattler, as found here for the K atoms, may open new possibilities for phonon engineering in thermoelectric materials. © 2014, IOP Publishing Ltd
Hirshfeld atom refinement for modelling strong hydrogen bonds
No full textHigh-resolution low-temperature synchrotron X-ray diffraction data of the salt L-phenylalaninium hydrogen maleate are used to test the new automated iterative Hirshfeld atom refinement (HAR) procedure for the modelling of strong hydrogen bonds. The HAR models used present the first examples of Z' > 1 treatments in the framework of wavefunction-based refinement methods. L-Phenylalaninium hydrogen maleate exhibits several hydrogen bonds in its crystal structure, of which the shortest and the most challenging to model is the O-H...O intramolecular hydrogen bond present in the hydrogen maleate anion (O...O distance is about 2.41 Å). In particular, the reconstruction of the electron density in the hydrogen maleate moiety and the determination of hydrogen-atom properties [positions, bond distances and anisotropic displacement parameters (ADPs)] are the focus of the study. For comparison to the HAR results, different spherical (independent atom model, IAM) and aspherical (free multipole model, MM; transferable aspherical atom model, TAAM) X-ray refinement techniques as well as results from a low-temperature neutron-diffraction experiment are employed. Hydrogen-atom ADPs are furthermore compared to those derived from a TLS/rigid-body (SHADE) treatment of the X-ray structures. The reference neutron-diffraction experiment reveals a truly symmetric hydrogen bond in the hydrogen maleate anion. Only with HAR is it possible to freely refine hydrogen-atom positions and ADPs from the X-ray data, which leads to the best electron-density model and the closest agreement with the structural parameters derived from the neutron-diffraction experiment, e.g. the symmetric hydrogen position can be reproduced. The multipole-based refinement techniques (MM and TAAM) yield slightly asymmetric positions, whereas the IAM yields a significantly asymmetric position. © 2014, International Union of Crystallography
The hydrological legacy of deforestation on global wetlands
No full textIncreased catchment erosion and nutrient loading are commonly recognized impacts of deforestation on global wetlands. In contrast, an increase in water availability in deforested catchments is well known in modern studies but is rarely considered when evaluating past human impacts. We used a Budyko water balance approach, a meta-analysis of global wetland response to deforestation, and paleoecological studies from Australasia to explore this issue. After complete deforestation, we demonstrated that water available to wetlands increases by up to 15% of annual precipitation. This can convert ephemeral swamps to permanent lakes or even create new wetlands. This effect is globally significant, with 9 to 12% of wetlands affected, including 20 to 40% of Ramsar wetlands, but is widely unrecognized because human impact studies rarely test for it. © 2014, American Association for the Advancement of Science
Lignin degradation in a coastal groundwater aquifer: a useful tracer?
No full textLignin as a biomarker in soils, peat, lakes and intertidal and marine sediment cores has been widely researched in the last four decades. The biogeochemical processes controlling their distribution and composition include fractionation due to phase changes, mineral binding, and abiotic and biotic decay. However, there appears to be no studies in the literature describing the concentration and composition of lignin in groundwater aquifers, despite lignin tracing having the potential to differentiate between types of vegetation and recharge source. In the latter case aquifers could potentially be a source of old, degradation resistant lignin. In this study, we characterise the lignin composition in groundwater samples from a coastal sand aquifer, in SE Australia. We compare these data with lignin composition of fresh vegetation samples from the study site, and with lignin data from other environments in the literature. Groundwater samples were also analysed for Dissolved Organic Carbon (DOC) and inorganic chemistry (major ions, Dissolved Inorganic Carbon (DIC) and redox sensitive species) to investigate lignin fractionation processes. To achieve this, the groundwater lignin composition was compared to the total DOC and DIC in the samples and the prevailing redox reactions. The lignin composition in groundwater was found to be unrelated to the surrounding surface vegetation, indicating significant alteration by biogeochemical processes along its flow paths. We identify potential lignin degradation zones, via determination of total OC consumed through redox reactions and microbial activity. In conclusion, this study, by closely examining the correlations of lignin phenols in groundwater with lignin in surface waters, as well as biogeochemical processes in the aquifer is shedding a new light on the ability of lignin as a biomarker in these subsurface systems. To our knowledge, this is the first attempt to assess the usefulness of lignin as a tracer in groundwater
Mild conditions for Deuteration of primary and secondary Arylamines for the synthesis of deuterated optoelectronic organic molecules
No full textDeuterated arylamines demonstrate great potential for use in optoelectronic devices, but their widespread utility requires a method for large-scale synthesis. The incorporation of these deuterated materials into optoelectronic devices also provides the opportunity for studies of the functioning device using neutron reflectometry based on the difference in the scattering length density between protonated and deuterated compounds. Here we report mild deuteration conditions utilising standard laboratory glassware for the deuteration of: diphenylamine, N-phenylnaphthylamine, N-phenyl-o-phenylenediamine and 1-naphthylamine (via H/D exchange in D2O at 80 °C, catalysed by Pt/C and Pd/C). These conditions were not successful in the deuteration of triphenylamine or N,N-dimethylaniline, suggesting that these mild conditions are not suitable for the deuteration of tertiary arylamines, but are likely to be applicable for the deuteration of other primary and secondary arylamines. The deuterated arylamines can then be used for synthesis of larger organic molecules or polymers with optoelectronic applications. © 2014, Creative Commons
Phase relations between the water-rich sulfuric acid hydrates, potential markers of thermal history on Jupiter’s icy moons
No full textSynchrotron X-ray powder diffraction has been used to explore the water-rich (<50 wt.% H2SO4) region of the sulfuric acid and water binary phase diagram at temperatures between 80 and 285 K. The phase relations that are determined demonstrate that, on laboratory timescales, sulfuric acid hydrates crystallize as mixtures of phases. Four forms of sulfuric acid hydrates were observed along with ice Ih, with their proportions dependent on temperature and sample H2SO4 wt.%. The charting of these phase relations has revealed a transformation between hydrate forms, which could be utilized as a marker for areas of higher heat flow on the surfaces of the Galilean ice moons. © 2014, Published by Elsevier Inc
What difference does a methyl group make: pentamethylbenzene?
No full textThe crystal structure of pentamethylbenzene has been obtained for the first time with the use of synchrotron radiation, whilst the low-energy spectrum of lattice dynamics, dominated by the methyl group torsions, was obtained using inelastic neutron scattering. The effect of symmetry lowering by the removal of a single methyl group relative to hexamethylbenzene has been investigated, including the role that this plays in the charge-transfer characteristics of complexes formed with tetracyanoethylene. © 2014, WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Oxide ion transport in (Nd2−xZrx)Zr2O7+δ electrolytes by an interstitial mechanism
No full textWe have studied the structure and transport properties of ten (Nd2−xZrx)Zr2O7+x/2 (x = 0–1.27) solid solutions, which lie in the ZrO2–Nd2Zr2O7 isomorphous miscibility range. Major attention has been focused on the pyrochlore-like (Nd2−xZrx)Zr2O7+x/2 solid solutions with x = 0–0.78, which are thought to be potential interstitial oxide ion conductors. The X-ray and neutron diffraction results demonstrate that the (Nd2−xZrx)Zr2O7+x/2 (x = 0–1.27) solid solutions undergo an order–disorder (pyrochlore–defect fluorite) structural phase transition. The (Nd2−xZrx)Zr2O7+x/2 (x = 0.2–0.78) have the bulk conductivity, ∼(1.2–4) × 10–3 S/cm at 750 °C, which is two orders of magnitude higher than that of the ordered pyrochlore Nd2Zr2O7. An attempt has been made to determine the interstitial oxygen content of (Nd2−xZrx)Zr2O7+x/2 (x = 0.2; 0.67) in a reducing atmosphere using thermogravimetry and mass spectrometry. It has been shown that no reduction occurs in the NdZrO system, where neodymium has only one oxidation state, 3+. © 2014, Elsevier B.V
Measurement and analysis of field-induced crystallographic texture using curved position-sensitive diffraction detectors
No full textThis paper outlines measurement and analysis methodologies created for determining the structural responses of electroceramics to an electric field. A sample stage is developed to apply electric fields to ceramic materials at elevated temperatures during neutron diffraction experiments. The tested voltages and temperatures range from −20 kV to +20 kV and room temperature to 200 °C, respectively. The use of the sample environment for measuring the response of ferroelectric ceramics to an electrical stimulus is demonstrated on the instrument Wombat, a monochromatic neutron diffractometer employing a curved positive sensitive detector. Methodologies are proposed to account for the geometrical effects when vector fields are applied to textured materials with angularly dispersive detector geometries. Representative results are presented for the ferroelectric (Bi1/2Na1/2)TiO3-6%BaTiO3 (BNT-6BT) which show both phase transformation and ferroelectric domain texturing under the application of an electric field. This experimental and analysis approach is well suited for time-resolved measurements such as stroboscopic and in situ studies on a variety of electro-active materials.© 2014, Springer Science+Business Media New York
Location of hydrogen atoms in hydronium jarosite
No full textVarious models for the crystal structure of hydronium jarosite were determined from Rietveld refinements against neutron powder diffraction patterns collected at ambient temperature and also single-crystal X-ray diffraction data. The possibility of a lower symmetry space group for hydronium jarosite that has been suggested by the literature was investigated. It was found the space group is best described as R3 ¯ m
R3¯m, the same for other jarosite minerals. The hydronium oxygen atom was found to occupy the 3 ¯ ¯ ¯ m
3¯m
site (3a Wyckoff site). Inadequately refined hydronium bond angles and bond distances without the use of restraints are due to thermal motion and disorder of the hydronium hydrogen atoms across numerous orientations. However, the acquired data do not permit a precise determination of these orientations; the main feature up/down disorder of hydronium is clear. Thus, the highest symmetry model with the least disorder necessary to explain all data was chosen: The hydronium hydrogen atoms were modeled to occupy an m (18 h Wyckoff site) with 50 % fractional occupancy, leading to disorder across two orientations. A rigid body description of the hydronium ion rotated by 60° with H–O–H bond angles of 112° and O–H distances of 0.96 Å was optimal. This rigid body refinement suggests that hydrogen bonds between hydronium hydrogen atoms and basal sulfate oxygen atoms are not predominant. Instead, hydrogen bonds are formed between hydronium hydrogen atoms and hydroxyl oxygen atoms. The structure of hydronium alunite is expected to be similar given that alunite supergroup minerals are isostructural.© 2014, Springer-Verlag Berlin Heidelberg