Structural Study of an Unusual Cubic Pyrochlore Bi1.5Zn0.92Nb1.5O6.92

Single-phase pyrochlore-type specimens of Bi_1.5Zn_0.92Nb_1.5O_6.92 were studied using combined electron, X-ray and neutron powder diffraction techniques. Rietveld refinements using neutron powder diffraction data confirmed an average pyrochlore structure A₂B₂O₆O′ (Fd&3macr;m, a=10.5616(1) Å) with both Bi and Zn mixed on the A-sites. However, refinements revealed significant local deviations from the ideal pyrochlore arrangement which were caused by apparent displacive disorder on both the A and O′ sites. The best fit was obtained with a disordered model in which the A-cations were randomly displaced by ∼0.39 Å from the ideal eight-fold coordinated positions. The displacements occur along the six 〈112〉 directions perpendicular to the O′-A-O′ links. In addition, the O′ ions were randomly displaced by ∼0.46 Å along all 12 〈110〉 directions. Crystal-chemical considerations suggest the existence of short-range correlations between the O′ displacements and both the occupancy of the A-sites (i.e., Bi or Zn) and the directions of the A-cation displacements. The combined A-cation and O′ displacements change the coordination sphere of the A-cations from 8 to (5+3); the resulting coordination environment of the A-cations bears similarities to that of the (5+1)coordinated Zn in zirconolite-like Bi₂Zn_2/3Nb_4/3O₇. The observed displacive disorder in the A₂O′ network of the Bi_1.5Zn_0.92Nb_1.5O_6.92 structure involves atoms associated with the lowest-frequency vibrational bending mode, and is likely responsible for both the high dielectric constant and the dielectric relaxation reported for this compound.     

C-terminal processing of yeast Spt7 occurs in the absence of functional SAGA complex

Background  

Spt7 is an integral component of the multi-subunit SAGA complex that is required for the expression of ~10% of yeast genes. Two forms of Spt7 have been identified, the second of which is truncated at its C-terminus and found in the SAGA-like (SLIK) complex.     

Cold Sintering: A Paradigm Shift for Processing and Integration of Ceramics

This paper describes a sintering technique for ceramics and ceramic‐based composites, using water as a transient solvent to effect densification (i.e. sintering) at temperatures between room temperature and 200 °C. To emphasize the incredible reduction in sintering temperature relative to conventional thermal sintering this new approach is named the “Cold Sintering Process” (CSP). Basically CSP uses a transient aqueous environment to effect densification by a mediated dissolution–precipitation process. CSP of NaCl, alkali molybdates and V₂O₅ with small concentrations of water are described in detail, but the process is extended and demonstrated for a diverse range of chemistries (oxides, carbonates, bromides, fluorides, chlorides and phosphates), multiple crystal structures, and multimaterial applications. Furthermore, the properties of selected CSP samples are demonstrated to be essentially equivalent as samples made by conventional thermal sintering.     

Thermally stimulated depolarization current spectra of cross-linked polyethylene and the influence of cross-linking byproducts

Cross-linked polyethylene (XLPE) is notable for its use as power cable insulation. Its longevity is limited by space charge buildup linked to impurities such as the byproducts left behind by the cross-linking agent dicumyl peroxide (DCP). The goal of this work is to determine the impacts of these byproducts on charge trapping and detrapping in XLPE using the thermally stimulated depolarization current technique. XLPE with byproducts has one source of trapped charge, which originates from the byproducts. XLPE that was thermally treated via degassing exhibits two other sources of trapped charge, which are charge injection and dipolar relaxations. Oxidation from degassing was shown to control the trapping from these sources, which is useful knowledge for processing this material prior to its use. Reintroducing acetophenone, one of the major byproducts of DCP, suppresses those two peaks once more, showing that it controls the overall space charge buildup characteristics in XLPE.     

Influence of experimental conditions on the electric field effect in the ceramic (BiPb)2Sr2Ca2Cu3Ox

An experimental study is reported of the influence of temperature (T), electric field polarity (±E), as well as of changes in the electrode/insulator/superconductor (E/I/S) measuring system on the field effect in the ceramic (BiPb)₂Sr₂Ca₂Cu₃O_x. It has been established that at 77 K and for E⩾60 MV/m the critical current I _c and conductivity of the sample increase for I>I _c, irrespective of the field polarity. For lower fields and a negative electrode potential the conductivity in an electric field may decrease. The field effect decreases with increasing temperature, to practically vanish near T _c where the sample is still in superconducting state. Experiments carried out with more complex systems E/I/M/I/S and E/I/M/S (M stands for a metallic foil) support the conclusion that it is the external electric field that is responsible for the observed effects. Fiz. Tverd. Tela (St. Petersburg) 39, 1967–1970 (December 1997)     

Effects of interfacial modifications on electrical properties of laminar composite dielectrics

The reported work highlights that both polarizibility and quasi-DC conductivity, the two most important parameters for high energy density materials, can be influenced by the surface polarity of an oxide and interfacial surface tension between the oxide and polymer in a laminar composite. Surface modification of laminar composites, composed of thermally grown silica and vapor phase grown Parylene C thin films using organosilanes, was used to control silica surface polarity and interfacial surface tension. Surface polarity of thermally grown silica was found to control the interfacial dipolar energy states.     

High Q calcium titanate cylindrical dielectric resonators for magnetic resonance microimaging

At high magnetic fields radiation losses, wavelength effects, self-resonance, and the high resistance of typical components all contribute to increased losses in conventional RF coil designs. High permittivity ceramic dielectric resonators create strong uniform magnetic fields in a compact structure at high frequencies and can potentially solve some of the challenges of high field coil design. In this study an NMR probe was constructed for operation at 600 MHz (14.1 T) using an inductively fed CaTiO₃ (relative permittivity of 156) cylindrical hollow bore dielectric resonator. The design has an unmatched Q value greater than 2000, and the electric field is largely confined to the dielectric itself, with near zero values in the hollow bore which accommodates the sample. Experimental and simulation mapping of the RF field show good agreement, with the ceramic resonator giving a pulse width approximately 25% less than a loop gap resonator of similar inner dimensions. High resolution images, with voxel dimensions less than 50 μm³, have been acquired from fixed zebrafish samples, showing excellent delineation of several fine structures.