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Sample records for al ba ca

  1. New insights into the application of the valence rules in Zintl phases-Crystal and electronic structures of Ba7Ga4P9, Ba7Ga4As9, Ba7Al4Sb9, Ba6CaAl4Sb9, and Ba6CaGa4Sb9

    NASA Astrophysics Data System (ADS)

    He, Hua; Stoyko, Stanislav; Bobev, Svilen

    2016-04-01

    Crystals of three new ternary pnictides-Ba7Al4Sb9, Ba7Ga4P9, and Ba7Ga4As9 have been prepared by reactions of the respective elements in molten Al or Pb fluxes. Single-crystal X-ray diffraction studies reveal that the three phases are isotypic, crystallizing in the orthorhombic Ba7Ga4Sb9-type structure (space group Pmmn, Pearson symbol oP40, Z=2), for which only the prototype is known. The structure is based on TrPn4 tetrahedra (Tr=Al, Ga; Pn=P, As, Sb), connected in an intricate scheme into 1D-ribbons. Long interchain Pn-Pn bonds (dP-P>3.0 Å; dAs-As>3.1 Å; dSb-Sb>3.3 Å) account for the realization of 2D-layers, separated by Ba2+ cations. Applying the classic valance rules to rationalize the bonding apparently fails, and Ba7Ga4Sb9 has long been known as a metallic Zintl phase. Earlier theoretical calculations, both empirical and ab-initio, suggest that the possible metallic properties originate from filled anti-bonding Pn-Pn states, and the special roles of the "cations" in this crystal structure. To experimentally probe this hypothesis, we sought to synthesize the ordered quaternary phases Ba6CaTr4Sb9 (Tr=Al, Ga). Single-crystal X-ray diffraction work confirms Ba6.145(3)Ca0.855Al4Sb9 and Ba6.235(3)Ca0.765Ga4Sb9, with Ca atoms preferably substituting Ba on one of the three available sites. The nuances of the five crystal structures are discussed, and the chemical bonding in Ba7Ga4As9 is interrogated by tight-binding linear muffin-tin orbital calculations.

  2. Conductor-backed coplanar waveguide resonators of Y-Ba-Cu-O and Tl-Ba-Ca-Cu-O on LaAlO3

    NASA Technical Reports Server (NTRS)

    Miranda, F. A.; Bhasin, K. B.; Stan, M. A.; Kong, K. S.; Itoh, T.

    1992-01-01

    Conductor-backed coplanar waveguide (CBCPW) resonators operating at 10.8 GHz have been fabricated from Tl-Ba-Ca-O (TBCCO) and Y-Ba-Cu-O (YBCO) thin films on LaAlO3. The resonators consist of a coplanar waveguide (CPW) patterned on the superconducting film side of the LaAlO3 substrate with a gold ground plane coated on the opposite side. These resonators were tested in the temperature range from 14 to 106 K. At 77 K, the best of our TBCCO and YBCO resonators have an unloaded quality factor (Qo) 7 and 4 times, respectively, larger than that of a similar all-gold resonator. In this study, the Qo's of the TBCCO resonators were larger than those of their YBCO counterparts throughout the aforementioned temperature range.

  3. Charge-compensation effect of Al on luminescence properties of M2(Si, Al)5N8:Ce3+ (M = Ca, Sr, Ba)

    NASA Astrophysics Data System (ADS)

    Kuramoto, Daiki; Horikawa, Takashi; Hanzawa, Hiromasa; Machida, Ken-ichi

    2013-09-01

    The charge-compensated materials, M2AlxSi5-xN8:Ce3+ (M = Ca, Sr, Ba), were synthesized from appropriate mixtures of MSi, MAlSi, (MSiHy, MAlSiHy), Si3N4 and CeF3 by a direct nitriding process in a N2 gas and the luminescence properties were characterized. The resultant phosphors showed green emission suitable for LED illumination by optimizing the mixing ratio of metal elements. These phosphors were effectively excited by violet or blue light (400-430 nm) and the emission bands were observed at various wavelength regions for Ca: 489-528 nm, Sr: 511-520 nm, and Ba: 508-514 nm. Although the emission intensity of Ca2(Si, Al)5N8:Ce3+ was decreased with increasing amount of Al, those of Sr- and Ba-analogues were maximized at x = 0.5 of Al content in M2Si5-xAlxN8:Ce3+.

  4. Blue, yellow and orange color emitting rare earth doped BaCa2Al8O15 phosphors prepared by combustion method

    NASA Astrophysics Data System (ADS)

    Yerpude, A. N.; Dhoble, S. J.; Reddy, B. Sudhakar

    2014-12-01

    Eu2+, Dy3+, Sm3+ activated BaCa2Al8O15 phosphors were prepared by the combustion method. The phosphor powders were well characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) and photoluminescence (PL) spectrophotometer. Photoluminescence spectra of BaCa2Al8O15:Eu2+ phosphors show emission wavelength at 435 nm that corresponds to 4f65d1→4f7 transition of Eu2+ ion by keeping excitation wavelength extending broad-band from 270 to 400 nm centered at 334 nm. The Dy3+ doped BaCa2Al8O15 phosphors shows blue emission (485 nm) and yellow emission (566 nm) under the excitation of 347 nm, corresponding to the 4F9/2→6H15/2 transition and 4F9/2→6H13/2 transition of Dy3+ ions, respectively. The Sm3+ doped BaCa2Al8O15 phosphors have shown strong orange emission at 604 nm corresponding to the 4G5/2→6H7/2 transition of Sm3+ with intense excitation wavelength at 406 nm. Scanning electron microscopy has been used for exploring the size and morphological properties of the prepared phosphors. The obtained results show that the phosphors have potential application in the field of solid state lighting.

  5. Optically stimulated luminescence (OSL) response of Al2O3:C, BaFCl:Eu and K2Ca2(SO4)3:Eu phosphors.

    PubMed

    Kumar, Pratik; Bahl, Shaila; Sahare, P D; Kumar, Surender; Singh, Manveer

    2015-12-01

    This paper investigates the optically stimulated luminescence (OSL) response of BaFCl:Eu and K2Ca2(SO4)3:Eu phosphors for different doses and bleaching durations. The results have also been compared with the commercially available Landauer Al2O3:C (Luxel®) dosemeter. Nanocrystalline K2Ca2(SO4)3:Eu is known to be a sensitive thermoluminescent phosphor, but its OSL response is hardly reported. At first, pellets of nanocrystalline K2Ca2(SO4)3:Eu powder were prepared by adding Teflon as a binder. Their OSL signal was compared with that of the material in pure form, i.e. without adding the binder (in 100:1 ratio). It was observed that adding the binder does not appreciably affect the OSL intensity. On comparison with the commercially available Al2O3:C from Landauer, it was found that K2Ca2(SO4)3:Eu is around 15 times less sensitive than Al2O3:C. 'Homemade' BaFCl:Eu phosphor has also been studied. The intensity of BaFCl:Eu was ∼20 times more than the standard Al2O3:C dosemeter and ∼200 times more sensitive than K2Ca2(SO4)3:Eu in the dose range of 13-200 cGy. OSL dosemeters are believed to give luminescence signal even if they are read before, i.e. multiple reading may be possible under suitable conditions after single exposure. This was also checked for all the prepared dosemeters and it was found that Al2O3:C showed the least decrease of <2 %, followed by BaFCl:Eu of 15 % and K2Ca2(SO4)3:Eu with 20 %. Finally, Al2O3:C and BaFCl:Eu phosphors were also studied for their optical bleaching durations to which the respective signals get completely removed so that the phosphor can be re-used. It was observed that BaFCl:Eu is bleached faster and more easily than Al2O3:C. PMID:25646524

  6. Synthesis and properties of superconducting (Hg,Re)-Ba-Ca-Cu-O thick films on polycrystalline LaAlO 3 substrate obtained by screen-printing method

    NASA Astrophysics Data System (ADS)

    Przybylski, K.; Brylewski, T.; Bućko, M.; Prażuch, J.; Morawski, A.; Łada, T.

    2003-05-01

    A superconducting Hg 0.7Re 0.3Ba 2Ca 2Cu 3O 8+ δ thick film on a polycrystalline LaAlO 3 (LAO) substrate was obtained by a two-step method by screen-printing a Re 0.3Ba 2Ca 2Cu 3O x precursor coating on the substrate followed by high-pressure gas firing in Hg vapour. Morphological observations have revealed that the adherent to the ceramic substrate film exhibited highly porous microstructure composed of plate-like crystallites characterized by a superconducting transition temperature of about 110 K. The major phases identified were a high- Tc (Hg,Re)-1223 phase and a low- Tc (Hg,Re)-1212 phase. Non-superconducting secondary impurity phases were also identified. Energy dispersion X-ray spectroscopy analyses at the substrate/film boundary showed a thin continuous layer of BaLa 2O 4 compound, the presence of which confirmed chemical interaction between the LAO substrate and (Hg,Re)-Ba-Ca-Cu-O film.

  7. Preparation and characterization of Tl sub 2 Ba sub 2 CaCu sub 2 O sub 8 films on (100) LaAlO sub 3

    SciTech Connect

    Holstein, W.L.; Parisi, L.A.; Kountz, D.J.; Wilker, C.; Matthews, A.L. ); Arendt, P.N. ); Taber, R.C. )

    1991-03-01

    A two-step process for the fabrication of 0.12-1.20 {mu}m-thick Tl{sub 2}Ba{sub 2}CaCu{sub 2}O{sub 8} films on (100) LaAlO{sub 3} has been developed. The process involves the deposition of a BaCaCuO precursor film at low temperature by rf magnetron sputtering, followed by annealing in the presence of Tl{sub 2}O vapor to convert the precursor film into Tl{sub 2}Ba{sub 2}CaCu{sub 2}O{sub 8}. Over a distance of 4 cm, film composition was Tl:Ba:Ca:Cu = 2.05 {plus minus} 0.09:2.05 {plus minus} 0.06:1.0 {plus minus} 0.3:1.94 {plus minus} 0.6 and thickness was uniform to within 6%. The films contain only trace quantities of secondary phases and are epitaxially oriented, with the c-axis of Tl{sub 2}Ba{sub 2}CaCu{sub 2}O{sub 8} perpendicular to the surface and the two a-axes aligned with the pseudo-cubic a-axes of the underlying LaAlO{sub 3} substrate. Films had a T{sub c} for zero dc resistivity of 106.5 {plus minus} 0.5 K,a transport critical current density for continuous current of 2.9 {times} 10{sup 6} A-cm{sup {minus}2} at 77 K, and a sharp ({lt}0.3{degrees} C) ac inductance transition with an onset temperature of 105 {plus minus} 2 K. Surface resistance at 20 GHz less than 2 m{Omega}, about 10X lower than Cu, was routinely achieved for temperatures below 90 K and, for the best films, at temperatures up to 100 K. Surface resistance at about 10 GHz on one film was 0.067 m{Omega} at 4.2 K, 0.36 m{Omega} at 77 K, and 0.74 m{Omega} at 90 K. Films have been reproducibly fabricated on substrates up to 2.54 cm square.

  8. NOx uptake on alkaline earth oxides (BaO, MgO, CaO and SrO) supported on γ-Al2O3

    SciTech Connect

    Verrier, Christelle LM; Kwak, Ja Hun; Kim, Do Heui; Peden, Charles HF; Szanyi, Janos

    2008-07-15

    NOx uptake experiments were performed on a series of alkaline earth oxide (AEO) (MgO, CaO, SrO, BaO) on γ-alumina materials. Temperature Programmed Desorption (TPD) conducted on He flow revealed the presence of two kinds of nitrate species: i.e. bulk and surface nitrates. The ratio of these two types of nitrate species strongly depends on the nature of the alkaline earth oxide. The amount of bulk nitrate species increases with the basicity of the alkaline earth oxide. This conclusion was supported by the results of infrared and 15N solid state NMR studies of NO2 adsorption. Due to the low melting point of the precursor used for the preparation of MgO/Al2O3 material (Mg(NO3)2), a significant amount of Mg was lost during sample activation (high temperature annealing) resulting in a material with properties were very similar to that of the γ-Al2O3 support. The effect of water on the NOx species formed in the exposure of the AEO-s to NO2 was also investigated. In agreement with our previous findings for the BaO/γ-Al2O3 system, an increase of the bulk nitrate species and the simultaneous decrease of the surface nitrate phase were observed for all of these materials.

  9. Influences of CaO on Crystallization, Microstructures, and Properties of BaO-Al2O3-B2O3-SiO2 Glass-Ceramics

    NASA Astrophysics Data System (ADS)

    Li, Bo; Tang, Bo; Xu, Mingjiang

    2015-10-01

    We have developed BaO-CaO-Al2O3-B2O3-SiO2 glass-ceramics with high thermal coefficient of expansion (TCE) to overcome thermal mismatch at board level. The crystalline phases include quartz (major), cristobalite (minor), and bazirite BaZrSi3O9 (minor). Calculations from whole-pattern fitting show that the crystallinity varies slightly within the range of 33.48% to 34.89%, while the mass fraction of the phases changes remarkably with the CaO content. This indicates that CaO cannot promote crystallization of Ba-Al-B-Si glass, but effectively suppresses the phase transformation from quartz to cristobalite, making the thermal expansion curves linear. An empirical equation for the TCE versus the temperature and the amount of CaO is established. Furthermore, the densification mechanism of Ca modifiers is revealed. Due to its higher field strength than Ba, substitution of Ca increases the glass viscosity and inhibits ion diffusion. Excessive CaO is thus harmful to the density, bending strength, and electrical properties. The sample with 10 wt.% CaO sintered at 950°C exhibited high bending strength (154.1 MPa) and high TCE (12.38 ppm/°C) as well as good electrical properties ( ɛ = 6.2, tan δ = 5 × 10-4, ρ = 3.8 × 1012 Ω cm).

  10. High-Temperature Vaporization Behavior of Oxides II. Oxides of Be, Mg, Ca, Sr, Ba, B, Al, Ga, In, Tl, Si, Ge, Sn, Pb, Zn, Cd, and Hg

    NASA Astrophysics Data System (ADS)

    Lamoreaux, R. H.; Hildenbrand, D. L.; Brewer, L.

    1987-07-01

    In order to assess the high-temperature vaporization behavior and equilibrium gas phase compositions over the condensed oxides of Be, Mg, Ca, Sr, Ba, B, Al, Ga, In, Tl, Si, Ge, Sn, Pb, Zn, Cd, and Hg, the relevant thermodynamic and molecular constant data have been compiled and critically evaluated. Selected values of the Gibbs energy functions of condensed and vapor phases are given in the form of equations valid over wide temperature ranges, along with the standard entropies and enthalpies of formation. These data were used to generate plots of equilibrium partial pressures of vapor species as functions of temperature for representative environmental conditions ranging from reducing to oxidizing. The calculated partial pressures and compositions agree, for the most part, with experimental results obtained under comparable conditions. Maximum vaporization rates have been calculated using the Hertz-Knudsen equation. Literature references are given.

  11. An Investigation of Armenite, BaCa2Al6Si9O302H2O.H2O Molecules and H Bonding in Microporous Silicates

    NASA Astrophysics Data System (ADS)

    Geiger, C. A.; Gatta, G.; Xue, X.; McIntyre, G.

    2012-12-01

    The crystal chemistry of armenite, ideally BaCa2Al6Si9O30.2H2O, a double-ring structure belonging to the milarite group, was studied to better understand the nature of extra-framework "Ca-oxygen-anion-H2O-molecule quasi-clusters" and H bonding behavior in microporous silicates. Neutron and X-ray single-crystal diffraction and IR powder and 1H NMR spectroscopic measurements were made. Four crystallographically independent Ca and H2O molecule sites were refined from the diffraction data, whereby both sites appear to have partial occupancies such that locally a Ca atom can have only a single H2O molecule bonded to it through an ion-dipole interaction. The Ca cation is further bonded to six O atoms of the framework forming a quasi cluster around it. The neutron results give the first static description of the protons in armenite, allowing bond distances and angles relating to the H2O molecules and H bonds to be determined. The IR spectrum of armenite is characterized in the OH-stretching region at RT by two broad bands at roughly 3470 and 3410 cm-1 and by a single H2O bending mode at 1654 cm-1. At 10 K four intense OH bands are located at 3479, 3454, 3401 and 3384 cm-1 and two H2O bending modes at 1650 and 1606 cm-1. The 1H MAS NMR spectrum shows a single strong resonance near 5.3 ppm and a smaller one near 2.7 ppm. The former can be assigned to H2O molecules bonded to Ca and the latter to weakly bonded H2O located at a site at the center of the structural double ring and it is partially occupied. The nature of H bonding in the microporous Ca-bearing zeolites scolecite, wairakite and epistilbite are also analyzed. The average OH stretching wavenumber shown by the IR spectra of armenite (~3435 cm-1) and scolecite (~3430 cm-1) are similar, while the average OH wavenumbers for wairakite (~3475 cm-1) and epistilbite (~3500 cm-1) are greater. In all cases the average OH stretching wavenumber is more similar to that of liquid water (~3400 cm-1) than of ice (~3220 cm-1). The

  12. Crystalline orientations of Tl2Ba2Ca2Cu3O(x) grains on MgO, SrTiO3, and LaAlO3 substrates

    NASA Technical Reports Server (NTRS)

    Liou, S. H.; Wu, C. Y.

    1992-01-01

    Crystalline orientations of Tl2Ba2Ca2Cu3O(x) grains in magnetron sputtered films on MgO (001), SrTiO3 (001), and LaAlO3 (001) substrates were investigated by scanning electron microscopy. In contrast to the nearly single crystalline films on the lattice matched substrates SrTiO3 and LaAlO3, films on the MgO (001) substrate, being polycrystalline in nature, exhibit several preferred in-plane grain orientations. These orientations agree well with a simplified theory of near-coincidence site lattices between Tl2Ba2Ca2Cu3O(x) and MgO.

  13. Electronic structure of Ca, Sr, and Ba under pressure.

    NASA Technical Reports Server (NTRS)

    Animalu, A. O. E.; Heine, V.; Vasvari, B.

    1967-01-01

    Electronic band structure calculations phase of Ca, Sr and Ba over wide range of atomic volumes under pressure electronic band structure calculations for fcc phase of Ca, Sr and Ba over wide range of atomic volumes under pressure electronic band structure calculations for fcc phase of Ca, Sr and Ba over wide range of atomic volumes under pressure

  14. Thermally stable green Ba(3)Y(PO(4))3:Ce(3+),Tb(3+) and red Ca(3)Y(AlO)(3)(BO(3))4:Eu(3+) phosphors for white-light fluorescent lamps.

    PubMed

    Huang, Chien-Hao; Kuo, Te-Wen; Chen, Teng-Ming

    2011-01-01

    A class of thermal stable of green-emitting phosphors Ba(3)Y(PO(4))(3):Ce(3+),Tb(3+) (BYP:Ce(3+),Tb(3+)) and red-emitting phosphors Ca(3)Y(AlO)(3)(BO(3))(4):Eu(3+) (CYAB:Eu(3+)) for white-light fluorescent lamps were synthesized by high temperature solid-state reaction. We observed a decay of only 3% at 150 °C for BYP:0.25Ce3+,0.25Tb3+ (3% for LaPO4:Ce(3+),Tb(3+)), and a decay of 4% for CYAB:0.5Eu(3+) (7% for Y(2)O(3):Eu(3+), 24% for Y(2)O(2)S:Eu(3+)). The emission intensity of composition-optimized Ba(3)(Y(0.5)Ce(0.25)Tb(0.25))(PO(4))(3) is 70% of that of commercial LaPO(4):Ce(3+),Tb(3+) phosphors, and the CIE chromaticity coordinates are found to be (0.323, 0.534). The emission intensity of Ca(3)(Y(0.5)Eu(0.5))(AlO)(3)(BO(3))(4) is 70% and 83% of those of Y(2)O(3):Eu(3+) and Y(2)O(2)S:Eu(3+) phosphors, respectively, and the CIE chromaticity coordinates are redder (0.652, 0.342) than those of Y(2)O(3):Eu(3+) (0.645, 0.347) and Y(2)O(2)S:Eu(3+) (0.647, 0.343). A white-light fluorescent lamp is fabricated using composition-optimized Ba(3)(Y(0.5)Ce(0.25)Tb(0.25))(PO(4))(3) and Ca(3)(Y(0.5)Eu(0.5))(AlO)(3)(BO(3))(4) phosphors and matching blue-emitting phosphors. The results indicate that the quality of the brightness and color reproduction is suitable for application in shortwave UV fluorescent lamps. The white-light fluorescent lamp displays CIE chromaticity coordinates of x = 0.33, y = 0.35, a warm white light with a correlated color temperature of 5646 K, and a color-rendering index of Ra = 70.

  15. Performance of two-pole bandpass filters photodefined on double-sided Y-Ba-Cu-O and Tl-Ba-Ca-Cu-O thin films

    NASA Technical Reports Server (NTRS)

    Miranda, F. A.; Toncich, S. S.; Bhasin, K. B.

    1993-01-01

    The performance of 7.3-GHz two-pole bandpass filters (5% bandwidth) fabricated on double-sided Y-Ba-Cu-O and Tl-Ba-Ca-Cu-O thin films deposited on LaAlO3 is discussed. At 77 K, the Tl-Ba-Ca-Cu-O and Y-Ba-Cu-O superconducting filters exhibited minimum passband insertion losses of 0.3 and 1.2 dB, respectively. An insertion loss of 3.4 dB was measured for an all-gold filter at 77 K.

  16. Cross sections for the production of residual nuclides by low- and medium-energy protons from the target elements C, N, O, Mg, Al, Si, Ca, Ti, V, Mn, Fe, Co, Ni, Cu, Sr, Y, Zr, Nb, Ba and Au

    NASA Astrophysics Data System (ADS)

    Michel, R.; Bodemann, R.; Busemann, H.; Daunke, R.; Gloris, M.; Lange, H.-J.; Klug, B.; Krins, A.; Leya, I.; Lüpke, M.; Neumann, S.; Reinhardt, H.; Schnatz-Büttgen, M.; Herpers, U.; Schiekel, Th.; Sudbrock, F.; Holmqvist, B.; Condé, H.; Malmborg, P.; Suter, M.; Dittrich-Hannen, B.; Kubik, P.-W.; Synal, H.-A.; Filges, D.

    1997-07-01

    Cross sections for residual nuclide production by p-induced reactions were measured from thresholds up to 2.6 GeV using accelerators at CERN/Geneve, IPN/Orsay, KFA/Jülich, LANL/Los Alamos, LNS/Saclay, PSI/Villigen, TSL/Uppsala, LUC/Louvain La Neuve. The target elements C, N, O, Mg, Al, Si, Ca, Ti, V, Mn, Fe, Co, Ni, Cu, Sr, Y, Zr, Nb, Ba and Au were investigated. Residual nuclides were measured by X- and γ-spectrometry and by Accelerator Mass Spectrometry (AMS). The measured cross sections were corrected for interfering secondary particles in experiments with primary proton energies above 200 MeV. Our consistent database covers presently ca 550 nuclear reactions and contains nearly 15000 individual cross sections of which about 10000 are reported here for the first time. They provide a basis for model calculations of the production of cosmogenic nuclides in extraterrestrial matter by solar and galactic cosmic ray protons. They are of importance for many other applications in which medium energy nuclear reactions have to be considered ranging from astrophysics over space and environmental sciences to accelerator technology and accelerator-based nuclear waste transmutation and energy amplification. The experimental data are compared with theoretical ones based on calculations using an INC/E model in form of the HETC/KFA2 code and on the hybrid model of preequilibrium reactions in form of the AREL code.>

  17. Synthesis and structural characterization of the ternary Zintl phases AE{sub 3}Al{sub 2}Pn{sub 4} and AE{sub 3}Ga{sub 2}Pn{sub 4} (AE=Ca, Sr, Ba, Eu; Pn=P, As)

    SciTech Connect

    He, Hua; Tyson, Chauntae; Saito, Maia; Bobev, Svilen

    2012-04-15

    Ten new ternary phosphides and arsenides with empirical formulae AE{sub 3}Al{sub 2}Pn{sub 4} and AE{sub 3}Ga{sub 2}Pn{sub 4} (AE=Ca, Sr, Ba, Eu; Pn=P, As) have been synthesized using molten Ga, Al, and Pb fluxes. They have been structurally characterized by single-crystal and powder X-ray diffraction to form with two different structures-Ca{sub 3}Al{sub 2}P{sub 4}, Sr{sub 3}Al{sub 2}As{sub 4}, Eu{sub 3}Al{sub 2}P{sub 4}, Eu{sub 3}Al{sub 2}As{sub 4}, Ca{sub 3}Ga{sub 2}P{sub 4}, Sr{sub 3}Ga{sub 2}P{sub 4}, Sr{sub 3}Ga{sub 2}As{sub 4}, and Eu{sub 3}Ga{sub 2}As{sub 4} crystallize with the Ca{sub 3}Al{sub 2}As{sub 4} structure type (space group C2/c, Z=4); Ba{sub 3}Al{sub 2}P{sub 4} and Ba{sub 3}Al{sub 2}As{sub 4} adopt the Na{sub 3}Fe{sub 2}S{sub 4} structure type (space group Pnma, Z=4). The polyanions in both structures are made up of TrPn{sub 4} tetrahedra, which share common corners and edges to form {sup 2}{sub {infinity}}[TrPn{sub 2}]{sub 3-} layers in the phases with the Ca{sub 3}Al{sub 2}As{sub 4} structure, and {sup 1}{sub {infinity}}[TrPn{sub 2}]{sub 3-} chains in Ba{sub 3}Al{sub 2}P{sub 4} and Ba{sub 3}Al{sub 2}As{sub 4} with the Na{sub 3}Fe{sub 2}S{sub 4} structure type. The valence electron count for all of these compounds follows the Zintl-Klemm rules. Electronic band structure calculations confirm them to be semiconductors. - Graphical abstract: AE{sub 3}Al{sub 2}Pn{sub 4} and AE{sub 3}Ga{sub 2}Pn{sub 4} (AE=Ca, Sr, Ba, Eu; Pn=P, As) crystallize in two different structures-Ca{sub 3}Al{sub 2}P{sub 4}, Sr{sub 3}Al{sub 2}As{sub 4}, Eu{sub 3}Al{sub 2}P{sub 4}, Eu{sub 3}Al{sub 2}As{sub 4}, Ca{sub 3}Ga{sub 2}P{sub 4}, Sr{sub 3}Ga{sub 2}P{sub 4}, Sr{sub 3}Ga{sub 2}As{sub 4}, and Eu{sub 3}Ga{sub 2}As{sub 4}, are isotypic with the previously reported Ca{sub 3}Al{sub 2}As{sub 4} (space group C2/c (No. 15)), while Ba{sub 3}Al{sub 2}P{sub 4} and Ba{sub 3}Al{sub 2}As{sub 4} adopt a different structure known for Na{sub 3}Fe{sub 2}S{sub 4} (space group Pnma (No. 62

  18. Processing, electrical and microwave properties of sputtered Tl-Ca-Ba-Cu-O superconducting thin films

    NASA Technical Reports Server (NTRS)

    Subramanyam, G.; Kapoor, V. J.; Chorey, C. M.; Bhasin, K. B.

    1993-01-01

    A reproducible fabrication process has been established for TlCaBaCuO thin films on LaAlO3 substrates by RF magnetron sputtering and post-deposition processing methods. Electrical transport properties of the thin films were measured on patterned four-probe test devices. Microwave properties of the films were obtained from unloaded Q measurements of all-superconducting ring resonators. This paper describes the processing, electrical and microwave properties of Tl2Ca1Ba2Cu2O(x) 2122-plane phase thin films.

  19. Magnetic characterization of Ca substituted Ba and Sr hexaferrites

    NASA Astrophysics Data System (ADS)

    Asti, G.; Carbucicchio, M.; Deriu, A.; Lucchini, E.; Slokar, G.

    1980-04-01

    A magnetic characterization has been worked out for the solid solution from Ba and Sr hexaferrites (BaFe 1 2O 1 9, SrFe 1 2O 1 9) towards CaO- xFe 2O 3 (2 ⪕ x ⪕5.5). Measurements of Curie temperature, saturation magnetization, magnetic anisotropy, together with Mössbauer characterization indicate that the intrinsic properties of the studied compounds do not change appreciably with increasing Ca content. These results, together with the X-ray data, are consistent with the formation of an undistorted M-type cell with a low content of iron and oxygen vacancies.

  20. Incorporation of Ba in Al and Fe pollucite

    NASA Astrophysics Data System (ADS)

    Vance, Eric R.; Gregg, Daniel J.; Griffiths, Grant J.; Gaugliardo, Paul R.; Grant, Charmaine

    2016-09-01

    Ba, the transmutation product of radioactive Cs, can be incorporated at levels of up to ∼0.07 formula units in Cs(1-2x)BaxAlSi2O6 aluminium pollucite formed by sol-gel methods and sintering at 1400 °C, with more Ba forming BaAl2Si2O8 phases. The effect of Ba substitution in pollucite-structured CsFeSi2O6 was also studied and no evidence of Ba substitution in the pollucite structure via cation vacancies or Fe2+ formation was obtained. The Ba entered a Fe-silicate glass structure. Charge compensation was also attempted with a Cs+ + Fe3+ ↔ Ba2+ + Ni2+ scheme but again the Ba formed a glass and NiO was evident. PCT leaching data showed CsFeSi2O6 to be very leach resistant.

  1. Ca/Ba/Sr-induced conformational changes of ciliary axonemes.

    PubMed

    Tamm, S; Tamm, S

    1990-01-01

    Macrocilia of the ctenophore Beroë undergo Ca/Ba/Sr-dependent activation of ciliary beating and microtubule sliding disintegration [Tamm, J. Comp. Physiol. A163:23-31, 1988a; Tamm, Cell Motil. Cytoskeleton 11:126-138, 1988b; Tamm, Cell Motil. Cytoskeleton 12:104-112, 1989; Tamm and Tamm, Proc. Natl. Acad. Sci. U.S.A. 86:6987-6991, 1989]. Here we report that detergent-extracted macrocilia show an ATP-independent conformational change in response to high concentrations of Ca, Ba, or Sr ions. When applied locally by iontophoresis, these ions induce a rapid planar curvature of the distal end of the macrociliary shaft, followed by a slower relaxation to the rest position. Tip curling occurs in a direction opposite to the physiological Ca/Ba/Sr response. When applied uniformly in the bath, a threshold concentration of 10(-1) M Sr is required to induce curling of the tip, and the distal ends remain curved. Calmodulin antagonists do not inhibit the tip curling response. Previous workers found that Ca induces changes in the helical shape of isolated doublet microtubules [Miki-Noumura and Kamiya, Exp. Cell Res. 97:451-453, 1976; Miki-Noumura and Kamiya, J. Cell Biol. 81:355-360, 1979; Takasaki and Miki-Noumura, J. Mol. Biol. 158:317-324, 1982] and sperm axonemes [Okuno and Brokaw, Cell Motil. 1:349-362, 1981] and suggested that conformational changes in microtubules may play a role in Ca regulation of ciliary motility. We propose that the Ca/Ba/Sr-induced curling of the macrociliary tip is due to similar helical changes of doublet microtubules, some of which in macrocilia are prevented from sliding by permanent connections (compartmenting lamellae) between adjacent axonemes within the shaft. Although the tip curling response does not appear to be directly relevant to the physiological Ca response of macrocilia, it provides a novel system for investigating Ca-induced conformational changes of microtubules independent of dynein-powered active sliding.

  2. Luminescence and site occupancy of Ce3+ in Ba2Ca(BO3)2

    NASA Astrophysics Data System (ADS)

    Lin, Huihong; Liang, Hongbin; Han, Bing; Zhong, Jiuping; Su, Qiang; Dorenbos, Pieter; Birowosuto, M. Danang; Zhang, Guobin; Fu, Yibing; Wu, Wenqing

    2007-07-01

    The phosphors of Ce3+ activated Ba2Ca(BO3)2 with chemical formulas Ba2(1-x)CexNaxCa(BO3)2 and Ba2Ca1-2xCexNax(BO3)2 were prepared. The luminescence properties have been investigated under vacuum ultraviolet UV and x-ray excitation. Though the point defects CeBa• and NaBa' are expected to occur in samples Ba2(1-x)CexNaxCa(BO3)2 , and CeCa• and NaCa' are expected to appear in samples Ba2Ca1-2xCexNax(BO3)2 according to the formulas of the compounds, however, two types of Ce3+ centers were found in all samples due to the occupancy of both Ba2+ and Ca2+ sites. So the influence of doping concentration on the preferential site occupancy was studied, and it was found that Ce3+ ions always preferentially enter Ba2+ sites at low doping concentration for both samples Ba2(1-x)CexNaxCa(BO3)2 and Ba2Ca1-2xCexNax(BO3)2 . In addition, the 5d energy levels and decay behaviors for Ce3+ in Ba2+ and Ca2+ sites, the concentration quenching, and the x-ray excited photon output were evaluated to clearly reveal the luminescence features.

  3. Electrical-transport properties and microwave device performance of sputtered TlCaBaCuO superconducting thin films

    NASA Technical Reports Server (NTRS)

    Subramanyam, G.; Kapoor, V. J.; Chorey, C. M.; Bhasin, K. B.

    1992-01-01

    The paper describes the processing and electrical transport measurements for achieving reproducible high-Tc and high-Jc sputtered TlCaBaCuO thin films on LaAlO3 substrates, for microelectronic applications. The microwave properties of TlCaBaCuO thin films were investigated by designing, fabricating, and characterizing microstrip ring resonators with a fundamental resonance frequency of 12 GHz on 10-mil-thick LaAlO3 substrates. Typical unloaded quality factors for a ring resonator with a superconducting ground plane of 0.3 micron-thickness and a gold ground plane of 1-micron-thickness were above 1500 at 65 K. Typical values of penetration depth at 0 K in the TlCaBaCuO thin films were between 7000 and 8000 A.

  4. Vacuum ultraviolet thin films. I - Optical constants of BaF2, CaF2, LaF3, MgF2, Al2O3, HfO2, and SiO2 thin films. II - Vacuum ultraviolet all-dielectric narrowband filters

    NASA Technical Reports Server (NTRS)

    Zukic, Muamer; Torr, Douglas G.; Spann, James F.; Torr, Marsha R.

    1990-01-01

    An iteration process matching calculated and measured reflectance and transmittance values in the 120-230 nm VUV region is presently used to ascertain the optical constants of bulk MgF2, as well as films of BaF2, CaF2, LaF3, MgF2, Al2O3, HfO2, and SiO2 deposited on MgF2 substrates. In the second part of this work, a design concept is demonstrated for two filters, employing rapidly changing extinction coefficients, centered at 135 nm for BaF2 and 141 nm for SiO2. These filters are shown to yield excellent narrowband spectral performance in combination with narrowband reflection filters.

  5. Piezoelectric and Dielectric Properties of Multilayered BaTiO3/(Ba,Ca)TiO3/CaTiO3 Thin Films.

    PubMed

    Zhu, Xiao Na; Gao, Ting Ting; Xu, Xing; Liang, Wei Zheng; Lin, Yuan; Chen, Chonglin; Chen, Xiang Ming

    2016-08-31

    Highly oriented multilayered BaTiO3-(Ba,Ca)TiO3-CaTiO3 thin films were fabricated on Nb-doped (001) SrTiO3 (Nb:STO) substrates by pulsed laser deposition. The configurations of multilayered BaTiO3-(Ba,Ca)TiO3-CaTiO3 thin films are designed with the thickness ratio of 1:1:1 and 2:1:1 and total thickness ∼300 nm. Microstructural characterization by X-ray diffraction indicates that the as-deposited thin films are highly c-axis oriented and large in-plane strain is determined in BaTiO3 and CaTiO3 layers. Piezoresponse force microscopy (PFM) studies reveal an intense in-plane polarization component, whereas the out-of-plane shows inferior phase contrast. The optimized combination is found to be the BaTiO3-(Ba0.85Ca0.15)TiO3-CaTiO3 structure with combination ratio 2:1:1, which displays the largest domain switching amplitude under DC electric field, the largest room-temperature dielectric constant ∼646, a small dielectric loss of 0.03, and the largest dielectric tunability of ∼50% at 400 kV/cm. These results suggest that the enhanced dielectric and tunability performance are greatly associated with the large in-plane polarization component and domain switching.

  6. Piezoelectric and Dielectric Properties of Multilayered BaTiO3/(Ba,Ca)TiO3/CaTiO3 Thin Films.

    PubMed

    Zhu, Xiao Na; Gao, Ting Ting; Xu, Xing; Liang, Wei Zheng; Lin, Yuan; Chen, Chonglin; Chen, Xiang Ming

    2016-08-31

    Highly oriented multilayered BaTiO3-(Ba,Ca)TiO3-CaTiO3 thin films were fabricated on Nb-doped (001) SrTiO3 (Nb:STO) substrates by pulsed laser deposition. The configurations of multilayered BaTiO3-(Ba,Ca)TiO3-CaTiO3 thin films are designed with the thickness ratio of 1:1:1 and 2:1:1 and total thickness ∼300 nm. Microstructural characterization by X-ray diffraction indicates that the as-deposited thin films are highly c-axis oriented and large in-plane strain is determined in BaTiO3 and CaTiO3 layers. Piezoresponse force microscopy (PFM) studies reveal an intense in-plane polarization component, whereas the out-of-plane shows inferior phase contrast. The optimized combination is found to be the BaTiO3-(Ba0.85Ca0.15)TiO3-CaTiO3 structure with combination ratio 2:1:1, which displays the largest domain switching amplitude under DC electric field, the largest room-temperature dielectric constant ∼646, a small dielectric loss of 0.03, and the largest dielectric tunability of ∼50% at 400 kV/cm. These results suggest that the enhanced dielectric and tunability performance are greatly associated with the large in-plane polarization component and domain switching. PMID:27514235

  7. Cu/Ba/bauxite: an Inexpensive and Efficient Alternative for Pt/Ba/Al2O3 in NOx Removal

    PubMed Central

    Wang, Xiuyun; Chen, Zhilin; Luo, Yongjin; Jiang, Lilong; Wang, Ruihu

    2013-01-01

    Cu/Ba/bauxite possesses superior NOx storage and reduction (NSR) performances, high thermal stability, strong resistance against SO2 poisoning and outstanding regeneration ability in comparison with Pt/Ba/Al2O3. It can serve as a cheap and promising alternative for traditional Pt/Ba/Al2O3 in NOx removal from lean-burn engines. PMID:23536149

  8. Method of forming superconducting Tl-Ba-Ca-Cu-O films

    DOEpatents

    Wessels, Bruce W.; Marks, Tobin J.; Richeson, Darrin S.; Tonge, Lauren M.; Zhang, Jiming

    1993-01-01

    A method of forming a superconducting Tl-Ba-Ca-Cu-O film is disclosed, which comprises depositing a Ba-Ca-Cu-O film on a substrate by MOCVD, annealing the deposited film and heat-treating the annealed film in a closed circular vessel with TlBa.sub.2 Ca.sub.2 Cu.sub.3 O.sub.x and cooling to form said superconducting film of TlO.sub.m Ba.sub.2 Ca.sub.n-1 Cu.sub.n O.sub.2n+2, wherein m=1,2 and n=1,2,3.

  9. Crystal and electronic structures, luminescence properties of Eu{sup 2+}-doped Si{sub 6-z}Al{sub z}O{sub z}N{sub 8-z} and M{sub y}Si{sub 6-z}Al{sub z-y}O{sub z+y}N{sub 8-z-y} (M=2Li, Mg, Ca, Sr, Ba)

    SciTech Connect

    Li, Y.Q. Hirosaki, N.; Xie, R.J.; Takeda, T.; Mitomo, M.

    2008-12-15

    The crystal structure, electronic structure, and photoluminescence properties of Eu{sub x}Si{sub 6-z}Al{sub z-x}O{sub z+x}N{sub 8-z-x} (x=0-0.1, 0Al{sub z-x-y}O{sub z+x+y}N{sub 8-z-x-y} (M=2Li, Mg, Ca, Sr, Ba) have been studied. Single-phase Eu{sub x}Si{sub 6-z}Al{sub z-x}O{sub z+x}N{sub 8-z-x} can be obtained in very narrow ranges of x{<=}0.06 (z=0.15) and z<0.5 (x=0.3), indicating that limited Eu{sup 2+} ions can be incorporated into nitrogen-rich Si{sub 6-z}Al{sub z}O{sub z}N{sub 8-z}. The Eu{sup 2+} ion is found to occupy the 2b site in a hexagonal unit cell (P6{sub 3}/m) and directly connected by six adjacent nitrogen/oxygen atoms ranging 2.4850-2.5089 A. The calculated host band gaps by the relativistic DV-X{alpha} method are about 5.55 and 5.45 eV (without Eu{sup 2+} 4f5d levels) for x=0 and 0.013 in Eu{sub x}Si{sub 6-z}Al{sub z-x}O{sub z+x}N{sub 8-z-x} (z=0.15), in which the top of the 5d orbitals overlap with the Si-3s3p and N-2p orbitals within the bottom of the conduction band of the host. Eu{sub x}Si{sub 6-z}Al{sub z-x}O{sub z+x}N{sub 8-z-x} shows a strong green emission with a broad Eu{sup 2+} band centered at about 530 nm under UV to near-UV excitation range. The excitation and emission spectra are hardly modified by Eu concentration and dual-doping ions of Li and other alkaline-earth ions with Eu. Higher Eu concentrations can significantly quench the luminescence of Eu{sup 2+} and decrease the thermal quenching temperature. In addition, the emission spectrum can only be slightly tuned to the longer wavelengths ({approx}529-545 nm) by increasing z within the solid solution range of z<0.5. Furthermore, the luminescence intensity of Eu{sub x}Si{sub 6-z}Al{sub z-x}O{sub z+x}N{sub 8-z-x} can be improved by increasing z and the dual-doping of Li and Ba. - Graphical abstract: Excitation and emission spectra of Eu{sub x}Si{sub 6-z}Al{sub z-x}O{sub z+x}N{sub 8-z-x} with the project of a 2x2x2 supercell crystal structure

  10. Luminescence and Site Occupancy of Eu2+ in Ba2 Ca(BO3)2

    NASA Astrophysics Data System (ADS)

    Li, Pan-Lai; Wang, Zhi-Jun; Yang, Zhi-Ping; Guo, Qing-Lin

    2011-01-01

    A green phosphor Ba2Ca(BO3)2:Eu2+ was synthesized by a high temperature solid-state reaction method under a reductive atmosphere. The luminescence and site occupancy of Eu2+ in Ba2Ca(BO3)2 are investigated. Ba2Ca(BO3)2:Eu2+ shows one green band (537 nm) under 400 nm near ultraviolet excitation which is suitable for UV LED. Ca2+ and Ba2+ ions in Ba2Ca(BO3)2 are replaced by Eu2+ ions, the Ba2Ca(BO3)2:Eu2+ shows a dissymmetrical emission band. The influence of Eu2+ doping concentrations on the emission intensity of Ba2Ca(BO3)2:Eu2+ is studied. It is found that the emission intensity is influenced by the Eu2+ concentration and reaches the maximum value at 2% Eu2+. According to the Dexter theory, the concentration quenching mechanisms of Eu2+ in Ba2Ca(BO3)2 are the d-dinteraction.

  11. The unusual chemical bonding and thermoelectric properties of a new type Zintl phase compounds Ba3Al2As4

    NASA Astrophysics Data System (ADS)

    Yang, Gui; Zhang, Guangbiao; Wang, Chao; Wang, Yuanxu

    2016-07-01

    Ba3Al2As4 exhibits an unusual anisotropic electrical conductivity, that is, the electrical conductivity along the chain is smaller than those along other two directions. The results is conflict with previous conclusion for Ca5M2Pn6. Earlier studies on Ca5M2Pn6 showed that a higher electrical conductivity could be obtained along the chain. The band decomposed charge density is used to explain such unusual behavior. Our calculations indicate the existence of a conductive pathway near the Fermi level is responsible for the electrons transport. Further, the Ba-As bonding of Ba3Al2As4 has some degree covalency which is novel for the Zintl compounds.

  12. Consequences of Ca multisite occupation for the conducting properties of BaTiO3

    NASA Astrophysics Data System (ADS)

    Zulueta, Y. A.; Dawson, J. A.; Leyet, Y.; Anglada-Rivera, J.; Guerrero, F.; Silva, R. S.; Nguyen, Minh Tho

    2016-11-01

    In combination with the dielectric modulus formalism and theoretical calculations, a newly developed defect incorporation mode, which is a combination of the standard A- and B-site doping mechanisms, is used to explain the conducting properties in 5 mol% Ca-doped BaTiO3. Simulation results for Ca solution energies in the BaTiO3 lattice show that the new oxygen vacancy inducing mixed mode exhibits low defect energies. A reduction in dc conductivity compared with undoped BaTiO3 is witnessed for the incorporation of Ca. The conducting properties of 5 mol% Ca-doped BaTiO3 are analyzed using molecular dynamics and impedance spectroscopy. The ionic conductivity activation energies for each incorporation mode are calculated and good agreement with experimental data for oxygen migration is observed. The likely existence of the proposed defect configuration is also analyzed on the basis of these methods.

  13. Ba/Ca Reproducibility and Growth Banding in Gulf of Alaska Bamboo Corals

    NASA Astrophysics Data System (ADS)

    Serrato Marks, G.; LaVigne, M.; Hill, T. M.; Sauthoff, W.; Guilderson, T. P.; Roark, E. B.; Dunbar, R. B.

    2014-12-01

    Deep-sea bamboo corals have been proposed as deep-ocean paleoceanographic archives because of their longevity and radial growth bands. Previous work has shown that bamboo coral Ba/Ca is a promising proxy for seawater barium, however, validation of Ba/Ca reproducibility is required. In addition, the growth band formation mechanism is uncertain, with some proposing that crystal orientation causes banding visible under light microscopy. The objective of this study was to evaluate Ba/Ca reproducibility and characterize growth band crystal orientation. Visible bands measured with a petrographic microscope were used to align LA-ICP-MS data collected along three replicate radii of the calcitic internodes of two well-dated corals from the Gulf of Alaska (collected live at 720m and 643m; 48°3'N, 132°44'W). Ba/Ca signals smoothed to ~annual resolution were reproducible within each coral (r=0.6-0.7; p<0.0001; n=3 radii/coral), suggesting that Ba/Ca varies in response to the external environment on annual timescales. Ba/Ca in the 720m coral increased from 1977 to 1998, a warm Pacific Decadal Oscillation (PDO) regime, possibly due to increased export production. The shallower coral (634m) revealed the inverse trend, suggesting variability in seawater barium dynamics with depth. Electron backscatter diffraction analysis of visible growth bands showed a preferred crystal orientation that does not correspond to location of visible bands or elemental composition, suggesting that crystal orientation does not cause bamboo coral banding. Overall, results show that regional oceanic signals are recorded as reproducible Ba/Ca variability in these corals. Comparison of these data to other well-dated records from the northeast Pacific would determine whether the relationship between Ba/Ca and PDO is regional. Additional archives of trace element variability will strengthen our understanding of how rapid climate change impacts intermediate ocean biogeochemistry.

  14. Ba/Ca Ratios in North Pacific Bamboo Corals Record Changes in Intermediate Water Biogeochemistry

    NASA Astrophysics Data System (ADS)

    Serrato Marks, G.; LaVigne, M.; Hill, T. M.; Sauthoff, W.; Guilderson, T. P.; Roark, E. B.; Dunbar, R. B.

    2015-12-01

    Trace elemental ratios preserved in the skeleton of bamboo corals, which live for hundreds of years at >500m depth, have been utilized as archives of deep-ocean conditions. However, it was previously unclear whether trace element data from these corals were internally reproducible and could therefore be used as reliable climate proxies. This study tests the internal reproducibility of Ba/Ca in the calcite of nine bamboo corals to further develop a new proxy for dissolved Ba in seawater (BaSW). Trace element LA-ICP-MS data were collected along three replicate radii of varying lengths of the calcitic internodes of well-dated corals collected live from the Gulf of Alaska (720m and 643m) and the California Margin (870m, 1012m, 1295m, 1500m, 1521m, 1954m, and 2054m; samples from 1295-1521m are not yet dated). Data were aligned using visible bands measured with a petrographic microscope to account for irregular growth. Ba/Ca data filtered with a 50μm (1.5-2 year) moving average were reproducible within each coral to 2.9 ± 2.1% (n=3 radii/coral, 9 corals), suggesting that regional geochemical signals are recorded as reproducible Ba/Ca signals on >annual timescales. Coral Ba/Ca presents an excellent proxy for BaSW, which has been found to be correlated with refractory nutrients (e.g. silicate) and oxygen minima. Increasing BaSW with depth and increased variability near 1000m suggests that BaSW is not constant with depth or with time. Several factors, including barite saturation state, particulate organic carbon (POC) remineralization rate, and particle sinking time, may be involved in the observed changes in BaSW. Further examination of such mechanisms could provide new insights into modern changes in deep-sea biogeochemistry.

  15. Co2FeAl based magnetic tunnel junctions with BaO and MgO/BaO barriers

    NASA Astrophysics Data System (ADS)

    Rogge, J.; Hetaba, W.; Schmalhorst, J.; Bouchikhaoui, H.; Stender, P.; Baither, D.; Schmitz, G.; Hütten, A.

    2015-07-01

    We succeed to integrate BaO as a tunneling barrier into Co2FeAl based magnetic tunnel junctions (MTJs). By means of Auger electron spectroscopy it could be proven that the applied annealing temperatures during BaO deposition and afterwards do not cause any diffusion of Ba neither into the lower Heusler compound lead nor into the upper Fe counter electrode. Nevertheless, a negative tunnel magnetoresistance (TMR) ratio of -10% is found for Co2FeAl (24 nm) / BaO (5 nm) / Fe (7 nm) MTJs, which can be attributed to the preparation procedure and can be explained by the formation of Co- and Fe-oxides at the interfaces between the Heusler and the crystalline BaO barrier by comparing with theory. Although an amorphous structure of the BaO barrier seems to be confirmed by high-resolution transmission electron microscopy (TEM), it cannot entirely be ruled out that this is an artifact of TEM sample preparation due to the sensitivity of BaO to moisture. By replacing the BaO tunneling barrier with an MgO/BaO double layer barrier, the electric stability could effectively be increased by a factor of five. The resulting TMR effect is found to be about +20% at room temperature, although a fully antiparallel state has not been realized.

  16. High-pressure densified solid solutions of alkaline earth hexaborides (Ca/Sr, Ca/Ba, Sr/Ba) and their high-temperature thermoelectric properties

    SciTech Connect

    Gürsoy, M.; Takeda, M.; Albert, B.

    2015-01-15

    Solid solutions of alkaline earth hexaborides were synthesized and densified by spark plasma sintering at 100 MPa. The high-temperature thermoelectric properties (Seebeck coefficients, electrical and thermal diffusivities, heat capacities) were measured between room temperature and 1073 K. CaB{sub 6}, SrB{sub 6}, BaB{sub 6} and the ternary hexaborides Ca{sub x}Sr{sub 1−x}B{sub 6}, Ca{sub x}Ba{sub 1−x}B{sub 6}, Sr{sub x}Ba{sub 1−x}B{sub 6} (x = 0.25, 0.5, 0.75) are n-type conducting compounds over the whole compositional and thermal ranges. The values of the figure of merit ZT for CaB{sub 6} (ca. 0.3 at 1073 K) were found to be significantly increased compared to earlier investigations which is attributed to the densification process. - Highlights: • Solid solutions of alkaline earth hexaborides were synthesized. • High-temperature thermoelectric properties of mixed calcium borides are excellent. • Spark plasma source densification results in high ZT values. • Borides are rare-earth free and refractory materials.

  17. Migration behaviour of twaite shad Alosa fallax assessed by otolith Sr:Ca and Ba:Ca profiles.

    PubMed

    Magath, V; Marohn, L; Fietzke, J; Frische, M; Thiel, R; Dierking, J

    2013-06-01

    Individual migration behaviour during the juvenile and adult life phase of the anadromous twaite shad Alosa fallax in the Elbe estuary was examined using otolith Sr:Ca and Ba:Ca profiles. Between hatching and the end of the first year of life, juveniles showed two migration patterns. Pattern one exhibited a single downstream migration from fresh water to the sea with no return into fresh water. In contrast, pattern two showed a first migration into the sea, then a return into fresh water and, finally, a second downstream migration into marine water. This first report of migration plasticity for A. fallax points to different exposure times to estuarine threats depending on the migration strategy. In adults, high Sr:Ca and low Ba:Ca in the majority of individuals confirmed prior reports of a primarily marine habitat use. Patterns reflecting spawning migrations were rarely observed on otoliths, possibly due to the short duration of visits to fresh water.

  18. Adsorption of Ba2+ by Ca-exchange clinoptilolite tuff and montmorillonite clay.

    PubMed

    Chávez, M L; de Pablo, L; García, T A

    2010-03-15

    The adsorption of barium by Ca-exchanged clinoptilolite and montmorillonite is presented. The kinetics of adsorption of Ba(2+) were evaluated contacting 1g portion of each adsorber with 100mL 0.1N BaCl(2) for 200 h. Adsorption by Ca-clinoptilolite is defined by second-order kinetics of rate constant K(v) 8.232 x 10(-2) g mg(-1)h(-1) and maximum removal of 71.885 mg g(-1). It is a two-stage process initiated by a rapid uptake of Ba(2+) followed by more moderate kinetics. The adsorption isotherms were determined contacting 0.2g of each adsorber with 10 mL 0.1-0.005N BaCl(2)+CaCl(2) solution, Ba(2+)/Ca(2+) ratio 1, for periods of 7 days for the tuff and 2 days for the clay. The equilibrium adsorption is described by the Langmuir model, of equilibrium constant K 0.0151 L mg(-1) and maximum adsorption of 15.29 mg g(-1). The adsorption of Ba(2+) by Ca-exchanged montmorillonite also follows a second-order reaction of rate constant K(v) 3.179 x 10(-2) g mg(-1)h(-1), and calculated separation of 36.74 mg g(-1); the Langmuir isotherm is defined by the constant K 0.034 L mg(-1) and maximum adsorption of 15.29 mg g(-1). X-ray diffraction shows that the exchange of Ba(2+) modifies the d(001) of Ca-montmorillonite from 15.4 to 12.4A. PMID:19926210

  19. Pulsed laser deposition of Tl-Ca-Ba-Cu-O films

    NASA Technical Reports Server (NTRS)

    Ianno, N. J.; Liou, S. H.; Woollam, John A.; Thompson, D.; Johs, B.

    1990-01-01

    Pulsed laser deposition is a technique commonly used to deposit high quality thin films of high temperature superconductors. This paper discusses the results obtained when this technique is applied to the deposition of Tl-Ca-Ba-Cu-O thin films using a frequency doubled Nd:YAG laser operating at 532 nm and an excimer laser operating at 248 nm. Films with onset temperatures of 125 K and zero resistance temperatures of 110 K deposited on (100) oriented MgO from a composite Tl2Ca2Ba2Cu3Ox target were obtained at both wavelengths upon appropriate post deposition annealing. Films deposited at 532 nm exhibit a rough surface, while those deposited at 248 nm are smooth and homogeneous. Upon annealing, films deposited at both wavelengths are single phase Tl2Ca2Ba2Cu3Ox.

  20. Kinetics of Sr/Ba and Sr/Ca ion exchange in synthetic zeolite A

    SciTech Connect

    Gaus, H.; Lutze, W.

    1981-01-08

    The isotopic exchange kinetics of Sr, Ba, and Ca have been measured in zeolites with different compositions and found to be describable as self-diffusion. The self-diffusion coefficients are strongly dependent on the composition. Also the Sr/Ba and Sr/Ca ion exchanges are measured in both directions and described as interdiffusion. While for Sr/Ba tolerable agreement is reached, for Sr/Ca a modification is necessary. The interdiffusion coefficient is multiplied by a factor which takes into account the activity, i.e., the selectivity of the zeolite. As a continuation of an earlier paper the zeolite is described as a mixture of microcells and free water. The above-mentioned factor must be calculated for a nonequilibrium state with respect to the water content in order to get agreement with the measurements.

  1. Thermoluminescence studies of bismuth doped Ba xCa 1- xS nanostructures

    NASA Astrophysics Data System (ADS)

    Singh, Surender; Lochab, S. P.; Kumar, Ravi; Singh, Nafa

    2011-01-01

    Bismuth doped Ba 1- xCa xS:Bi ( x=0-1) nanocrystallities have been prepared by the solid state reaction method and characterized by XRD and TEM. X-ray diffraction analysis shows the formation of the compounds in cubic structure at room temperature. Only partial replacement of Ba is possible and we found that Ba 0.5Ca 0.5S:Bi could not be prepared due to the difference between ionic radii of barium and calcium. Thermoluminescence studies of these samples after exposure to UV radiation have been carried out. The TL glow curve of Ba xCa 1 -xS:Bi has been found to be a simple structure with a single peak at 405, 428 and 503 K for x=1, 0.8 and 0, respectively. The kinetic parameters at various heating rates namely activation energy ( E), order of kinetics ( b) and frequency factor ( s) of the Ba 1- xCa xS:Bi ( x=0.2) (0.4 mol%) sample have been determined using Chen’s method. The deconvolution of curve was done using the GCD function suggested by Kitis. The effect of different heating rates and different amount of dose has also been discussed.

  2. Critical currents of aligned grains of Tl-Ba-Ca-Cu-O compounds

    NASA Technical Reports Server (NTRS)

    Fang, M. M.; Finnemore, D. K.; Farrell, D. E.; Bansal, N. R.

    1989-01-01

    A study of irreversibility in the magnetization curves of Tl2Ba2Ca2Cu3O10 and Tl2Ba2Ca1Cu2O8 was undertaken to determine the intragranular critical currents and the effects of flux-creep in grain-aligned samples of these materials. For fields of greater than 0.3 T, and H parallel to c axis, the critical supercurrent falls approximately exponentially with both magnetic field and temperature. Flux-creep is found to be linear in the logarithm of time at low fields over a wide temperature range.

  3. Anomalous Ba/Ca signals associated with low temperature stresses in Porites corals from Daya Bay, northern South China Sea.

    PubMed

    Chen, Tianran; Yu, Kefu; Li, Shu; Chen, Tegu; Shi, Qi

    2011-01-01

    Barium to calcium (Ba/Ca) ratio in corals has been considered as a useful geochemical proxy for upwelling, river flood and other oceanic processes. However, recent studies indicated that additional environmental or biological factors can influence the incorporation of Ba into coral skeletons. In this study, Ba/Ca ratios of two Porites corals collected from Daya Bay, northern South China Sea were analyzed. Ba/Ca signals in the two corals were 'anomalous' in comparison with Ba behaviors seen in other near-shore corals influenced by upwelling or riverine runoff. Our Ba/Ca profiles displayed similar and remarkable patterns characterized by low and randomly fluctuating background signals periodically interrupted by sharp and large synchronous peaks, clearly indicating an environmental forcing. Further analysis indicated that the Ba/Ca profiles were not correlated with previously claimed environmental factors such as precipitation, coastal upwelling, anthropogenic activities or phytoplankton blooms in other areas. The maxima of Ba/Ca appeared to occur in the period of Sr/Ca maxima, coinciding with the winter minimum temperatures, which suggests that the anomalous high Ba/Ca signals were related to winter-time low sea surface temperature. We speculated that the Ba/Ca peaks in corals of the Daya Bay were most likely the results of enrichment of Ba-rich particles in their skeletons when coral polyps retracted under the stresses of anomalous winter low temperatures. In this case, Ba/Ca ratio in relatively high-latitude corals can be a potential proxy for tracing the low temperature stress.

  4. Analysis of Ca in BaCl 2 matrix using laser-induced breakdown spectroscopy

    NASA Astrophysics Data System (ADS)

    Rinaldi, C. A.; Ferrero, J. C.

    2001-08-01

    The simplicity of the sample preparation and the use of an internal standardization method for the quantitative analysis of Ca has been investigated. The experimental set-up allowed the measurement of the intensity of ionic emission lines from Ca(II) and Ba(II), as a function of the composition in the matrix sample. The intensity ratios of the emission of Ca(II) to three different lines of Ba(II) were measured as a function of the distance (time) from the ablation point. With this information, the best experimental conditions for the analysis were determined. The method was then applied to the quantitative analysis of Ca in soils and baby food and the results compared with those obtained with conventional chemical and atomic absorption analysis.

  5. Atomized BaF2-CaF7 for Better-Flowing Plasma-Spray Feedstock

    NASA Technical Reports Server (NTRS)

    DellaCorte, Christopher; Stanford, Malcolm K.

    2008-01-01

    Atomization of a molten mixture of BaF2 and CaF2 has been found to be superior to crushing of bulk solid BaF2- CaF2 as a means of producing eutectic BaF2-CaF2 powder for use as an ingredient of the powder feedstock of a high-temperature solid lubricant material known as PS304. Developed to reduce friction and wear in turbomachines that incorporate foil air bearings, PS304 is applied to metal substrates by plasma spraying. The constituents of PS304 are: a) An alloy of 80 weight percent Ni and 20 weight percent Cr, b) Cr2O3, c) Ag, and d) The BaF2-CaF2 eutectic, specifically, 62 weight percent BaF2 and 38 weight percent CaF2. The superiority of atomization as a means of producing the eutectic BaF2-CaF2 powder lies in (1) the shapes of the BaF2-CaF2 particles produced and (2) the resulting flow properties of the PS304 feedstock powder: The particles produced through crushing are angular, whereas those produced through atomization are more rounded. PS304 feedstock powder containing the more rounded BaF2-CaF2 particles flows more freely and more predictably, as is preferable for plasma spraying.

  6. Ca, Sr and Ba stable isotopes reveal the fate of soil nutrients along a tropical climosequence

    USGS Publications Warehouse

    Bullen, Thomas D.; Chadwick, Oliver A.

    2016-01-01

    Nutrient biolifting is an important pedogenic process in which plant roots obtain inorganic nutrients such as phosphorus (P) and calcium (Ca) from minerals at depth and concentrate those nutrients at the surface. Here we use soil chemistry and stable isotopes of the alkaline earth elements Ca, strontium (Sr) and barium (Ba) to test the hypothesis that biolifting of P has been an important pedogenic process across a soil climosequence developed on volcanic deposits at Kohala Mountain, Hawaii. The geochemical linkage between these elements is revealed as generally positive site-specific relationships in soil mass gains and losses, particularly for P, Ba and Ca, using the ratio of immobile elements titanium and niobium (Ti/Nb) to link individual soil samples to a restricted compositional range of the chemically and isotopically diverse volcanic parent materials. At sites where P is enriched in surface soils relative to abundances in deeper soils, the isotope compositions of exchangeable Ca, Sr and Ba in the shallowest soil horizons (< 10 cm depth) are lighter than those of the volcanic parent materials and trend toward those of plants growing on fresh volcanic deposits. In contrast the isotope composition of exchangeable Ba in deeper soil horizons (> 10 cm depth) at those sites is consistently heavier than the volcanic parent materials. The isotope compositions of exchangeable Ca and Sr trend toward heavier compositions with depth more gradually, reflecting increasing leakiness from these soils in the order Ba < Sr < Ca and downward transfer of light biocycled Ca and Sr to deeper exchange sites. Given the long-term stability of ecosystem properties at the sites where P is enriched in surface soils, a simple box model demonstrates that persistence of isotopically light exchangeable Ca, Sr and Ba in the shallowest soil horizons requires that the uptake flux to plants from those near-surface layers is less than the recycling flux returned to the surface as

  7. Is otolith microchemistry (Sr: Ca and Ba:Ca ratios) useful to identify Mugil curema populations in the southeastern Caribbean Sea?

    PubMed

    Avigliano, E; Callicó-Fortunato, R; Buitrago, J; Volpedo, A V

    2015-11-01

    The aim of the present study was to evaluate the potential use of otolith microchemistry (Sr:Ca and Ba:Ca ratios) to identify silver mullet, Mugil curema, populations in Southeastern Caribbean Sea. Fish samples were collected in 7 areas of Nueva Esparta State (Venezuela). The otolith Sr:Ca and Ba:Ca ratios and water Sr:Ca were determined (by ICP-OES and EDTA volumetric method). Otoliths Sr:Ca and Ba:Ca ratios and Sr:Ca partition coefficient of mullets in Cubagua island (south of the State) were significantly different from ratios in La Guardia (north of the State). A discriminant analysis of otolith Sr:Ca and Ba:Ca ratios separated Cubagua Island from La Guardia values. These results suggest the existence of different mullet groups in the Southeastern Caribbean Sea. For this, the simultaneous use of Sr:Ca and Ba:Ca ratios could be a potential tool to identify populations in the study area. PMID:26628220

  8. Is otolith microchemistry (Sr: Ca and Ba:Ca ratios) useful to identify Mugil curema populations in the southeastern Caribbean Sea?

    PubMed

    Avigliano, E; Callicó-Fortunato, R; Buitrago, J; Volpedo, A V

    2015-11-01

    The aim of the present study was to evaluate the potential use of otolith microchemistry (Sr:Ca and Ba:Ca ratios) to identify silver mullet, Mugil curema, populations in Southeastern Caribbean Sea. Fish samples were collected in 7 areas of Nueva Esparta State (Venezuela). The otolith Sr:Ca and Ba:Ca ratios and water Sr:Ca were determined (by ICP-OES and EDTA volumetric method). Otoliths Sr:Ca and Ba:Ca ratios and Sr:Ca partition coefficient of mullets in Cubagua island (south of the State) were significantly different from ratios in La Guardia (north of the State). A discriminant analysis of otolith Sr:Ca and Ba:Ca ratios separated Cubagua Island from La Guardia values. These results suggest the existence of different mullet groups in the Southeastern Caribbean Sea. For this, the simultaneous use of Sr:Ca and Ba:Ca ratios could be a potential tool to identify populations in the study area.

  9. Solubility of BaS in BaO-BaF2 slag and the Influence of FeOx, SiO2, Cr2O3, BaCI2, CaO, and MgO on the sulfide capacity of this system

    NASA Astrophysics Data System (ADS)

    Rachev, Ivan P.; Tsukihashi, Fumitaka; Sano, Nobuo

    1992-03-01

    The influence of SiO2, FeOx, Cr2O3, BaCl2, CaO, and MgO on the sulfide capacity of the BaO-BaF2 system was measured at 1473 K, using a gas-slag-metal equilibration technique. It was found that the substitution of BaF2 by SiO2, FeOx, Cr2O3, and BaCl2 decreases the sulfide capacity of the BaO-BaF2 system. Similar results were obtained for the carbonate capacity. The CaO-saturated BaO-BaF2 flux, however, was found to have slightly higher sulfide and carbonate capacities than the pure BaO-BaF2 flux. The solubility of CaO increased with increasing BaF2 content and was 18 mol pet in BaF2 at 1473 K. The solubility of MgO in the BaO-BaF2 system at the same temperature is very low, and it has no effect on the sulfide and carbonate capacities. The solubility of BaS in the BaO-BaF2 system was also measured at 1473 K and had its maximum for the slag containing 40 mass pet BaO. The activity of BaO in the system was calculated from those data.

  10. Synthesis and superconducting properties of Tl-Ba-Ca-Cu-O films

    NASA Technical Reports Server (NTRS)

    Liou, S. H.; Chan, V. K.; Foong, F.; Lee, W. Y.; Gou, Y. S.

    1991-01-01

    Tl-Ba-Ca-Cu-O superconducting films were synthesized by sputtering either from a single target or from two oxide targets in a symmetric configuration. Films with zero resistance Tc of up to 122 K were obtained after various postannealing treatments at 870-950 C under an oxygen atmosphere. The composition of the films is not very homogeneous on the submicrometer scale. The critical current of these films at 77 K is in the 1000 A/sq cm to 10,000 A/sq cm range, which is much smaller than that of films prepared on SrTiO3 and LaAlO3 substrates. The low critical current density in these films is probably due to the granularity in the films. The morphology, structure, and magnetic and superconducting properties of the films were studied. Films prepared by two different sputtering techniques have similar results which depend mostly on the film compositions and their annealing conditions. It is found that the induced magnetic flux in the film decreases rapidly with increasing temperature, indicating weak flux pinning.

  11. High temperature superconductor step-edge Josephson junctions using Ti-Ca-Ba-Cu-O

    DOEpatents

    Ginley, D.S.; Hietala, V.M.; Hohenwarter, G.K.G.; Martens, J.S.; Plut, T.A.; Tigges, C.P.; Vawter, G.A.; Zipperian, T.E.

    1994-10-25

    A process is disclosed for formulating non-hysteretic and hysteretic Josephson junctions using HTS materials which results in junctions having the ability to operate at high temperatures while maintaining high uniformity and quality. The non-hysteretic Josephson junction is formed by step-etching a LaAlO[sub 3] crystal substrate and then depositing a thin film of TlCaBaCuO on the substrate, covering the step, and forming a grain boundary at the step and a subsequent Josephson junction. Once the non-hysteretic junction is formed the next step to form the hysteretic Josephson junction is to add capacitance to the system. In the current embodiment, this is accomplished by adding a thin dielectric layer, LaA1O[sub 3], followed by a cap layer of a normal metal where the cap layer is formed by first depositing a thin layer of titanium (Ti) followed by a layer of gold (Au). The dielectric layer and the normal metal cap are patterned to the desired geometry. 8 figs.

  12. High temperature superconductor step-edge Josephson junctions using Ti-Ca-Ba-Cu-O

    DOEpatents

    Ginley, David S.; Hietala, Vincent M.; Hohenwarter, Gert K. G.; Martens, Jon S.; Plut, Thomas A.; Tigges, Chris P.; Vawter, Gregory A.; Zipperian, Thomas E.

    1994-10-25

    A process for formulating non-hysteretic and hysteretic Josephson junctions using HTS materials which results in junctions having the ability to operate at high temperatures while maintaining high uniformity and quality. The non-hysteretic Josephson junction is formed by step-etching a LaAlO.sub.3 crystal substrate and then depositing a thin film of TlCaBaCuO on the substrate, covering the step, and forming a grain boundary at the step and a subsequent Josephson junction. Once the non-hysteretic junction is formed the next step to form the hysteretic Josephson junction is to add capacitance to the system. In the current embodiment, this is accomplished by adding a thin dielectric layer, LaA1O.sub.3, followed by a cap layer of a normal metal where the cap layer is formed by first depositing a thin layer of titanium (Ti) followed by a layer of gold (Au). The dielectric layer and the normal metal cap are patterned to the desired geometry.

  13. Structural and photoluminescence properties of Dy3+ co-doped and Eu2+ activated MAl2O4 (M = Ba, Ca, Sr) nanophosphors

    NASA Astrophysics Data System (ADS)

    Dejene, F. B.; Kebede, M. A.; Redi-Abshiro, M.; Kgarebe, B. V.

    2013-09-01

    Long afterglow alkaline earth aluminates MAl2O4:Eu, Dy (M: Ca, Sr, Ba) phosphors are generally synthesized by the solid-state process which is more feasible than other conventional processes in terms of operation and large-scale production. However, the constituents of phosphors synthesized using this process are usually not mixed well, the particles agglomerates and very high temperature requirement to synthesize the final powder make it undesirable. In order to circumvent these problems, MAl2O4:Eu, Dy (Ca, Ba, Sr) phosphors were prepared at low temperatures (500 °C) by the solution-combustion of corresponding metal nitrate-urea solution mixtures, over a time of 5-10 min. In order to elucidate the relationship between the constituent, structure and PL properties product's particle size, morphological and structural properties were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive X-ray spectrometer (EDS), while the characteristic luminescence properties were investigated using emission spectra. The low temperature monoclinic structure for both CaAl2O4 and SrAl2O4 and the hexagonal structure of BaAl2O4 were observed. The emission spectra of these phosphors indicated that all of them are broad band, and the only emission peaks around 448, 490 and 515 nm of CaAl2O4:Eu, Dy, BaAl2O4:Eu, Dy and SrAl2O4:Eu, Dy, respectively, are due to 5d → 4f transition of Eu2+. The decay curves implied that these phosphors contain fast, medium and slow-decay process. The Dy3+ trap levels may be considered to be responsible for the long afterglow phosphorescence at room temperature.

  14. Barium aluminides Ba{sub x}Al{sub 5}(x=3,3.5,4)

    SciTech Connect

    Jehle, Michael; Scherer, Harald; Wendorff, Marco; Roehr, Caroline

    2009-05-15

    Three aluminides of the series Ba{sub x}Al{sub 5}(x=3,3.5,4) were synthesized from stoichiometric ratios of the elements in Ta crucibles. The crystal structure of the new compound Ba{sub 7}Al{sub 10} was determined using single crystal X-ray data (space group R3-barm, a=604.23(9), c=4879.0(12)pm, Z=3, R1=0.0325). The compound exhibits Al Kagome (3.6.3.6.) nets in which half of the triangles form the basis of trigonal bipyramids Al{sub 5}. The apical Al are thus three-bonded assuming a charge of -2 ({sup 27}Al-NMR chemical shift delta=660pm), whereas the Al atoms of the basal triangle (i.e. of the Kagome net) are four-bonded and thus of formal charge -1(delta=490ppm). The total charge of the anion is thus exactly compensated by the Ba cations, i.e. the compound can be interpreted as an electron precise Zintl phase, exhibiting a distinct pseudo-band gap at the Fermi level of the calculated tDOS. According to the total formula, the structure displays a combination the stacking sequences of Ba{sub 3}Al{sub 5} and Ba{sub 4}Al{sub 5}, the structures of which have been redetermined with current methods (both hexagonal with space group P6{sub 3}/mmc; Ba{sub 3}Al{sub 5}: a=606.55(7), c=1461.8(2)pm, Z=2, R1=0.0239; Ba{sub 4}Al{sub 5}: a=609.21(7), c=1775.8(3)pm, Z=2, R1=0.0300). These three compounds with slightly different electron counts but similar polyanions allow to compare the bond lengths, the electronic structures and the overall bonding situation in dependence of positive or negative deviation of the electron count in relation to the novel formally electron precise Zintl compound Ba{sub 7}Al{sub 10}. - Al{sub 5} layers of Kagome nets in the new binary electron precise Zintl compound Ba{sub 3.5}Al{sub 5}, also found in Ba{sub 3}Al{sub 5} and Ba{sub 4}Al{sub 5}.

  15. Multi-colony calibrations of coral Ba/Ca with a contemporaneous in situ seawater barium record

    NASA Astrophysics Data System (ADS)

    LaVigne, Michèle; Grottoli, Andréa G.; Palardy, James E.; Sherrell, Robert M.

    2016-04-01

    The coral skeleton barium to calcium ratio (Ba/Cacoral), a proxy for seawater barium concentrations (BaSW), has been interpreted as a tracer of upwelling based on the characteristic "nutrient like" depth profile of BaSW. However, in some tropical regions, such as the Gulf of Panamá, substantial influence of terrestrial runoff inputs and differences between the vertical distribution of BaSW and that of the major nutrients (nitrate and phosphate) in the upper water column can complicate the interpretation of Ba/Cacoral as an upwelled nutrient proxy. In the Gulf of Panamá, contemporaneous Ba/Cacoral records from multiple colonies of Porites lobata, Pavona gigantea, and Pavona clavus corals record a nearly twofold change in surface water BaSW as a 20-70% increase in skeletal Ba/Ca with excellent correlation among Ba/Ca records from co-located colonies (r = 0.86-0.99). These results provide, for the first time, an absolute calibration of the coral Ba proxy with a contemporaneous BaSW record. Compiling the Ba/Cacoral records from three co-located colonies of each species into taxon-specific composite regressions reveals strong statistically significant correlations with the BaSW time-series record (p < 0.001). Differences among taxa in regression slope, y-intercept, and average distribution coefficient, as well as a demonstration of the application of the P. clavus calibration to a previously published Ba/Cacoral record, emphasize the necessity of using taxon-specific calibrations to reconstruct changes in BaSW with accuracy. These results support the application of Ba/Cacoral to reconstruct past changes in absolute BaSW concentrations, adding an important tool to the collection of geochemical proxies for reconstructing surface ocean biogeochemical processes in the past.

  16. Seawater nutrient and carbonate ion concentrations recorded as P/Ca, Ba/Ca, and U/Ca in the deep-sea coral Desmophyllum dianthus

    NASA Astrophysics Data System (ADS)

    Anagnostou, Eleni; Sherrell, Robert M.; Gagnon, Alex; LaVigne, Michele; Field, M. Paul; McDonough, William F.

    2011-05-01

    As paleoceanographic archives, deep sea coral skeletons offer the potential for high temporal resolution and precise absolute dating, but have not been fully investigated for geochemical reconstructions of past ocean conditions. Here we assess the utility of skeletal P/Ca, Ba/Ca and U/Ca in the deep sea coral D. dianthus as proxies of dissolved phosphate (remineralized at shallow depths), dissolved barium (trace element with silicate-type distribution) and carbonate ion concentrations, respectively. Measurements of these proxies in globally distributed D. dianthus specimens show clear dependence on corresponding seawater properties. Linear regression fits of mean coral Element/Ca ratios against seawater properties yield the equations: P/Ca coral (μmol/mol) = (0.6 ± 0.1) P/Ca sw(μmol/mol) - (23 ± 18), R2 = 0.6, n = 16 and Ba/Ca coral(μmol/mol) = (1.4 ± 0.3) Ba/Ca sw(μmol/mol) + (0 ± 2), R2 = 0.6, n = 17; no significant relationship is observed between the residuals of each regression and seawater temperature, salinity, pressure, pH or carbonate ion concentrations, suggesting that these variables were not significant secondary dependencies of these proxies. Four D. dianthus specimens growing at locations with Ωarag ⩽ 0.6 displayed markedly depleted P/Ca compared to the regression based on the remaining samples, a behavior attributed to an undersaturation effect. These corals were excluded from the calibration. Coral U/Ca correlates with seawater carbonate ion: U/Ca coral(μmol/mol) = (-0.016 ± 0.003) [CO32-] (μmol/kg) + (3.2 ± 0.3), R2 = 0.6, n = 17. The residuals of the U/Ca calibration are not significantly related to temperature, salinity, or pressure. Scatter about the linear calibration lines is attributed to imperfect spatial-temporal matches between the selected globally distributed specimens and available water column chemical data, and potentially to unresolved additional effects. The uncertainties of these initial proxy calibration regressions

  17. Mechanochemical synthesis of MgF2 - MF2 composite systems (M = Ca, Sr, Ba)

    NASA Astrophysics Data System (ADS)

    Scholz, G.; Breitfeld, S.; Krahl, T.; Düvel, A.; Heitjans, P.; Kemnitz, E.

    2015-12-01

    The capability of mechanochemical synthesis for the formation of MgF2-MF2 (M: Ca, Sr, Ba) composites, solid solutions or well-defined compounds was tested applying a fluorination of different fluorine-free metal sources with NH4F directly at milling. No evidence was found for a substitution of Mg2+ with Ca2+ (Sr2+, Ba2+) ions, or vice versa, in rutile or fluorite structure. However, an equimolar ratio of Mg2+ to the second cation allows the mechanochemical synthesis of tetrafluoromagnesates, MMgF4, which is more and more hampered the smaller the radius of the cation M2+ is. BaMgF4 is formed even phase pure from the acetates, SrMgF4 can only be observed in a mixture accompanied by the binary fluorides. In addition, 19F MAS NMR spectra along with calculations of 19F isotropic chemical shift values according to the superposition model point to the formation of a metastable phase of CaMgF4, which disappears at thermal treatment and decomposes into the binary fluorides CaF2 and MgF2.

  18. Superconductivity in the Tl-Ca-Ba-Cu-O System:. Synthesis, Characterization and Mechanism

    NASA Astrophysics Data System (ADS)

    Ganguli, A. K.; Swamy, K. S. Nanjunda; Subbanna, G. N.; Rajumon, M. K.; Sarma, D. D.; Rao, C. N. R.

    Synthesis and characterization of some of the members of the Tl-Ca-Ba-Cu-O system are presented. Tc in both the TlCan-1Ba2CunO2n+3 and Tl2Can-1Ba2CunO2n+4 series increase with the number of Cu-O layers, n; Tc in the latter series with two Tl-O layers are generally higher than in the former with a single Tl-O layer. Tl in the cuprates is in the 3+ state while Cu is in the 1+ and 2+ states, showing the importance of oxygen holes. The concentration of these holes seems to increase with the number of Tl-O layers.

  19. Observations of Al, Fe and Ca(+) in Mercury's Exosphere

    NASA Technical Reports Server (NTRS)

    Bida, Thomas A.; Killen, Rosemary M.

    2011-01-01

    We report 5-(sigma) tangent column detections of Al and Fe, and strict 3-(sigma) tangent column upper limits for Ca(+) in Mercury's exosphere obtained using the HIRES spectrometer on the Keck I telescope. These are the first direct detections of Al and Fe in Mercury's exosphere. Our Ca(-) observation is consistent with that reported by The Mercury Atmospheric and Surface Composition Spectrometer (MASCS) on the MErcury Surface, Space ENvironment, GEochemistry, and Ranging (MESSENGER) spacecraft.

  20. Submillimeter and microwave residual losses in epitaxial films of Y-Ba-Cu-O and Tl-Ca-Ba-Cu-O

    SciTech Connect

    Miller, D.; Richards, P.L. ); Garrison, S.M.; Newman, N. ); Eom, C.B.; Geballe, T.H. . Dept. of Applied Physics); Etemad, S.; Inam, A.; Venkatesan, T. ); Martens, J.S. (Sandia National Labs., Albuquerque, NM (Unite

    1992-03-01

    We have used a novel bolometric technique and a resonant technique to obtain accurate submillimeter and microwave residual loss data for epitaxial thin films of YBa{sub 2}Cu{sub 3}O{sub 7}, Tl{sub 2}Ca{sub 2}Ba{sub 2}Cu{sub 3}O{sub 10} and Tl{sub 2}CaBa{sub 2}Cu{sub 2}O{sub 8}. For all films we obtain good agreement between the submillimeter and microwave data, with the residual losses in both the Y-Ba-Cu-O and Tl-Ca-Ba-Cu-O films scaling approximately as frequency squared below {approximately} 1 THz. We are able to fit the losses in the Y-Ba-Cu-O films to a weakly coupled grain model for the a-b plane conductivity, in good agreement with results from a Kramers-Kronig analysis of the loss data. We observe strong phonon structure in the Tl-Ca-Ba-Cu-O films for frequencies between 2 and 21 THz, and are unable to fit these losses to the simple weakly coupled grain model. This is in strong contrast to the case for other high {Tc} superconductors such as YBa{sub 2}Cu{sub 3}O{sub 7}, where phonon structure observed in ceramic samples is absent in epitaxial oriented films and crystals because of the electronic screening due to the high conductivity of the a-b planes.

  1. Crystal structure and superconductivity in (Cu,Hg)Ba2Ca4Cu5Oy

    NASA Astrophysics Data System (ADS)

    Akimoto, J.; Kawaguchi, K.; Sohma, M.; Hayakawa, H.; Gotoh, Y.; Oosawa, Y.; Tokiwa, K.; Iyo, A.; Ihara, H.

    1997-02-01

    A new solid-solution superconductor, (Cu,Hg)Ba2Ca4Cu5Oy with the tetragonal lattice parameters a = 3.849(2) Å and c = 21.496(3) Å, has been synthesized by the high-temperature and high-pressure technique. The structure refinement of the as-prepared (Cu,Hg)-1245 by the single-crystal X-ray diffraction method confirmed the substitutional composition (Cu0.76Hg0.24)Ba2Ca4Cu5O12.45, whose cationic composition was close to that obtained by chemical analysis. The additional Cu atoms at the mercury site construct the chain-like oxygen coordination. The superstructure observed in Cu-1245 disappeared by the partial substitution of mercury for copper in the present (Cu,Hg)-1245. The structure refinement of the as-prepared Hg-1245 revealed the mercury-site deficiency of about 20%.

  2. Stability of Tl-Ba-Ca-Cu-O Superconducting Thin Films

    SciTech Connect

    Siegal, M.P.; Overmyer, D.L.; Venturini, E.L.; Padilla, R.R.; Provencio, P.N.

    1999-08-23

    We report the stability of TlBa{sub 2}CaCu{sub 2}O{sub 7} (Tl-1212) and Tl{sub 2}Ba{sub 2}CaCu{sub 2}O{sub 8} (T1-2212) thin films and by inference, the stability of TlBa{sub 2}Ca{sub 2}Cu{sub 3}O{sub 9} (Tl-1223) and Tl{sub 2}Ba{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10} (Tl-2223) thin films, under a variety of conditions. In general, we observe that the stability behavior of the single Tl-O layer materials (Tl-1212 and Tl-1223)are similar and the double Tl-O layer materials (Tl-2212 and Tl-2223) are similar. All films are stable with repeated thermal cycling to cryogenic temperatures. Films are also stable in acetone and methanol. Moisture degrades film quality rapidly, especially in the form of vapor. Tl-1212 is more sensitive to vapor than Tl-2212. These materials are stable to high temperatures in either N{sub 2}, similar to vacuum for the cuprates, and O{sub 2} ambients. While total degradation of properties (superconducting and structural) occur at the same temperatures for all phases, 600 C in N{sub 2} and 700 C in O{sub 2}, the onset of degradation occurs at somewhat lower temperatures for Tl-1212 than for Tl-2212 films. In all cases, sample degradation is associated with Tl depletion from the films.

  3. Enhanced ultrasonic attenuation of Tl-Ca-Ba-Cu-O at the superconducting transition

    NASA Technical Reports Server (NTRS)

    Sun, K. J.; Winfree, W. P.; Xu, M.-F.; Levy, M.; Sarma, Bimal K.

    1990-01-01

    Temperature-dependent ultrasonic attenuation measurements have been performed on polycrystalline samples of Tl-Ca-Ba-Cu-O at various frequencies. An attenuation anomaly was observed close to the superconducting transition temperature T(c) (103 K) whose temperature position was frequency-independent. The attenuation decreased exponentially with temperature in the superconducting state for both transverse and longitudinal waves. It was also found that the temperature-dependent sound velocity showed a slope change around T(c).

  4. NOx Uptake Mechanism on Pt/BaO/Al2O3 Catalysts

    SciTech Connect

    Kwak, Ja Hun; Kim, Do Heui; Szailer, Tamas; Peden, Charles HF; Szanyi, Janos

    2006-11-01

    The NOx adsorption mechanism on Pt/BaO/Al2O3 catalysts was investigated by performing NOx storage/reduction cycles, NO2 adsorption and NO + O2 adsorption on 2%Pt/(x)BaO/Al2O3 (x = 2, 8 and 20 wt%) catalysts. NOx uptake profiles on 2%Pt/20%BaO/Al2O3 at 523 K show complete uptake behavior for almost 5 min, and then the NOx level starts gradually increasing with time and it reaches 75% of the inlet NOx concentration after 30 min time-on-stream. Although this catalyst shows fairly high NOx conversion at 523 K, only ~ 2.4 wt% out of 20 wt% BaO is converted to Ba(NO3)2. Adsorption studies by using NO2 and NO + O2 suggest two different NOx adsorption mechanisms. The NO2 uptake profile on 2%Pt/20%BaO/Al2O3 shows the absence of a complete NOx uptake period at the beginning of adsorption and the overall NOx uptake is controlled by the gas-solid equilibrium between NO2 and BaO/Ba(NO3)2 phase. When we use NO + O2, complete initial NOx uptake occurs and the time it takes to convert ~ 4 % of BaO to Ba(NO3)2 is independent of the NO concentration. These NOx uptake characteristics suggest that the NO + O2 reaction on the surface of Pt particles produces NO2 that is subsequently transferred to the neighboring BaO phase by spill over. At the beginning of the NOx uptake, this spill-over process is very fast and so it is able to provide complete NOx storage. However, the NOx uptake by this mechanism slows down as BaO in the vicinity of Pt particles are converted to Ba(NO3)2. The formation of Ba(NO3)2 around the Pt particles results in the development of a diffusion barrier for NO2, and increases the probability of NO2 desorption and consequently, the beginning of NOx slip. As NOx uptake by NO2 spill-over mechanism slows down due to the diffusion barrier formation, the rate and extent of NO2 uptake are determined by the diffusion rate of nitrate ions into the BaO bulk, which, in turn, is determined by the gas phase NO2 concentration.

  5. Barium Cycling During the Paleocene-Eocene Thermal Maximum: Evidence From Ba/Ca in Foraminifera

    NASA Astrophysics Data System (ADS)

    Hall, J. M.; Zachos, J. C.; Turekian, K. K.

    2004-12-01

    The Paleocene-Eocene thermal maximum (PETM) around 55 Ma reflects short-term, rapid climate change during a period of intense greenhouse climate. This interval is characterized by a negative carbon isotopic shift, interpreted as a release of methane from seafloor gas hydrate reservoirs. This perturbation of the carbon cycle is accompanied by significantly greater rates of euhedral barite accumulation in deep sea sediment commonly believed to be a reflection of elevated primary productivity in surface waters. An interpretation of higher productivity during the PETM, however, is contrary to microfossil assemblage data which indicates a decrease in primary productivity. It has also been suggested that the increase in barite accumulation during the PETM may have been the result of an increase in dissolved barium concentrations in the deep ocean coeval with methane release. This supposition has support from the fact that modern gas hydrate reservoirs are surrounded by pore waters with dissolved barium concentrations considerably higher than that of seawater. This investigation utilizes the barium content of foraminifera as a proxy to reconstruct changes in the barium concentration of the ocean. At 55 Ma, Ba/Ca decreases between 25 to 28% in the planktic foraminifer \\textit{Morozovella velascoensis}, indicating a decrease in the barium concentration of the surface ocean. These results bolster the theory that there was increased biogenic barite precipitation during the PETM. Changes in surface water temperature and pH may have altered species assemblages such that celestite (SrSO4) precipitating organisms enriched in barium as BaSO4 (possibly acantharia) were dominant, modifying the barite precipitation pathways, which affected water column barite cycling. Ba/Ca and Cd/Ca measurements on benthic foraminifera show a positive correlation with Mn/Ca, indicating contamination of manganese oxide coatings. This contamination is in part due to the greater surface to volume

  6. 120 K superconductor TlBaCaCu/sub 2/O/sub y/

    SciTech Connect

    Zhao, Z.X.; Chen, L.Q.; Mai, Z.H.; Huang, Y.Z.; Xiao, Z.L.; Chu, X.; Zheng, D.N.; Jia, S.L.; Wang, J.H.; Chen, G.H.

    1988-01-01

    The author have prepared 120K superconductor in Tl-Ba-Ca-Cu oxide system. This 120K superconductor has been investigated by x-ray diffraction and EDAX micro-analysis. EDAX analysis shows that the composition of this superconductor is very close to TLBa(Ca/sub 1/-/sub x/Cu/sub x/)CuO/sub y/(chi - 0.3). Most of the x-ray powder diffractions including all the strong ones can be indexed according to a tetragonal structure with /alpha/ = 5.46 A and c = 36.2A which means that the sample is nearly a single phase material.

  7. Thick film of HgBa 2Ca 2Cu 3O 8+δ via the sol-gel technique

    NASA Astrophysics Data System (ADS)

    Yoo, S. H.; Wong, K. W.; Xin, Y.

    1997-02-01

    We have prepared superconducting HgBa 2Ca 2Cu 3O 8+δ thick films on polycrystalline MgO substrate via the sol-gel technique together with a slow annealing method. A precursor film of Ba 2Ca 2Cu 3O 7 was annealed with a bulk mixture of unreacted HgBa 2Ca 2Cu 3O 8+δ and a precursor, Ba 2Ca 2Cu 3O 7, pellet that was employed to control the HgO vapor pressure. Our films show an onset superconducting transition temperature of 140 K and a zero resistance temperature of 130 K after oxygen annealing. The high Tc thick films are consistently reproducible.

  8. Genesis of basalt magmas and their derivatives under the Izu Islands, Japan, inferred from Sr/Ca-Ba/Ca systematics

    NASA Astrophysics Data System (ADS)

    Onuma, Naoki; Hirano, Masataka; Isshiki, Naoki

    1983-10-01

    The Sr/Ca-Ba/Ca systematics defined for a series of volcanic rocks provided by volcanoes of the Izu Islands, Japan, have cast a new light on the origin and evolution of basalt magmas and their derivatives: (1) The mantle material in the source region of primary basalt magmas beneath the Izu Islands shows a chondritic value of Sr/Ca and Ba/Ca ratios. (2) Both the tholeiite magma and the high-alumina/calc-alkali basalt magma are primary with higher degrees (15-20% for the former) and lower degrees (8-11% for the latter) of partial melting of a common mantle material. (3) The primary basalt magmas evolve independently via crystal fractionation process in respective magma chambers at shallower depths each providing a series of andesite and dacite magmas corresponding to respective primary basalt magmas. (4) The crystal fractionation process in magma chamber is controlled mainly by plagioclase and clinopyroxene crystallization in terms of the alkaline earth elements. The plagioclase/clinopyroxene ratio decreases during crystal fractionation process. The chemical environments of magma chambers are similar to each other in the tholeiite series and in the high-alumina basalt/calc-alkali rock series. (5) The end products provided by the crystal fractionation process lie within Bowen's petrogeny's residua system, making a thin, silicic crust under the volcanic islands near the Izu Peninsula. The calc-alkali rhyolites in these islands are derived from the thin silicic crust via melting process by the heat of intruded primary basalt magmas. (6) The regional distribution of degree of partial melting indicates variations from 15 to 20% along the volcanic front and from 8 to 11% in the region behind it. The fact suggests that an interaction between the mantle wedge under the Philippine Sea Plate and the subducting slab of the Pacific Plate beneath the Izu Islands is different from place to place, with respect to temperature distribution and/or water supply from the subducting

  9. A first principles study on newly proposed (Ca/Sr/Ba)Fe2Bi2 compounds with their parent compounds

    NASA Astrophysics Data System (ADS)

    Sundareswari, M.; Jayalakshmi, D. S.; Viswanathan, E.

    2016-02-01

    The structural, electronic, bonding and magnetic properties of newly proposed iron-based compounds viz., CaFe2Bi2, SrFe2Bi2, BaFe2Bi2 with their Fermi surface topology are reported here for the first time by means of first principles calculation. All these properties of newly proposed compounds are compared and analysed along with their respective parent compounds namely (Ca,Sr,Ba)Fe2As2.

  10. Activity and diffusivity of oxygen in liquid Ag-Yb1Ba2Cu3 and Tl1Ba2Ca2Cu3 alloys

    NASA Astrophysics Data System (ADS)

    Chou, H.; Chen, H. S.; Fang, W. C.; Wu, M. K.

    1992-12-01

    We have measured the activity and diffusivity of oxygen in liquid Ag-Yb1Ba2Cu3 and Tl1Ba2Ca2Cu3 at 930 and 900 °C, respectively, by a modified coulometric titration method on the galvanic cell: O_ in liquid alloys/yttria stabilized zirconia/air, Pt. The standard Gibbs formation energy and the diffusivity of oxygen in liquid Ag-Yb1Ba2Cu3 alloy for 1/2O2(1 atm)→O_(1 at. %) are determined to be ΔG=-247.4 kJ/g atom, and D=1.52×10-4 cm2/s. The oxygen solubility Cs in the Ag-Yb1Ba2Cu3 alloy is 0.0913 at. %, a factor of 5.5 higher than that in Yb1Ba2Cu3 alloy. The addition of Ag does not alter the growth mechanism and the oxygen diffusion controls the film growth. The growth speed is enhanced as a result of the enhanced oxygen solubility. ΔG and the diffusion coefficient of oxygen in the Tl1Ba2Ca2Cu3 liquid alloy are -257 kJ/g atom and 1.2×10-4 cm2/s, respectively. The oxygen solubility of the Tl1Ba2Ca2Cu3 alloy at 900 °C is found to be very high at ˜5.74 at. %. All thermodynamic data for oxygen in the precursor alloys are consistent with each other but there is a deviation of activity coefficient with composition for the different alloys from the theoretical model.

  11. Microwave surface resistance of bulk Tl-Ba-Ca-Cu-O superconductors

    SciTech Connect

    Newman, H.S.; Singh, A.K.; Sadananda, K.; Imam, M.A.

    1989-01-23

    The first measurements of the microwave surface resistance at 18 GHz of bulk Tl-Ba-Ca-Cu-O superconductors produced by the hot isostatic pressing (HIP) process are reported. The superconducting samples, prepared by solid-state reaction with subsequent sintering and consolidation to obtain ideal density, were measured by replacing the end wall of a TE/sub 011/ circular mode gold-plated copper cavity with the sample and determining the cavity Q for the temperature range 4--300 K. Results indicated that HIP samples which underwent subsequent annealing exhibit, below the critical temperature, a surface resistance approaching an order of magnitude less than copper.

  12. Hyper- and hypobaric processing of Tl-Ba-Ca-Cu-O superconductors

    SciTech Connect

    Goretta, K.C.; Routbort, J.L.; Shi, Donglu; Chen, J.G.; Hash, M.C.

    1989-11-01

    Tl-based superconductors of initial composition Tl:Ca:Ba:Cu equal to 2:2:2:3 and 1:3:1:3 were heated in oxygen at pressures of 10{sup 4} to 6 {times} 10{sup 5} Pa. The 2:2:2:3 composition formed primarily the 2-layer superconductor with zero resistance from 77 to 104 K. The 1:3:1:3 composition formed nearly phase pure 3-layer superconductor with a maximum zero resistance temperature of 120 K. Application of hyperbaric pressure influenced phase purities and transition temperatures slightly; phase purities decreased significantly with application of hypobaric pressures. 10 refs., 1 fig.

  13. Hyper- and hypobaric processing of Tl-Ba-Ca-Cu-O superconductors

    NASA Astrophysics Data System (ADS)

    Goretta, K. C.; Routbort, J. L.; Shi, Donglu; Chen, J. G.; Hash, M. C.

    1989-11-01

    Tl-based superconductors of initial composition Tl:Ca:Ba:Cu equal to 2:2:2:3 and 1:3:1:3 were heated in oxygen at pressures of 10(sup 4) to 6 (times) 10(sup 5) Pa. The 2:2:2:3 composition formed primarily the 2-layer superconductor with zero resistance from 77 to 104 K. The 1:3:1:3 composition formed nearly phase pure 3-layer superconductor with a maximum zero resistance temperature of 120 K. Application of hyperbaric pressure influenced phase purities and transition temperatures slightly; phase purities decreased significantly with application of hypobaric pressures.

  14. Fabrication and chemical composition of RF magnetron sputtered Tl-Ca-Ba-Cu-O high Tc superconducting thin films

    NASA Technical Reports Server (NTRS)

    Subramanyam, G.; Radpour, F.; Kapoor, V. J.; Lemon, G. H.

    1990-01-01

    The preparation of TlCaBaCuO superconducting thin films on (100) SrTiO3 substrates is described, and the results of their characterization are presented. Sintering and annealing the thin films in a Tl-rich ambient yielded superconductivity with a Tc of 107 K. The results of an XPS study support two possible mechanisms for the creation of holes in the TlCaBaCuO compound: (1) partial substitution of Ca(2+) for Tl(3+), resulting in hole creation, and (2) charge transfer from Tl(3+) to the CuO layers, resulting in a Tl valence between +3 and +1.

  15. A new (Ba, Ca) (Ti, Zr)O3 based multiferroic composite with large magnetoelectric effect

    PubMed Central

    Naveed-Ul-Haq, M.; Shvartsman, Vladimir V.; Salamon, Soma; Wende, Heiko; Trivedi, Harsh; Mumtaz, Arif; Lupascu, Doru C.

    2016-01-01

    The lead-free ferroelectric 0.5Ba(Zr0.2Ti0.8)O3 − 0.5(Ba0.7Ca0.3)TiO3 (BCZT) is a promising component for multifunctional multiferroics due to its excellent room temperature piezoelectric properties. Having a composition close to the polymorphic phase boundary between the orthorhombic and tetragonal phases, it deserves a case study for analysis of its potential for modern electronics applications. To obtain magnetoelectric coupling, the piezoelectric phase needs to be combined with a suitable magnetostrictive phase. In the current article, we report on the synthesis, dielectric, magnetic, and magnetoelectric characterization of a new magnetoelectric multiferroic composite consisting of BCZT as a piezoelectric phase and CoFe2O4 (CFO) as the magnetostrictive phase. We found that this material is multiferroic at room temperature and manifests a magnetoelectric effect larger than that of BaTiO3 −CoFe2O4 bulk composites with similar content of the ferrite phase. PMID:27555563

  16. A new (Ba, Ca) (Ti, Zr)O3 based multiferroic composite with large magnetoelectric effect

    NASA Astrophysics Data System (ADS)

    Naveed-Ul-Haq, M.; Shvartsman, Vladimir V.; Salamon, Soma; Wende, Heiko; Trivedi, Harsh; Mumtaz, Arif; Lupascu, Doru C.

    2016-08-01

    The lead-free ferroelectric 0.5Ba(Zr0.2Ti0.8)O3 ‑ 0.5(Ba0.7Ca0.3)TiO3 (BCZT) is a promising component for multifunctional multiferroics due to its excellent room temperature piezoelectric properties. Having a composition close to the polymorphic phase boundary between the orthorhombic and tetragonal phases, it deserves a case study for analysis of its potential for modern electronics applications. To obtain magnetoelectric coupling, the piezoelectric phase needs to be combined with a suitable magnetostrictive phase. In the current article, we report on the synthesis, dielectric, magnetic, and magnetoelectric characterization of a new magnetoelectric multiferroic composite consisting of BCZT as a piezoelectric phase and CoFe2O4 (CFO) as the magnetostrictive phase. We found that this material is multiferroic at room temperature and manifests a magnetoelectric effect larger than that of BaTiO3 ‑CoFe2O4 bulk composites with similar content of the ferrite phase.

  17. A new (Ba, Ca) (Ti, Zr)O3 based multiferroic composite with large magnetoelectric effect.

    PubMed

    Naveed-Ul-Haq, M; Shvartsman, Vladimir V; Salamon, Soma; Wende, Heiko; Trivedi, Harsh; Mumtaz, Arif; Lupascu, Doru C

    2016-01-01

    The lead-free ferroelectric 0.5Ba(Zr0.2Ti0.8)O3 - 0.5(Ba0.7Ca0.3)TiO3 (BCZT) is a promising component for multifunctional multiferroics due to its excellent room temperature piezoelectric properties. Having a composition close to the polymorphic phase boundary between the orthorhombic and tetragonal phases, it deserves a case study for analysis of its potential for modern electronics applications. To obtain magnetoelectric coupling, the piezoelectric phase needs to be combined with a suitable magnetostrictive phase. In the current article, we report on the synthesis, dielectric, magnetic, and magnetoelectric characterization of a new magnetoelectric multiferroic composite consisting of BCZT as a piezoelectric phase and CoFe2O4 (CFO) as the magnetostrictive phase. We found that this material is multiferroic at room temperature and manifests a magnetoelectric effect larger than that of BaTiO3 -CoFe2O4 bulk composites with similar content of the ferrite phase. PMID:27555563

  18. Thermodynamic stability of radiogenic Ba in CsAlSi2O6 pollucite

    NASA Astrophysics Data System (ADS)

    Jaffe, John; van Ginhoven, Renée; Jiang, Weilin

    2013-03-01

    Pollucite, a zeolite-like nanoporous aluminosilicate structure with nominal composition CsAlSi2O6, has been suggested as a nuclear waste storage form for fission-product radioactive isotopes of cesium, especially 137Cs. One factor affecting the long-term stability of this waste form is the valence change associated with the beta decay that converts Cs into barium. We have used first-principles density functional total energy calculations to evaluate the thermodynamic stability of pollucite with Ba replacing Cs at regular lattice sites with respect to the precipitation of Ba, Cs or their oxides. We included small clusters of substitutional BaCs as well as localized complexes of BaCs with compensating electron donor defects, specifically Cs vacancies and interstitial oxygen. We conclude that Cs-Ba pollucite is thermodynamically stable against precipitation of Cs or its oxide, but that partial precipitation of Ba or BaO may be thermodynamically favored under some conditions. Even this change may be kinetically limited, however. Fuel Cycle Research and Development, U.S. Department of Energy Waste Form Campaign

  19. Magnetic behaviour of the MTbF{sub 6} fluoroterbates (M=Cd, Ca, Sr, ({alpha}/{beta})-Ba)

    SciTech Connect

    Josse, M.; El-Ghozzi, M.; Avignant, D.; Andre, G.; Bouree, F.; Isnard, O.

    2012-01-15

    Neutron powder diffraction has been performed on the MTbF{sub 6} fluorides (M=Cd, Ca, Sr, ({alpha}/{beta})-Ba). Four of these fluorides (Cd, Ca, Sr, {beta}-Ba) are built of a (pseudo-) tetragonal packing of [TbF{sub 6}]{sup 2-} chains and only differs by the chains relative orientations. Thus this series represents a valuable opportunity to evaluate the Tb{sup 4+}-Tb{sup 4+} magnetic interactions. All the compounds displayed antiferromagnetic order (T{sub N}=2.70 K (Cd), 2.15 K (Ca), 2.60 K (Sr), 2.10 K ({beta}-Ba)), except for the {alpha} form of BaTbF{sub 6}. The crystal structure of this latter fluoroterbate has also been investigated by means of high-resolution neutron powder diffraction. From Neutron Powder Diffraction data, CdTbF{sub 6} and {beta}-BaTbF{sub 6} magnetic structures were determined, together with the metamagnetic behaviour of {beta}-BaTbF{sub 6} as a function of an external magnetic field. A tentative phase diagram is then given for {beta}-BaTbF{sub 6}. Advantage was taken of the polymorphism of the BaTbF{sub 6} fluoroterbate to analyse, on the basis of topological parameters such as bond distances and angles, the magnetic behaviour of its {alpha} and {beta} forms. It was shown that superexchange interactions are present in {beta}-BaTbF{sub 6}, and that these interactions may also rule the magnetic behaviour of the other MTbF{sub 6} (M=Ca, Sr, Cd) tetravalent terbium fluorides. - Graphical abstract: Powder neutron diffraction revealed magnetic order in four of the five investigated fluoroterbates, while crystal chemical analyses of {alpha} and {beta} forms of BaTbF{sub 6} evidenced the existence of superexchange interactions. Highlights: Black-Right-Pointing-Pointer Five fluoroterbates are investigated by Powder Neutron Diffraction (PND). Black-Right-Pointing-Pointer Four of them are antiferromagnetically ordered at 1.4 K. Black-Right-Pointing-Pointer Magnetic structures of {beta}-BaTbF{sub 6} and CdTbF{sub 6} are determined. Black

  20. Synthesis and characterization of high-Tc superconductors in the Tl-Ca-Ba-Cu-O system

    NASA Technical Reports Server (NTRS)

    Bansal, Narottam P.; Farrell, D. E.

    1989-01-01

    Both Tl2Ca2Ba2Cu3O10 and TlCa3BaCu3O8.5 are investigated for superconductivity as a function of the sintering temperature, time, atmosphere, and quench rate in an effort to synthesize the high-Tc superconducting phase in the thallium system. The samples are characterized by electrical resistivity measurements, X-ray diffraction, and scanning electron microscopy. Samples of starting composition Tl2Ca2Ba2Cu3O10 fired in air at 860-900 C and rapidly quenched show a Tc of 96-107 K. In contrast, specimens of starting composition TlCa3BaCu3O8.5 when baked at 900 C and slowly cooled in oxygen superconduct at 116 K and above and consist of Tl2Ca2Ba2Cu3O(10+x) as the dominant phase. The results also show that, in contrast to the case of YBa2Cu3O(7-x), doping with a small concentration of fluorine sharpens the resistive transition and produces a large Tc increase in thallium-based superconductors.

  1. Synthesis and characterization of high-Tc superconductors in the Tl-Ca-Ba-Cu-O system

    NASA Astrophysics Data System (ADS)

    Bansal, Narottam P.; Farrell, D. E.

    1989-05-01

    Both Tl2Ca2Ba2Cu3O10 and TlCa3BaCu3O8.5 are investigated for superconductivity as a function of the sintering temperature, time, atmosphere, and quench rate in an effort to synthesize the high-Tc superconducting phase in the thallium system. The samples are characterized by electrical resistivity measurements, X-ray diffraction, and scanning electron microscopy. Samples of starting composition Tl2Ca2Ba2Cu3O10 fired in air at 860-900 C and rapidly quenched show a Tc of 96-107 K. In contrast, specimens of starting composition TlCa3BaCu3O8.5 when baked at 900 C and slowly cooled in oxygen superconduct at 116 K and above and consist of Tl2Ca2Ba2Cu3O(10+x) as the dominant phase. The results also show that, in contrast to the case of YBa2Cu3O(7-x), doping with a small concentration of fluorine sharpens the resistive transition and produces a large Tc increase in thallium-based superconductors.

  2. Hardness of CaF2 and BaF2 solid lubricants at 25 to 670 deg C

    NASA Technical Reports Server (NTRS)

    Deadmore, Daniel L.; Sliney, Harold E.

    1987-01-01

    Plastic deformation is a prominent factor in determining the lubricating value of solid lubricants. Little information is available and its direct measurement is difficult so hardness, which is an indirect measure of this property was determined for fluoride solid lubricant compositions. The Vickers hardness of BaF2 and CaF2 single crystals was measured up to 670 C in a vacuum. The orientation of the BaF2 was near the (013) plane and the CaF2 was about 16 degrees from the degrees from the (1'11) plane. The BaF2 has a hardness of 83 kg/sq mm at the 25 C and 9 at the 600 C. The CaF2 is 170 at 25 C and 13 at 670 C. The decrease in hardness in the temperature range of 25 to 100 C is very rapid and amounts to 40% for both materials. Melts of BaF2 and CaF2 were made in a platinum crucible in ambient air with compositions of 50 to 100 wt% BaF2. The Vickers hardness of these polycrystalline binary compositions at 25 C increased with increasing CaF2 reaching a maximum of 150 kn/sq mm near the eutectic. The polycrystalline CaF2 was 14% softer than that of the single crystal surface and BsF2 was 30% harder than the single crystal surface. It is estimated that the brittle to ductile transition temperature for CaF2 and BaF2 is less than 100 C for the conditions present in the hardness tester.

  3. Co{sub 2}FeAl based magnetic tunnel junctions with BaO and MgO/BaO barriers

    SciTech Connect

    Rogge, J.; Schmalhorst, J.; Hütten, A.; Hetaba, W.

    2015-07-15

    We succeed to integrate BaO as a tunneling barrier into Co{sub 2}FeAl based magnetic tunnel junctions (MTJs). By means of Auger electron spectroscopy it could be proven that the applied annealing temperatures during BaO deposition and afterwards do not cause any diffusion of Ba neither into the lower Heusler compound lead nor into the upper Fe counter electrode. Nevertheless, a negative tunnel magnetoresistance (TMR) ratio of -10% is found for Co{sub 2}FeAl (24 nm) / BaO (5 nm) / Fe (7 nm) MTJs, which can be attributed to the preparation procedure and can be explained by the formation of Co- and Fe-oxides at the interfaces between the Heusler and the crystalline BaO barrier by comparing with theory. Although an amorphous structure of the BaO barrier seems to be confirmed by high-resolution transmission electron microscopy (TEM), it cannot entirely be ruled out that this is an artifact of TEM sample preparation due to the sensitivity of BaO to moisture. By replacing the BaO tunneling barrier with an MgO/BaO double layer barrier, the electric stability could effectively be increased by a factor of five. The resulting TMR effect is found to be about +20% at room temperature, although a fully antiparallel state has not been realized.

  4. Preparation of high T(c) Tl-Ba-Ca-Cu-O thin films by pulsed laser evaporation and Tl2O3 vapor processing

    NASA Technical Reports Server (NTRS)

    Johs, B.; Thompson, D.; Ianno, N. J.; Woollam, John A.; Liou, S. H.

    1989-01-01

    Tl-Ba-Ca-Cu-O superconducting thin films with zero-resistance temperatures up to 115 K have been prepared using a Tl2O3 vapor process on Ba-Ca-Cu-O precursor thin films. The Ba-Ca-Cu-O thin films were made by laser deposition on Y-stabilized ZrO2 substrates. This technique minimizes problems caused by the toxicity of Tl2O3, and its subsequent decomposition to the volatile and toxic Tl2O upon heating. Therefore, it may have practical application in the fabrication of high T(c) Tl-Ba-Ca-Cu-O superconducting thin-film devices.

  5. Synthesis and luminous characteristics of Ba3CaSi2-xAlxO8:Eu, Mn phosphor for white LED

    NASA Astrophysics Data System (ADS)

    Shen, Changyu; Yang, Yi; Jin, Shangzhong; Ming, Jiangzhou

    2008-12-01

    Ba3CaSi1.7Al0.3O8: Eu, Mn white-emitting phosphor was prepared by solid reaction and X-ray powder diffraction (XRD) analysis confirmed the formation of Ba3CaSi1.7Al0.3O8: 0.1Eu, 0.1Mn. It was found experimentally that, its three-color emission peaks situated at 621, 491 and 435 nm respectively under excitation of 350-450nm irradiation. The 435nm and 491nm emission bands are attributed to 4f to 5d transition of Eu2+ ions. The emission band peaking at 621nm originates from the 4T1-6A1 transition of Mn2+ ions after the energy transferring from Eu2+ to Mn2+ ions. When the concentrations of the Al3+, Eu2+ and Mn2+ ions were 0.8 mol, 0.1mol and 0.1mol respectively, the sample presented intense white emitting. The addition of Al ion to the host leads to a substantial change of intensity ratio between blue to green emission.

  6. Theoretical studies of the osmium based perovskites AOsO3 (A=Ca, Sr and Ba)

    NASA Astrophysics Data System (ADS)

    Ali, Zahid; Sattar, Abdul; Asadabadi, S. Jalali; Ahmad, Iftikhar

    2015-11-01

    Osmium based perovskites AOsO3 (A=Ca, Sr and Ba) have been studied theoretically using density functional theory approach. These studies show that CaOsO3 and SrOsO3 are orthorhombic and BaOsO3 is cubic and are consistent with the experiments. The electronic band structures demonstrate that these compounds are metals. The magnetic studies verify the experimental observations at low temperature, where the spin effects are canceled by the orbitals. The stable magnetic phase optimizations and magnetic susceptibilities calculations by the post-DFT treatment confirm that CaOsO3 and SrOsO3 are weak ferromagnetic whereas BaOsO3 is a paramagnetic material. The directional magnetic study shows that these compounds are magnetically anisotropic, and reveals that the easy magnetization axis is [001] direction.

  7. Frustration of Negative Capacitance in Al2O3/BaTiO3 Bilayer Structure

    PubMed Central

    Kim, Yu Jin; Park, Min Hyuk; Lee, Young Hwan; Kim, Han Joon; Jeon, Woojin; Moon, Taehwan; Do Kim, Keum; Jeong, Doo Seok; Yamada, Hiroyuki; Hwang, Cheol Seong

    2016-01-01

    Enhancement of capacitance by negative capacitance (NC) effect in a dielectric/ferroelectric (DE/FE) stacked film is gaining a greater interest. While the previous theory on NC effect was based on the Landau-Ginzburg-Devonshire theory, this work adopted a modified formalism to incorporate the depolarization effect to describe the energy of the general DE/FE system. The model predicted that the SrTiO3/BaTiO3 system will show a capacitance boost effect. It was also predicted that the 5 nm-thick Al2O3/150 nm-thick BaTiO3 system shows the capacitance boost effect with no FE-like hysteresis behavior, which was inconsistent with the experimental results; the amorphous-Al2O3/epitaxial-BaTiO3 system showed a typical FE-like hysteresis loop in the polarization – voltage test. This was due to the involvement of the trapped charges at the DE/FE interface, originating from the very high field across the thin Al2O3 layer when the BaTiO3 layer played a role as the NC layer. Therefore, the NC effect in the Al2O3/BaTiO3 system was frustrated by the involvement of reversible interface charge; the highly stored charge by the NC effect of the BaTiO3 during the charging period could not be retrieved during the discharging process because integral part of the polarization charge was retained within the system as a remanent polarization. PMID:26742878

  8. Giant thermal vibrations in the framework compounds Ba1 -xSrxAl2O4

    NASA Astrophysics Data System (ADS)

    Kawaguchi, S.; Ishii, Y.; Tanaka, E.; Tsukasaki, H.; Kubota, Y.; Mori, S.

    2016-08-01

    Synchrotron x-ray diffraction experiments were performed on the network compounds Ba1 -xSrxAl2O4 at temperatures between 15 and 800 K. The ferroelectric phase of the parent BaAl2O4 is largely suppressed by substituting a small amount of Sr for Ba and disappears for x ≥0.1 . Structural refinements reveal that the isotropic atomic displacement parameter Biso in the bridging oxygen atom is largely independent of temperature and retains an anomalously large value in the adjacent paraelectric phase even at the lowest temperature. The Biso systematically increases as x increases, exhibiting an especially large value for x =0.5 . According to previous electron diffraction experiments for Ba1 -xSrxAl2O4 with x ≥0.1 , strong thermal diffuse scattering occurs at two reciprocal points relating to two distinct soft modes at the M and K points over a wide range of temperatures below 800 K [Y. Ishii et al., Sci. Rep. 6, 19154 (2016), 10.1038/srep19154]. Although the latter mode disappears at approximately 200 K, the former does not condense, at least down to 100 K. The anomalously large Biso observed in this study is ascribed to these soft modes existing in a wide temperature range.

  9. Fluorescence and phosphorescence properties of the low temperature forms of the MAl{sub 2}Si{sub 2}O{sub 8}:Eu{sup 2+} (M=Ca, Sr, Ba) compounds

    SciTech Connect

    Clabau, Frederic; Garcia, Alain; Bonville, Pierre; Gonbeau, Danielle; Le Mercier, Thierry; Deniard, Philippe; Jobic, Stephane

    2008-06-15

    The fluorescence and phosphorescence properties of Europium-doped MAl{sub 2}Si{sub 2}O{sub 8} (M=Ca, Sr, Ba) are reinvestigated and discussed on the basis of the propensity of an activator to agglomerate with an oxygen vacancy. Due to a stronger attraction of the anion vacancy towards Eu{sup 2+} cations going from BaAl{sub 2}Si{sub 2}O{sub 8} to SrAl{sub 2}Si{sub 2}O{sub 8} and CaAl{sub 2}Si{sub 2}O{sub 8} host lattices, the interpretation of the fluorescence spectra turns out to be less trivial in the Ca and Sr host lattices than in the Ba one and requests the account for Eu{sup 2+} cations lying at alkaline-earth sites with or without vacancy in their neighborhood. Phosphorescence in these compounds is highlighted. - Graphical abstract: The Eu{sup 2+}-doped MAl{sub 2}Si{sub 2}O{sub 8} (M=Ca, Sr, and Ba) aluminosilicates exhibit a bluish white luminescence, which can last several minutes after the removal of the excitation. The account for Eu{sup 2+} cations coupled with defects is required to explain fluorescence spectra.

  10. Preparation and physical properties of (M1-xYbx) Fe2As2 (M = Ca, Ba) single crystals

    NASA Astrophysics Data System (ADS)

    Chen, S. C.; Syu, K. J.; Lee, W. H.; Chen, Y. Y.

    2014-03-01

    As judged by x-ray diffraction data, single crystals in the series (M1-xYbx) Fe2As2 (M = Ca, Ba) with 0 < x <0.22 have been made by flux method. Magnetic and electrical properties as well as the specific heat data in the systems (M1-xYbx) Fe2As2 (M = Ca, Ba) investigated will be discussed. Supported by the National Science Council of Republic of China under Contract Number NSC-102-2112-M-194-005-MY3.

  11. Al-Ca and Al-Fe metal-metal composite strength, conductivity, and microstructure relationships

    SciTech Connect

    Kim, Hyong June

    2011-01-01

    Deformation processed metal-metal composites (DMMC’s) are composites formed by mechanical working (i.e., rolling, swaging, or wire drawing) of two-phase, ductile metal mixtures. Since both the matrix and reinforcing phase are ductile metals, the composites can be heavily deformed to reduce the thickness and spacing of the two phases. Recent studies have shown that heavily drawn DMMCs can achieve anomalously high strength and outstanding combinations of strength and conductivity. In this study, Al-Fe wire composite with 0.07, 0.1, and 0.2 volume fractions of Fe filaments and Al-Ca wire composite with 0.03, 0.06, and 0.09 volume fractions of Ca filaments were produced in situ, and their mechanical properties were measured as a function of deformation true strain. The Al-Fe composites displayed limited deformation of the Fe phase even at high true strains, resulting in little strengthening effect in those composites. Al-9vol%Ca wire was deformed to a deformation true strain of 13.76. The resulting Ca second-phase filaments were deformed to thicknesses on the order of one micrometer. The ultimate tensile strength increased exponentially with increasing deformation true strain, reaching a value of 197 MPa at a true strain of 13.76. This value is 2.5 times higher than the value predicted by the rule of mixtures. A quantitative relationship between UTS and deformation true strain was determined. X-ray diffraction data on transformation of Al + Ca microstructures to Al + various Al-Ca intermetallic compounds were obtained at the Advanced Photon Source at Argonne National Laboratory. Electrical conductivity was measured over a range of true strains and post-deformation heat treatment schedules.

  12. Linking large piezoelectric coefficients to highly flexible polarization of lead free BaTiO3-CaTiO3-BaZrO3 ceramics

    NASA Astrophysics Data System (ADS)

    Benabdallah, F.; Simon, A.; Khemakhem, H.; Elissalde, C.; Maglione, M.

    2011-06-01

    We report a large d31 piezoelectric coefficient and corresponding electromechanical coupling factor, Kp, of 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 (BCTZ50) and 0.68Ba(Zr0.2Ti0.8)O3-0.32(Ba0.7Ca0.3)TiO3 (BCTZ32) lead-free piezoceramics. The piezoelectric coefficient, d31, reaches a high value of 200 pC/N for BCTZ50 at room temperature which is comparable to the one of the soft PZT. This confirms the previously reported d33 for the same material. A useful way to achieve such performances at the expense of a smaller thermal budget is suggested, enabling better control of the ceramics composition and microstructure. Based on pyroelectric and ferroelectric hysteresis loops measurements, we show that such outstanding properties are likely due to the high flexibility of polarization under thermal and electric stresses.

  13. Multiple caloric effects in geometrically frustrated "114" CaBaCo4O7 Cobaltite

    NASA Astrophysics Data System (ADS)

    Dhanasekhar, C.; Das, A. K.; Venimadhav, A.

    2016-11-01

    We have investigated the magnetocaloric and electrocaloric effects in "114" CaBaCo4O7 (CBCO) sample prepared by solid state method. Magnetization study has revealed the ferrimagnetic transition (TC) at 60 K and another transition at 66 K. Observation of irreversibility and first order nature of magnetic transition above TC has suggested a complicated magnetic nature of the system. A maximum magnetic entropy change of ~6.8 J/Kg-K has been found at TC and further a broadening of the entropy peak with the increase of magnetic field indicates the field induced transition above TC. From temperature dependent pyrocurrent measurements, we have measured the electric polarization under different electric fields and the change in isothermal electrocaloric entropy is found to be ~0.50 J-m-3 K-1 (for 150 kV/m) just above magnetic transition temperature.

  14. TlCaBaCuO high Tc superconducting microstrip ring resonators designed for 12 GHz

    NASA Technical Reports Server (NTRS)

    Subramanyam, G.; Kapoor, V. J.; Chorey, C. M.; Bhasin, K. B.

    1993-01-01

    Microwave properties of sputtered Tl-Ca-Ba-Cu-O thin films were investigated by designing, fabricating, and testing microstrip ring resonators. Ring resonators designed for 12 GHz fundamental resonance frequency, were fabricated and tested. From the unloaded Q values for the resonators, the surface resistance was calculated by separating the conductor losses from the total losses. The penetration depth was obtained from the temperature dependence of resonance frequency, assuming that the shift in resonance frequency is mainly due to the temperature dependence of penetration depth. The effective surface resistance at 12 GHz and 77 K was determined to be between 1.5 and 2.75 mOmega, almost an order lower than Cu at the same temperature and frequency. The effective penetration depth at 0 K is approximately 7000 A.

  15. Performance of TlCaBaCuO 30 GHz 64 element antenna array

    NASA Technical Reports Server (NTRS)

    Lewis, L. L.; Koepf, G.; Bhasin, K. B.; Richard, M. A.

    1993-01-01

    A 64-element, 30-GHz microstrip antenna array with corporate feed network was designed and built on a 0.254-mm (10-mil) thick lanthanum aluminate substrate. One antenna pattern was fabricated from gold film, and a second pattern used TlCaBaCuO high-temperature superconductor. Both antennas used gold ground planes deposited on the reverse side of the substrate. Gain and radiation patterns were measured for both antennas at room temperature and at cryogenic temperatures. Observations agree well with simple models for loss and microwave beam width, with a gain on boresight of 20.3 dB and beam width of 15 deg for the superconducting antenna. The antenna loss is only 1.9 dB.

  16. Vortex fluctuation in HgBa 2Ca 3Cu 4O 10+δ

    NASA Astrophysics Data System (ADS)

    Kim, Mun-Seog; Kim, Wan-Seon; Lee, Sung-Ik; Yu, Seong-Cho; Itskevich, E. S.; Kuzemskaya, I.

    1997-08-01

    Reversible magnetization with the external magnetic fields of 1 T ≤ H ≤ 5 T parallel to the c-axis has been measured for the grain aligned HgBa2Ca3Cu4O10+δ. A strong vortex fluctuation effect was clearly observed and the magnetization is well described by the vortex fluctuation model. From this analysis, the penetration depth λab(0) = 1583 Å and the effective interlayer spacing s = 44.6 Å were estimated. However, the value of s is significantly larger than the lattice parameter c = 19 Å, which is different from the prediction of the vortex fluctuation model. From the model on superconducting fluctuations proposed by Koshelev, in which not only the critical fluctuations at the lowest Landau level but also the Gaussian fluctuations at higher Landau levels were considered, the different value of s = 15.4 Å was obtained.

  17. Density functional theory study of phonons in graphene doped with Li, Ca and Ba

    NASA Astrophysics Data System (ADS)

    Pešić, Jelena; Damljanović, Vladimir; Gajić, Radoš; Hingerl, Kurt; Belić, Milivoj

    2015-12-01

    Vibrational frequencies and phonon displacement patterns of the H-site doped graphene are calculated by the density functional theory (DFT). DFT calculations, as well as the group theory study, are used to describe these structures as interesting materials for single layer superconductivity. In this paper, graphene doped with Li, Ca and Ba adatoms is systematically analysed and compared. Due to the effect of zone folding, displacement patterns of calculated modes correspond to the ones of the K and Γ point phonons of graphene and this offers the possibility for comparison with the experimental results for graphene. Our objective was to provide compendious and practical guidelines for the experimental research and characterization of these structures.

  18. Liquid Be, Ca and Ba. An orbital-free ab-initio molecular dynamics study

    SciTech Connect

    Rio, B. G. del; González, L. E.

    2015-08-17

    Several static and dynamic properties of liquid beryllium (l-Be), liquid calcium (l-Ca) and liquid barium (l-Ba) near their triple point have been evaluated by the orbital-free ab initio molecular dynamics method (OF-AIMD), where the interaction between valence electrons and ions is described by means of local pseudopotentials. These local pseudopotentials used were constructed through a force-matching process with those obtained from a Kohn-Sham ab initio molecular dynamics study (KS-AIMD) of a reduced system with non-local pseudopotentials. The calculated static structures show good agreement with the available experimental data, including an asymmetric second peak in the structure factor which has been linked to the existence of a marked icosahedral short-range order in the liquid. As for the dynamic properties, we obtain collective density excitations whose associated dispersion relations exhibit a positive dispersion.

  19. Synthesis, crystal and electronic structures of the new Zintl phases Ba3Al3Pn5 (Pn = P, As) and Ba3Ga3P5.

    PubMed

    He, Hua; Tyson, Chauntae; Saito, Maia; Bobev, Svilen

    2013-01-01

    The new Zintl compounds Ba(3)Al(3)P(5), Ba(3)Al(3)As(5,) and Ba(3)Ga(3)P(5) have been synthesized using molten metal fluxes. They are isoelectronic and isotypic, crystallizing with a novel rhombohedral structure type in the space group R3c with unit cell constants a = 14.5886(9) Å, c = 28.990(3) Å for Ba(3)Al(3)P(5), a = 14.613(3) Å, c = 28.884(8) Å for Ba(3)Ga(3)P(5), and a = 14.9727(13) Å, c = 29.689(4) Å for Ba(3)Al(3)As(5), respectively. The structures are based on TrPn(4) (Tr = Al, Ga; Pn = P, As) tetrahedra that share both edges and corners, leading to intricate arrangements embodied in the [Tr(4)Pn(9)](15-) and [Tr(3)Pn(6)](9-) strands, interconnected by dimeric [Tr(2)Pn(6)](12-) units. The Ba(2+) cations reside within cylindrical channels within the polyanionic framework and provide the valence electrons needed for Tr-Pn covalent bonding. In spite of the large and complex structure, there are no homoatomic Tr-Tr or Pn-Pn interactions, hence, the structures can be readily rationalized in the context of the Zintl-Klemm formalism as follows [Ba(2+)](3)[Tr(3+)](3)[Pn(3-)](5); calculations on their electronic band-structures confirm this reasoning and reveal about 1.4-1.9 eV energy band gaps, that is, semiconducting behavior. Structural parallels with other known Zintl compounds are also presented.

  20. Polymorphic structure evolution and large piezoelectric response of lead-free (Ba,Ca)(Zr,Ti)O{sub 3} ceramics

    SciTech Connect

    Tian, Ye; Chao, Xiaolian E-mail: yangzp@snnu.edu.cn; Wei, Lingling; Liang, Pengfei; Yang, Zupei E-mail: yangzp@snnu.edu.cn; Jin, Li

    2014-03-17

    The polymorphic structure evolution of (Ba,Ca)(Zr,Ti)O{sub 3} piezoelectric ceramics was investigated by analysis of the in situ X-ray diffraction and dielectric spectra. The results indicated that a confined orthorhombic (O) phase region induced by the approach of the rhombohedral (R) and tetragonal (T) phases existed in an extremely narrow temperature range of (Ba{sub 0.85}Ca{sub 0.15})(Zr{sub 0.1}Ti{sub 0.9})O{sub 3} composition. The electric properties near the O–T phase boundaries of (Ba{sub 0.95}Ca{sub 0.05})(Zr{sub 0.05}Ti{sub 0.95})O{sub 3} and (Ba{sub 0.85}Ca{sub 0.15})(Zr{sub 0.1}Ti{sub 0.9})O{sub 3} were compared. The results suggested that the confined O phase region is an important factor that contributes to the extremely large piezoelectric response.

  1. LiCaAl/sub 6/:Cr/sup 3+/

    SciTech Connect

    Payne, S.A.; Chase, L.L.; Newkirk, H.W.; Smith, L.K.; Krupke, W.F. )

    1988-11-01

    The authors report the discovery of a new laser, LiCaAIF/sub 6/:Cr/sup 3/ (Cr/sup 3+/ :LiCAF). The intrinsic (extrapolated maximum) slope efficiency was found to be 67 percent. For comparison, they also measured the intrinsic slope efficiencies of BeAl/sub 2/O/sub 4/:Cr/sup 3+/ (alexandrite), Na/sub 3/Ga/sub 2/Li/sub 3/F/sub 12/:Cr/sup 3+/, and ScBO/sub 3/:Cr/sup 3+/, and obtained values of 65,28, and 26 percent, respectively. The tuning range of LiCaAIF/sub 6/:Cr/sup 3+/ was determined to be at least 720-840 nm. The conventional spectroscopic properties, such as the absorption, emission, and emission lifetimes as a function of temperature, are reported as well.

  2. Superconducting and normal-state properties of APd2As2 (A = Ca, Sr, Ba) single crystals

    NASA Astrophysics Data System (ADS)

    Anand, V. K.; Kim, H.; Tanatar, M. A.; Prozorov, R.; Johnston, D. C.

    2013-06-01

    The synthesis and crystallography, magnetic susceptibility χ, magnetization M, specific heat Cp, in-plane electrical resistivity ρ, and in-plane magnetic penetration depth measurements are reported for single crystals of APd2As2 (A = Ca, Sr, Ba) versus temperature T and magnetic field H. The crystals were grown using PdAs self-flux. CaPd2As2 and SrPd2As2 crystallize in a collapsed body-centered tetragonal ThCr2Si2-type structure (I4/mmm), whereas BaPd2As2 crystallizes in the primitive tetragonal CeMg2Si2-type structure (P4/mmm), in agreement with literature data. The ρ(T) data exhibit metallic behavior for all three compounds. Bulk superconductivity is reported for CaPd2As2 and SrPd2As2 below Tc=1.27 and 0.92 K, respectively, whereas only a trace of superconductivity is found in BaPd2As2. No other phase transitions were observed. The χ(T) and M(H) data reveal anisotropic diamagnetism in the normal state, with χc>χab for CaPd2As2 and BaPd2As2, and χc<χab for SrPd2As2. The normal and superconducting state data indicate that CaPd2As2 and SrPd2As2 are conventional type-II nodeless s-wave electron-phonon superconductors. The electronic superconducting state heat capacity data for CaPd2As2, which has an extremely sharp heat capacity jump at Tc, are analyzed using our recent elaboration of the α-model of the BCS theory of superconductivity, which indicates that the s-wave gap in this compound is anisotropic in momentum space.

  3. Energy transfer between Eu-Mn and photoluminescence properties of Ba0.75Al11O17.25-BaMgAl10O17:Eu2+,Mn2+ solid solution

    NASA Astrophysics Data System (ADS)

    Zhou, Jun; Wang, Yuhua; Liu, Bitao; Li, Feng

    2010-08-01

    In order to evaluate the energy transfer between Eu-Mn in Ba0.75Al11O17.25-BaMgAl10O17 solid solution, Ba0.75Al11O17.25-BaMgAl10O17:Eu2+,Mn2+ phosphors were prepared by flux method. The crystal structure and the morphology of the solid solution were demonstrated by x-ray dirrfactometer and scanning electron microscopy. The photoluminescence mechanisms were explained by the energy transfer of Eu2+ to Mn2+ and the Dexter theory. A redshift of green emission peak and a decrease in decay time with the increase in Mn2+ concentration were observed. These phenomena are attributed to the formation of Mn2+ paired centers after analysis by a method of Pade approximations.

  4. Effect of reaction time and (Ca+Mg)/Al molar ratios on crystallinity of Ca-Mg-Al layered double Hydroxide

    NASA Astrophysics Data System (ADS)

    Heraldy, E.; Nugrahaningtyas, K. D.; Sanjaya, F. B.; Darojat, A. A.; Handayani, D. S.; Hidayat, Y.

    2016-02-01

    Ca-Mg-Al Layered Double Hydroxides (Ca-Mg-Al-LDH) compounds were successfully synthesized from brine water and AlCl3.6H2O as the starting materials by coprecipitation method. The product result was characterized by X-ray powder diffraction (XRD) and Fourier transform infrared (FT-IR). The effects of the reaction time and the molar ratios of the raw material on the crystallinity of Ca-Mg-Al-LDH were examining. Results show that increasing reaction time (30; 60 and 90 min.) could improve the crystallinity and monodispersity of layered double hydroxide compounds particles. The well-defined Ca-Mg- Al-LDH could be prepared with (Ca+Mg)/Al molar ratios 0.5.

  5. Electric Properties of [(BaO)1.00(XO)x](Ti0.95Zr0.05)O2 (X = Ca, Sr, Ba) Ceramics Fired under Reduced Atmosphere

    NASA Astrophysics Data System (ADS)

    Sakai, Yuichi; Futakuchi, Tomoaki; Adachi, Masatoshi

    2009-09-01

    Ba(Ti0.95Zr0.05)O3 doped with CaO, SrO, or BaO was investigated in order to develop materials suitable for lead-free actuators with resistance to reduction. The grain sizes of [(BaO)1.00(XO)x](Ti0.95Zr0.05)O2 (X = Ca, Sr, Ba; x = 0-0.05) ceramics decreased with increasing amount of dopant concentration x. The grain sizes of the ceramics with a dopant concentration x in the range of 0.005 to 0.05 are approximately 1-2 µm. The crystalline phases of the ceramics with a dopant concentration x = 0.01 or less were perovskite single phases. CaO, SrO, or BaO doping concentrations of x = 0.005 or more were effective for preventing the reduction of Ba(Ti0.95Zr0.05)O3 during firing under 3% H2-N2 atmosphere. The remanent polarizations and dynamic piezoelectric constants of the ceramics decreased with increasing dopant concentration of CaO, SrO, or BaO. The dynamic piezoelectric constant of the ceramics with BaO dopant concentration x of 0.005 was approximately 640 pm/V. The Curie temperature was approximately 109 °C in this composition.

  6. Ion beam modification of Tl-Ba-Ca-Cu-O type high temperature superconductors during irradiation

    SciTech Connect

    Newcomer, P.P.; Morosin, B.; Wang, L.M.

    1994-12-31

    Microstructural modification of high temperature superconductor (HTS) single-crystal plates of Tl-1212 and Tl-2212 (numbers designate the Tl/Ba/Ca/Cu cation ratio) was studied during 1.5 MeV Kr{sup +} and Xe{sup +} ion irradiation with in-situ electron diffraction and after ion irradiation with high resolution TEM (HRTEM). Similar in-situ temperature dependence effects are seen for both phases. During irradiations from 22K to 673K, an amorphous halo develops after very low ion dose or fluence (1.7 {times} 10{sup 12} ions/cm{sup 2}). During irradiation at 100 and 300K, complete amorphization is obtained, while at 22 and {ge}533K, the halo fades slightly and a polycrystalline ring pattern develops, indicating ion irradiation induced crystallization occurred. After a low ion dose (8.5 {times} 10{sup 12} ions/cm{sup 2}) at 100 and 300K, HRTEM reveals amorphous regions 5-20 nm in size which are not columnar and do not all penetrate the entire sample thickness. At 22 and {ge}533K, Moire fringes and misoriented crystallites of cascade size are observed. The 4-6nm crystallites are thallium-rich.

  7. Estimation Model for Electrical Conductivity of CaF2-CaO-Al2O3 Slags

    NASA Astrophysics Data System (ADS)

    Shi, Guan-yong; Zhang, Ting-an; Dou, Zhi-he; Niu, Li-ping

    2016-09-01

    Electrical conductivity is one of the most important properties of molten slags. It has an important influence on process parameter selection of the electroslag remelting process. In the present work, a new model for estimating electrical conductivity of high-temperature slags has been proposed via calculating the conductivity by electrical conductivity of pure substances and interaction parameters between the different components in the slag has been proposed. In this model, the Arrhenius law is used to describe the relationship between electrical conductivity and temperature of slags. This model has been successfully applied to the CaF2-Al2O3, CaF2-CaO, and CaO-Al2O3, as well as CaF2-CaO-Al2O3 systems, and the calculated results are in good agreement with the measured values.

  8. Electronic Structure of HgBa2CaCu2O(6+delta) Epitaxial films measured by x-ray Photoemission

    NASA Technical Reports Server (NTRS)

    Vasquez, R. P.; Rupp, M.; Gupta, A.; Tsuei, C. C.

    1995-01-01

    The electronic structure and chemical states of HgBa2CaCu20(sub 6 + delta), epitaxial films have been studied with x-ray photelectron spectroscopy. Signals from the superconducting phase dominate all the core-level spectra, and a clear Fermi edge is observed in the valence-band region. The Ba, Ca, Cu, and O core levels are similar to those of Tl2Ba2CaCu208(+)O(sub 6 + delta), but distinct differences are observed in the valence bands which are consistent with differences in the calculated densities of states.

  9. Actinide chemistry in Allende Ca-Al-rich inclusions

    NASA Technical Reports Server (NTRS)

    Murrell, M. T.; Burnett, D. S.

    1987-01-01

    Fission track radiography is used to investigate the U and Th microscale distribution in a set of Allende-meteorite Ca-Al-rich inclusions. In the Type B inclusions, the major phases melilite and fassaite are important actinide host phases, and on the rims of Type B inclusions and throughout all other inclusions studied, perovskite is the dominant actinide host phase. Results suggest that neither alteration nor loss or gain of an actinide-rich phase appears to have been an important Th/U fractionation mechanism, and that volatility differences may be the dominant factor. Th/U and rare earth element abundance patterns for the spinel and perovskite rim suggest rim formation by volatilization of interior material, and within the constraints of the brief time scale required for this heating, several mechanisms for spinel-perovskite rim formation are possible.

  10. Magnetic dependent proximity effects of superconductivity and ferromagnetism in Y BaCuO/LaCaMnO bilayers

    NASA Astrophysics Data System (ADS)

    Peng, Lin; Cai, Chuanbing; Chen, Changzhao; Gao, Bo; Ying, Liliang; Liu, Zhiyong

    2008-12-01

    The Y BaCuO/ La 0.88Ca 0.12MnO 3 (YBCO/LCMOi) and Y BaCuO/ La 0.33Ca 0.67MnO 3 (YBCO/LCMOj) bilayers are fabricated with the method of pulsed laser deposition, and the magnetic dependent proximity effects are investigated. The magnetic fields were applied parallel (in-plane) and perpendicular (out-of-plane) to the film plane. Magnetic properties curves in different temperature range and magnetic field along two crystal orientation show a complex behavior due to the interplay between Meissner currents in YBCO layer and the magnetic fields present in LCMOi (or LCMOj) layer. Ac susceptibility measurements show that the suppression of superconductivity in LCMOi and LCMOj bilayers. The obtained results are discussed in terms of the effect of hole charge transfer from YBCO to LCMOi (or LCMOj) on the proximity between superconductivity and ferromagnetism.

  11. Pb-DOPING Effects in Hg1-xPbxBa2Ca2Cu3O8+δ

    NASA Astrophysics Data System (ADS)

    Xue, Y. Y.; Huang, Z. J.; Qiu, X. D.; Beauvais, L.; Zhang, X. N.; Sun, Y. Y.; Meng, R.; Chu, C. W.

    Samples with a nominal composition of Hg1-xPbxBa2Ca2Cu3O8+δ (x~0.1, 0.2, and 0.3) have been synthesized and characterized. The Pb-doping promotes the formation of the three CuO2-layer compound Hg1-xPbxBa2Ca2Cu3O8+δ, and reduces the release of Hg vapor at the synthesis temperature. The intergrain electric coupling is also significantly enhanced by the doping, resulting in lower normal-state resistivity and higher intergrain critical current density. The carrier concentration of the as-synthesized samples increases with the increase of x, ranging from underdoped (x~0) to overdoped (x≥0.2).

  12. Highly oriented Tl2Ba2Ca2Cu3O10 thin films by pulsed laser evaporation

    NASA Technical Reports Server (NTRS)

    Liou, S. H.; Aylesworth, K. D.; Ianno, N. J.; Johs, B.; Thompson, D.

    1989-01-01

    Superconducting thin films on MgO (100) substrates with nearly pure Tl2Ba2Ca2Cu3O10 (2:2:2:3) phase using pulsed laser evaporation and postannealing have been fabricated. The films had c axes perpendicular to the substrates. Superconducting films with onset temperatures of 125 K and zero resistance at 110 K were obtained. X-ray microprobe fluorescence measurements indicate that a typical composition of films is Tl(0.66)Ba(1.77)Ca(1.46)Cu3O(x) which is low in Tl compared to that expected for the 2:2:2:3 phase. A typical grain size is greater than 10 microns revealed by scanning electron microscopy.

  13. Electrochemical properties of mixed conducting (La,M)(CoFe) oxide perovskites (M=3DSr, Ca, and Ba)

    SciTech Connect

    Stevenson, J.W.; Armstrong, T.R.; Bates, J.L.

    1996-04-01

    Electrical properties and oxygen permeation properties of solid mixed-conducting electrolytes (La,M)(CoFe) oxide perovskites (M=3DSr, Ca, and Ba) have been characterized. These materials are potentially useful as passive membranes to separate high purity oxygen from air and as the cathode in a fuel cell. Dilatometric linear expansion measurements were performed as a function of temperature and oxygen partial pressure to evaluate the stability.

  14. Cluster Chemistry in Electron-Poor Ae-Pt-Cd Systems (Ae=Ca, Sr, Ba): (Sr,Ba)Pt2Cd4, Ca6Pt8Cd16, and Its Known Antitype Er6Pd16Sb8

    SciTech Connect

    Samal, Saroj L.; Gulo, Fakhili; Corbett, John D.

    2013-02-18

    Three new ternary polar intermetallic compounds, cubic Ca6Pt8Cd16, and tetragonal (Sr, Ba)Pt2Cd4 have been discovered during explorations of the Ae–Pt–Cd systems. Cubic Ca6Pt8Cd16 (Fm-3m, Z = 4, a = 13.513(1) Å) contains a 3D array of separate Cd8 tetrahedral stars (TS) that are both face capped along the axes and diagonally bridged by Pt atoms to generate the 3D anionic network Cd8[Pt(1)]6/2[Pt(2)]4/8. The complementary cationic surface of the cell consists of a face-centered cube of Pt(3)@Ca6 octahedra. This structure is an ordered ternary variant of Sc11Ir4 (Sc6Ir8Sc16), a stuffed version of the close relative Na6Au7Cd16, and a network inverse of the recent Er6Sb8Pd16 (compare Ca6Pt8Cd16). The three groups of elements each occur in only one structural version. The new AePt2Cd4, Ae = Sr, Ba, are tetragonal (P42/mnm,Z = 2, a ≈ 8.30 Å, c ≈ 4.47 Å) and contain chains of edge-sharing Cd4 tetrahedra along c that are bridged by four-bonded Ba/Sr. LMTO-ASA and ICOHP calculation results and comparisons show that the major bonding (Hamilton) populations in Ca6Pt8Cd16 and Er6Sb8Pd16 come from polar Pt–Cd and Pd–Sb interactions, that Pt exhibits larger relativistic contributions than Pd, that characteristic size and orbital differences are most evident for Sb 5s, Pt8, and Pd16, and that some terms remain incomparable, Ca–Cd versus Er–Pd.

  15. A Comparative Study of Si-BaSO4 and Si-CaSO4 Pyrotechnic Time-Delay Compositions

    NASA Astrophysics Data System (ADS)

    Tichapondwa, Shepherd M.; Focke, Walter W.; del Fabbro, Olinto; Gisby, John; Kelly, Cheryl

    2016-07-01

    Slow-burning Si-BaSO4 pyrotechnic delay compositions are employed commercially for intermediate to long-time delays. However, there is very little information on this composition available in open literature. The reactivity of this composition was therefore characterized and compared to that of Si-CaSO4. The Si-BaSO4 composition supported combustion in the range of 20-60 wt% Si in the bomb calorimeter. However, burning was only sustained between 20 and 40 wt% Si in rigid aluminum tubes, with burning rates of between 8.4 and 16 mm s-1. These values are comparable to those for the Si-CaSO4 system (6.9-12.5 mm s-1). However, the CaSO4-based formulations tended to have higher energy output and produced more transient pressure compared to the barium sulfate compositions. Both formulations were insensitive to impact, friction, and electrostatic discharge stimuli. The reaction products were a complex mixture that contained crystalline phases in addition to an amorphous phase. Although barium sulfate is insoluble in water and decidedly nontoxic, the reaction products produced by the Si-BaSO4 compositions were found to release soluble barium ions when contacted with water. This ranged from 50 to 140 mg per gram of barium sulfate reacted.

  16. Ultracold magnetically tunable interactions without radiative-charge-transfer losses between Ca+, Sr+, Ba+, and Yb+ ions and Cr atoms

    NASA Astrophysics Data System (ADS)

    Tomza, Michał

    2015-12-01

    The Ca+, Sr+, Ba+, and Yb+ ions immersed in an ultracold gas of the Cr atoms are proposed as experimentally feasible heteronuclear systems in which ion-atom interactions at ultralow temperatures can be controlled with magnetically tunable Feshbach resonances without charge transfer and radiative losses. Ab initio techniques are applied to investigate electronic-ground-state properties of the (CaCr)+, (SrCr)+, (BaCr)+, and (YbCr)+ molecular ions. The potential energy curves, permanent electric dipole moments, and static electric dipole polarizabilities are computed. The spin-restricted open-shell coupled-cluster method restricted to single, double, and noniterative triple excitations and the multireference configuration-interaction method restricted to single and double excitations are employed. The scalar relativistic effects are included within the small-core energy-consistent pseudopotentials. The leading long-range induction and dispersion interaction coefficients are also reported. Finally, magnetic Feshbach resonances between the Ca+, Sr+, Ba+, and Yb+ ions interacting with the Cr atoms are analyzed. The present proposal opens the way towards robust quantum simulations and computations with ultracold ion-atom systems free of radiative charge-transfer losses.

  17. Enthalpies of formation of CaAl4O7 and CaAl12O19 (hibonite) by high temperature, alkali borate solution calorimetry

    NASA Technical Reports Server (NTRS)

    Geiger, C. A.; Kleppa, O. J.; Grossman, L.; Mysen, B. O.; Lattimer, J. M.

    1988-01-01

    Enthalpies of formation were determined for two calcium aluminate phases, CaAl4O7 and CaAl12O19, using high-temperature alkali borate solution calorimetry. The aluminates were synthesized by multiple-cycle heating and grinding stoichiometric mixtures of CaCO3 and Al2O3, and the products were characteized by X-ray diffraction and SEM microbeam analysis. The data on impurities (CaAl4O7 was found to be about 89.00 percent pure by weight and the CaAl12O19 samples about 91.48 percent pure) were used to correct the heat of solution values of the synthetic products. The enthalpies of formation, at 1063 K, from oxides, were found to be equal to -(25.6 + or - 4.7) kJ/g.f.w. for CaAl4O7 and -(33.0 + or - 9.7) kJ/g.f.w. for CaAl12O19; the respective standard enthalpies of formation from elements, at 298 K, were estimated to be -4007 + or - 5.2 kJ/g.f.w. and -10,722 + or - 12 kJ/g.f.w.

  18. Different binding sites for Bacillus thuringiensis Cry1Ba and Cry9Ca proteins in the European corn borer, Ostrinia nubilalis (Hübner).

    PubMed

    Hernández-Martínez, Patricia; Hernández-Rodríguez, Carmen Sara; Van Rie, Jeroen; Escriche, Baltasar; Ferré, Juan

    2014-07-01

    Binding studies using (125)I-Cry9Ca and biotinylated-Cry1Ba proteins showed the occurrence of independent binding sites for these proteins in Ostrinia nubilalis. Our results, along with previously available binding data, indicate that combinations of Cry1A or Cry1Fa proteins with Cry1Ba and/or Cry9Ca could be a good strategy for the resistance management of O. nubilalis. PMID:24799046

  19. Interfacial chemical reaction and multiple gap state formation on three layer cathode in organic light-emitting diode: Ca/BaF2/Alq3

    NASA Astrophysics Data System (ADS)

    Kim, Tae Gun; Lee, Hyunbok; Yi, Yeonjin; Lee, Seung Mi; Kim, Jeong Won

    2015-07-01

    A three layer cathode is a promising stack structure for long lifetime and high efficiency in organic light-emitting diodes. The interfacial chemical reactions and their effects on electronic structures for alkaline-earth metal (Ca, Ba)/Alq3 [tris(8-hydroxyquinolinato)aluminum] and Ca/BaF2/Alq3 are investigated using in-situ X-ray and ultraviolet photoelectron spectroscopy, as well as molecular model calculation. The BaF2 interlayer initially prevents direct contact between Alq3 and the reactive Ca metal, but it is dissociated into Ba and CaF2 by the addition of Ca. As the Ca thickness increases, the Ca penetrates the interlayer to directly participate in the reaction with the underlying Alq3. This series of chemical reactions takes place irrespective of the BaF2 buffer layer thickness as long as the Ca overlayer thickness is sufficient. The interface reaction between the alkaline-earth metal and Alq3 generates two energetically separated gap states in a sequential manner. This phenomenon is explained by step-by-step charge transfer from the alkaline-earth metal to the lowest unoccupied molecular orbital states of Alq3, forming new occupied states below the Fermi level.

  20. Interfacial chemical reaction and multiple gap state formation on three layer cathode in organic light-emitting diode: Ca/BaF{sub 2}/Alq{sub 3}

    SciTech Connect

    Kim, Tae Gun; Kim, Jeong Won; Lee, Hyunbok; Yi, Yeonjin; Lee, Seung Mi

    2015-07-14

    A three layer cathode is a promising stack structure for long lifetime and high efficiency in organic light-emitting diodes. The interfacial chemical reactions and their effects on electronic structures for alkaline-earth metal (Ca, Ba)/Alq{sub 3} [tris(8-hydroxyquinolinato)aluminum] and Ca/BaF{sub 2}/Alq{sub 3} are investigated using in-situ X-ray and ultraviolet photoelectron spectroscopy, as well as molecular model calculation. The BaF{sub 2} interlayer initially prevents direct contact between Alq{sub 3} and the reactive Ca metal, but it is dissociated into Ba and CaF{sub 2} by the addition of Ca. As the Ca thickness increases, the Ca penetrates the interlayer to directly participate in the reaction with the underlying Alq{sub 3}. This series of chemical reactions takes place irrespective of the BaF{sub 2} buffer layer thickness as long as the Ca overlayer thickness is sufficient. The interface reaction between the alkaline-earth metal and Alq{sub 3} generates two energetically separated gap states in a sequential manner. This phenomenon is explained by step-by-step charge transfer from the alkaline-earth metal to the lowest unoccupied molecular orbital states of Alq{sub 3}, forming new occupied states below the Fermi level.

  1. BaCoCa--a heuristic software tool for the parallel assessment of sequence biases in hundreds of gene and taxon partitions.

    PubMed

    Kück, Patrick; Struck, Torsten H

    2014-01-01

    BaCoCa (BAse COmposition CAlculator) is a user-friendly software that combines multiple statistical approaches (like RCFV and C value calculations) to identify biases in aligned sequence data which potentially mislead phylogenetic reconstructions. As a result of its speed and flexibility, the program provides the possibility to analyze hundreds of pre-defined gene partitions and taxon subsets in one single process run. BaCoCa is command-line driven and can be easily integrated into automatic process pipelines of phylogenomic studies. Moreover, given the tab-delimited output style the results can be easily used for further analyses in programs like Excel or statistical packages like R. A built-in option of BaCoCa is the generation of heat maps with hierarchical clustering of certain results using R. As input files BaCoCa can handle FASTA and relaxed PHYLIP, which are commonly used in phylogenomic pipelines. BaCoCa is implemented in Perl and works on Windows PCs, Macs and Linux operating systems. The executable source code as well as example test files and a detailed documentation of BaCoCa are freely available at http://software.zfmk.de. PMID:24076250

  2. BaCoCa--a heuristic software tool for the parallel assessment of sequence biases in hundreds of gene and taxon partitions.

    PubMed

    Kück, Patrick; Struck, Torsten H

    2014-01-01

    BaCoCa (BAse COmposition CAlculator) is a user-friendly software that combines multiple statistical approaches (like RCFV and C value calculations) to identify biases in aligned sequence data which potentially mislead phylogenetic reconstructions. As a result of its speed and flexibility, the program provides the possibility to analyze hundreds of pre-defined gene partitions and taxon subsets in one single process run. BaCoCa is command-line driven and can be easily integrated into automatic process pipelines of phylogenomic studies. Moreover, given the tab-delimited output style the results can be easily used for further analyses in programs like Excel or statistical packages like R. A built-in option of BaCoCa is the generation of heat maps with hierarchical clustering of certain results using R. As input files BaCoCa can handle FASTA and relaxed PHYLIP, which are commonly used in phylogenomic pipelines. BaCoCa is implemented in Perl and works on Windows PCs, Macs and Linux operating systems. The executable source code as well as example test files and a detailed documentation of BaCoCa are freely available at http://software.zfmk.de.

  3. Preparation, photoluminescent properties and luminescent dynamics of BaAlF{sub 5}:Eu{sup 2+} nanophosphors

    SciTech Connect

    Zhang, Wei; Hua, Ruinian; Liu, Tianqing; Zhao, Jun; Na, Liyan; Chen, Baojiu

    2014-12-15

    Graphical abstract: Rice-shaped BaAlF{sub 5}:Eu{sup 2+} nanophosphors were synthesized via one-pot hydrothermal process. The as-prepared BaAlF{sub 5}:Eu{sup 2+} are composed of many particles with an average diameter of 40 nm. When excited at 260 nm, the sharp line emission located at 361 nm of Eu{sup 2+} was observed. The optimum doping concentration of Eu{sup 2+} was confirmed to be 5 mol%. The strong ultraviolet emission of Eu{sup 2+} ions in BaAlF{sub 5}:Eu{sup 2+} nanoparticles suggests that these nanoparticles may have potential applications for sensing, solid-state lasers and spectrometer calibration. - Highlights: • BaAlF{sub 5}:Eu{sup 2+} nanophosphors were synthesized via a mild hydrothermal process. • The Van and Huang models were used to research the mechanism of concentration quenching. • The optimum doping concentration of Eu2+ was confirmed to be 5 mol%. - Abstract: Eu{sup 2+}-doped BaAlF{sub 5} nanophosphors were synthesized via a facile one-pot hydrothermal method. The final products were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and photoluminescence (PL) spectroscopy. XRD results showed that the prepared samples are single-phase. The FE-SEM and TEM images indicated that the prepared BaAlF{sub 5}:Eu{sup 2+} nanophosphors are composed of many rice-shaped particles with an average diameter of 40 nm. When excited at 260 nm, BaAlF{sub 5}:Eu{sup 2+} nanophosphors exhibit the sharp line emissions of Eu{sup 2+} at room temperature. The optimum doping concentration of Eu{sup 2+} was confirmed to be 5 mol%. The Van and Huang models were used to study the mechanism of concentration quenching and the electric dipole–dipole interaction between Eu{sup 2+} can be deduced to be a dominant for quenching fluorescence in BaAlF{sub 5}:Eu{sup 2+} nanophosphors. The strong ultraviolet emission of Eu{sup 2+} in BaAlF{sub 5}:Eu{sup 2+} nanophosphors suggests that

  4. Tracing Environmental Variation Over The Past 130 Years In The Barents Sea: Mineral Ratio (Mg/Ca, Sr/Ca, Ba/Ca, And Mn/Ca) Evidence In Shells Of The Circumpolar Greenland Cockle, Serripes groenlandicus

    NASA Astrophysics Data System (ADS)

    Henkes, G. A.; Ambrose, W. G.; Johnson, B. J.; Carroll, M. L.; McMahon, K. W.; Denisenko, S. G.; Thorrold, S. R.

    2007-12-01

    In order to quantify the impacts of human induced climate change on Arctic marine ecosystems it is crucial to establish high-resolution proxies to record regional environmental variability. The Barents Sea region is highly influenced by the annual recession and precession of Arctic sea ice and, as an ecosystem is extremely sensitive to seasonal to decadal climatic changes. Long-lived, sessile, marine bivalves have the potential to provide detailed oceanographic and biological proxy information from the Barents Sea in locations where historic, long- term data logging does not exist. Here, we present preliminary mineral ratio evidence (Mg, Sr, Ba, Mn) for Barents Sea environmental variation from shells of the circumpolar Greenland cockle, Serripes groenlandicus, over the past 130 years from 4 different locations in Norwegian and Russian waters. For all mineral ratios there are clear seasonal trends corresponding with dark winter growth checks on the external surface of each individual. The seasonal patterns of Mg and Sr show progressive change. On average for 9 individuals, Mg/Ca was 10.6 percent greater and Sr/Ca was 5.5 percent lower on the winter checks compared to other values, while Ba/Ca and Mn/Ca ratios show peaks during the middle of the summer growth period. Mineral patterns from the Pechora Sea region are particularly pronounced, which may be related to the influence freshwater from summer river discharge. While the mineral data are initially compelling enough to demonstrate clear seasonal periodicity and inter-annual variation, we believe that a multi-proxy approach to interpreting the information obtained from these bivalves is critical. Therefore, parallel to this study, we are examining external, incremental growth and organic carbon isotopes of shell material from the same collection of bivalves.

  5. Sulfation and Desulfation Behavior of Pt-BaO/MgO-Al2O3 NOx Storage Reduction Catalyst.

    PubMed

    Jeong, Soyeon; Kim, Do Heui

    2016-05-01

    The comparative study between Pt-BaO/Al2O3 and Pt-BaO/MgO-Al2O3 gives the information about the effect of MgO addition to Al2O3 support on the sulfation and desulfation behavior of Pt-BaO/MgO-Al2O3 NOx storage reduction catalyst. The sulfated two samples were analyzed by using element analysis (EA), X-ray diffraction (XRD), H2 temperature programmed reaction (H2 TPRX) and NOx uptake measurement. The amount of sulfur uptake on 2 wt% Pt-20 wt% BaO/Al2O3 and 2 wt% Pt-20 wt% BaO/MgO-Al2O3 are almost identical as 0.45 and 0.40 of S/Ba, respectively, which yields the drastic decrease in NOx uptake for both sulfated samples. However, after desulfa- tion with H2 at 600 degrees C, the residual sulfur amount on MgO-Al2O3 supported catalyst is three times larger than that on Al2O3 supported one, indicating that sulfur species formed on the former are more stable than those on the latter. It is also well corresponding to the H2 TPRX results where the main H2S peak from MgO-Al2O3 supported sample is observed at higher temperature than Al2O3 supported one, resulting in the lower NOx uptake activity of former sample than the latter one. Meanwhile, after desulfation of MgO-Al2O3 supported sample at 700 degrees C and 800 degrees C, the activity is recovered more significantly due to the removal of the large amount of sulfur while Al2O3 supported one decreases monotonically due to the sintering of Pt crystallite and the formation of BaAl2O4 phase. It is summarized that MgO-Al2O3 supported catalyst enhances the thermal stability of the catalyst, however, forms the stable sulfate species, which needs to be improved to develop the more sulfur resistant NSR catalyst system. PMID:27483765

  6. Sulfation and Desulfation Behavior of Pt-BaO/MgO-Al2O3 NOx Storage Reduction Catalyst.

    PubMed

    Jeong, Soyeon; Kim, Do Heui

    2016-05-01

    The comparative study between Pt-BaO/Al2O3 and Pt-BaO/MgO-Al2O3 gives the information about the effect of MgO addition to Al2O3 support on the sulfation and desulfation behavior of Pt-BaO/MgO-Al2O3 NOx storage reduction catalyst. The sulfated two samples were analyzed by using element analysis (EA), X-ray diffraction (XRD), H2 temperature programmed reaction (H2 TPRX) and NOx uptake measurement. The amount of sulfur uptake on 2 wt% Pt-20 wt% BaO/Al2O3 and 2 wt% Pt-20 wt% BaO/MgO-Al2O3 are almost identical as 0.45 and 0.40 of S/Ba, respectively, which yields the drastic decrease in NOx uptake for both sulfated samples. However, after desulfa- tion with H2 at 600 degrees C, the residual sulfur amount on MgO-Al2O3 supported catalyst is three times larger than that on Al2O3 supported one, indicating that sulfur species formed on the former are more stable than those on the latter. It is also well corresponding to the H2 TPRX results where the main H2S peak from MgO-Al2O3 supported sample is observed at higher temperature than Al2O3 supported one, resulting in the lower NOx uptake activity of former sample than the latter one. Meanwhile, after desulfation of MgO-Al2O3 supported sample at 700 degrees C and 800 degrees C, the activity is recovered more significantly due to the removal of the large amount of sulfur while Al2O3 supported one decreases monotonically due to the sintering of Pt crystallite and the formation of BaAl2O4 phase. It is summarized that MgO-Al2O3 supported catalyst enhances the thermal stability of the catalyst, however, forms the stable sulfate species, which needs to be improved to develop the more sulfur resistant NSR catalyst system.

  7. Influence of Cu-site substitution on La2Ca1Ba2Cu5Oz superconducting system

    NASA Astrophysics Data System (ADS)

    Bhalodia, J. A.; Mankadia, S. R.; Dalsaniya, S. M.; Gonal, M. R.

    2012-07-01

    We have prepared a series of La2CaBa2Cu5-xCoxOz; x = 0.0, 0.1, 0.2, 0.5, 1.0, 2.0, 5.0 (La-2125) compounds by the standard solid state reaction method and characterized for their structural, superconducting, magnetic properties and oxygen content through X-ray diffraction, scanning electron microscopy, d. c. resistivity, magnetic susceptibility and iodometric titration respectively. All the compounds crystallize with the tetragonal LaBa2Cu3Oz type structure, space group P4/mmm. Here the effect of higher Co substitution for Cu in the La2CaBa2Cu5-xCoxOz system has been studied. It is observed that only 2 at. % Co substitution for Cu destroys the superconductivity of the sample. For heavily doped samples (with x >= 0.1) are found non-superconducting presumably because of magnetic pair- breaking effect. These samples do not show superconductivity but are of interest for understanding the interplay between superconductivity and magnetism. Possible reasons for destruction of superconductivity are discussed in this communication.

  8. Improvement of critical current density in thallium-based (Tl,Bi)Sr(1.6)Ba(0.4)Ca2Cu3O(x) superconductors

    NASA Technical Reports Server (NTRS)

    Ren, Z. F.; Wang, C. A.; Wang, J. H.; Miller, D. J.; Goretta, K. C.

    1995-01-01

    Epitaxial (Tl,Bi)Sr(1.6)Ba(0.4)Ca2Cu3O(x) ((Tl,Bi)-1223) thin films on (100) single crystal LaAlO3 substrates were synthesized by a two-step procedure. Phase development, microstructure, and relationships between film and substrate were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Resistance versus temperature, zero-field-cooled and field cooled magnetization, and transport critical current density (J(sub c)) were measured. The zero-resistance temperature was 105-111 K. J(sub c) at 77 K and zero field was greater than 2 x 10(exp 6) A/sq cm. The films exhibited good flux pinning properties.

  9. Luminescent Characteristics of Ba(1--x)Al2Si2O8:xTb3+ Green Phosphors.

    PubMed

    Hakeem, D A; Kim, Y; Park, K

    2016-02-01

    Ba(1--x)Al2Si2O8:xTb3+ (0.03 < or = x < or = 0.12) green phosphors are prepared by solution combustion method. The photoluminescence properties of the Ba(1--x)Al2Si2O8:xTb3+ phosphors are studied as a function of Tb3+ concentration. The Ba(1--x)Al2Si2O8:xTb3+ phosphors crystallize in a hexagonal crystal structure. The excitation spectra consist of two broad bands with maxima at 238 nm and 265 nm and several weak peaks in the range of 310-500 nm. Strong emission peaks are observed at 484, 540, 589, and 612 nm due to the (5)D4 --> (7)F6, (5)D4 --> (7)F5, (5)D4 --> (7)F4, and (5)D4 --> (7)F3 tran- sitions of the Tb3+, respectively. The emission peak (540 nm) from the (5)D4 --> (7)F3 transition is dominant, indicating green light emission. Ba(1--x)Al2Si2O8:xTb3+ phosphor shows the strongest green emission intensity. The Ba(1--x)Al2Si2O8:xTb3+ can be considered a promising green phosphor for white LEDs applications. PMID:27433666

  10. Suppression of structural phase transition by Sr substitution in the improper ferroelectric BaAl2O4

    NASA Astrophysics Data System (ADS)

    Mori, Shigeo; Ishii, Yui; Tanaka, Eri; Tsukasaki, Hirofumi; Kawaguchi, Shogo

    2015-10-01

    To clarify lattice fluctuations and precursor phenomena accompanied by structural phase transition in stuffed tridymite compounds, changes in diffuse scattering as a function of temperature in Ba0.6Sr0.4Al2O4 have been carefully investigated by powder X-ray diffraction using synchrotron radiation, electron diffraction and transmission electron microscopy (TEM) experiments. In situ electron diffraction experiments revealed that Ba0.6Sr0.4Al2O4 exhibits lattice fluctuation manifested as a unique honeycomb-shaped diffuse scattering in the wide temperature range between 298 and 100 K. Unlike in the case of BaAl2O4, Ba0.6Sr0.4Al2O4 shows no structural phase transition to the ferroelectric structure with the hexagonal P63 space group in the temperature range. In contrast, it is revealed that the electron beam irradiation to the Ba0.6Sr0.4Al2O4 sample inside the transmission electron microscope induced structural change from the hexagonal P6322 structure to the modulated structure with double periodicity in the three equivalent <110> directions in the low-temperature region. This implies that the total energy difference between these two structures is small. The hexagonal P6322 structure transforms into the modulated one with short correlation length owing to some small external perturbations.

  11. Structure, phase composition, and strengthening of cast Al-Ca-Mg-Sc alloys

    NASA Astrophysics Data System (ADS)

    Belov, N. A.; Naumova, E. A.; Bazlova, T. A.; Alekseeva, E. V.

    2016-02-01

    The structure and phase composition of Al-Ca-Mg-Sc alloys containing 0.3 wt % Sc, up to 10 wt % Ca, and up to 10 wt % Mg have been investigated in the cast state and state after heat treatment. It has been shown that only binary phases Al4Ca, Al3Sc, and Al3Mg2 can be in equilibrium with the aluminum solid solution. It has been found that the maximum strengthening effect caused by the precipitation of Al3Sc nanoparticles for all investigated alloys is attained after annealing at 300-350°C.

  12. Mechanism of particle growth of a BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphor by firing with AlF{sub 3}

    SciTech Connect

    Oshio, Shozo; Matsuoka, Tomizo; Tanaka, Shosaku; Kobayashi, Hiroshi

    1998-11-01

    The mechanism of particle growth of the blue emitting BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphor by firing with AlF{sub 3} has been clarified. It was found that the reaction between BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} and AlF{sub 3} during firing, on the basis of the following chemical equation, results in recreation of BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} with particle growth BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} + (4/3)AlF{sub 3} {l_reversible} BaMgF{sub 4}:Eu{sup 2+} + (17/3)Al{sub 2}O{sub 3}, the firing of Ba/MgAl{sub 10}O{sub 17}:Eu{sup 2+} with AlF{sub 3} first converts the phosphor into a mixture of the two compounds, BaMgF{sub 4}:Eu{sup 2+} and Al{sub 2}O{sub 3}, at around 1200 C. The BaMgF{sub 4}:Eu{sup 2+} melts at temperatures over 1000 C, then reacts with Al{sub 2}O{sub 3}, and participates in the recreation of both BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} and AlF{sub 3} through a chemical reaction between the two compounds at 1200 C in BaMgF{sub 4}:Eu{sup 2+} solutions. Recreated AlF{sub 3} appears to sublime immediately because it is a material which sublimates with heating. This paper proposes a mechanism for the growth of particle of recreated BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} by the melting of BaMgF{sub 4}:Eu{sup 2+}.

  13. Phase, Dielectric and Ferroelectric Properties of Microwave Sintered La and Ca Modified BaTiO{sub 3} Ceramics

    SciTech Connect

    Sonia, S.; Patel, R. K.; Kumar, P.; Prakash, Chandra; Agrawal, D. K.

    2011-11-22

    Lanthanum and calcium modified barium titanate, Ba{sub (1-x)}La{sub x}Ti{sub (1-x/4)}O{sub 3}/BLT and Ba({sub 1-x})Ca{sub x}TiO{sub 3}/BCT, where x = 0.02, ferroelectric ceramic samples were synthesized in single perovskite phase by microwave processing technique. Sintering temperature was optimized at 1100 deg. C for 1h. Presence of pore free micron size uniform grains suggested the advantage of using microwave sintering process. Transition temperature (T{sub c}) decreases with the substitution of La content in BT system. Temperature coefficient of capacitance is negligible from RT temperature to 75 deg. C for BLT ceramic samples. Polarization vs. electric field (P-E) hysteresis loop study confirms the ferroelectric nature of the modified BT ceramic samples.

  14. Ba3Pt4Al4-Structure, Properties, and Theoretical and NMR Spectroscopic Investigations of a Complex Platinide Featuring Heterocubane [Pt4Al4] Units.

    PubMed

    Stegemann, Frank; Benndorf, Christopher; Bartsch, Timo; Touzani, Rachid St; Bartsch, Manfred; Zacharias, Helmut; Fokwa, Boniface P T; Eckert, Hellmut; Janka, Oliver

    2015-11-16

    Ba3Pt4Al4 was prepared from the elements in niobium ampules and crystallizes in an orthorhombic structure, space group Cmcm (oP44, a = 1073.07(3), b = 812.30(3), c = 1182.69(3) pm) isopointal to the Zintl phase A2Zn5As4 (A = K, Rb). The structure features strands of distorted [Pt4Al4] heterocubane-like units connected by condensation over Pt/Al edges. These are arranged in a hexagonal rod packing by further condensation over Pt and Al atoms with the barium atoms located inside cavities of the [Pt4Al4](δ-) framework. Structural relaxation confirmed the electronic stability of the new phase, while band structure calculations indicate metallic behavior. Crystal orbital Hamilton bonding analysis coupled with Bader effective charge analysis suggest a polar intermetallic phase in which strong Al-Pt covalent bonds are present, while a significant electron transfer from Ba to the [Pt4Al4](δ-) network is found. By X-ray photoelectron spectroscopy measurements the Pt 4f5/2 and 4f7/2 energies for Ba3Pt4Al4 were found in the range of those of elemental Pt due to the electron transfer of Ba, while PtAl and PtAl2 show a pronounced shift toward a more cationic platinum state. (27)Al magic-angle spinning NMR investigations verified the two independent crystallographic Al sites with differently distorted tetrahedrally coordinated [AlPt4] units. Peak assignments could be made based on both geometrical considerations and in relation to electric field gradient calculations. PMID:26536164

  15. Photoluminescence and phosphorescence properties of MAl 2O 4:Eu 2+, Dy 3+ (M=Ca, Ba, Sr) phosphors prepared at an initiating combustion temperature of 500 °C

    NASA Astrophysics Data System (ADS)

    Mothudi, B. M.; Ntwaeaborwa, O. M.; Botha, J. R.; Swart, H. C.

    2009-12-01

    Eu 2+ and Dy 3+ co-doped calcium aluminate, barium aluminate and strontium aluminate phosphors were synthesized at an initiating combustion temperature of 500 °C using urea as an organic fuel. The crystallinity of the phosphors was investigated by using X-ray diffraction (XRD) and the morphology was determined by a scanning electron microscope (SEM). The low temperature monoclinic structure for both CaAl 2O 4 and SrAl 2O 4 and the hexagonal structure of BaAl 2O 4 were observed. The effect of the host materials on the photoluminescence (PL) and phosphorescence properties were investigated by using a He-Cd Laser and a Cary Eclipse fluorescence spectrophotometer, respectively. The broad band emission spectra observed at 449 nm for CaAl 2O 4:Eu 2+, Dy 3+, 450 nm (with a shoulder-peak at 500 nm) for BaAl 2O 4:Eu 2+, Dy 3+ and 528 nm for SrAl 2O 4:Eu 2+, Dy 3+ are attributed to the 4f 65d 1 to 4f 7 transition in the Eu 2+ ion in the different hosts.

  16. Effect of sintering temperature on the luminescence properties of Ca0.8Ba0.2TiO3:Pr(3+) red-emitting phosphor.

    PubMed

    Mu, Yannan; Qiu, Min; Zhou, Xiaoming; Li, Qian; Sun, Meiling; Yang, Haibin; Fu, Wuyou; Yang, Lihua; Ma, Jinwen

    2015-08-01

    Nanoparticles with the nominal composition Ca0.8Ba0.2Ti03:Pr(3+) were prepared using the sol-gel process. Barium nitrate, 4-hydrated calcium nitrate and praseodymium oxide were used as raw materials. The structural evolution and decomposition processes of the precursors were investigated by powder X-ray diffraction, differential thermal analysis and thermogravimetric analysis. Crystalline Ca0.8Ba0.2Ti03:Pr(3+) could be obtained at 700°C. The photoluminescence properties of the samples were investigated using excitation and emission spectra. Ca0.8Ba0.2Ti03:Pr(3+) nanoparticles showed strong red emission, which could be assigned to the typical (1) D2 →(3) H4 transition of Pr(3+). Furthermore, the study found that sintering temperature and the introduction of Ba(2+) influence the decay time of persistent luminescence. PMID:25209628

  17. Continuous cross-over from ferroelectric to relaxor state and piezoelectric properties of BaTiO3-BaZrO3-CaTiO3 single crystals

    NASA Astrophysics Data System (ADS)

    Benabdallah, F.; Veber, P.; Prakasam, M.; Viraphong, O.; Shimamura, K.; Maglione, M.

    2014-04-01

    Optimal properties like piezoelectricity can be found in polarizable materials for which the structure changes sharply under small composition variations in the vicinity of their morphotropic phase boundary or the triple point in their isobaric temperature-composition phase diagram. In the latter, lead-free (Ba0.850Ca0.150)(Ti0.900Zr0.100)O3 ceramics exhibit outstanding piezoelectric coefficients. For the first time, we report the growth of piezoelectric lead-free single crystals in the BaTiO3-BaZrO3-CaTiO3 pseudo-ternary system. The stoichiometry control in the CaO-BaO-TiO2-ZrO2 solid solution led to single crystals with various compositions ranging from (Ba0.857Ca0.143)(Ti0.928Zr0.072)O3 to (Ba0.953Ca0.047)(Ti0.427Zr0.573)O3. We evidenced a continuous cross-over from a ferroelectric state at high titanium content to a relaxor one on increasing the zirconium content. Such a property tuning is rather seldom observed in lead-free ferroelectrics and confirms what was already reported for ceramics. Single crystal with (Ba0.838Ca0.162)(Ti0.854Zr0.146)O3 composition, which has been grown and oriented along [001] crystallographic direction, displayed electromechanical coefficients d31 and k31 of 93 pC.N-1 and 0.18, respectively, near the room temperature (T = 305 K).

  18. Continuous cross-over from ferroelectric to relaxor state and piezoelectric properties of BaTiO{sub 3}-BaZrO{sub 3}-CaTiO{sub 3} single crystals

    SciTech Connect

    Benabdallah, F.; Veber, P. Prakasam, M.; Viraphong, O.; Maglione, M.; Shimamura, K.

    2014-04-14

    Optimal properties like piezoelectricity can be found in polarizable materials for which the structure changes sharply under small composition variations in the vicinity of their morphotropic phase boundary or the triple point in their isobaric temperature-composition phase diagram. In the latter, lead-free (Ba{sub 0.850}Ca{sub 0.150})(Ti{sub 0.900}Zr{sub 0.100})O{sub 3} ceramics exhibit outstanding piezoelectric coefficients. For the first time, we report the growth of piezoelectric lead-free single crystals in the BaTiO{sub 3}-BaZrO{sub 3}-CaTiO{sub 3} pseudo-ternary system. The stoichiometry control in the CaO-BaO-TiO{sub 2}-ZrO{sub 2} solid solution led to single crystals with various compositions ranging from (Ba{sub 0.857}Ca{sub 0.143})(Ti{sub 0.928}Zr{sub 0.072})O{sub 3} to (Ba{sub 0.953}Ca{sub 0.047})(Ti{sub 0.427}Zr{sub 0.573})O{sub 3}. We evidenced a continuous cross-over from a ferroelectric state at high titanium content to a relaxor one on increasing the zirconium content. Such a property tuning is rather seldom observed in lead-free ferroelectrics and confirms what was already reported for ceramics. Single crystal with (Ba{sub 0.838}Ca{sub 0.162})(Ti{sub 0.854}Zr{sub 0.146})O{sub 3} composition, which has been grown and oriented along [001] crystallographic direction, displayed electromechanical coefficients d{sub 31} and k{sub 31} of 93 pC.N{sup −1} and 0.18, respectively, near the room temperature (T = 305 K)

  19. Ca(2+) and CaM are involved in Al(3+) pretreatment-promoted fluoride accumulation in tea plants (Camellia sinesis L.).

    PubMed

    Zhang, Xian-Chen; Gao, Hong-Jian; Wu, Hong-Hong; Yang, Tian-Yuan; Zhang, Zheng-Zhu; Mao, Jing-Dong; Wan, Xiao-Chun

    2015-11-01

    Tea plant (Camellia sinensis (L.) O. kuntze) is known to be a fluoride (F) and aluminum (Al(3+)) hyper-accumulator. Previous study showed that pre-treatment of Al(3+) caused a significant increase of F accumulation in tea plants. However, less is known about the intricate network of Al(3+) promoted F accumulation in tea plants. In this study, the involvement of endogenous Ca(2+) and CaM in Al(3+) pretreatment-promoted F accumulation in tea plants was investigated. Our results showed that Al(3+) induced the inverse change of intracellular Ca(2+) fluorescence intensity and stimulated Ca(2+) trans-membrane transport in the mature zone of tea root. Also, a link between internal Ca(2+) and CaM was found in tea roots under the presence of Al(3+). In order to investigate whether Ca(2+) and CaM were related to F accumulation promoted by Al(3+) pretreatment, Ca(2+) chelator EGTA and CaM antagonists CPZ and TFP were used. EGTA, CPZ, and TFP pretreatment inhibited Al(3+)-induced increase of Ca(2+) fluorescence intensity and CaM content in tea roots, and also significantly reduced Al(3+)-promoted F accumulation in tea plants. Taken together, our results suggested that the endogenous Ca(2+) and CaM are involved in Al(3+) pretreatment-promoted F accumulation in tea roots. PMID:26318146

  20. Structural changes and microstructures in stuffed tridymite-type compounds Ba1-xSrxAl2O4

    NASA Astrophysics Data System (ADS)

    Tanaka, Eri; Ishii, Yui; Tsukasaki, Hirofumi; Taniguchi, Hiroki; Mori, Shigeo

    2014-09-01

    Crystal structures and microstructures in Ba1-xSrxAl2O4 solid solutions between the end members of BaAl2O4 and SrAl2O4 have been carefully investigated by powder X-ray diffraction, electron diffraction and transmission electron microscopy (TEM) imaging experiments. With the help of fast Fourier transform (FFT) calculation, high-resolution TEM images suggested that diffuse streaks along three equivalent <110> directions in the (001) plane, which appear in the P63 structure of Ba1-xSrxAl2O4 for x = 0.4, originate from the large structural fluctuation of the AlO4 tetrahedral network. On the other hand, the monoclinic P21 structure in Ba1-xSrxAl2O4 with x = 0.7 was found to consist of a modulated structure with \\boldsymbol{{q}} = 0,1/2,0. The present experimental results reveal that a structural phase boundary exists at approximately x = 0.6 between the P63 structure with a large structural fluctuation and a monoclinic P21 phase with the single-q modulated structure.

  1. Study of the electronic structure and half-metallicity of CaMnO3/BaTiO3 superlattice

    NASA Astrophysics Data System (ADS)

    Wang, Kai; Jiang, Wei; Chen, Jun-Nan; Huang, Jian-Qi

    2016-09-01

    In this paper, the electronic structure, magnetic properties and half-metallicity of the CaMnO3/BaTiO3 superlattice are investigated by employing the first-principle calculation based on density functional theory within the GGA or GGA + U exchange-correlation functional. The CaMnO3/BaTiO3 superlattice is constructed by the cubic CaMnO3 and the tetragonal ferroelectric BaTiO3 growing alternately along (0 0 1) direction. The cubic CaMnO3 presents a robust half-metallicity and a metastable ferromagnetic phase. Its magnetic moment is an integral number of 3.000 μB per unit cell. However, the CaMnO3/BaTiO3 superlattice has a stable ferromagnetic phase, for which the magnetic moment is 12.000 μB per unit cell. It also retains the robust half-metallicity which mainly results from the strong hybridization between Mn and O atoms. The results show that the constructed CaMnO3/BaTiO3 superlattice exhibits superior magnetoelectric properties. It may provide a theoretical reference for the design and preparation of new multiferroic materials.

  2. Yb{sup 3+}:BaCaBO{sub 3}F: A potential new self-frequency-doubling laser material

    SciTech Connect

    Schaffers, K.I.; DeLoach, L.D.; Ebbers, C.A.; Payne, S.A.

    1995-03-09

    Yb:BaCaBO{sub 3}F (Yb:BCBF) has been investigated as a new laser crystal with potential for self-frequency-doubling. An YB:BCBF laser has been pumped at 912 mm, and a measured slope efficiency of 38% has been obtained for the fundamental laser output at 1034 nm. Single crystal powders of BCBF have been compared with K*P for a relative measure of the second harmonic generating potential, yielding d{sub eff}[BCBF]= (0-66)d{sub eff}[K*P]. The growth, spectroscopy, laser performance, and linear and nonlinear optical properties of YB:BCBF are reported here.

  3. Mechanism of X-ray excited optical luminescence (XEOL) in europium doped BaAl2O4 phosphor.

    PubMed

    Rezende, Marcos V Dos S; Montes, Paulo J R; Andrade, Adriano B; Macedo, Zelia S; Valerio, Mário E G

    2016-06-29

    This paper reports a luminescence mechanism in Eu-doped BaAl2O4 excited with monochromatic X-rays (also known as X-ray excited optical luminescence - XEOL) from synchrotron radiation. The material was prepared via a proteic sol-gel methodology. The X-ray absorption near edge structures (XANES) at the Ba LIII- and Eu LIII-edges exhibit typical absorption spectra. XEOL spectra recorded in energy ranges, either around the Ba LIII- or Eu LIII-edges, showed important differences concerning the intensity of the Eu(2+) or Eu(3+) emission bands. Nevertheless, the total area under the XEOL spectra increases as the energy of the X-ray photons increases in both ranges (Ba LIII- and Eu LIII-edges). PMID:27306425

  4. Phase Compositions of Self Reinforcement Al2O3/CaAl12O19 Composite using X-ray Diffraction Data and Rietveld Technique

    NASA Astrophysics Data System (ADS)

    Asmi, D.; Low, I. M.; O'Connor, B.

    2008-03-01

    The analysis of x-ray diffraction (XRD) patterns by the Rietveld technique was tested to the quantitatively phase compositions of self reinforcement Al2O3/CaAl12O19 composite. Room-temperature XRD patterns revealed that α-Al2O3 was the only phase presence in the CA0 sample, whereas the α-Al2O3 and CaAl12O19 phases were found for CA5, CA15, CA30, and CA50 samples. The peak intensity of CA6 in the self reinforcement Al2O3/CaAl12O19 composites increased in proportion with increase in CaAl12O19 content in contrast to α-Al2O3. The diffraction patterns for CA100 sample shows minor traces of α-Al2O3 even in relatively low peak intensity. It is suggesting that the in-situ reaction sintering of raw materials were not react completely to form 100 wt% CaAl12O19 at temperature 1650 °C. Quantitative phase compositions of self reinforcement Al2O3/CaAl12O19 composites by Rietveld analysis with XRD data has been well demonstrated. The results showed that the GOF values are relatively low and the fluctuation in the difference plots shows a reasonable fit between the observed and the calculated plot.

  5. Theoretical investigation of superconductivity in Ba(AlSn) under pressure

    NASA Astrophysics Data System (ADS)

    Parlak, Cihan

    2016-10-01

    The compound of Ba(AlSn) from ternary superconductors exhibits the superconductivity behaviour below the temperature 2.9 K. We report the results of an ab initio study based on electronic, and detailed lattice dynamical properties as a function of pressure of superconducting material. The phonon dispersion curves along the high-symmetry directions and phonon frequencies parameters at the Brillouin zone center are computed by using density functional perturbation theory while the elastic constants are calculated in metric-tensor formulation. The Vickers hardness belonging to the compound is also evaluated clearly. The band structure, partial densities of states and Fermi surface topology are also discussed in detail. At the same time we describe the relationship between the properties determined and superconducting characteristic.

  6. Theoretical survey on M@C80 (M = Ca, Sr, and Ba): Behavior of different alkaline earth metal impacting the chemical stability and electronic properties

    NASA Astrophysics Data System (ADS)

    Cui, Jin-Bo; Guo, Yi-Jun; Li, Qiao-Zhi; Zhao, Pei; Zhao, Xiang

    2016-08-01

    Structures of mono-metallofullerenes M@C80 (M = Ca, Sr, and Ba) that separated in early experiment are determined owning the C2v(31920)-C80 cage. The change rule of properties for M@C80 (M = Ca, Sr, and Ba) influenced by different inner metal are discussed. As the trapped metal changes from calcium to barium, performance of thermodynamic stabilities for M@C2v(31920)-C80, M@C2v(31922)-C80, and M@D5h(31923)-C80 are significantly different. Orbital analysis suggests that the lowest unoccupied molecular orbitals (LUMOs) of Ca@C2v(31920)-C80 and Ca@D5h(31923)-C80 are mostly located on the trapped metal, whereas reduction reactions of Ca@C2v(31920)-C80 and Ca@D5h(31923)-C80 occur on the fullerene cage. Natural electron configuration analyses demonstrates that the decentralized electron back-donation of Ba@C2v(31920)-C80 would take responsible for the instability of itself. Electronic properties such as electron affinities and ionization potentials are significantly affected by encapsulated metal are also found. Computational UV-visible-NIR spectra for M@C2v(31920)-C80 (M = Ca, Sr, Ba) are in perfect accord with the spectra obtained experimentally.

  7. Research and analysis on the thin films sputtered by the Ba-Al-S:Eu target fabricated by powder sintering

    NASA Astrophysics Data System (ADS)

    Zhang, Dongpu; Xu, Fang; Yu, Zhinong; Xue, Wei

    2014-11-01

    Europium-doped barium thioaluminate (BaAl2S4:Eu) is currently the most efficient blue phosphor for inorganic thin film electroluminescent (iEL) device. To produce the full-color EL device, several kinds of blue-emitting layer were attempted and tested. As a key point of blue-emitting layer fabrication, single target sputtering deposition is an effective method. In this work, new structural target is introduced and the fabricated process is expatiated. The PL spectra of as fabricated targets show that both of two, 3mol% and 5mol% europium-doped, have blue emitting property. According to the PL spectra excited by 290nm, 300nm and 320nm ultraviolet, emission peaks located in the region near 470nm. So the as-fabricated targets can be used in single target sputtering deposition on thin film of BaAl2S4:Eu. XRD pattern indicates that there are 4 different phases, barium tetraaluminum sulfide (BaAl4S7), barium sulfide (BaS), europium sulfide (EuS) and barium aluminum oxide (BaAl2O4), in target 1. Besides these four compounds, other two phases, aluminum sulfide (Al2S3) and barium thioaluminate (BaAl2S4), are detected in target 2. Considering the analysis results, especially the hydrolyzation of Al2S3, target 1 is more suitable for sputtering deposition of BaAl2S4:Eu thin film. XPS and X-ray Fluorescence patterns describe the precise molar ratio of each element. In target 1 the relative atom concentration of barium, aluminum, sulfur and oxygen can be calculated from the pattern and molar ratio is about 9:33:41:17. Molar ratio of barium and europium is about 1:0.03. In short, the barium thioaluminate doped by europium sputtering target 1 is better to be applied in the fabrication of blue-emitting layer in inorganic electro-luminescent devices.

  8. Solvothermal synthesis of well-dispersed MF(2) (M = Ca,Sr,Ba) nanocrystals and their optical properties.

    PubMed

    Zhang, Xiaoming; Quan, Zewei; Yang, Jun; Yang, Piaoping; Lian, Hongzhou; Lin, Jun

    2008-02-20

    MF(2) (M = Ca,Sr,Ba) nanocrystals (NCs) were synthesized via a solvothermal process in the presence of oleic acid and characterized by x-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectra, UV/vis absorption spectra, photoluminescence (PL) excitation and emission spectra, and lifetimes, respectively. In the synthetic process, oleic acid as a surfactant played a crucial role in confining the growth and solubility of the MF(2) NCs. The as-prepared CaF(2), SrF(2) and BaF(2) NCs present morphologies of truncated octahedron, cube and sheet in a narrow distribution, respectively. Possible growth mechanisms were proposed to explain these results. The as-prepared NCs are highly crystalline and can be well dispersed in cyclohexane to form stable and clear colloidal solutions, which demonstrate strong emission bands centred at 400 nm in photoluminescence (PL) spectra compared with the cyclohexane solvent. The PL properties of the colloidal solutions of the as-prepared NCs can be ascribed to the trap states of surface defects.

  9. Bonding, moment formation, and magnetic interactions in Ca14MnBi11 and Ba14MnBi11

    NASA Astrophysics Data System (ADS)

    Sánchez-Portal, D.; Martin, Richard M.; Kauzlarich, S. M.; Pickett, W. E.

    2002-04-01

    ``14-1-11'' phase compounds, based on magnetic Mn ions and typified by Ca14MnBi11 and Ba14MnBi11, show an unusual magnetic behavior, but the large number (104) of atoms in the primitive cell has precluded any previous full electronic structure study. Using an efficient, local-orbital-based method within the local-spin-density approximation to study the electronic structure, we find a gap between a bonding valence-band complex and an antibonding conduction-band continuum. The bonding bands lack one electron per formula unit of being filled, making them low carrier density p-type metals. The hole resides in the MnBi4 tetrahedral unit, and partially compensates for the high-spin d5 Mn moment, leaving a net spin near 4μB that is consistent with experiment. These manganites are composed of two disjoint but interpenetrating ``jungle gym'' networks of spin-4/2 MnBi9-4 units with ferromagnetic interactions within the same network, and weaker couplings between the networks whose sign and magnitude is sensitive to materials parameters. Ca14MnBi11 is calculated to be ferromagnetic as observed, while for Ba14MnBi11 (which is antiferromagnetic) the ferromagnetic and antiferromagnetic states are calculated to be essentially degenerate. The band structure of the ferromagnetic states is very close to half metallic.

  10. P- T- X controls on Ca and Na distribution between Mg-Al tourmaline and fluid

    NASA Astrophysics Data System (ADS)

    Berryman, Eleanor J.; Wunder, Bernd; Rhede, Dieter; Schettler, Georg; Franz, Gerhard; Heinrich, Wilhelm

    2016-04-01

    Ca-Na partitioning between tourmaline and a coexisting fluid is investigated in the system CaO-Na2O-B2O3-Al2O3-MgO-SiO2-H2O-Cl between 0.2-4.0 GPa and 500-700 °C. The synthesis experiments produced a mineral assemblage of tourmaline, coesite/quartz, and in some cases additional phases, typically comprising <1 wt% of the solid product. The synthesized tourmalines are solid solutions of dravite [NaMg3Al6Si6O18(BO3)3(OH)3(OH)], "oxy-uvite" (i.e. "Ca-Mg-O root name") [CaMg3Al6Si6O18(BO3)3(OH)3O], and magnesio-foitite [☐(Mg2Al)Al6Si6O18(BO3)3(OH)3(OH)]. Starting materials comprised a fluid of constant ionic strength (2.00 m) and an oxide mixture with a constant Mg/Al ratio. As a result, the number of vacancies at the X site and the Mg/Al ratio of tourmaline crystals synthesized at the same temperature vary only slightly. The major solid solution is Ca-Na exchange at the X site via the exchange vector X Ca W O[ X Na W (OH)]-1, with the exchange vector X (Ca☐)[ X Na2]-1 serving as a secondary Ca-incorporation mechanism. Tourmaline's X-site composition reflects the fluid composition, whereby the Ca (or Na) concentration in the fluid corresponds with the Ca (or Na) content in tourmaline at each pressure and temperature. At 0.2 GPa, 700 °C, Ca preferentially partitions into tourmaline, producing the most Ca-rich tourmaline crystals synthesized here. At pressures >1.0 GPa, Ca partitions preferentially into the fluid, resulting in Na-dominant tourmaline compositions. Temperature has a secondary effect on Ca-Na partitioning, with higher temperatures correlating with increased Ca incorporation in tourmaline. Based on the experimental findings, tourmaline is expected to have Ca-rich compositions when it forms in low pressure, high-temperature Ca-rich rocks, consistent with the current record of tourmaline occurrence. The bulk Mg/Al ratio and the pH of the tourmaline-forming system may also affect Ca incorporation in tourmaline, but remain to be investigated experimentally.

  11. CaFeAl mixed oxide derived heterogeneous catalysts for transesterification of soybean oil to biodiesel.

    PubMed

    Lu, Yongsheng; Zhang, Zaiwu; Xu, Yunfeng; Liu, Qiang; Qian, Guangren

    2015-08-01

    CaAl layered double oxides (LDO) were prepared by co-precipitation and calcined at 750°C, and then applied to biodiesel production by transesterification reaction between methanol and soybean oil. Compared with characteristics of CaFe/LDO and CaAl/LDO, CaFeAl/LDO had the best performance based on prominent catalytic activity and stability, and achieved over 90% biodiesel yield, which stayed stable (over 85%) even after 8 cycles of reaction. The optimal catalytic reaction condition was 12:1M-ratio of methanol/oil, reaction temperatures of 60°C, 270rpm stirring rate, 60min reaction time, and 6% weight-ratio of catalyst/oil. In addition, the CaFeAl/LDO catalyst is insoluble in both methanol and methyl esters and can be easily separated for further reaction, turning it into an excellent alternative for biodiesel synthesis.

  12. CaFeAl mixed oxide derived heterogeneous catalysts for transesterification of soybean oil to biodiesel.

    PubMed

    Lu, Yongsheng; Zhang, Zaiwu; Xu, Yunfeng; Liu, Qiang; Qian, Guangren

    2015-08-01

    CaAl layered double oxides (LDO) were prepared by co-precipitation and calcined at 750°C, and then applied to biodiesel production by transesterification reaction between methanol and soybean oil. Compared with characteristics of CaFe/LDO and CaAl/LDO, CaFeAl/LDO had the best performance based on prominent catalytic activity and stability, and achieved over 90% biodiesel yield, which stayed stable (over 85%) even after 8 cycles of reaction. The optimal catalytic reaction condition was 12:1M-ratio of methanol/oil, reaction temperatures of 60°C, 270rpm stirring rate, 60min reaction time, and 6% weight-ratio of catalyst/oil. In addition, the CaFeAl/LDO catalyst is insoluble in both methanol and methyl esters and can be easily separated for further reaction, turning it into an excellent alternative for biodiesel synthesis. PMID:25740001

  13. Intracavity dye laser spectroscopy studies of the Ba + N(2)O, Ca + N(2)O + CO, and Sr + N(2)O + CO reactions.

    PubMed

    Eckstrom, D J; Barker, J R; Hawley, J G; Reilly, J P

    1977-08-01

    A search for gain or absorption on several candidate visible chemical laser transitions has been carried out using the intracavity dye laser probe technique. Absorption was found on the following v'' ? v' bands of the BaO(A(1)Sigma ? X(1)Sigma) bands in the Ba + N(2)O reaction: 0 ? 1; 0 ? 4; 1 ? 1; 1 ? 2, and 5 ? 1. No gain or absorption could be detected on the 7 ? 1, 6 ? 0, and 4 ? 0 bands (sensitivity ~10(-4)/cm). In Ca, Sr + N(2)O + CO flames, absorption was found in the green arc bands of CaO and the red arc bands of SrO. Several new bandhead wavelengths are reported. Our results support assignment of the arc bands to the diatomic metal oxides. Absorptions and enhancements were found on various Sr, Ba, and Ba(+) transitions. PMID:20168881

  14. Laser soldering of sapphire substrates using a BaTiAl6O12 thin-film glass sealant

    NASA Astrophysics Data System (ADS)

    de Pablos-Martin, A.; Tismer, S.; Benndorf, G.; Mittag, M.; Lorenz, M.; Grundmann, M.; Höche, Th.

    2016-07-01

    Two sapphire substrates are tightly bonded through a BaTiAl6O12-glass thin film, by irradiation with a nanosecond laser. After the laser process, the composition of the glass sealant changes, due to incorporation of Al2O3 from the upper substrate. After annealing of the bonded samples (950 °C for 30 minutes) crystalline structures are observed by TEM which are attributed to crystalline BaTiAl6O12. These crystals together with Al2O3:Ti centers are the responsible of the observed strong blue luminescence of the laser irradiated region upon UV excitation. The structural and optical characterizations of the bonded samples clarify the laser soldering procedure as well as the origin of the luminescence. Bond quality and bond strength were evaluated by scanning acoustic microscopy (SAM) and tensile tests, which results in a tensile stress of nearly 13 MPa, which is an acceptable value for glass sealants.

  15. A Fluctuating State in the Framework Compounds (Ba,Sr)Al2O4

    PubMed Central

    Ishii, Yui; Tsukasaki, Hirofumi; Tanaka, Eri; Mori, Shigeo

    2016-01-01

    The structural fluctuation in hexagonal Ba1−xSrxAl2O4 with a corner-sharing AlO4 tetrahedral network was characterized at various temperatures using transmission electron microscopy experiments. For x ≤ 0.05, soft modes of q ~ (1/2, 1/2, 0) and equivalent wave vectors condense at a transition temperature (TC) and form a superstructure with a cell volume of 2a × 2b × c. However, TC is largely suppressed by Sr-substitution, and disappears for x ≥ 0.1. Furthermore, the q ~ (1/2, 1/2, 0) soft mode deviates from the commensurate value as temperature decreases and survives in nanoscaled regions below ~200 K. These results strongly suggest the presence of a new quantum criticality induced by the soft mode. Two distinct soft modes were observed as honeycomb-type diffuse scatterings in the high-temperature region up to 800 K. This intrinsic structural instability is a unique characteristic of the framework compound and is responsible for this unusually fluctuating state. PMID:26758625

  16. Macroscopic magnetic properties in TlBa{sub 2}Ca{sub 3}Cu{sub 4}O{sub 11-{delta}} single crystals

    SciTech Connect

    Zhang, Lu; Collins, C.; Liu, J.Z.; Shelton, R.N.

    1996-11-01

    The four-CuO{sub 2}-layer TlBa{sub 2}Ca{sub 3}Cu{sub 4}O{sub 11{minus}{delta}} compound has a high superconducting transition temperature of 128 K and strong interlayer coupling. The authors have performed magnetic experiments on single crystals of TlBa{sub 2}Ca{sub 3}Cu{sub 4}O{sub 11{minus}{delta}}, which include hysteresis loop, irreversibility line and time relaxation measurements. From these measurements, the authors observed the large critical current density, high irreversibility line and strongly temperature dependent flux creep rate in the TlBa{sub 2}Ca{sub 3}Cu{sub 4}O{sub 11{minus}{delta}} single crystals.

  17. Magnetic and magnetocaloric properties of La 0.7Ca 0.3- xBa xMnO 3 compounds

    NASA Astrophysics Data System (ADS)

    Phan, Manh-Huong; Tian, Sheng-Bo; Yu, Seong-Cho; Ulyanov, A. N.

    2003-01-01

    Magnetic properties and magnetocaloric effect in La 0.7Ca 0.3- xBa xMnO 3 ( x=0.12, 0.24, 0.3) compounds were investigated. It is shown that there is a large magnetic entropy change associated with the ferromagnetic-paramagnetic transition. The Curie temperature ( TC) increases with the barium addition, while the maximum entropy change ( ΔS Mmax) slightly decreases. La 0.7Ca 0.18Ba 0.12MnO 3 exhibits the largest ΔS Mmax value of 1.85 J/kg/K at 298 K among the compounds investigated up to 10 kOe applied field. Through these results, La 0.7Ca 0.3- xBa xMnO 3 materials are strongly suggested for the use of active refrigerants for magnetic refrigeration technology near and above room temperature.

  18. Surface modification of MAl2O4:Eu2+,Dy3+ (M = Sr, Ca, Ba) phosphors to enhance water resistance by combustion method

    NASA Astrophysics Data System (ADS)

    Deng, Suqing; Xue, Zhiping; Yang, Qu; Liu, Yingliang; Lei, Bingfu; Xiao, Yong; Zheng, Mingtao

    2013-10-01

    A facile combustion method was introduced into surface modification of MAl2O4:Eu2+,Dy3+ (M = Sr, Ca, Ba) phosphors to improve their water resistance. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), pH measurements and photoluminescence (PL) spectrophotometry were used to characterize the phosphors before and after modification, respectively. Experimental results showed that compact layer of MAl2B2O7 (M = Sr, Ca, Ba) substance was formed on the surface of aluminate phosphors by direct chemical reaction between aluminate and boracic acid. MAl2B2O7 (M = Sr, Ca, Ba) substance is chemically stable in water and could improve water resistance of aluminate phosphors effectively with little influence of luminescence property. It was considered that the versatility of combustion method for surface modification of aluminate phosphors has been confirmed.

  19. Defect-induced wetting on BaF 2(111) and CaF 2(111) at ambient conditions

    NASA Astrophysics Data System (ADS)

    Cardellach, M.; Verdaguer, A.; Fraxedas, J.

    2011-12-01

    The interaction of water with freshly cleaved (111) surfaces of isostructural BaF2 and CaF2 single crystals at ambient conditions (room temperature and under controlled humidity) has been studied using scanning force microscopy in different operation modes and optical microscopy. Such surfaces exhibit contrasting behaviors for both materials: while on BaF2(111) two-dimensional water layers are formed after accumulation at step edges, CaF2(111) does not promote the formation of such layers. We attribute such opposed behavior to lattice match (mismatch) between hexagonal water ice and the hexagonal (111) surfaces of BaF2(CaF2). Optical microscope images reveal that this behavior also determines the way the surfaces become wetted at a macroscopic level.

  20. Pressure-induced amorphous-to-amorphous configuration change in Ca-Al metallic glasses

    PubMed Central

    Lou, H. B.; Fang, Y. K.; Zeng, Q. S.; Lu, Y. H.; Wang, X. D.; Cao, Q. P.; Yang, K.; Yu, X. H.; Zheng, L.; Zhao, Y. D.; Chu, W. S.; Hu, T. D.; Wu, Z. Y.; Ahuja, R.; Jiang, J. Z.

    2012-01-01

    Pressure-induced amorphous-to-amorphous configuration changes in Ca-Al metallic glasses (MGs) were studied by performing in-situ room-temperature high-pressure x-ray diffraction up to about 40 GPa. Changes in compressibility at about 18 GPa, 15.5 GPa and 7.5 GPa during compression are detected in Ca80Al20, Ca72.7Al27.3, and Ca66.4Al33.6 MGs, respectively, whereas no clear change has been detected in the Ca50Al50 MG. The transfer of s electrons into d orbitals under pressure, reported for the pressure-induced phase transformations in pure polycrystalline Ca, is suggested to explain the observation of an amorphous-to-amorphous configuration change in this Ca-Al MG system. Results presented here show that the pressure induced amorphous-to-amorphous configuration is not limited to f electron-containing MGs. PMID:22530094

  1. Synthesis, Crystal and Electronic Structures of the Pnictides AE3TrPn3 (AE = Sr, Ba; Tr = Al, Ga; Pn = P, As)

    DOE PAGES

    Stoyko, Stanislav; Voss, Leonard; He, Hua; Bobev, Svilen

    2015-09-24

    New ternary arsenides AE3TrAs3 (AE = Sr, Ba; Tr = Al, Ga) and their phosphide analogs Sr3GaP3 and Ba3AlP3 have been prepared by reactions of the respective elements at high temperatures. Single-crystal X-ray diffraction studies reveal that Sr3AlAs3 and Ba3AlAs3 adopt the Ba3AlSb3-type structure (Pearson symbol oC56, space group Cmce, Z = 8). This structure is also realized for Sr3GaP3 and Ba3AlP3. Likewise, the compounds Sr3GaAs3 and Ba3GaAs3 crystallize with the Ba3GaSb3-type structure (Pearson symbol oP56, space group Pnma, Z = 8). Both structures are made up of isolated pairs of edge-shared AlPn4 and GaPn4 tetrahedra (Pn = pnictogen, i.e.,more » P or As), separated by the alkaline-earth Sr2+ and Ba2+ cations. In both cases, there are no homoatomic bonds, hence, regardless of the slightly different atomic arrangements, both structures can be rationalized as valence-precise [AE2+]3[Tr3+][Pn3-]3, or rather [AE2+]6[Tr2Pn6]12-, i.e., as Zintl phases.« less

  2. Effect of Phosphatidylserine on Unitary Conductance and Ba2+ Block of the BK Ca2+–activated K+ Channel

    PubMed Central

    Park, Jin Bong; Kim, Hee Jeong; Ryu, Pan Dong; Moczydlowski, Edward

    2003-01-01

    Incorporation of BK Ca2+–activated K+ channels into planar bilayers composed of negatively charged phospholipids such as phosphatidylserine (PS) or phosphatidylinositol (PI) results in a large enhancement of unitary conductance (gch) in comparison to BK channels in bilayers formed from the neutral zwitterionic lipid, phospatidylethanolamine (PE). Enhancement of gch by PS or PI is inversely dependent on KCl concentration, decreasing from 70% at 10 mM KCl to 8% at 1,000 mM KCl. This effect was explained previously by a surface charge hypothesis (Moczydlowski, E., O. Alvarez, C. Vergara, and R. Latorre. 1985. J. Membr. Biol. 83:273–282), which attributed the conductance enhancement to an increase in local K+ concentration near the entryways of the channel. To test this hypothesis, we measured the kinetics of block by external and internal Ba2+, a divalent cation that is expected to respond strongly to changes in surface electrostatics. We observed little or no effect of PS on discrete blocking kinetics by external and internal Ba2+ at 100 mM KCl and only a small enhancement of discrete and fast block by external Ba2+ in PS-containing membranes at 20 mM KCl. Model calculations of effective surface potential sensed by the K+ conduction and Ba2+-blocking reactions using the Gouy-Chapman-Stern theory of lipid surface charge do not lend support to a simple electrostatic mechanism that predicts valence-dependent increase of local cation concentration. The results imply that the conduction pore of the BK channel is electrostatically insulated from the lipid surface, presumably by a lateral distance of separation (>20 Å) from the lipid head groups. The lack of effect of PS on apparent association and dissociation rates of Ba2+ suggest that lipid modulation of K+ conductance is preferentially coupled through conformational changes of the selectivity filter region that determine the high K+ flux rate of this channel relative to other cations. We discuss possible mechanisms

  3. The atomic structure of lead-free Ba(Zr0.2Ti0.8)O3-(Ba0.7Ca0.3)TiO3 by using neutron total scattering analysis

    NASA Astrophysics Data System (ADS)

    Jeong, I.-K.; Ahn, J. S.

    2012-12-01

    We conducted neutron total scattering measurements on lead-free Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 (BZT-0.5BCT) ceramic at 300 K and 150 K, and studied both long-range and local structures near the morphotropic phase boundary. Despite the long-range phase transition from tetragonal to rhombohedral structures, we found that local atomic structure of BZT-0.5BCT barely changes between 300 K and 150 K. To incorporate both long-range and local structures in a consistent way, we performed reverse Monte Carlo modeling. In BZT-0.5BCT, we found that the Ca substitution on Ba sites causes little impact on the local displacement of Ti ion but enhances octahedral tilting of ZrO6, resulting in nonuniform lattice distortion.

  4. The microstructure-strength relationship in a deformation processed Al-Ca composite

    SciTech Connect

    Tian, Liang; Kim, Hyongjune; Anderson, Iver; Russell, Alan

    2013-02-07

    An Al-9 vol% Ca composite was produced by powder metallurgy and deformation processing. The Al–Ca composite was extruded, swaged and wire drawn to a deformation true strain of 13.8. Both Al and Ca are face-centered cubic, so the Ca second phase deformed into continuous, nearly cylindrical filaments in the Al matrix. The formation of intermetallic compounds, filament coarsening, and spheriodization at elevated temperature was observed by scanning electron microscopy, differential scanning calorimetry, and X-ray diffraction. Both the thickness and spacing of the Ca filaments decreased exponentially with increasing deformation. The ultimate tensile strength of the composite increased rapidly with increased deformation, especially at high deformation processing strains. The relation between deformation true strain and ultimate tensile strength is underestimated by the rule of mixtures; a modified Hall–Petch barrier strengthening model was found to fit the data better.

  5. Crystal and Magnetic Structures of the Oxide Sulfides CaCoSO and BaCoSO.

    PubMed

    Salter, Edward J T; Blandy, Jack N; Clarke, Simon J

    2016-02-15

    CaCoSO, synthesized from CaO, Co, and S at 900 °C, is isostructural with CaZnSO and CaFeSO. The structure is non-centrosymmetric by virtue of the arrangement of the vertex-sharing CoS3O tetrahedra which are linked by their sulfide vertices to form layers. The crystal structure adopts space group P63mc (No. 186), and the lattice parameters are a = 3.7524(9) Å and c = 11.138(3) Å at room temperature with two formula units in the unit cell. The compound is highly insulating, and powder neutron diffraction measurements reveal long-range antiferromagnetic order with a propagation vector k = (1/3, 1/3, 1/2). The magnetic scattering from a powder sample can be modeled starting from a 120° arrangement of Co(2+) spin vectors in the triangular planes and then applying a canting out of the planes which can be modeled in the magnetic space group C(c)c (space group 9.40 in the Belov, Neronova, and Smirnova (BNS) scheme) with Co(2+) moments of 2.72(5) μ(B). The antiferromagnetic structure of the recently reported compound BaCoSO, which has a very different crystal structure from CaCoSO, is also described, and this magnetic structure and the magnitude of the ordered moment (2.75(2) μ(B)) are found by experiment to be similar to those predicted computationally.

  6. Ca-rich Ca-Al-oxide, high-temperature-stable sorbents prepared from hydrotalcite precursors: synthesis, characterization, and CO2 capture capacity.

    PubMed

    Chang, Po-Hsueh; Chang, Yen-Po; Chen, San-Yuan; Yu, Ching-Tsung; Chyou, Yau-Pin

    2011-12-16

    We present the design and synthesis of Ca-rich Ca-Al-O oxides, with Ca(2+)/Al(3+) ratios of 1:1, 3:1, 5:1, and 7:1, which were prepared by hydrothermal decomposition of coprecipitated hydrotalcite-like Ca-Al-CO(3) precursors, for high-temperature CO(2) adsorption at 500-700 °C. In situ X-ray diffraction measurements indicate that the coprecipitated, Ca-rich, hydrotalcite-like powders with Ca(2+)/Al(3+) ratios of 5:1 and 7:1 contained Ca(OH)(2) and layered double hydroxide (LDH) phases. Upon annealing, LDH was first destroyed at approximately 200 °C to form an amorphous matrix, and then at 450-550 °C, the Ca(OH)(2) phase was converted into a CaO matrix with incorporated Al(3+) to form a homogeneous solid solution without a disrupted lattice structure. CaO nanocrystals were grown by thermal treatment of the weakly crystalline Ca-Al-O oxide matrix. Thermogravimetric analysis indicates that a CO(2) adsorption capacity of approximately 51 wt. % can be obtained from Ca-rich Ca-Al-O oxides prepared by calcination of 7:1 Ca-Al-CO(3) LDH phases at 600-700 °C. Furthermore, a relatively high CO(2) capture capability can be achieved, even with gas flows containing very low CO(2) concentrations (CO(2)/N(2) = 10 %). Approximately 95.6 % of the initial CO(2) adsorption capacity of the adsorbent is retained after 30 cycles of carbonation-calcination. TEM analysis indicates that carbonation-promoted CaCO(3) formation in the Ca-Al-O oxide matrix at 600 °C, but a subsequent desorption in N(2) at 700 °C, caused the formation CaO nanocrystals of approximately 10 nm. The CaO nanocrystals are widely distributed in the weakly crystalline Ca-Al-O oxide matrix and are present during the carbonation-calcination cycles. This demonstrates that Ca-Al-O sorbents that developed through the synthesis and calcination of Ca-rich Ca-Al LDH phases are suitable for long-term cyclic operation in severe temperature environments.

  7. Stabilization of metastable ferroelectric Ba1−xCaxTi2O5 by breaking Ca-site selectivity via crystallization from glass

    PubMed Central

    Masuno, Atsunobu; Moriyoshi, Chikako; Mizoguchi, Teruyasu; Okajima, Toshihiro; Kuroiwa, Yoshihiro; Arai, Yasutomo; Yu, Jianding; Inoue, Hiroyuki; Watanabe, Yasuhiro

    2013-01-01

    The thermal stability and dielectric and structural properties of ferroelectric Ba1−xCaxTi2O5 (0 ≤ x ≤ 0.30) prepared by crystallization from glass are investigated. The Ba1−xCaxTi2O5 compounds with x < 0.10 are thermally stable phases, while those with x ≥ 0.10 are metastable phases. The ferroelectric transition temperature drastically decreases from 470 to 220°C with increasing x. Crystal structure analyses reveal that one of two possible Ba sites is occupied by Ca in the stable phase region, while Ca-site selectivity is broken in the metastable phase region. The Ca-site selectivity introduces local distortion and makes the crystal lattice unstable. However, the local distortion is suppressed by the occupancy of Ca into both Ba sites. Accordingly, the metastable ferroelectric phase can be obtained beyond the substitution limit of Ca by crystallization from the glassy state. The stabilization mechanism provides possible wide control of the functionality of materials by expanding the composition range. PMID:24145958

  8. Investigation on photoluminescence properties and defect chemistry of GdAlO3:Dy3+ Ba2+ phosphors

    NASA Astrophysics Data System (ADS)

    Selvalakshmi, Thangaraj; Sellaiyan, Selvakumar; Uedono, Akira; Semba, Takaaki; Bose, Arumugam Chandra

    2016-08-01

    GdAlO3:Dy3+ Ba2+ phosphors are synthesized by citrate-based sol-gel method. Photoluminescence and positron annihilation studies are used to investigate the emission and defect chemistry of the phosphors respectively. The strong yellow (Dy3+) emission properties of phosphors are discussed for various concentrations of Dy3+ ions. Upon the addition of Ba2+ ion, an enhancement in emission intensity is observed due to the lattice distortions around Dy3+ ion. The positron studies indicate the presence of defects at crystallite boundaries, vacancy clusters and large voids in the materials. The influence of Ba2+ ion on the photoluminescence and lattice distortion around Dy3+ is also explored.

  9. Ba/Ca in Planktonic Foraminifera as a Recorder of Freshwater Input to the Ocean: Proxy Refinement in the Gulf of Papua, Papua New Guinea

    NASA Astrophysics Data System (ADS)

    Gibson, K.

    2015-12-01

    In the study of paleoclimate, the past several decades have seen large strides in the advancement of proxies designed to reconstruct changes in sea surface temperature (SST); however, techniques for reconstructing ocean salinity are less well developed. The ratio of Ba/Ca in planktic foraminiferal tests has shown initial promise as a tool for reconstructing salinity in continental margin sites near river mouths. In these environments, Ba/Ca shows an inverse correlation with salinity, and often a less clear correlation to nutrients or indicators of productivity, as is more typical in open-ocean settings. An ideal area in which to apply and test foraminiferal Ba/Ca as a proxy for freshwater input is the Western Pacific Warm Pool (WPWP), where temperatures are relatively stable, but large variations in precipitation are today driven by the El Nino Southern Oscillation (ENSO) and strength of the Australian-Indonesian monsoon. Foraminiferal Ba/Ca in sediments proximal to a river mouth should therefore reflect changes in riverine input, which in turn reflect variations in precipitation on different timescales. We present here planktic foraminiferal δ18O, Ba/Ca, and Mg/Ca records spanning the last glacial-interglacial transition from marine sediment cores in the Gulf of Papua, located in the WPWP. The δ18O records show an increase in the magnitude of glacial-interglacial (G-IG) δ18O change (∆18O) moving away from the coastline and the mouth of the primary local freshwater source, the Fly River. The reduced amplitude in G-IG ∆18O in the cores closer to shore, manifested by more negative δ18O values before ~20 kyr ago, is likely due to freshwater input from the Fly River, with the effects diminishing with distance from the Fly River source. Temperature and sea level are also changing over the deglaciation, however, contributing to the signal recorded in the calcite δ18O. We use planktic Mg/Ca analyses and independent records of sea level change to isolate the

  10. Dielectric and piezoelectric properties of lead-free 0.5Ba(Zr0.2 Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 piezoelectric ceramics with glass additive.

    PubMed

    Im, In-Ho; Chung, Kwang-Hyun

    2014-12-01

    We have investigated the dielectric and piezoelectric properties of lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics with BaO-CaO-SiO2 glass additive as a function of sintering temperatures. With adding BaO-CaO-SiO2 glass additive, diffusivity of lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics was increased. The dispersion constant γ of BZT-BCT ceramics with BaO-CaO-SiO2 glass was changed from 1.9683 to 1.7673 by decreasing sintering temperature ranging from 1450 degrees C to 1350 degrees C, while 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics at sintered 1450 degrees C showed γ = 1.5055. The piezoelectric properties such as electromechanical coupling factor (k(p)) and piezoelectric constant (d33) of lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics with BaO-CaO-SiO2 glass additive sintered at 1400 degrees C showed similar values compared with 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics without BaO-CaO-SiO2 glass additive sintered at 1450 degrees C. The addition of BaO-CaO-SiO2 glass additive can be of help to decrease sintering temperature of lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics.

  11. Dielectric and piezoelectric properties of lead-free 0.5Ba(Zr0.2 Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 piezoelectric ceramics with glass additive.

    PubMed

    Im, In-Ho; Chung, Kwang-Hyun

    2014-12-01

    We have investigated the dielectric and piezoelectric properties of lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics with BaO-CaO-SiO2 glass additive as a function of sintering temperatures. With adding BaO-CaO-SiO2 glass additive, diffusivity of lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics was increased. The dispersion constant γ of BZT-BCT ceramics with BaO-CaO-SiO2 glass was changed from 1.9683 to 1.7673 by decreasing sintering temperature ranging from 1450 degrees C to 1350 degrees C, while 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics at sintered 1450 degrees C showed γ = 1.5055. The piezoelectric properties such as electromechanical coupling factor (k(p)) and piezoelectric constant (d33) of lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics with BaO-CaO-SiO2 glass additive sintered at 1400 degrees C showed similar values compared with 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics without BaO-CaO-SiO2 glass additive sintered at 1450 degrees C. The addition of BaO-CaO-SiO2 glass additive can be of help to decrease sintering temperature of lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics. PMID:25970982

  12. Yb(3+):BaCaBO3F: A potential new self-frequency-doubling laser material

    NASA Astrophysics Data System (ADS)

    Schaffers, K. I.; Deloach, L. D.; Ebbers, C. A.; Payne, S. A.

    1995-03-01

    Yb:BaCaBO3F (Yb:BCBF) has been investigated as a new laser crystal with potential for self-frequency-doubling. A Yb:BCBF laser has been pumped at 912 mm, and a measured slope efficiency of 38% has been obtained for the fundamental laser output at 1034 nm. Single crystal powders of BCBF have been compared with KD*P (KD2PO4) for a relative measure of the second harmonic generating potential, yielding d(sub eff)(BCBF) = (0.66)d(sub eff)(KD*P). The growth, spectroscopy, laser performance, and linear and nonlinear optical properties of Yb:BCBF are reported here.

  13. Structural and Optoelectronic Properties of X3ZN (X = Ca, Sr, Ba; Z = As, Sb, Bi) Anti-Perovskite Compounds

    NASA Astrophysics Data System (ADS)

    Ullah, Imran; Murtaza, G.; Khenata, R.; Mahmood, Asif; Muzzamil, M.; Amin, N.; Saleh, M.

    2016-06-01

    We employed first-principles calculations to predict the structural and optoelectronic properties of X3ZN (X = Ca, Sr, Ba; Z = As, Sb, Bi) anti-perovskite compounds using an all-electron full-potential linearized augmented plane-wave method. Optimized structural parameters are found to be in good agreement with the available experimental measurements. The electronic band structure is calculated using different exchange-correlation potentials which reveal that the investigated compounds are narrow direct band gap semiconductors. A direct narrow band gap at the center of the Brillouin zone emphasises the optical activity of these compounds. Prediction of the optical properties, such as the real and imaginary parts of the dielectric function and refractive index along with reflectivity and optical conductivity, reveals the importance of these compounds in the visible and near UV optoelectronic devices industry.

  14. Synthesis and investigation of (Hg 1- xCu x)Ba 2Ca 2Cu 3O 8+ δ

    NASA Astrophysics Data System (ADS)

    Lokshin, K. A.; Pavlov, D. A.; Kovba, M. L.; Putilin, S. N.; Antipov, E. V.; Bryntse, I.

    2002-02-01

    A reproducible synthesis method for superconducting HgBa 2Ca 2Cu 3O 8+ δ (Hg-1223) has been developed, using sealed silica tubes and a CoO/Co 3O 4 mixture as oxygen getter to achieve a controlled partial pressure of oxygen. Samples containing more than 95% of Hg-1223 were prepared with this technique. A significant range of substitution of Cu for Hg was revealed by EDS analysis in samples synthesized at 900°C. After post-anneal in oxygen the lattice parameters were calculated from XRD data and Tc was determined to be 135 K, by susceptibility methods. We suggest that a high synthesis temperature and a low partial pressure of mercury promote substitution in the Hg-1223 phase.

  15. Relaxor behavior of ferroelectric Ca0.22Sr0.12Ba0.66Nb2O6

    NASA Astrophysics Data System (ADS)

    Shekhar Pandey, Chandra; Schreuer, Jürgen; Burianek, Manfred; Mühlberg, Manfred

    2013-01-01

    The relaxor behavior of tetragonal tungsten bronze uniaxial relaxor ferroelectric calcium strontium barium niobate (Ca0.22Sr0.12Ba0.66Nb2O6 or CSBN-22) single crystal was studied by measuring elastic constants and thermal expansion with the aid of resonant ultrasound spectroscopy and dilatometry, respectively, in the temperature range 300 K-1503 K. Thermal expansion yields evidence of the Burns temperature TB and the intermediate characteristic temperature T*, which was also supported by the temperature evolutions of the elastic constants cij. CSBN-22 was found to be ˜2%-3% elastically stiffer than CBN-28. The presented results open the perspective to understand the relaxor behavior of CSBN.

  16. Contrasting Effects of Ca{sup 2+} and Ho{sup 3+} Substitutions on Superconductivity and Excess conductivity of (Ho{sub 1-x}Ca{sub x})(Ba{sub 2-y}Ho{sub y})Cu{sub 3}O{sub 7-{delta}}

    SciTech Connect

    Maulud, M. F.; Hamidi, Z. S.; Yusof, A. A.; Yusof, M. I. M.; Yahya, A. K.

    2010-07-07

    Effects of Ho{sup 3+} and Ca{sup 2+} substitutions in (Ho{sub 1-x}Ca{sub x})(Ba{sub 2-y}Ho{sub y})Cu{sub 3}O{sub 7-{delta}}ceramics on normal and superconducting state behaviour were investigated. Electrical resistivity measurements showed increasing Ho{sup 3+} substitution at Ba{sup 2+} site (x = 0, 0.4, y = 0-0.4) caused normal state resistivity to change from metal-like to semimetal/semiconductor-like behaviour and suppressed T{sub c} from 89 K (y = 0) to 72 K (y = 0.4) while substitution of Ca{sup 2+} for Ho{sup 3+}((x = 0.2) 0.4, (y 0.4)) revives metallic behaviour of the normal state with increasing x. Excess conductivity analysis based on Asmalazov-Larkin theory showed 2D to 3D transition for all superconducting samples but with contrasting effects of the substitutions on AL{sub 2D} and AL{sub 3D} constants. The resistivity and excess conductivity results indicate effective hole filling Ho{sup 3+} and hole doping by by Ca{sup 2+} substitutions.

  17. Fabrication and chemical composition of rf magnetron sputtered Tl-Ca-Ba-Cu-O high T sub c superconducting thin films

    SciTech Connect

    Subramanyam, G.; Radpour, F.; Kapoor, V.J.; Lemon, G.H. )

    1990-08-01

    High-temperature superconducing Tl-Ca-Ba-Cu-O (TlCaBaCuO) thin films were fabricated by rf magnetron sputtering on strontium titanate (SrTiO{sub 3}) substrates. Thin films of 0.5--0.7-{mu}m thickness were deposited by pure argon sputtering from a single composite powder target of Tl{sub 2}Ca{sub 2}Ba{sub 2}Cu{sub 3}O{sub {ital x}} at an rf power of 250 W and a pressure of 5 mTorr. As-deposited thin films were sintered and annealed in a thallium-rich ambient to obtain superconductivity with a zero resistance temperature ({ital T}{sub {ital c}0}) at 107 K. X-ray diffraction results showed highly {ital c}-axis oriented films with Tl{sub 2}Ca{sub 2}Ba{sub 2}Cu{sub 3}O{sub {ital x}} (2223) and Tl{sub 2}Ca{sub 1}Ba{sub 2}Cu{sub 2}O{sub {ital x}} (2122) phases present. Auger electron spectroscopy survey and depth profiles were performed to determine the compositional uniformity and impurity contents of the thin films. X ray photoelectron spectroscopy high-resolution spectra were obtained at the surface, in the bulk, and near the interface with the substrate. Our XPS results support two possible mechanisms for the creation of holes in the TlCaBaCuO compound: (1) partial substitution of Ca{sup 2+} for Tl{sup 3+} and (2) charge transfer from Tl{sup 3+} to the CuO layers resulting in a valence of Tl between +3 and +1 states and the creation of holes in the CuO layers. In addition, a wet chemical etching process was developed for patterning the as-deposited TlCaBaCuO thin films. A 125-{mu}m-wide line was formed using standard photolithography and wet chemical etching which, after heat treatments, showed superconductivity with a {ital T}{sub {ital c}0} of 80 K.

  18. Ferroelectric property of (Ba,Bi)(Ti,M)O3 (M; Cu, Mn, Al, Fe, In, Y, Yb) ceramics

    NASA Astrophysics Data System (ADS)

    Shiroki, K.; Kumada, N.; Ogiso, H.; Yonesaki, Y.; Takei, T.; Kinomura, N.; Wada, S.

    2011-10-01

    Two types of solid solutions, (Ba1-2xBi2x)(CuxTi1-x)O3 (x <= 0.04) and (Ba1-xBix)(MxTi1-x)O3 (M; Al, Mn, Fe, In, Y, Yb; x <= 0.03) were prepared by conventional high temperature reaction. For the solid solution of (Ba1-2xBi2x)(CuxTi1-x)O3 single phases with the tetragonal cell was obtained in the region of x <= 0.04 and for the solid solutions of (Ba1-xBix)(MxTi1-x)O3 (M; Al, Mn, Fe, In, Y, Yb) single phases with the tetragonal cell was observed in the region of x <= 0.03 except the sample of M = Al in which a small amount of the second phase was contained. In these solid solutions the Tc increased with the value of x except for M = Al, and was 144.7°C for x = 0.020 of M = Cu, and the highest Tc was observed for x = 0.020 of every M atom and the order of the highest Tc was Cu (144.7°C), Y (141.4°C), Yb (140.8°C), In (138.5°C), Mn (135.5°C) and Fe (131.3°C). The highest apparent piezoelectric constant, (d33 = 258 pm/V) in these solid solutions was observed for x = 0.010 of Al.

  19. Relaxor behavior of CaxBa1-xNb2O6 (0.18≤x≤0.35) tuned by Ca/Ba ratio and investigated by resonant ultrasound spectroscopy

    NASA Astrophysics Data System (ADS)

    Pandey, Chandra Shekhar; Schreuer, Jürgen; Burianek, Manfred; Mühlberg, Manfred

    2013-03-01

    Dependence of relaxor behavior of incompletely filled tetragonal tungsten bronze uniaxial relaxor ferroelectric calcium barium niobate (CaxBa1-xNb2O6, CBN-x) on its composition was investigated by varying Ca/Ba ratio (0.18 ≤ x ≤ 0.35) and studying its thermal and elastic properties. Recently, we have reported the relaxor behavior CBN-28 with the evidence of the existence of the Burns temperature TB, and the intermediate characteristic temperature T* [Pandey , Phys. Rev. BPRBMDO1098-012110.1103/PhysRevB.84.174102 84, 174102 (2011)]. In this work, we show that the dynamics of polar nanoregions (and hence the relaxor behavior) strongly varies with the Ca/Ba ratio. Evidence is found for a more pronounced relaxor behavior with increasing x. The Curie temperature and the Burns temperature are also very sensitive to the composition, whereas the characteristic temperature T* appears unaffected from the Ca/Ba ratio. The bonding interaction has been explained on the basis of bulk modulus, Poisson's ratio, and deviation from Cauchy relations. Presented results open the perspective to understand the variation of relaxor behavior of CBN-x (˜0.18≤x≤˜0.35) above Curie temperature.

  20. Determining Solute Sources and Water Flowpaths in a Forested Headwater Catchment: Advances With the Ca-Sr-Ba Multi-tracer

    NASA Astrophysics Data System (ADS)

    Bullen, T. D.; Bailey, S. W.; McGuire, K. J.; Zimmer, M. A.; Ross, D. S.

    2011-12-01

    Determining solute sources and water flowpaths in catchments is of critical importance to development of models that effectively describe catchment function. For solutes in soil water and stream water, simple mass balance models that compare precipitation input to catchment outlet compositions can predict average mineral weathering contributions for the catchment as a whole, but fail to provide information about either variability of contributions from different portions of the catchment and different soil depths or processes such as ion exchange and biological cycling. In order to better understand how forested headwater catchments function, we are interpreting concentration and isotope ratios of the alkaline earth elements Ca, Sr and Ba in streamwater, groundwater, the soil ion exchange pool and plants in a hydropedologic context at the 41 hectare hydrologic reference catchment (Watershed 3) at the Hubbard Brook Experimental Forest, New Hampshire, USA. This forested headwater catchment consists of a beech-birch-maple-spruce forest growing on vertically- and laterally-developed Spodosols and Inceptisols formed on granitoid glacial till that mantles Paleozoic metamorphic bedrock. Across the watershed in terms of the soil ion exchange pool, the forest floor has high Sr/Ba and Ca/Sr ratios, mineral soils have intermediate Sr/Ba and low Ca/Sr, and relatively unweathered till in the C horizon has low Sr/Ba and high Ca/Sr. Waters moving through these various compartments will obtain Sr/Ba and Ca/Sr ratios reflecting these characteristics, and thus variations of Sr/Ba and Ca/Sr of streamwater provide evidence of the depth of water flowpaths feeding the streams. 87Sr/86Sr of exchangeable Sr spans a broad range from 0.715 to 0.725, with highest values along the mid-to upper flanks of the catchment and lowest values in a broad zone along the central axis of the catchment associated with numerous groundwater seeps. Thus, variations of 87Sr/86Sr in streamwater provide

  1. Phosphate-sulfide assemblages and Al/Ca ratios in type-3 chondrites

    NASA Astrophysics Data System (ADS)

    Rubin, A. E.; Grossman, J. N.

    1985-09-01

    Electron microscopic examinations were carried out on various chondrites to re-examine previously reported anomalously high Al/Ca ratios. Polished thin sections of the three CV3, two CO3 and the Krymka LL3 chondrites were scanned to characterize the phosphate-sulfide inclusions. The formation of the assemblages was interpreted as proceeding in five steps, starting with the formation of metal grains with early nebular material and finishing with a reaction between schreibersite with Ca, O and Cl to form merrillite and chloropatite. The abundances of the observed assemblages were not high enough to imply Al/Ca ratios similar to whole-rocks. It is concluded that the specimens were originally examined with a broader electron beam than used to examine standard samples, and resulted in the anomalously high Al/Ca ratios.

  2. Phosphate-sulfide assemblages and Al/Ca ratios in type-3 chondrites

    NASA Technical Reports Server (NTRS)

    Rubin, A. E.; Grossman, J. N.

    1985-01-01

    Electron microscopic examinations were carried out on various chondrites to re-examine previously reported anomalously high Al/Ca ratios. Polished thin sections of the three CV3, two CO3 and the Krymka LL3 chondrites were scanned to characterize the phosphate-sulfide inclusions. The formation of the assemblages was interpreted as proceeding in five steps, starting with the formation of metal grains with early nebular material and finishing with a reaction between schreibersite with Ca, O and Cl to form merrillite and chloropatite. The abundances of the observed assemblages were not high enough to imply Al/Ca ratios similar to whole-rocks. It is concluded that the specimens were originally examined with a broader electron beam than used to examine standard samples, and resulted in the anomalously high Al/Ca ratios.

  3. In vitro synthesis of amorphous Mg-, Ca-, Sr- and Ba-carbonates: What do we learn about intracellular calcification by cyanobacteria?

    NASA Astrophysics Data System (ADS)

    Cam, N.; Georgelin, T.; Jaber, M.; Lambert, J.-F.; Benzerara, K.

    2015-07-01

    Some cyanobacteria, including Candidatus Gloeomargarita lithophora, which was isolated from Lake Alchichica (Mexico), can form intracellular carbonates. This contradicts the common paradigm that cyanobacterial calcification is always extracellular and suggests that calcification might be controlled by these cyanobacterial species. Intracellular carbonates have several peculiar characteristics: they are relatively small (between 60 and 500 nm), they are poorly crystalline, and they have Sr/Ca and Ba/Ca ratios much higher than the solution in which the cells grow. It is therefore crucial to understand whether these unique features may indicate the involvement of specific biological processes. Here, in vitro abiotic syntheses were performed to synthesize Mg-, Ca-, Sr- and Ba-containing carbonates with compositions, crystallinities and sizes close to those observed in intracellularly calcifying cyanobacteria. Precipitates were characterized by scanning and transmission electron microscopies coupled with energy dispersive X-ray spectroscopy, thermogravimetric analysis and X-ray diffraction. The size and the poor crystallinity of cyanobacterial intracellular carbonates could be mimicked under these abiotic conditions. It was shown that similarly to Mg, elements such as Sr and Ba can favor stabilization of poorly crystalline carbonates. In contrast, the differential partitioning of Sr, Ba and Ca between the solution and the solids as observed in cyanobacteria could not be mimicked in vitro. This provides keys to a better understanding of biological processes involved in the formation of intracellular carbonates by some cyanobacteria, including the involvement of membrane transporters.

  4. Mechanochemical synthesis, structure, and properties of solid solutions of alkaline earth metal fluorides: Ma1-xMbxF2 (M: Ca, Sr, Ba)

    NASA Astrophysics Data System (ADS)

    Heise, M.; Scholz, G.; Düvel, A.; Heitjans, P.; Kemnitz, E.

    2016-10-01

    The capability of mechanochemical synthesis for the formation of solid solutions of alkaline earth metal fluorides Ma1-xMbxF2 (M: Ca, Sr, Ba) was tested by fluorination of metal acetates and metal hydroxides with ammonium fluoride directly at milling. Evidence was found for a mutual substitution of cations on their lattice positions in Ca1-xSrxF2 and Ba1-xSrxF2 samples. For the Ba/Ca-system this synthesis route is only partially successful. X-ray diffraction and 19F MAS NMR spectroscopy were used to characterize all samples concerning their crystal structure and local fluorine coordination. Calculations of 19F chemical shifts with the superposition model along with probability calculations for the intensity of the individual 19F lines, performed in dependence on the molar composition of the samples, perfectly agree with the experimental findings. The fluoride ion conductivity of as-prepared samples, determined by temperature dependent DC conductivity measurements, is significantly higher than those of crystalline binary fluorides. Moreover, a higher F- ion conductivity is observed for samples with higher mixing grade in the Ca/Sr-and the Ba/Sr-systems.

  5. Single Phase Melt Processed Powellite (Ba,Ca) MoO{sub 4} For The Immobilization Of Mo-Rich Nuclear Waste

    SciTech Connect

    Brinkman, Kyle; Marra, James; Fox, Kevin; Reppert, Jason; Crum, Jarrod; Tang, Ming

    2012-09-17

    Crystalline and glass composite materials are currently being investigated for the immobilization of combined High Level Waste (HLW) streams resulting from potential commercial fuel reprocessing scenarios. Several of these potential waste streams contain elevated levels of transition metal elements such as molybdenum (Mo). Molybdenum has limited solubility in typical silicate glasses used for nuclear waste immobilization. Under certain chemical and controlled cooling conditions, a powellite (Ba,Ca)MoO{sub 4} crystalline structure can be formed by reaction with alkaline earth elements. In this study, single phase BaMoO{sub 4} and CaMoO{sub 4} were formed from carbonate and oxide precursors demonstrating the viability of Mo incorporation into glass, crystalline or glass composite materials by a melt and crystallization process. X-ray diffraction, photoluminescence, and Raman spectroscopy indicated a long range ordered crystalline structure. In-situ electron irradiation studies indicated that both CaMoO{sub 4} and BaMoO{sub 4} powellite phases exhibit radiation stability up to 1000 years at anticipated doses with a crystalline to amorphous transition observed after 1 X 10{sup 13} Gy. Aqueous durability determined from product consistency tests (PCT) showed low normalized release rates for Ba, Ca, and Mo (<0.05 g/m{sup 2}).

  6. Thermal stability of the luminescence of Ca6Ba(PO4)4O:Eu2+ yellow phosphor for white light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Meng, Yingjun; Zhao, Weiren; Chen, Junhua; Wang, Nenghuo; Zhou, Yiyang; Zhang, Wei; Yi, Shuangping

    2016-07-01

    Yellow-emitting Ca6Ba(PO4)4O:Eu2+ phosphors were synthesized by solid-state reaction method. The phase composition was checked by X-ray powder diffraction. The photoluminescence properties of Ca6Ba(PO4)4O:Eu2+ and their thermal properties of photoluminescence were explored. The excitation spectra ranging from 230 to 450 nm and an intense broad yellow emission band centered at 530 nm can be observed under the excitation at 375 nm. Ca6Ba(PO4)4O:0.07Eu2+ phosphor maintains 45 % of the photoluminescence intensity of room temperature when heated up to 150 °C, exhibiting a relatively good thermal quenching resistance. The optimum concentration of Eu2+ in Ca6- x Ba(PO4)4O: xEu2+ was found with x = 0.07, and the concentration quenching mechanism was illustrated by configurational coordinate diagram. The luminescence decay of Eu2+ ions was also studied carefully, showing the decrease of the lifetime with the increase of Eu2+ concentration.

  7. Single phase melt processed powellite (Ba,Ca)MoO4 for the immobilization of Mo-rich nuclear waste

    SciTech Connect

    Brinkman, Kyle; Fox, Kevin M.; Marra, James C.; Reppert, Jason; Crum, Jarrod V.; Tang, Ming

    2012-10-02

    Crystalline and glass composite materials are currently being investigated for the immobilization of combined High Level Waste (HLW) streams resulting from potential commercial fuel reprocessing scenarios. Several of these potential waste streams contain elevated levels of transition metal elements such as molybdenum (Mo). Molybdenum has limited solubility in typical silicate glasses used for nuclear waste immobilization. Under certain chemical and controlled cooling conditions, a powellite (Ba,Ca)MoO4 crystalline structure can be formed by reaction with alkaline earth elements. In this study, single phase BaMoO4 and CaMoO4 were formed from carbonate and oxide precursors demonstrating the viability of Mo incorporation into glass, crystalline or glass composite materials by a melt and crystallization process. X-ray diffraction, photoluminescence, and Raman spectroscopy indicated a long range ordered crystalline structure. In situ electron irradiation studies indicated that both CaMoO4 and BaMoO4 powellite phases exhibit radiation stability up to 1000 years at anticipated doses with a crystalline to amorphous transition observed after 1 x 1013 Gy. Aqueous durability determined from product consistency tests (PCT) showed low normalized release rates for Ba, Ca, and Mo (<0.05 g/m2).

  8. Metal-semiconductor-transition observed in Bi{sub 2}Ca(Sr, Ba){sub 2}Co{sub 2}O{sub 8+δ} single crystals

    SciTech Connect

    Dong, Song-Tao; Zhang, Bin-Bin; Zhang, Lun-Yong; Yao, Shu-Hua E-mail: shyao@nju.edu.cn; Zhou, Jian; Zhang, Shan-Tao; Gu, Zheng-Bin; Chen, Yan-Feng; Chen, Y. B. E-mail: shyao@nju.edu.cn

    2014-07-28

    Electrical property evolution of Bi{sub 2}AE{sub 2}Co{sub 2}O{sub 8+δ} single crystals (AE = Ca, Sr and Ba) is systematically explored. When AE changes from Ca to Ba, the electrical property of Bi{sub 2}Ca{sub 2}Co{sub 2}O{sub 8+δ} and Bi{sub 2}Sr{sub 2}Co{sub 2}O{sub 8+δ} demonstrates semiconductor-like properties. But Bi{sub 2}Ba{sub 2}Co{sub 2}O{sub 8+δ} shows the metallic behavior. Analysis of temperature-dependent resistance substantiates that from metallic Bi{sub 2}Ba{sub 2}Co{sub 2}O{sub 8+δ} to semiconductor-like Bi{sub 2}Sr{sub 2}Co{sub 2}O{sub 8+δ} can be attributed to Anderson localization. However the semiconductor behaviour of Bi{sub 2}Sr{sub 2}Co{sub 2}O{sub 8+δ} and Bi{sub 2}Ca{sub 2}Co{sub 2}O{sub 8+δ} is related to electronic correlations effect that is inferred by large negative magnetoresistance (∼70%). The theoretical electronic structures and valence X-ray photoemission spectroscopy substantiate that there is a relative large density of state around Fermi level in Bi{sub 2}Ba{sub 2}Co{sub 2}O{sub 8+δ} compared with other two compounds. It suggests that Bi{sub 2}Ba{sub 2}Co{sub 2}O{sub 8+δ} is more apt to be metal in this material system.

  9. Formation Mechanism of CaS-Bearing Inclusions and the Rolling Deformation in Al-Killed, Low-Alloy Steel with Ca Treatment

    NASA Astrophysics Data System (ADS)

    Xu, Guang; Jiang, Zhouhua; Li, Yang

    2016-08-01

    The existing form of CaS inclusion in Ca-treated, Al-killed steel during secondary refining process was investigated with scanning electron microscopy and an energy-dispersive spectrometer (EDS). The results of 12 heats industrial tests showed that CaS has two kinds of precipitation forms. One form takes place by the direct reaction of Ca and S, and the other takes place by the reaction of CaO in calcium aluminates with dissolved Al and S in liquid steel. Thermodynamic research for different precipitation modes of CaS under different temperature was carried out. In particular, CaO-Al2O3-CaS isothermal section diagrams and component activities of calcium aluminates were calculated by the thermodynamic software FactSage. By thermodynamic calculation, a precipitation-area diagram of oxide-sulfide duplex inclusion was established by fixing the sulfur content. The quantity of CaS, which was precipitated in a reaction between [Al], [S] and (CaO), can be calculated and predicted based on the precipitation-area diagram of oxide-sulfide duplex inclusion. Electron probe microanalysis and EDS were used for observing rolling deformation of different types of CaS-bearing inclusions during the rolling process. Low modification of calcium aluminates wrapped by CaS has different degrees of harm to steel in the rolling process. A thick CaS layer can prevent some fragile calcium aluminates from being crushed during the rolling process. Some oxide-sulfide duplex inclusion contains little CaS performed better deformation during the rolling process, but when CaS in oxide-sulfide duplex inclusion becomes more, it will cause the whole inclusion to lose plastic yielding ability. The plastic deformation region of CaS-bearing inclusion in a CaO-Al2O3-CaS isothermal section diagram is confirmed.

  10. Photoluminescence properties of AlN-doped BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphors

    SciTech Connect

    Wang, Yong; Tang, Jianfeng; Ouyang, Xicheng; Liu, Buqiong; Lin, Rong Han

    2013-06-01

    Highlights: ► Ideal hexagonal shape particle size in 5 μm and 2.5–3 μm in thickness are obtained. ► The growth mechanism is studied by a computer simulation. ► The influence of introduced AlN on the sites of Eu{sup 2+} and photoluminescence properties was investigated. - Abstract: The AlN-doped BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphors were synthesized by conventional solid-state reaction. Powder X-ray diffraction (XRD), scanning electron microscope (SEM) and photoluminescence spectrum (PL) were used for characterization. The growth mechanism was carried out by computer simulation with CASTEP application, and revealed that an ideal hexagonal shape, particle size in 5 μm and 2.5–3 μm in thickness, could be obtained by AlN doping. Additionally, due to the low electronegativity of N{sup 3−}, the AlN-doped sample showed 35% increase in PL intensity and improvement of thermal stability. These fine particle size and better photoluminescence properties are expected to be applicable to industrial production of BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphors.

  11. Coexisting charge and magnetic orders in the dimer-chain iridate Ba5AlIr2O11

    DOE PAGES

    Terzic, J.; Wang, J. C.; Ye, Feng; Song, W. H.; Yuan, S. J.; Aswartham, S.; DeLong, L. E.; Streltsov, S. V.; Khomskii, Daniel I.; Cao, G.

    2015-06-29

    In this paper, we have synthesized and studied single-crystal Ba5AlIr2O11 that features dimer chains of two inequivalent octahedra occupied by tetravalent Ir4+(5d5) and pentavalent Ir5+(5d4) ions, respectively. Ba5AlIr2O11 is a Mott insulator that undergoes a subtle structural phase transition near TS=210K and a magnetic transition at TM=4.5K; the latter transition is surprisingly resistant to applied magnetic fields μoH≤12T but more sensitive to modest applied pressure (dTM/dp ≈ +0.61K/GPa). All results indicate that the phase transition at TS signals an enhanced charge order that induces electrical dipoles and strong dielectric response near TS. It is clear that the strong covalency andmore » spin-orbit interaction (SOI) suppress double exchange in Ir dimers and stabilize a novel magnetic state that is neither S=3/2 nor J=1/2, but rather lies in an “intermediate” regime between these two states. Finally, the novel behavior of Ba5AlIr2O11 therefore provides unique insights into the physics of SOI along with strong covalency in competition with double-exchange interactions of comparable strength.« less

  12. Chemical spray pyrolysis of Tl-Ba-Ca-Cu-O high-T(sub c) superconductors for high-field bitter magnets

    NASA Technical Reports Server (NTRS)

    Derochemont, L. Pierre; Zhang, John G.; Squillante, Michael R.; Hermann, A. M.; Duan, H. M.; Andrews, Robert J.; Kelliher, Warren C.

    1991-01-01

    The deposition of Tl-Ba-Ca-Cu-O thick films by spray pyrolyzing a Ba-Ca-Cu-O precursor film and diffusing thallium into the film to form the superconducting phase is examined. This approach was taken to reduce exposure to thallium and its health and safety hazards. The Tl-Ba-Ca-Cu-O system was selected because it has very attractive features which make it appealing to device and manufacturing engineering. Tl-Ba-Ca-Cu-O will accommodate a number of superconducting phases. This attribute makes it very forgiving to stoichiometric fluctuations in the bulk and film. It has excellent thermal and chemical stability, and appears to be relatively insensitive to chemical impurities. Oxygen is tightly bound into the systems, consequently there is no orthorhombic (conductor) to tetragonal (insulator) transition which would affect a component's lifetime. More significantly, the thallium based superconductors appear to have harder magnetic properties than the other high-Tc oxide ceramics. Estimates using magnetoresistance measurements indicate that at 77 K Tl2Ba2CaCu2O10 will have an upper critical field, H(sub c2) fo 26 Tesla for applied fields parallel to the c-axis and approximately 1000 Tesla for fields oriented in the a-b plane. Results to date have shown that superconducting films can be reproducibly deposited on 100 oriented MgO substrates. One film had a zero resistance temperature of 111.5 K. Furthermore, x ray diffraction analysis of the films showed preferential c-axis orientation parallel to the plane of the substrate. These results have now made it possible to consider the manufacture of a superconducting tape wire which can be configured into a topology useful for high-field magnet designs. The research which leads to the preparation of these films and plans for further development are reviewed.

  13. Effect of NiCr Clad BaF2·CaF2 Addition on Wear Performance of Plasma Sprayed Chromium Carbide-Nichrome Coating

    NASA Astrophysics Data System (ADS)

    Du, Lingzhong; Huang, Chuanbing; Zhang, Weigang; Zhang, Jingmin; Liu, Wei

    2010-03-01

    NiCr clad BaF2·CaF2 fluoride eutectic powders were added into chromium carbide-nichrome feedstock to improve the tribological properties of NiCr-Cr3C2 coating, and the structures, mechanical, and ball-on-disk sliding wear performance of the coating were characterized. The results show that NiCr cladding can effectively decrease the density and thermophysical difference between the feedstock components, while alleviate the decarburization and oxidization of the constituent phases, and form the coating with a uniform and dense microstructure. However, the addition of BaF2·CaF2 has a negative effect on mechanical properties of the coating. When the temperature reaches 500 °C, the BaF2·CaF2 eutectic is soften by the heat and smeared by the counterpart, thus the low shear stress lubricating film forms between the contact surface, that improves the tribological properties dramatically. At this temperature, the dominant wear mechanisms also change from splats spallation and abrasive wear at room temperature to plastic deformation and plawing by the counterpart. Within the temperature range from 600 to 800 °C, the friction coefficient, the wear rates of NiCr/Cr3C2-10% BaF2·CaF2 coating and its coupled Si3N4 ball are 20%, 40%, and 75% lower than those of the NiCr/Cr3C2 coating, respectively. The NiCr/Cr3C2-BaF2·CaF2 coating shows superior wear performance to the NiCr/Cr3C2 coating without lubricant additive.

  14. Synthesis, characterization and optical properties of ATiO{sub 3}–Pr thin films prepared by a photochemical method (where A = Ba and Ca)

    SciTech Connect

    Cabello, G.; Lillo, L.; Caro, C.; Seguel, M.; Buono-Core, G.E.; Huentupil, Y.; Chornik, B.; Carrasco, C.; Rodríguez, C.A.

    2015-10-15

    Highlights: • A method of photochemical deposition has been used to the preparation of (Ba,Ca)TiO{sub 3} thin films doped Pr(III). • The (Ba,Ca)TiO{sub 3}/Pr(III) films under 375 nm excitation shows emissions attributable to {sup 1}D{sub 2} → {sup 3}H{sub 4} transition of Pr ion. • These PL signals decreased above 10 mol% of Pr(III). • Analysis suggests the presence of intermediate energy levels in the band gap influences in the PL processes. - Abstract: This article reports the characterization and optical properties of (Ba,Ca)TiO{sub 3} thin films doped with Pr at different proportions (0–15 mol%). The films were deposited on Si (1 0 0) and quartz substrates using a photochemical method and post-annealed at 900 °C. The evaluation of photo-reactivity of the precursor complexes was monitored by UV–vis and FT-IR spectroscopy. The obtained films were characterized by X-ray diffraction and X-ray photoelectron spectroscopy. The results indicate that Ba, Ca, Ti, O and Pr are present in the form of perovskite. Under UV light excitation (375 nm) the (Ba,Ca)TiO{sub 3}–Pr films show the characteristic emissions ascribed to {sup 1}D{sub 2} → {sup 3}H{sub 4} transition of Pr{sup 3+} ion. The optical measurements show the presence of intermediate energy levels in the band gap which influence the emission processes.

  15. Pedogeochemical mapping of Al, Ba, Pb, Ti and V in soils of the Barcelona Province (Catalonia, NE Spain): relationships with soil physico-chemical properties.

    NASA Astrophysics Data System (ADS)

    Bech, J.; Reverter, F.; Tume, P.; Sokolowska, M.; Sanchez, P.; Longan, L.; Bech, J.; Zhiyanski, M.; Lansac, A.; Oliver, M. T.

    2009-04-01

    Pedogeochemical mapping is a useful tool for estimating the local background of potentially toxic elements (PTE), wich is essential for environmental regulation. The aim of this study is to estimate the levels and distribution of Al, Ba, Pb, Ti and V in surface soils of the Barcelona province (Catalonia, NE Spain) and their relationships with administrative-geographic districts, texture, pH, organic carbon and CaCO3. The studied region has a surface area of 7731 Km2. The geology is varied: granites and Paleozoic shales predominate in SE-E. and Mesozoic and Cenozoic limestones, dolomites, marlstones, gypsum and sandstones in the remainder of the studied area. 319 top soil samples (0-20 cm) were collected at 5 km intervals on a regular grid, dried and sieved (2mm). General soil properties were analysed by standard methods. Aqua regia digests (DIN 38414-S7) of Al, Ba, Pb, Ti and V were determined by Inductively Coupled Plasma Spectrometry. Statistical data treatment was carried out using SPSS 12.0 and Statgraphics Plus 5.1. We applied Exploratory Data Analysis (EDA) techniques to statistically describe the data. The software used for mapping was ESRI's Arc Wiew 9.0, Desktop version. Analytical data is represented using growing dot maps. The values of every mapped variable were grouped into a few cartographic classes in order to produce limited legends. The limits for the cartographic classes were chosen by the percentile method (5th, 25th, 50th, 75th, 90th, and 98th). Some results are: Al mg kg-1min 4410.0, max 194786.0, mean 18145.6, sd 12112.1, med 16273.3 ; Ba mgkg-1min 7.32, max 1709.0, mean 128.4, sd 149.2, med 91.7; Pb mg kg-1min 2.76, max 485.7, mean 52.2, sd 46.3, med 46.0; Ti mg kg-1min 11.6, max 3540.0, mean 268.0, sd 421.6, med 132.2, and V mg kg-1min 2.15, max 289.2, mean 31.4, sd 25.7, med 26.0. . The highest mean value of Ba (328mkg-1), Pb (139.6 mgkg-1) and V (54.7 mgkg-1) corresponds to the Barcelonés district with mainly urban soils. The Al contents

  16. Revised structural phase diagram of (Ba{sub 0.7}Ca{sub 0.3}TiO{sub 3})-(BaZr{sub 0.2}Ti{sub 0.8}O{sub 3})

    SciTech Connect

    Keeble, Dean S.; Thomas, Pam A.; Benabdallah, Feres; Maglione, Mario; Kreisel, Jens

    2013-03-04

    The temperature-composition phase diagram of barium calcium titanate zirconate (x(Ba{sub 0.7}Ca{sub 0.3}TiO{sub 3})-(1 - x)(BaZr{sub 0.2}Ti{sub 0.8}O{sub 3}); BCTZ) has been reinvestigated using high-resolution synchrotron x-ray powder diffraction. Contrary to previous reports of an unusual rhombohedral-tetragonal phase transition in this system, we have observed an intermediate orthorhombic phase, isostructural to that present in the parent phase, BaTiO{sub 3}, and we identify the previously assigned T-R transition as a T-O transition. We also observe the O-R transition coalescing with the previously observed triple point, forming a phase convergence region. The implication of the orthorhombic phase in reconciling the exceptional piezoelectric properties with the surrounding phase diagram is discussed.

  17. Structural, dielectric and electrocaloric properties in lead-free Zr-doped Ba0.8Ca0.2TiO3 solid solution

    NASA Astrophysics Data System (ADS)

    Asbani, B.; Gagou, Y.; Dellis, J.-L.; Lahmar, A.; Amjoud, M.; Mezzane, D.; Kutnjak, Z.; El Marssi, M.

    2016-07-01

    We investigate in the present work the additional data points (x=0.02, 0.06 and 0.08) to the previous reported paper (Asbani et al., 2015) [21] that sufficiently enrich to understand the EC properties and underlying phase diagram of the lead-free Ba0.8Ca0.2Ti(1-x)ZrxO3 (xBCTZ) system. X-ray diffraction analysis performed at room temperature, confirms a continuous tetragonal solid solution with P4mm (No. 99) space group that evolved to pseudo-cubic symmetry for the high Zr-content compounds. Ferroelectric and paraelectric behaviors were highlighted using P-E hysteresis data versus temperature. Phase transition was confirmed by dielectric permittivity measurements versus temperature showing a decrease of the Curie temperature when Zr-content increases. From P-E hysteresis recording the electrocaloric temperature change (ΔT) was calculated that ranged in between 0.12 and 0.27 K and the electrocaloric responsivity (ξ) in 0.15 to 0.34×10-6 K·m/V under 7.95 kV/cm applied electric field. The zero-field entropy is compared to electrocaloric isothermal entropy to estimate the extent the EC is being under-driven.

  18. Temperature variation of the size effect in dilute AlMg and AlCa alloys: Measurement and theory

    NASA Astrophysics Data System (ADS)

    Gilder, H. M.; Asty, M.; Audit, Ph.

    1980-12-01

    Optical-interferometric-differential-length and x-ray lattice-parameter measurements performed at low temperatures in dilute AlMg and AlCa alloys indicate that the temperature variation of the size effect corresponds to a relatively large difference between the intrinsic coefficient of thermal expansion βi of the solute atom structure and that, β, of the solvent. This result is another example of the surprising expansive properties of point defects previously described by Gilder and co-workers (high-temperature vacancy diffusion) and more recently by Ganne (low-temperature dilatometry on irradiated specimens). Specifically, in the temperature range 0.2Ca)β~-4. This, as well as the fact that the sign of the change in the coefficient of thermal expansion Δβ of the host metal caused by the introduction of the solute atom is positive for Mg and negative for Ca, indicates that solute-solvent valence effects play a minor role in determining the coefficient of thermal expansion of the dilute alloy. It is also found, to within the experimental precision, that Δβ(Mg) and Δβ(Ca) are temperature independent, suggesting a type of Matthiessen's rule for thermal expansion. A model calculation of the size effect and its temperature variation in the infinitely dilute alloy is presented. The volume-dependent forces are treated by means of a term describing the elastic energy associated with the solute-solvent volume misfit, whereas the temperature-dependent potential of Dagens et al. is used to calculate the pairwise interaction between the solvent ions and the solute ion. Good agreement with the experimental data is obtained for the size effect in both AlMg and AlCa. The calculated values of Δβ(Mg)Ci, Ci being the solute concentration, and βi(Mg) fall between the measured values in the two AlMg alloys studied. The calculation of Δβ(Ca)Ci and βi(Ca) is not possible due to a lack of elastic-constants data for pure, metallic

  19. Concentrations and ratios of Sr, Ba and Ca along an estuarine river to the Gulf of Mexico - implication for sea level rise effects on trace metal distribution

    NASA Astrophysics Data System (ADS)

    He, S.; Xu, Y. J.

    2015-11-01

    Strontium and barium to calcium ratios are often used as proxies for tracking animal movement across salinity gradients. As sea level rise continues, many estuarine rivers in the world face saltwater intrusion, which may cause changes in mobility and distribution of these metals upstream. Despite intensive research on metal adsorption and desorption in marine systems, knowledge of the spatiotemporal distribution of these elements along estuarine rivers is still limited. In this study, we conducted an intensive monitoring of Sr and Ba dynamics along an 88 km long estuary, the Calcasieu River in South Louisiana, USA, which has been strongly affected by saltwater intrusion. Over the period from May 2013 to August 2015, we collected monthly water samples and performed in-situ water quality measurements at six sites from the upstream to the river mouth, with a salinity range from 0.02 to 29.50 ppt. Water samples were analyzed for Sr, Ba, and Ca concentrations. In-situ measurements were made on salinity, pH, water temperature, dissolved oxygen concentration, and specific conductance. We found that the Sr and Ca concentrations and the Sr / Ca ratio all increased significantly with increasing salinity. The average Sr concentration at the site closest to the Gulf of Mexico (site 6) was 46.21 μmol L-1, which was about 130 times higher than that of the site furthest upstream (site 1, 0.35 μmol L-1). The average Ca concentration at site 6 was 8.19 mmol L-1, which was about 60 times higher than that of site 1 (0.13 mmol L-1). The average Sr / Ca ratio at site 6 (8.41 mmol mol-1) was about 3 times the average Sr / Ca ratio at site 1 (2.89 mmol mol-1). However, the spatial variation in Ba concentration was marginal, varying from 0.36 μmol L-1 at site 6 to 0.47 at site 5. The average Ba / Ca ratio at site 1 (4.82 mmol mol-1) was about 54 times the average Ba / Ca ratio at site 6 (0.09 mmol mol-1), showing a clear negative relation between the Ba / Ca ratio and increasing

  20. First-Principles Studies of Pressure-Induced Structural and Insulator-To Transitions in Alkaline-Earth Dicarbides MC2 (M = Ca, Sr and Ba)

    NASA Astrophysics Data System (ADS)

    Jiang, Li-Na

    2013-12-01

    Pressure-induced phase transitions in MC2 (M = Ca, Sr and Ba) are investigated by using the first-principles plane wave pseudopotential method within the generalized gradient approximation. The first-order phase transition from tetragonal phase (CaC2-type, space group I4/mmm) to rhombohedral (CsCl-type, space group R/line{3}m) structure is predicted to occur at 22.2, 10.0 and 3.6 GPa, respectively, and transition pressure point of BaC2 agrees well with recent theoretical works. Based on the electronic analysis, the ionic Ca-C bond character becomes stronger with increasing pressure in both I4/mmm and R/line{3}m phases. In particular, there will occur a transition from insulator to metal with increasing pressure due to the reason that the calculated band gap gets narrower and finally closes at some high pressure.

  1. First principles study of magnetoelectric coupling in Co2FeAl/BaTiO3 tunnel junctions.

    PubMed

    Yu, Li; Gao, Guoying; Zhu, Lin; Deng, Lei; Yang, Zhizong; Yao, Kailun

    2015-06-14

    Critical thickness for ferroelectricity and the magnetoelectric effect of Co2FeAl/BaTiO3 multiferroic tunnel junctions (MFTJs) are investigated using first-principles calculations. The ferroelectric polarization of the barriers can be maintained upto a critical thickness of 1.7 nm for both the Co2/TiO2 and FeAl/TiO2 interfaces. The magnetoelectric effect is derived from the difference in the magnetic moments on interfacial atoms, which is sensitive to the reversal of electric polarization. The magnetoelectric coupling is found to be dependent on the interfacial electronic hybridizations. Compared with the Co2/TiO2 interface, more net magnetization change is achieved at the FeAl/TiO2 interface. In addition, the in-plane strain effect shows that in-plane compressive strain can lead to the enhancement of ferroelectric polarization stability and intensity of magnetoelectric coupling. These findings suggest that Co2FeAl/BaTiO3 MFTJs could be utilized in the area of electrically controlled magnetism, especially the MFTJ with loaded in-plane compressive strain with the FeAl/TiO2 interface. PMID:25987345

  2. Mössbauer spectroscopy study of Al distribution in BaAl{sub x}Fe{sub 12−x}O{sub 19} thin films

    SciTech Connect

    Przybylski, M. Żukrowski, J.; Harward, I.; Celiński, Z.

    2015-05-07

    Barium hexagonal ferrite (BaM) films grown on Si are a good candidate material for new-generations of on-wafer microwave devices operating at frequencies above 40 GHz. Doping BaM with Al increases the value of anisotropy field even more, and in combination with a large value of remanence, would allow one to create a self-biasing material/structure that would eliminate the need for permanent bias magnets in millimeter wave devices. To examine the occupation of Fe sublattices by Al ions, we carried out Conversion Electron Mössbauer Spectroscopy (CEMS) measurements at room temperature and zero magnetic field (after magnetizing the samples in a strong magnetic field). The spectra can be reasonably fitted with three components (sub-spectra) corresponding to different Fe sublattices. There are significant changes in the spectra with the addition of Al: The magnetic hyperfine field decreases for all three components, and their relative contributions also change remarkably. These observations are in agreement with the fact that the Al substitutes Fe, thus lowering the component contributions and the value of the hyperfine field. In addition, our previous XRD analysis indicates increasing grain misalignment with Al content, further supporting the CEMS data.

  3. Crystal Growth and Photoluminescence Properties of Truncated Cubic BaMgAl10O17:Eu2+ Phosphors for Three-Dimensional Plasma Display Panels.

    PubMed

    Liu, Bitao; Chen, Yuan; Peng, Lingling; Han, Tao; Yu, Hong; Tian, Liangliang; Tu, Mingjing

    2016-04-01

    Monodispersed, truncated cube BaMgAl10O17:Eu2+ phosphors were synthesized by the sol-gel process. Scanning electron microscope (SEM), photoluminescence spectrum, powder X-ray diffraction and decay curves were used to evaluate the truncated cubic BaMgAl10O17:Eu2+ phosphors. The crystal growth process and photoluminescence properties were discussed in detail. The results showed that this truncated cubic morphology can be achieved via a simple sinter process. These truncated cubic BaMgAl10O17:Eu2+ phosphors showed acceptable emission intensity and better thermal properties. This result indicates truncated cubic BaMgAl10O17:Eu2+ phosphors would meet the requirements of plasma display panels (PDPs). PMID:27451727

  4. Ca and In co-doped BaFeO3-δ as a cobalt-free cathode material for intermediate-temperature solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Wang, Jian; Lam, Kwun Yu; Saccoccio, Mattia; Gao, Yang; Chen, Dengjie; Ciucci, Francesco

    2016-08-01

    We report Ba0·95Ca0·05Fe0·95In0·05O3-δ (BCFI), a novel cobalt-free perovskite, as a promising cathode material for intermediate-temperature solid oxide fuel cells (IT-SOFCs). We synthesize this new material, and systematically characterize its lattice structure, thermal stability, chemical composition, electrical conductivity, and oxygen reduction reaction (ORR) activity. The cubic phase of BaFeO3-δ is stabilized by light isovalent and lower-valence substitution, i.e., 5% Ca2+ in the Ba2+ site and 5% In3+ in the Fe3+/Fe4+ site, in contrast with the typical approach of substituting elements of higher valence. Without resorting to co-doping strategy, the phase of BaFe0·95In0·05O3-δ (BFI) is rhombohedral, while Ba0·95Ca0·05FeO3-δ (BCF) is a mixture of the cubic phase together with BaFe2O4 impurities. The structure of BCFI is cubic from room temperature up to 900 °C with a moderate thermal expansion coefficient of 23.2 × 10-6 K-1. Thanks to the large oxygen vacancy concentration and fast oxygen mobility, BCFI exhibits a favorable ORR activity, i.e., we observe a polarization resistance as small as 0.038 Ω cm2 at 700 °C. The significantly enhanced performance, compared with BFI and BCF, is attributed to the presence of the cubic phase and the large oxygen vacancies brought by the isovalent substitution in the A-site and lower-valence doping in the B-site.

  5. Ca and In co-doped BaFeO3-δ as a cobalt-free cathode material for intermediate-temperature solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Wang, Jian; Lam, Kwun Yu; Saccoccio, Mattia; Gao, Yang; Chen, Dengjie; Ciucci, Francesco

    2016-08-01

    We report Ba0·95Ca0·05Fe0·95In0·05O3-δ (BCFI), a novel cobalt-free perovskite, as a promising cathode material for intermediate-temperature solid oxide fuel cells (IT-SOFCs). We synthesize this new material, and systematically characterize its lattice structure, thermal stability, chemical composition, electrical conductivity, and oxygen reduction reaction (ORR) activity. The cubic phase of BaFeO3-δ is stabilized by light isovalent and lower-valence substitution, i.e., 5% Ca2+ in the Ba2+ site and 5% In3+ in the Fe3+/Fe4+ site, in contrast with the typical approach of substituting elements of higher valence. Without resorting to co-doping strategy, the phase of BaFe0·95In0·05O3-δ (BFI) is rhombohedral, while Ba0·95Ca0·05FeO3-δ (BCF) is a mixture of the cubic phase together with BaFe2O4 impurities. The structure of BCFI is cubic from room temperature up to 900 °C with a moderate thermal expansion coefficient of 23.2 × 10-6 K-1. Thanks to the large oxygen vacancy concentration and fast oxygen mobility, BCFI exhibits a favorable ORR activity, i.e., we observe a polarization resistance as small as 0.038 Ω cm2 at 700 °C. The significantly enhanced performance, compared with BFI and BCF, is attributed to the presence of the cubic phase and the large oxygen vacancies brought by the isovalent substitution in the A-site and lower-valence doping in the B-site.

  6. Microstructural characterization of Ag-sheathed Tl-Ba-Ca-Cu-O and Bi-Sr-Ca-Cu-O superconducting tapes by analytical electron microscopy

    SciTech Connect

    Hu, J.G.; Miller, D.J.; Goretta, K.C.; Poeppel, R.B.

    1992-09-01

    The microstructures of Tl(1223) and Pb-doped Bi(2223) silver tapes produced by the powder-in-tube (PM) method have been examined by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and energy dispersive spectrometry (EDS). The Tl tapes annealed below the melting point exhibited fine grains and a high density of pores while tapes subjected to partial melting prior to solid state annealing were fully dense with large grains. However, these tapes also showed an increase in the size and density of impurity particles, particularly CaO and a Ba-Cu rich phase. Silver powders added to the precursors tended to promote the growth of Tl(1223) at lower temperatures but also interfered with the development of texture by providing nucleation sites of random orientations. In contrast, the Bi(2223) tape exhibited a high degree of texture and alignment. The incorporation of silver within the superconducting phase was found to be negligible for both the Tl(1223) and Bi(2223) tapes.

  7. Microwave Dielectric Properties for Ba(Mg1/3Ta2/3)O3 A(Mg1/2W1/2)O3 (A=Ba, Sr, and Ca) Ceramics

    NASA Astrophysics Data System (ADS)

    Furuya, Mitsuru; Ochi, Atsushi

    1994-09-01

    For a high-Q dielectric resonator at microwave frequencies, complex perovskite-structured Ba(Mg1/3Ta2/3)O3 A(Mg1/2W1/2)O3 (A=Ba, Sr, and Ca) ceramics have been developed. A(Mg1/2W1/2)O3 effects on the crystal structure, microstructure, and microwave characteristic of Ba(Mg1/3Ta2/3)O3 (BMT) were investigated. Ba(Mg1/2W1/2)O3 (BMW) decreased the temperature coefficient of resonant frequency ( TCF) for BMT. Sr(Mg1/2W1/2)O3 (SMW) and Ca(Mg1/2W1/2)O3 (CMW) increased it. Zero TCF was obtained for the BMT/BMW=95/5 composition. With 0.5 mol% BMW content, dielectric loss quality, Q d, reached a maximum (40000 at 10 GHz).

  8. Synthesis and Microwave Dielectric Properties of A16V18O61 (A = Ba, Sr and Ca) Ceramics for LTCC Applications

    NASA Astrophysics Data System (ADS)

    Suresh, E. K.; Prasad, K.; Arun, N. S.; Ratheesh, R.

    2016-06-01

    Low-temperature co-firable A16V18O61 (A = Ba, Sr, Ca) ceramics have been prepared through the solid state ceramic route. The structural features of these ceramics have been studied using the x-ray diffraction (XRD) technique. The existence of the A16V18O61 (A = Ba, Sr, Ca) ceramic phase was confirmed through laser Raman spectroscopic studies. Scanning electron microscopy analysis revealed a dense microstructure for the ceramics with closely packed polygonal grains. Among the samples studied, Ba16V18O61 ceramic was prepared in the ultralow sintering temperature of 620°C for 1 h, which can be co-firable with an aluminium electrode. XRD and electron dispersive spectroscopy analyses showed that the samples under study have excellent compatibility with metal electrodes. The microwave dielectric properties measured using a vector network analyzer revealed that A16V18O61 (A = Ba, Sr, Ca) ceramics have excellent unloaded quality factors.

  9. Effect of Ca addition on the corrosion behavior of Mg-Al-Mn alloy

    NASA Astrophysics Data System (ADS)

    Yang, Jiang; Peng, Jian; Nyberg, Eric A.; Pan, Fu-sheng

    2016-04-01

    The microstructures and corrosion resistance of magnesium-5 wt% aluminum-0.3 wt% manganese alloys (Mg-Al-Mn) with different Ca additions (0.2-4 wt%) were investigated. Results showed that with increasing Ca addition, the grain of the alloys became more refined, whereas the corrosion resistant ability of the alloys initially increased and then decreased. The alloy with 2 wt% Ca addition exhibited the best corrosion resistance, attributed to the effect of the oxide film and (Mg,Al)2Ca phases which were discontinuously distributed on the grain boundaries. These phases acted as micro-victims, they preferentially corroded to protect the α-Mg matrix. The oxide film formed on the alloy surface can hinder the solution further to protect the α-Mg matrix.

  10. Preparation and Electrochemical Characterization of Aluminium Liquid Battery Cells With Two Different Electrolytes (NaCl-BaCl2-AlF3-NaF and LiF-AlF3-BaF2).

    PubMed

    Napast, Viktor; Moškon, Jože; Homšak, Marko; Petek, Aljana; Gaberšček, Miran

    2015-01-01

    The possibility of preparation of operating rechargeable liquid battery cells based on aluminium and its alloys is systematically checked. In all cases we started from aluminium as the negative electrode whereas as the positive electrode three different metals were tested: Pb, Bi and Sn. Two types of electrolytes were selected: Na(3)AlF(6) -AlF(3) - BaCl(2) - NaCl and Li(3)AlF(3) - BaF(2). We show that some of these combinations allowed efficient separation of individual liquid layers. The cells exhibited expected voltages, relatively high current densities and could be charged and discharged several times. The capacities were relatively low (120 mAh in the case of Al-Pb system), mostly due to unoptimised cell construction. Improvements in various directions are possible, especially by hermetically sealing the cells thus preventing salt evaporation. Similarly, solubility of aluminium in alloys can be increased by optimising the composition of positive electrode. PMID:26680707

  11. Preparation and Electrochemical Characterization of Aluminium Liquid Battery Cells With Two Different Electrolytes (NaCl-BaCl2-AlF3-NaF and LiF-AlF3-BaF2).

    PubMed

    Napast, Viktor; Moškon, Jože; Homšak, Marko; Petek, Aljana; Gaberšček, Miran

    2015-01-01

    The possibility of preparation of operating rechargeable liquid battery cells based on aluminium and its alloys is systematically checked. In all cases we started from aluminium as the negative electrode whereas as the positive electrode three different metals were tested: Pb, Bi and Sn. Two types of electrolytes were selected: Na(3)AlF(6) -AlF(3) - BaCl(2) - NaCl and Li(3)AlF(3) - BaF(2). We show that some of these combinations allowed efficient separation of individual liquid layers. The cells exhibited expected voltages, relatively high current densities and could be charged and discharged several times. The capacities were relatively low (120 mAh in the case of Al-Pb system), mostly due to unoptimised cell construction. Improvements in various directions are possible, especially by hermetically sealing the cells thus preventing salt evaporation. Similarly, solubility of aluminium in alloys can be increased by optimising the composition of positive electrode.

  12. Density Measurements of Low Silica CaO-SiO2-Al2O3 Slags

    NASA Astrophysics Data System (ADS)

    Muhmood, Luckman; Seetharaman, Seshadri

    2010-08-01

    Density measurements of a low-silica CaO-SiO2-Al2O3 system were carried out using the Archimedes principle. A Pt 30 pct Rh bob and wire arrangement was used for this purpose. The results obtained were in good agreement with those obtained from the model developed in the current group as well as with other results reported earlier. The density for the CaO-SiO2 and the CaO-Al2O3 binary slag systems also was estimated from the ternary values. The extrapolation of density values for high-silica systems also showed good agreement with previous works. An estimation for the density value of CaO was made from the current experimental data. The density decrease at high temperatures was interpreted based on the silicate structure. As the mole percent of SiO2 was below the 33 pct required for the orthosilicate composition, discrete {text{SiO}}4^{4 - } tetrahedral units in the silicate melt would exist along with O2- ions. The change in melt expansivity may be attributed to the ionic expansions in the order of {text{Al}}^{ 3+ } - {text{O}}^{ 2- } < {text{Ca}}^{ 2+ } - {text{O}}^{ 2- } < {text{Ca}}^{ 2+ } - {text{O}}^{ - } Structural changes in the ternary slag also could be correlated to a drastic change in the value of enthalpy of mixing.

  13. Self-organized homo-epitaxial growth in nonlinear optical BaAlBO3F2 crystal crossing lines patterned by laser in glass

    NASA Astrophysics Data System (ADS)

    Shinozaki, K.; Abe, S.; Honma, T.; Komatsu, T.

    2015-11-01

    Crystallization processing of glasses is important as a novel technique for the development of new optical materials, and laser-induced crystallization provides a new challenge in science and technology of materials. Nonlinear optical BaAlBO3F2 crystal lines with crossing, bending, and spiral shapes were patterned at the surface of 2NiO-49BaF2-24.5Al2O3-24.5B2O3 (mol%) and 2.9NiO-48.5BaF2-24.3Al2O3-24.3B2O3 (mol%) glasses by laser irradiation (Yb:YVO4 laser with a wavelength of 1080 nm) and the orientation state of BaAlBO3F2 crystals was examined from birefringence image observations. The birefringence images indicate that the growth of highly c-axis oriented BaAlBO3F2 crystals follows along the laser scanning direction even if the laser scanning direction changes, and in particular the direction of the c-axis of BaAlBO3F2 crystals changes gradually at the crossing and bending points. The model of "self-organized homo-epitaxial growth" is proposed for the crystal orientation at the crossing and bending points, as a new crystal growth science and engineering beyond the wise providence of nature.

  14. Microstructure and dielectric properties of (Ba 0.6Sr 0.4)TiO 3 thin films grown on super smooth glazed-Al 2O 3 ceramics substrate

    NASA Astrophysics Data System (ADS)

    Chen, Hongwei; Yang, Chuanren; Zheng, Shanxue; Zhang, Jihua; Zhang, Qiaozhen; Lei, Guanhuan; Lou, Feizhi; Yang, Lijun

    2011-12-01

    Modified substrates with nanometer scale smooth surface were obtained via coating a layer of CaO-Al2O3-SiO2 (CaAlSi) high temperature glaze with proper additives on the rough-95% Al2O3 ceramics substrates. (Ba0.6Sr0.4)TiO3 (BST) thin films were deposited on modified Al2O3 substrates by radio-frequency magnetron sputtering. The microstructure, dielectric, and insulating properties of BST thin films grown on glazed-Al2O3 substrates were investigated by X-ray diffraction (XRD), atomic force microscope (AFM), and dielectric properties measurement. These results showed that microstructure and dielectric properties of BST thin films grown on glazed-Al2O3 substrates were almost consistent with that of BST thin films grown on LaAlO3 (1 0 0) single-crystal substrates. Thus, the expensive single-crystal substrates may be substituted by extremely cheap glazed-Al2O3 substrates.

  15. Experimental determination of the partition coefficient for Ba in Neogloboquadrina dutertrei suggests calcification occurs in a Ba-enriched microenvironment

    NASA Astrophysics Data System (ADS)

    Fehrenbacher, J. S.; Russell, A. D.; Davis, C. V.; Spero, H. J.; Chu, E.

    2015-12-01

    The Ba/Ca ratio in several spinose planktic foraminifer species varies as a function of the Ba/Ca concentration of seawater and is not affected by other parameters such as the seawater salinity, temperature and pH (Honisch et al., 2011). Since seawater Ba concentration is linearly related to Ba in nearshore environments, Ba/Ca ratios in spinose species shows promise as an indicator of past changes in monsoon strength and river runoff (e. g. Weldeab et al. 2007). In contrast, the non-spinose foraminifers often have intrashell variability in Ba/Ca, with Ba/Ca ratios much higher than expected for the range of Ba concentrations observed in the ocean. Furthermore, the Ba/Ca ratio can vary by over a factor of 10 within a single specimen. This suggests either 1) the partition coefficient for Ba in non-spinose species differs from that determined for spinose species, or 2) non-spinose species calcify in a micro-environment that is enriched in Ba. We conducted experiments on live specimens to determine the partition coefficient for Ba in the non-spinose foraminifer N. dutertrei. Specimens were collected via plankton net from the Southern California Bight and cultured at the Wrigley Marine Science Center, Santa Catalina Island during the summer of 2013-2015. We use isotopically labeled seawater (87Sr) to identify discrete portions of calcite that grew in culture. We use laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) for trace element analyses and to identify ocean grown vs. culture grown calcite. We show that the partition coefficient is similar to the spinose species: N. dutertrei incorporates Ba as a function of seawater chemistry. We conclude from these observations that N. dutertrei forms its calcite from fluids enriched in Ba, and hypothesize that this process occurs via attachment to organic-rich particles such as marine snow.

  16. Synthesis, Crystal and Electronic Structures of the Pnictides AE3TrPn3 (AE = Sr, Ba; Tr = Al, Ga; Pn = P, As)

    SciTech Connect

    Stoyko, Stanislav; Voss, Leonard; He, Hua; Bobev, Svilen

    2015-09-24

    New ternary arsenides AE3TrAs3 (AE = Sr, Ba; Tr = Al, Ga) and their phosphide analogs Sr3GaP3 and Ba3AlP3 have been prepared by reactions of the respective elements at high temperatures. Single-crystal X-ray diffraction studies reveal that Sr3AlAs3 and Ba3AlAs3 adopt the Ba3AlSb3-type structure (Pearson symbol oC56, space group Cmce, Z = 8). This structure is also realized for Sr3GaP3 and Ba3AlP3. Likewise, the compounds Sr3GaAs3 and Ba3GaAs3 crystallize with the Ba3GaSb3-type structure (Pearson symbol oP56, space group Pnma, Z = 8). Both structures are made up of isolated pairs of edge-shared AlPn4 and GaPn4 tetrahedra (Pn = pnictogen, i.e., P or As), separated by the alkaline-earth Sr2+ and Ba2+ cations. In both cases, there are no homoatomic bonds, hence, regardless of the slightly different atomic arrangements, both structures can be rationalized as valence-precise [AE2+]3[Tr3+][Pn3-]3, or rather [AE2+]6[Tr2Pn6]12-, i.e., as Zintl phases.

  17. Band alignment at epitaxial BaSnO3/SrTiO3(001) and BaSnO3/LaAlO3(001) heterojunctions

    NASA Astrophysics Data System (ADS)

    Chambers, Scott A.; Kaspar, Tiffany C.; Prakash, Abhinav; Haugstad, Greg; Jalan, Bharat

    2016-04-01

    We have spectroscopically determined the optical bandgaps and band offsets at epitaxial interfaces of BaSnO3 with SrTiO3(001) and LaAlO3(001). 28 u.c. BaSnO3 epitaxial films exhibit direct and indirect bandgaps of 3.56 ± 0.05 eV and 2.93 ± 0.05 eV, respectively. The lack of a significant Burstein-Moss shift corroborates the highly insulating, defect-free nature of the BaSnO3 films. The conduction band minimum is lower in electron energy in 5 u.c. films of BaSnO3 than in SrTiO3 and LaAlO3 by 0.4 ± 0.2 eV and 3.7 ± 0.2 eV, respectively. This result bodes well for the realization of oxide-based, high-mobility, two-dimensional electron systems that can operate at ambient temperature, since electrons generated in the SrTiO3 by modulation doping, or at the BaSnO3/LaAlO3 interface by polarization doping, can be transferred to and at least partially confined in the BaSnO3 film.

  18. Crystal growth, frequency doubling, and infrared laser performance of Yb{sup 3+}:BaCaBO{sub 3}F

    SciTech Connect

    Schaffers, K.I.; DeLoach, L.D.; Payne, S.A.

    1996-05-01

    Yb:BaCaBO{sub 3}F (Yb:BCBF) has been investigated as a new laser crystal with potential for self-frequency doubling. Yb{sup 3+} in BCBF exhibits a minimum absorption cross section at 912 nm of 1.1 {times} 10{sup {minus}20} cm{sup 2} with a bandwidth (FWHM) of 19 nm. The maximum emission cross section at 1034 nm is 1.3 {times} 10{sup {minus}20} cm{sup 2} with a transition bandwidth of 24 nm. The measured emission lifetime of Yb{sup 3+} is 1.17 ms. An Yb:BCBF laser has been demonstrated with a Ti:sapphire pump source, and a measured slope efficiency of 38% has been obtained for the fundamental laser output. Single crystal powders of BCBF have been compared with KD*P for a relative measure of the second-harmonic generating potential, yielding d{sub eff} (BCBF) {approximately}0.26 pm/V. The phasematching angle has been estimated from the refractive index data for type 1 second-harmonic generation of 0.517 {micro}m light; the predicted angle is 37{degree} from the c-axis. The growth, spectroscopy, laser performance, and linear and nonlinear optical properties of Yb:BCBF are reported.

  19. Geochemistry of Ca, Sr, Ba and Ra sulfates in some deep brines from the Palo Duro basin, Texas

    SciTech Connect

    Langmuir, D.; Melchior, D.

    1985-11-01

    The geochemistry of Ca, Sr, Ba and Ra sulfates in some deep brines from the Palo Duro Basin of north Texas, was studied to define geochemical controls on radionuclides such as /sup 90/Sr and /sup 226/Ra. Published solubility data for gypsum, anhydrite, celestite, barite and RaSO/sub 4/ were first reevaluated, in most cases using the ion interaction approach of Pitzer, to determine solubility products of the sulfates as a function of temperature and pressure. Ionic strengths of the brines were from 2.9 to 4.8 m, their temperatures and pressures up to 40/sup 0/C and 130 bars. Saturation indices of the sulfates were computed with the ion-interaction approach in one brine from the arkosic granite wash facies and four from the carbonate Wolfcamp Formation. All five brines are saturated with respect to gypsum, anhydrite and celestite, and three of the five with respect to barite. All are undersaturated by from 5 to 6 orders of magnitude with respect to pure RaSO/sub 4/. /sup 226/Ra concentrations in the brines, which ranged from 10/sup -11.3/ to 10/sup -12.7/ m, are not controlled by RaSO/sub 4/ solubility or adsorption, but possibly by the solubility of trace Ra solid solutions in sulfates including celestite and barite.

  20. The geochemistry of Ca, Sr, Ba and Ra sulfates in some deep brines from the Palo Duro Basin, Texas

    NASA Astrophysics Data System (ADS)

    Langmuir, Donald; Melchior, Daniel

    1985-11-01

    The geochemistry of Ca, Sr, Ba and Ra sulfates in some deep brines from the Palo Duro Basin of north Texas, was studied to define geochemical controls on radionuclides such as 90Sr and 226Ra. Published solubility data for gypsum, anhydrite, celestite, barite and RaSO 4 were first reevaluated, in most cases using the ion interaction approach of Pitzer, to determine solubility products of the sulfates as a function of temperature and pressure. Ionic strengths of the brines were from 2.9 to 4.8 m, their temperatures and pressures up to 40°C and 130 bars. Saturation indices of the sulfates were computed with the ion-interaction approach in one brine from the arkosic granite wash fades and four from the carbonate Wolfcamp Formation. All five brines are saturated with respect to gypsum, anhydrite and celestite, and three of the five with respect to barite. All are undersaturated by from 5 to 6 orders of magnitude with respect to pure RaSO 4. 226Ra concentrations in the brines, which ranged from 10 -11.3 to 10 -12.7 m, are not controlled by RaSO 4 solubility or adsorption, but possibly by the solubility of trace Ra solid solutions in sulfates including celestite and barite.

  1. Anomalous elastic behavior of relaxor ferroelectric Ca0.28Ba0.72Nb2O6 single crystals

    NASA Astrophysics Data System (ADS)

    Pandey, Chandra Shekhar; Schreuer, Jürgen; Burianek, Manfred; Mühlberg, Manfred

    2011-11-01

    Full sets of elastic constants cij of tetragonal tungsten bronze relaxor ferroelectric Ca0.28Ba0.72Nb2O6 (CBN-28) single crystals are measured above Curie temperature up to 1503 K employing resonant ultrasound spectroscopy. Thermal expansion measurements on as-grown unpoled CBN-28 reveal the existence of a characteristic temperature T * (˜800 K) for CBN-28 between the Burns temperature Tb (˜1100 K) and the temperature of maximum dielectric permittivity Tm (˜600 K). The influence of polar nanoregions (PNRs) on the elastic properties of CBN-28 is studied in detail. The temperature evolution of cij shows pronounced anomalies. All independent elastic constants evolved differently, with temperature reflecting their coupling to different types of the reorientational motion of PNRs through their interaction with acoustic waves. The anisotropy of longitudinal elastic stiffness coefficients and the deviation from Cauchy relations for CBN-28 are also studied, showing the evolution of material anisotropy and the nature of bonding interactions with temperature, respectively.

  2. Optical absorption and TEM studies of silver nanoparticle embedded BaO-CaF2-P2O5 glasses

    NASA Astrophysics Data System (ADS)

    Narayanan, Manoj Kumar; Shashikala, H. D.

    2016-05-01

    Silver nanoparticle embedded 30BaO-20CaF2-50P2O5-4Ag2O-4SnO glasses were prepared by melt-quenching and subsequent heat treatment process. Silver-doped glasses were heat treated at temperatures 500 °C, 525°C and 550 °C for a fixed duration of 10 hours to incorporate metal nanoparticles into the glass matrix. Appearance and shift in peak positions of the surface plasmon resonance (SPR) bands in the optical absorption spectra of heat treated glass samples indicated that both formation and growth of nanoparticle depended on heat treatment temperature. Glass sample heat treated at 525 °C showed a SPR peak around 3 eV, which indicated that spherical nanoparticles smaller than 20 nm were formed inside the glass matrix. Whereas sample heat treated at 550 °C showed a size dependent red shift in SPR peak due to the presence of silver nanoparticles of size larger than 20 nm. Size of the nanoparticles calculated using full-width at half-maximum (FWHM) of absorption band showed a good agreement with the particle size obtained from transmission electron microscopy (TEM) analysis.

  3. Magnetoelectric effect and magnetic phase diagram of a polar ferrimagnet CaBaFe4O7

    NASA Astrophysics Data System (ADS)

    Kocsis, V.; Tokunaga, Y.; Bordács, S.; Kriener, M.; Puri, A.; Zeitler, U.; Taguchi, Y.; Tokura, Y.; Kézsmárki, I.

    2016-01-01

    The magnetic phase diagram of a polar ferrimagnet CaBaFe4O7 with a magnetic easy axis has been investigated by measurements of magnetization, specific heat, and magnetoelectricity. A ferrimagnetic transition takes place at TC 1=275 K within the orthorhombic phase followed by a second magnetic transition at TC 2=211 K. Below TC 2, successive metamagnetic transitions occur for magnetic fields applied perpendicular to the easy axis, implying a sequential emergence of magnetic states which are neither collinear nor coplanar. The observation of the static magnetoelectric effect was limited to temperatures below 120 K due to the conducting nature of the crystals at higher temperatures. The magnitude of the ferroelectric polarization shows large changes between the different field-induced magnetic phases. The low-field state is characterized by a large linear magnetoelectric coefficient of αc c=39 ps/m, while a gigantic polarization change of Δ P =850 μ C /m2 is observed for μoH =14 T applied along the easy axis.

  4. Multi-Centennial Record of North Atlantic Freshwater Variability since the Little Ice Age Archived in Coralline Algal Ba/Ca

    NASA Astrophysics Data System (ADS)

    Chan, P. T. W.; Halfar, J.; Adey, W.; Zack, T.

    2014-12-01

    Declining Arctic sea-ice cover in recent decades has driven large-scale freshwater transport into the North Atlantic, possibly influencing the strength of the Meridional Overturning Circulation and even global climate. However, due to the lack of long-term oceanographic observations, little is known about the natural freshwater variability of the Northwestern Atlantic. Crustose coralline algae Clathromorphum compactum are extremely long-lived shallow marine calcareous plants that are abundant along the subarctic eastern Canadian coastline. They are particularly well-suited as recorders of paleoclimate signals due to the formation of annual growth increments, allowing for the precise calendar dating and geochemical sampling of hard tissue. Here, we provide the first annually-resolved multi-centennial record of coralline algal Ba/Ca from Labrador, Canada, as a proxy for North Atlantic freshwater variability extending well into the Little Ice Age (LIA) (1665 AD). Barium-to-calcium ratios (Ba/Ca) from coralline algae have previously been used as an indicator of freshwater runoff. This is because barium-rich clay sediments are transported by terrestrial runoff into coastal waters, and barium is released from the clay minerals upon encountering more alkaline elements present in seawater. We observe higher algal barium concentrations during the LIA, followed by a steady decline to recent times. In addition, coralline algal Ba/Ca shows significant positive relationships to Hudson Strait runoff, as well as Canadian Arctic and North Atlantic sea-ice extent. This suggests that more riverine Ba is transported from the Hudson Strait into the Labrador Sea during periods of increased sea-ice cover. Multiyear sea-ice can block incoming solar radiation thereby diminishing the effects of nutrient scavenging by phytoplankton, resulting in a more conservative transport of Ba into northern Labrador. However as sea-ice continues to thin, more sunlight is able to penetrate through the

  5. Chemical short-range order and the Meyer - Neldel rule for liquid alloys: AlCa and GaAlCa

    NASA Astrophysics Data System (ADS)

    You, D.; Schnyders, H. S.; Van Zytveld, J. B.

    1997-02-01

    We have measured the electrical resistivity, 0953-8984/9/7/006/img1, its specific temperature dependence, 0953-8984/9/7/006/img2, and the thermopower, S, of two series of ternary liquid alloys: 0953-8984/9/7/006/img3 and 0953-8984/9/7/006/img4. We also provide new analysis for the binary liquid alloy AlCa. We do not see the unusually large values for S that were found earlier for amorphous solid ternary alloys of the approximate composition 0953-8984/9/7/006/img5. We do find that, while chemical short-range order (CSRO) appears to occur in the liquid binary alloy 0953-8984/9/7/006/img6, CSRO is apparently destroyed by substitution of one Ga atom for one Al per complex: 0953-8984/9/7/006/img7. CSRO may exist in the liquid alloy 0953-8984/9/7/006/img8. And we find that the activated conductivities of these ternary liquid alloys (and also of liquid AlCa) are consistent with the Meyer - Neldel rule (MNR), extending the range of applicability of the MNR to systems with activation energies about an order of magnitude smaller than previously observed. These results appear to rule out two physical models as universal bases for the MNR, but are consistent with one based on a hopping conductivity whose characteristic energy is that of a polaron shift.

  6. Suppression of superconductivity with Pr substitution in Nd 1- xPr xBaCaCu 3O 7 system

    NASA Astrophysics Data System (ADS)

    Awana, V. P. S.; Cardoso, Claudio A.; de Lima, O. F.; Singh, Rajvir; Narlikar, A. V.; Yelon, W. B.; Malik, S. K.

    1999-05-01

    The structural, superconducting and magnetic properties of Nd 1- xPr xBaCaCu 3O 7 system with x=0.0, 0.10, 0.25, 0.35, 0.50, 0.75 and 1.0 have been investigated. X-ray diffraction results reveal that Pr substitutes isostructurally in NdBaCaCu 3O 7 (Nd:1113) superconductor with complete solubility. The superconducting transition temperature ( Tc), measured by ac susceptibility technique, decreases with increasing x. However, suppression of Tc with increasing Pr substitution is less in Nd:1113 superconductor compared to that reported for Nd 1- xPr xBa 2Cu 3O 7 system. Interestingly, in the fully Pr substituted compounds of the above series, i.e., in PrBaCaCu 3O 7 and PrBa 2Cu 3O 7, the Pr moments order antiferromagnetically with TN of 10 and 17 K, respectively. The present results along those reported earlier [V.P.S. Awana, J. Horvat, S.X. Dou, A. Sedky, A.V. Narlikar, J. Magn. Magn. Mater., 182 (1998) L280; V.P.S. Awana, S.X. Dou, S.K. Malik, Rajvir Singh, A.V. Narlikar, D.A. Landinez Tellez, J.M. Ferreira, J. Albino Aguiar, S. Uma, E. Gmelin, W.B. Yelon, J. Magn. Magn. Mater., 187 (1998) 192], clearly suggest that there is a correlation between the Tc suppression due to Pr and the magnetic ordering temperature of the fully substituted Pr moments in these systems. The TN may be taken to be a measure of the strength of hybridization between the Pr-4f electrons with Cu-O conduction band, and hence a lower TN may imply a less deleterious effect on superconductivity.

  7. Effects of Ca, Cu, Al and La on pectin gel strength: implications for plant cell walls.

    PubMed

    McKenna, Brigid A; Nicholson, Timothy M; Wehr, J Bernhard; Menzies, Neal W

    2010-06-16

    Rheology of Ca-pectate gels is widely studied, but the behaviour of pectate gels formed by Cu, Al and La is largely unknown. It is well known that gel strength increases with increasing Ca concentration, and it is hypothesised that this would also be the case for other cations. Pectins are a critical component of plant cell walls, imparting various physicochemical properties. Furthermore, the mechanism of metal toxicity in plants is hypothesised to be, in the short term, related to metal interactions with cell wall pectin. This study investigated the influence of Ca, Cu, Al and La ion concentrations at pH 4 on the storage modulus as a function of frequency for metal-pectin gels prepared from pectin (1%) with a degree of esterification of 30%. Gels were formed in situ over 6d in metal chloride solution adjusted daily to pH 4. Cation concentration was varied to develop a relationship between gel strength and cation concentration. At similar levels of cation saturation, gel strength increased in the order of La<Ca < or =AlCa gels being the most swollen.

  8. Effects of Ca, Cu, Al and La on pectin gel strength: implications for plant cell walls.

    PubMed

    McKenna, Brigid A; Nicholson, Timothy M; Wehr, J Bernhard; Menzies, Neal W

    2010-06-16

    Rheology of Ca-pectate gels is widely studied, but the behaviour of pectate gels formed by Cu, Al and La is largely unknown. It is well known that gel strength increases with increasing Ca concentration, and it is hypothesised that this would also be the case for other cations. Pectins are a critical component of plant cell walls, imparting various physicochemical properties. Furthermore, the mechanism of metal toxicity in plants is hypothesised to be, in the short term, related to metal interactions with cell wall pectin. This study investigated the influence of Ca, Cu, Al and La ion concentrations at pH 4 on the storage modulus as a function of frequency for metal-pectin gels prepared from pectin (1%) with a degree of esterification of 30%. Gels were formed in situ over 6d in metal chloride solution adjusted daily to pH 4. Cation concentration was varied to develop a relationship between gel strength and cation concentration. At similar levels of cation saturation, gel strength increased in the order of La<Ca < or =AlCa gels being the most swollen. PMID:20457449

  9. The Density and Compressibility of BaCO3-SrCO3-CaCO3-K2CO3-Na2CO3-Li2CO3 Liquids: New Measurements and a Systematic Trend with Cation Field Strength

    NASA Astrophysics Data System (ADS)

    Hurt, S. M.; Lange, R. A.; Ai, Y.

    2015-12-01

    The volumetric properties of multi-component carbonate liquids are required to extend thermodynamic models that describe partial melting of the deep mantle (e.g. pMELTS; Ghiorso et al., 2003) to carbonate-bearing lithologies. Carbonate in the mantle is an important reservoir of carbon, which is released to the atmosphere as CO2 through volcanism, and thus contributes to the carbon cycle. Although MgCO3 is the most important carbonate component in the mantle, it is not possible to directly measure the 1-bar density and compressibility of MgCO3 liquid because, like other alkaline-earth carbonates, it decomposes at a temperature lower than its melting temperature. Despite this challenge, Liu and Lange (2003) and O'Leary et al. (2015) showed that the one bar molar volume, thermal expansion and compressibility of the CaCO3 liquid component could be obtained by measuring the density and sound speeds of stable liquids in the CaCO3-Li2CO3-Na2CO3-K2CO3 quaternary system at one bar. In this study, this same strategy is employed on SrCO3- and BaCO3-bearing alkali carbonate liquids. The density and sound speed of seven liquids in the SrCO3-Li2CO3-Na2CO3-K2CO3 quaternary and three liquids in the BaCO3-Li2CO3-Na2CO3-K2CO3 quaternary were measured from 739-1367K, with SrCO3 and BaCO3 concentrations ranging from 10-50 mol%. The density measurements were made using the double-bob Archimedean method and sound speeds were obtained with a frequency-sweep acoustic interferometer. The molar volume and sound speed measurements were used to calculate the isothermal compressibility of each liquid, and the results show the volumetric properties mix ideally with composition. The partial molar volume and compressibility of the SrCO3 and BaCO3 components are compared to those obtained for the CaCO3 component as a function of cation field strength. The results reveal a systematic trend that allows the partial molar volume and compressibility of the MgCO3 liquid component to be estimated.

  10. Structures, phase transitions and microwave dielectric properties of the 6H perovskites Ba{sub 3}BSb{sub 2}O{sub 9}, B=Mg, Ca, Sr, Ba

    SciTech Connect

    Ling, Chris D. Rowda, Budwy; Avdeev, Maxim; Pullar, Robert

    2009-03-15

    We present a complete temperature-composition phase diagram for Ba{sub 3}BSb{sub 2}O{sub 9}, B=Mg, Ca, Sr, Ba, along with their electrical behavior as a function of B. These compounds have long been recognized as 6H-type perovskites, but (with the exception of B=Mg) their exact structures and properties were unknown due to their low symmetries, temperature-dependent phase transitions, and difficulties in synthesizing pure samples. The full range of possible space group symmetries is observed, from ideal hexagonal P6{sub 3}/mmc to monoclinic C2/c to triclinic P1-bar. Direct second-order transitions between these phases are plausible according to group theory, and no evidence was seen for any further intermediate phases. The phase diagram with respect to temperature and the effective ionic radius of B is remarkably symmetrical for B=Mg, Ca, and Sr. For B=Ba, a first-order phase transition to a locally distorted phase allows a metastable hexagonal phase to persist to lower temperatures than expected before decomposing around 600 K. Electrical measurements revealed that dielectric permittivity corrected for porosity does not change significantly as a function of B and is in a good agreement with the values predicted by the Clausius-Mossotti equation. - Graphical abstract: Thermodynamic phase diagram for Ba{sub 3}BSb{sub 2}O{sub 9}, B=Mg, Ca, and Sr, as a function of temperature T and effective ionic radius (IR) of the B{sup 2+} cation.

  11. Luminescence Properties of Self-Activated Mm(VO4)2 (M = Mg, Ca, Sr, and Ba) Phosphors Synthesized by Solid-State Reaction Method.

    PubMed

    Min, Xin; Huang, Zhaohui; Fang, Minghao; Liu, Yan'gai; Tang, Chao; Wu, Xiaowen

    2016-04-01

    In this paper, M3(VO4)2 (M = Mg, Ca, Sr, and Ba) self-activated phosphors were prepared by a solid-state reaction method at 1,000 °C for 5 h. The phase formation and micrographs were analyzed by X-ray diffraction and scanning electron microscopy. The Ca3(VO4)2 phosphor does not show any emission peaks under excitation with ultraviolet (UV) light. However, the M3(VO4)2 (M = Mg, Sr, and Ba) samples are effectively excited by UV light chips ranging from 200 nm to 400 nm and exhibit broad emission bands due to the charge transfer from the oxygen 2p orbital to the vacant 3d orbital of the vanadium in the VO4. The color of these phosphors changes from yellow to light blue via blue-green with increasing ionic radius from Mg to Sr to Ba. The luminescence lifetimes and quantum yield decrease with the increasing unit cell volume and V-V distance, in the order of Mg3(VO4)2 to Sr3(VO4)2 to Ba3(VO4)2. The emission intensity decreases with the increase of temperatures, but presents no color shift. This confirms that these self-activated M3(VO4)2 phosphors can be suggested as candidates of the single-phase phosphors for light using UV light emitting diodes (LEDs). PMID:27451689

  12. Optically stimulated luminescence in LiCaAlF6:Eu2+ phosphor.

    PubMed

    More, Y K; Wankhede, S P; Moharil, S V; Kumar, Munish; Chougaonkar, M P

    2015-09-01

    Results on optically stimulated luminescence (OSL) in LiCaAlF6:Eu(2+) are reported. Continuous wave OSL signal as recorded using blue (470 nm) stimulation was found to be ~31% that of standard phosphor lithium magnesium phosphate. The rate of OSL depletion for standard phosphor lithium magnesium phosphate is only three times less as compared with that of LiCaAlF6:Eu(2+). Strong photoluminescence (PL) in the near ultraviolet region is observed for LiCaAlF6:Eu(2+) with the characteristic Eu(2+) emission at 369 nm for 254 nm excitation. The thermoluminescence (TL) glow peak for LiCaAlF6:Eu(2+) was observed at around 180°C. The glow peak was about six times more intense compared with the dosimetric peak of the well known thermoluminescence dosimetric (TLD) phosphor LiF-TLD 100. Thus this phosphor deserves much more attention than it has received until now and may be useful as a dosimetric material in radiation dosimetry. PMID:25620581

  13. Formation Mechanism of CaS-Al2O3 Inclusions in Low Sulfur Al-Killed Steel After Calcium Treatment

    NASA Astrophysics Data System (ADS)

    Xu, Jianfei; Huang, Fuxiang; Wang, Xinhua

    2016-04-01

    The laboratory experiments of alumina inclusions modified by calcium treatment in Al-killed steel were carried out at 1873 K (1600 °C), and the inclusions in steel samples were characterized at 1, 5, and 10 minutes after calcium addition. The results show that the type of inclusions after calcium treatment was determined by the sulfur and T.O contents of steel. CaS-Al2O3 inclusions were obtained in steels with high sulfur and low T.O contents. The mass ratio between CaS and Al2O3 was determined by T.Ca and T.O contents of steel. The influence of holding time after calcium addition on the composition of inclusions was negligible. The thermodynamics for the formation of CaS-Al2O3 inclusions after calcium treatment was discussed, and a simple formation mechanism was proposed. Moreover, the CaO, Al2O3, and CaS contents in the inclusions were predicted through the sulfur, total calcium (T.Ca), and T.O contents, and it was found that the CaO content decreases with increasing S/T.O, while (pctCaS)/(pctAl2O3)1/3 increases with increasing T.Ca/T.O.

  14. Ca-,Al-rich inclusions in the unique chondrite ALH85085 - Petrology, chemistry, and isotopic compositions

    NASA Astrophysics Data System (ADS)

    Kimura, M.; El Goresy, A.; Palme, H.; Zinner, E.

    1993-05-01

    A comprehensive study is performed for the Ca-,Al-rich inclusions (CAIs) in the unique chondrite ALH85085. The ALH85085 inclusions are smaller (5-80 microns) and more refractory than their counterparts in carbonaceous chondrites. The study includes 42 inclusions for petrography and mineralogy, 15 for bulk major and minor element chemical composition, six for Mg-Al isotopic systematics, 10 for Ca isotopes, nine for Ti isotopes, and six for trace element abundances. In addition, oxygen-isotopic compositions were determined in minerals from a single inclusion. No correlation is found between mineralogy, major element chemistry, and trace element abundances. It is further shown that the high-temperature geochemical behavior of ultrarefractory trace elements is decoupled from that of the major elements Ca and Ti (Ti is correlated with the relatively volatile elements Nb and Yb) implying that perovskite is of only minor importance as carrier of ultrarefractories.

  15. Effect of alloying elements Al and Ca on corrosion resistance of plasma anodized Mg alloys

    NASA Astrophysics Data System (ADS)

    Anawati, Asoh, Hidetaka; Ono, Sachiko

    2016-04-01

    Plasma anodizing is a surface treatment used to form a ceramic-type oxide film on Mg alloys by the application of a high anodic voltage to create intense plasma near the metal surface. With proper selection of the process parameters, the technique can produce high quality oxide with superior adhesion, corrosion resistance, micro-hardness, wear resistance and strength. The effect of alloying element Al on plasma anodizing process of Mg alloys was studied by comparing the anodizing curves of pure Mg, AZ31, and AZ61 alloys while the effect of Ca were studied on AZ61 alloys containing 0, 1, and 2 wt% Ca. Anodizing was performed in 0.5 M Na3PO4 solution at a constant current density of 200 Am-2 at 25°C. Anodic oxide films with lava-like structure having mix composition of amorphous and crystal were formed on all of the alloys. The main crystal form of the oxide was Mg3(PO4)2 as analyzed by XRD. Alloying elements Al and Ca played role in modifying the plasma lifetime during anodization. Al tended to extend the strong plasma lifetime and therefore accelerated the film thickening. The effect of Ca on anodizing process was still unclear. The anodic film thickness and chemical composition were altered by the presence of Ca in the alloys. Electrochemical corrosion test in 0.9% NaCl solution showed that the corrosion behavior of the anodized specimens depend on the behavior of the substrate. Increasing Al and Ca content in the alloys tended to increase the corrosion resistance of the specimens. The corrosion resistance of the anodized specimens improved significantly about two orders of magnitude relative to the bare substrate.

  16. Thermochemistry of glasses and liquids in the systems CaMgSi 2O 6-CaAl 2Si 2O 8-NaAlSi 3O 8, SiO 2-CaAl 2Si 2O 8-NaAlSi 3O 8 and SiO 2-Al 2O 3-CaO-Na 2O

    NASA Astrophysics Data System (ADS)

    Navrotsky, A.; Hon, R.; Weill, D. F.; Henry, D. J.

    1980-10-01

    Enthalpies of solution in 2PbO· B 2O 3 at 712°C have been measured for glasses in the systems albite anorthite diopside, NaAlO 2-SiO 2, Ca 0.5AlO 2-SiO 2 and albite-anorthite-quartz. The systems albite-anorthite and diopside-anorthite show substantial negative enthalpies of mixing, albite-diopside shows significant positive heats of mixing. For compositions up to NaAlO2 = 0.42 (which includes the subsystem albite-silica) the system NaAlO 2-SiO 2 shows essentially zero heats of mixing. A negative ternary excess heat of mixing is found in the plagioclase-rich portion of the albite-anorthite-diopside system. The join Si 4O 8-CaAl 2Si 2O 8 shows small but significant heats of mixing. In albite-anorthite-quartz. ternary glasses, the ternary excess enthalpy of mixing is positive. Based on available heat capacity data and appropriate consideration of the glass transition, the enthalpy of the crystal-glass transition (vitrification) is a serious underestimate of the enthalpy of the crystal-liquid transition (fusion) especially when the melting point, Tf, is many hundreds of degrees higher than the glass transition temperature, Tg. On the other hand, the same heat capacity data suggest that the enthalpies of mixing in albite-anorthite-diopside liquids are calculated to be quite similar to those in the glasses. The enthalpies of mixing observed in general support the structural models proposed by TAYLOR and BROWN (1979a, b) and others for the structure of aluminosilicate glasses.

  17. Monolithic translucent BaMgAl10O17:Eu2+ phosphors for laser-driven solid state lighting

    NASA Astrophysics Data System (ADS)

    Cozzan, Clayton; Brady, Michael J.; O'Dea, Nicholas; Levin, Emily E.; Nakamura, Shuji; DenBaars, Steven P.; Seshadri, Ram

    2016-10-01

    With high power light emitting diodes and laser diodes being explored for white light generation and visible light communication, thermally robust encapsulation schemes for color-converting inorganic phosphors are essential. In the current work, the canonical blue-emitting phosphor, high purity Eu-doped BaMgAl10O17, has been prepared using microwave-assisted heating (25 min) and densified into translucent ceramic phosphor monoliths using spark plasma sintering (30 min). The resulting translucent ceramic monoliths convert UV laser light to blue light with the same efficiency as the starting powder and provide superior thermal management in comparison with silicone encapsulation.

  18. Co-Dopant Influence on the Persistent Luminescence of BaAl2O4:Eu2+,R3+

    NASA Astrophysics Data System (ADS)

    Rodrigues, Lucas C. V.; Hölsä, Jorma; Carvalho, José M.; Pedroso, Cássio C. S.; Lastusaari, Mika; Felinto, Maria C. F. C.; Watanabe, Shigeo; Brito, Hermi F.

    2014-04-01

    The R3+ (rare earth) co-dopants may have a surprisingly important role in persistent luminescence - enhancement of up to 1-3 orders of magnitude may be obtained in the performance of these phosphor materials - depending strongly on the R3+ ion, of course. In this work, the effects of the R3+ co-dopants in the BaAl2O4:Eu2+,R3+ materials were studied using mainly thermoluminescence (TL) and synchrotron radiation XANES methods. In BaAl2O4, the conventional and persistent luminescence both arise from the 4f7→4f65d1 transition of Eu2+, yielding blue-green emission color. The former, in the presence of humidity, turns to more bluish because of creation of an additional Eu2+ luminescence centre which is not, however, visible in persistent luminescence. The trap structure in the non-co-doped BaAl2O4:Eu2+ is rather complex with 4-5 TL bands above room temperature. With R3+ co-doping, this basic structure is modified though no drastic change can be observed. This underlines the fact that even very small changes in the trap depths can produce significant modifications in the persistent luminescence efficiency. It should be remembered that basically the persistent luminescence performance is controlled by the Boltzmann population law depending exponentially on both the temperature and trap depth. Some mechanisms for persistent luminescence have suggested the presence of either divalent R2+ or tetravalent RIV during the charging of the Eu2+ doped materials. The present XANES measurements on BaAl2O4:Eu2+,R3+ confirmed the presence of only the trivalent form of the R3+ co-dopants excluding both of these pathways. It must thus be concluded, that the energy is stored in intrinsic and extrinsic defects created by the synthesis conditions and charge compensation due to R3+ co-doping. Even though the effect of the R3+ co-dopants was carefully exploited and characterized, the differences in the effect of different R3+ ions with very similar chemical and spectroscopic properties could

  19. Single-component and white light-emitting phosphor BaAl2Si2O8: Dy3+, Eu3+ synthesis, luminescence, energy transfer, and tunable color

    NASA Astrophysics Data System (ADS)

    Ma, Pingchuan; Song, Yanhua; Sheng, Ye; Yuan, Bo; Guan, Hongxia; Xu, Chengyi; Zou, Haifeng

    2016-10-01

    A series of Dy3+ - Eu3+ co-doped BaAl2Si2O8 phosphors were prepared via the conventional solid-state reaction method. Their crystal structure, luminescent characteristic and lifetime were investigated. The optimum doping concentrations of Dy3+and Eu3+ are both 0.05 for Dy3+ or Eu3+ singly doped BaAl2Si2O8. Furthermore, BaAl2Si2O8: 0.05Dy3+ and BaAl2Si2O8: 0.05Eu3+ emits yellow and red light. The emission color of BaAl2Si2O8: Dy3+, Eu3+ could be tuned from yellow to white due to the energy transfer. This energy transfer from Dy3+ to Eu3+ was confirmed and investigated by photoluminescence spectra and the decay time of energy donor Dy3+ ions. With constantly increasing Eu3+ concentration, the energy transfer efficiency from Dy3+ to Eu3+ in BaAl2Si2O8 host increased gradually and reached as high as 81%, the quantum yield was about 47.43%. BaAl2Si2O8: Dy3+, Eu3+ phosphors can be effectively excited by UV (about 348 nm) light and emit visible light from yellow to white by altering the concentration ratio of Dy3+ and Eu3+, indicating that the phosphors have potential applications as a white light-emitting phosphor for display and lighting.

  20. Synthesis, structural characterization and properties of SrAl4-xGex, BaAl4-xGex, and EuAl4-xGex (x≈0.3-0.4)—Rare examples of electron-rich phases with the BaAl4 structure type

    NASA Astrophysics Data System (ADS)

    Zhang, Jiliang; Bobev, Svilen

    2013-09-01

    Three solid solutions with the general formula AEAl4-xGex (AE=Eu, Sr, Ba; 0.32(1)≤x≤0.41(1)) have been synthesized via the aluminum self-flux method, and their crystal structures have been established from powder and single-crystal X-ray diffraction. They are isotypic and crystallize with the well-known BaAl4 structure type, adopted by the three AEAl4 end members. In all structures, Ge substitutes Al only at the 4e Wyckoff site. Results from X-rays photoelectron spectroscopy on EuAl4-xGex and EuAl4 indicate that the interactions between the Eu2+ cations and the polyanionic framework are enhanced in the Ge-doped structure, despite the slightly elevated Fermi level. Magnetic susceptibility measurements confirm the local moment magnetism, expected for the [Xe]4f7 electronic configuration of Eu2+ and suggest strong ferromagnetic interactions at cryogenic temperatures. Resistivity data from single-crystalline samples show differences between the title compounds, implying different bonding characteristics despite the close Debye temperatures. A brief discussion on the observed electron count and homogeneity ranges for AEAl4-xGex (AE=Eu, Sr, Ba) is also presented.

  1. Coral Ba/Ca records of sediment input to the fringing reef of the southshore of Moloka'i, Hawai'i over the last several decades

    USGS Publications Warehouse

    Prouty, N.G.; Field, M.E.; Stock, J.D.; Jupiter, S.D.; McCulloch, M.

    2010-01-01

    The fringing reef of southern Moloka’i is perceived to be in decline because of land-based pollution. In the absence of historical records of sediment pollution, ratios of coral Ba/Ca were used to test the hypothesis that sedimentation has increased over time. Baseline Ba/Ca ratios co-vary with the abundance of red, terrigenous sediment visible in recent imagery. The highest values at One Ali’i are near one of the muddiest parts of the reef. This co-varies with the lowest growth rate of all the sites, perhaps because the upstream Kawela watershed was historically leveed all the way to the nearshore, providing a fast-path for sediment delivery. Sites adjacent to small, steep watersheds have ∼decadal periodicities whereas sites adjacent to mangrove forests have shorter-period fluctuations that correspond to the periodicity of sediment transport in the nearshore, rather than the watershed. All four sites show a statistically significant upward trend in Ba/Ca.

  2. Optically pumped cerium-doped LiSrAlF.sub.6 and LiCaAlF.sub.6

    DOEpatents

    Marshall, Christopher D.; Payne, Stephen A.; Krupke, William F.

    1996-01-01

    Ce.sup.3+ -doped LiSrAlF.sub.6 crystals are pumped by ultraviolet light which is polarized along the c axis of the crystals to effectively energize the laser system. In one embodiment, the polarized fourth harmonic light output from a conventional Nd:YAG laser operating at 266 nm is arranged to pump Ce:LiSrAlF.sub.6 with the pump light polarized along the c axis of the crystal. The Ce:LiSrAlF.sub.6 crystal may be placed in a laser cavity for generating tunable coherent ultraviolet radiation in the range of 280-320 nm. Additionally, Ce-doped crystals possessing the LiSrAlF.sub.6 type of chemical formula, e.g. Ce-doped LiCaAlF.sub.6 and LiSrGaF.sub.6, can be used. Alternative pump sources include an ultraviolet-capable krypton or argon laser, or ultraviolet emitting flashlamps. The polarization of the pump light will impact operation. The laser system will operate efficiently when light in the 280-320 nm gain region is injected or recirculated in the system such that the beam is also polarized along the c axis of the crystal. The Ce:LiSrAlF.sub.6 laser system can be configured to generate ultrashort pulses, and it may be used to pump other devices, such as an optical parametric oscillator.

  3. Optically pumped cerium-doped LiSrAlF{sub 6} and LiCaAlF{sub 6}

    DOEpatents

    Marshall, C.D.; Payne, S.A.; Krupke, W.F.

    1996-05-14

    Ce{sup 3+}-doped LiSrAlF{sub 6} crystals are pumped by ultraviolet light which is polarized along the c axis of the crystals to effectively energize the laser system. In one embodiment, the polarized fourth harmonic light output from a conventional Nd:YAG laser operating at 266 nm is arranged to pump Ce:LiSrAlF{sub 6} with the pump light polarized along the c axis of the crystal. The Ce:LiSrAlF{sub 6} crystal may be placed in a laser cavity for generating tunable coherent ultraviolet radiation in the range of 280-320 nm. Additionally, Ce-doped crystals possessing the LiSrAlF{sub 6} type of chemical formula, e.g. Ce-doped LiCaAlF{sub 6} and LiSrGaF{sub 6}, can be used. Alternative pump sources include an ultraviolet-capable krypton or argon laser, or ultraviolet emitting flashlamps. The polarization of the pump light will impact operation. The laser system will operate efficiently when light in the 280-320 nm gain region is injected or recirculated in the system such that the beam is also polarized along the c axis of the crystal. The Ce:LiSrAlF{sub 6} laser system can be configured to generate ultrashort pulses, and it may be used to pump other devices, such as an optical parametric oscillator. 10 figs.

  4. Combustion Synthesis of CaAl2Si2O8:Eu2+, Dy3+ And CaSrAl2SiO7:Eu2+ Long After Glow Phosphors

    NASA Astrophysics Data System (ADS)

    Talwar, Gurjeet; Joshi, C. P.; Moharil, S. V.; Kondawar, V. K.

    2011-10-01

    CaSrAl2SiO7:Eu2+ and CaAl2Si2O8:Eu2+, Dy3+ are prepared through modified combustion technique. The photoluminescence and long after glow decay characteristics are studied. PL emission spectra of both the phosphors are obtained in blue region.

  5. Aluminum-Magnesium and Oxygen Isotope Study of Relict Ca-Al-rich Inclusions in Chondrules

    NASA Astrophysics Data System (ADS)

    Krot, Alexander N.; McKeegan, Kevin D.; Huss, Gary R.; Liffman, Kurt; Sahijpal, Sandeep; Hutcheon, Ian D.; Srinivasan, Gopalan; Bischoff, Adolph; Keil, Klaus

    2006-03-01

    Relict Ca-Al-rich inclusions (CAIs) in chondrules crystallized before their host chondrules and were subsequently partly melted together with chondrule precursors during chondrule formation. Like most CAIs, relict CAIs are 16O enriched (Δ17O<-20‰) compared to their host chondrules (Δ17O>-9‰). Hibonite in a relict CAI from the ungrouped carbonaceous chondrite Adelaide has a large excess of radiogenic 26Mg (26Mg*) from the decay of 26Al, corresponding to an initial 26Al/27Al ratio [(26Al/27Al)I] of (3.7+/-0.5)×10-5 in contrast, melilite in this CAI and plagioclase in the host chondrule show no evidence for 26Mg* [(26Al/27Al)I of <5×10-6]. Grossite in a relict CAI from the CH carbonaceous chondrite PAT 91546 has little 26Mg*, corresponding to a (26Al/27Al)I of (1.7+/-1.3)×10-6. Three other relict CAIs and their host chondrules from the ungrouped carbonaceous chondrite Acfer 094, CH chondrite Acfer 182, and H3.4 ordinary chondrite Sharps do not have detectable 26Mg* [(26Al/27Al)I<1×10-5, <(4-6)×10-6, and <1.3×10-5, respectively]. Isotopic data combined with mineralogical observations suggest that relict CAIs formed in an 16O-rich gaseous reservoir before their host chondrules, which originated in an 16O-poor gas. The Adelaide CAI was incorporated into its host chondrule after 26Al had mostly decayed, at least 2 Myr after the CAI formed, and this event reset 26Al-26Mg systematics.

  6. Major contributor to the large piezoelectric response in (1 - x)Ba(Zr0.2Ti0.8)O3 - x(Ba0.7Ca0.3)TiO3 ceramics: Domain wall motion

    NASA Astrophysics Data System (ADS)

    Gao, Jinghui; Hu, Xinghao; Zhang, Le; Li, Fei; Zhang, Lixue; Wang, Yu; Hao, Yanshuang; Zhong, Lisheng; Ren, Xiaobing

    2014-06-01

    The piezoelectric activity of lead-free Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 (BZT-xBCT) ceramics has been investigated as a function of composition by using Rayleigh analysis under subswitching-electric-field in combination with large-electric-field strain measurement. The result shows that the intrinsic piezoelectric response exhibits peak values in the vicinity of composition-induced R (rhombohedral)-MPB (morphotropic phase boundary) and MPB-T (tetragonal) phase transitions, but being much less than total d33 value. On the other hand, the extrinsic piezoelectric response, especially the one associated with reversible domain wall motion, has been greatly enhanced in the phase instability regime. Our results indicate that the extrinsic piezoelectric activity is the major contributor to the high piezoelectricity in BZT-xBCT ceramics.

  7. Phase transitions and phase diagram of Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 Pb-free system by anelastic measurement

    NASA Astrophysics Data System (ADS)

    Xue, Dezhen; Gao, Jinghui; Zhou, Yumei; Ding, Xiangdong; Sun, Jun; Lookman, Turab; Ren, Xiaobing

    2015-03-01

    The internal friction and storage modulus of Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 (BZT-xBCT) Pb-free ceramics have been measured by dynamic mechanical analysis. The anelastic properties show clear anomalies with regard to the transformations between cubic (C), tetragonal (T), orthorhombic (O), and rhombohedral (R) phases, which are all of ferroelastic in nature. The previous reported T-R transition region in the BZT-xBCT system can be divided into the T-O and O-R transitions, consistent with recent studies on the appearance of an intermediate O phase. Based on the internal friction and storage modulus results, a revisited version of BZT-xBCT phase diagram is proposed.

  8. Electronic structure and x-ray magnetic circular dichroism in A2FeReO6 (A =Ca ,Sr ,andBa ) oxides

    NASA Astrophysics Data System (ADS)

    Antonov, V. N.; Bekenov, L. V.; Ernst, A.

    2016-07-01

    A systematic electronic structure study of A2FeReO6 (A =Ba ,Sr ,andCa ) has been performed by employing the local-spin-density approximation (LSDA) and LSDA +U methods using the fully relativistic spin-polarized Dirac linear muffin-tin orbital band-structure method. We investigated the effects of the subtle interplay between spin-orbit coupling, electron correlations, and lattice distortion on the electronic structure of double perovskites. Ca2FeReO6 has a large distortion in the Fe-O-Re bond, and the electronic structure is mainly determined by electron correlations and lattice distortion. In the Ba -Sr -Ca row, the correlation effects at the Fe site are increased. The correlations at the Re site are small in the Ba- and Sr-based compounds but significant in Ca2FeReO6 . Ca2FeReO6 behaves like an insulator only if considered with a relatively large value of Coulomb repulsion Ueff=2.3 eV at the Re site in addition to Ueff=3.1 eV at the Fe site. Ca2FeReO6 possesses a phase transition at 140 K where the metal-insulator transition (MIT) occurs between metallic high-temperature and insulating low-temperature phases. The spin and orbital magnetic moments are linear functions of temperature before and after the MIT but change abruptly at the point of the phase transition. From theoretically calculated magnetocrystalline anisotropy energy (MAE), we found that the easy axis of magnetization for the low-temperature phase is along the b direction, in agreement with experimental data. We found that the major contribution to the MAE is due to the orbital magnetic anisotropy at the Re site. X-ray-absorption spectra and x-ray magnetic circular dichroism at the Re, Fe, and Ba L2 ,3 and Fe, Ca, and O K edges were investigated theoretically in the frame of the LSDA +U method. A qualitative explanation of the x-ray magnetic circular dichroism spectra shape is provided by an analysis of the corresponding selection rules, orbital character, and occupation numbers of individual orbitals

  9. Low loss composition of BaxSryCa1-x-yTiO3: Ba0.12-0.25Sr0.35-0.47Ca0.32-0.53TiO3

    DOEpatents

    Xiang, Xiao-Dong; Chang, Hauyee; Takeuchi, Ichiro

    2001-01-01

    A dielectric thin-film material for microwave applications, including use as a capacitor, the thin-film comprising a composition of barium strontium calcium and titanium of perovskite type (Ba.sub.x Sr.sub.y Ca.sub.1-x-y)TiO.sub.3. Also provided is a method for making a dielectric thin film of that formula over a wide compositional range through a single deposition process.

  10. Photoluminescence of A- and B-site Eu3+-substituted (SrxBa1-x)2CaWyMo1-yO6 phosphors

    NASA Astrophysics Data System (ADS)

    Sletnes, M.; Lindgren, M.; Valmalette, J. C.; Wagner, N. P.; Grande, T.; Einarsrud, M.-A.

    2016-05-01

    The photoluminescence of two series of A- and B-site Eu3+ substituted (SrxBa1-x)2CaWyMo1-yO6 double perovskite phosphor materials, (SrxBa1-x)1.96Eu0.02K0.02CaWyMo1-yO6 and (SrxBa1-x)2Ca0.96Eu0.02Li0.02WyMo1-yO6 (x and y=0, 0.25, 0.50, 0.75, and 1), were studied systematically as a function of stoichiometry and crystal structure. The Eu3+ lattice sites controlled by co-doping with either K or Li were confirmed by Raman spectroscopy. The variation in integrated emission intensity and emission colour over the experimental matrix was examined using statistical tools, and the observed trends were rationalized based on the physical and electronic structure of the phosphors. Phosphors with Eu on B-site with maximum Sr content had remarkably higher emission intensities than all other materials, but the emission was more orange than red due to domination of the 5D0-7F1 (595 nm) transition of Eu3+. The relative intensities of the 5D0-7F2 (615 nm) and 5D0-7F1 transitions of Eu3+, and thus the red-shift of the emission, decreased linearly with increasing Sr content in the A-site Eu-substituted phosphors, and reached a maximum for Sr1.96Eu0.02K0.02CaW0.25Mo0.75O6. A maximum external quantum efficiency of 17% was obtained for the phosphor Sr2Ca0.7Eu0.15Li0.15W0.5Mo0.5O6 with Eu on B-site.

  11. The crystal structure of bøgvadite (Na2SrBa2Al4F20)

    NASA Astrophysics Data System (ADS)

    Balić-Žunić, Tonči

    2014-08-01

    The crystal structure of bøgvadite, Na2SrBa2Al4F20, has been solved and refined to a R1 factor of 4.4 % from single-crystal data (Mo Kα X-ray diffraction, CCD area detector) on a sample from the cryolite deposit at Ivittuut, SW Greenland. Bøgvadite is monoclinic, P21/ n space group, with unit cell parameters a = 7.134(1), b = 19.996(3) and c = 5.3440(8) Å, β = 90.02(1)o. A close proximity of the crystal structure to an orthorhombic symmetry and the presence of the two twin components in a nearly 1:1 ratio suggest that the investigated bøgvadite crystal has originally formed as a high-temperature orthorhombic polymorph which on cooling transformed to the stable low temperature monoclinic structure. The bøgvadite crystal structure has groupings of cation-fluoride coordination polyhedra similar to those found in the crystal structures of the genetically closely associated minerals jarlite and jørgensenite. However, its structure type is different from the latter two. The fluoridoaluminate framework of bøgvadite consists of infinite zig-zag chains of cis-connected AlF6 coordination octahedra. The 1 ∞[AlF5] chains are interconnected by infinite chains of Na-F coordination polyhedra which extend in the same direction. Na is coordinated by nine F atoms if its full surrounding is taken in consideration, but makes significant chemical bonds only to closest five. The chains of AlF6 and NaF9 coordination polyhedra form double layers. In the centre of layers, relatively large voids in the form of pentagonal antiprisms are occupied by Sr atoms which make chemical bonds with the closest six F atoms. Between the SrF10 coordinations in the centre of layers run empty channels. The double layers are interconnected by Ba atoms which are coordinated by eight F atoms and fill the spaces between the layers. Bøgvadite belongs to the group of fluoridoaluminates with infinite chains of cis-connected AlF6 coordination octahedra, alike those found in the crystal structures of Ba-fluoridoaluminates.

  12. Evolution of structure and physical properties in Al-substituted Ba-hexaferrites

    NASA Astrophysics Data System (ADS)

    Alex, Trukhanov; Larisa, Panina; Sergei, Trukhanov; Vitalii, Turchenko; Mohamed, Salem

    2016-01-01

    The investigations of the crystal and magnetic structures of the BaFe12-xAlxO19 (x = 0.1-1.2) solid solutions have been performed with powder neutron diffractometry. Magnetic properties of the BaFe12-xAlxO19 (x = 0.1-1.2) solid solutions have been measured by vibration sample magnetometry at different temperatures under different magnetic fields. The atomic coordinates and lattice parameters have been Rietveld refined. The invar effect is observed in low temperature range (from 4.2 K to 150 K). It is explained by the thermal oscillation anharmonicity of atoms. The increase of microstress with decreasing temperature is found from Rietveld refinement. The Curie temperature and the change of total magnetic moment per formula unit are found for all compositions of the BaFe12-xAlxO19 (x = 0.1-1.2) solid solutions. The magnetic structure model is proposed. The most likely reasons and the mechanism of magnetic structure formation are discussed. Project supported by the Ministry of Education and Science of the Russian Federation in the framework of Increase Competitiveness Program of NUST “MISiS” (Grant No. K4-2015-040). L. Panina acknowledges support under the Russian Federation State contract for organizing a scientific work.

  13. Crystal structure study of (Ca, Gd){sub 2}(Al, Ti)O{sub 4}

    SciTech Connect

    Sawada, Haruo; Marumo, Fumiyuki; Kodama, Nobuhiro

    1998-08-01

    The crystal structures of two crystals of (Ca, Gd){sub 2} (Al, Ti)O{sub 4} [tetragonal I4/mmm; Z = 4], one strongly fluorescent and the other weakly fluorescent, having minor differences in their precise compositions have been studied with single-crystal X-ray diffraction methods. The unit cell is significantly smaller for the weakly fluorescent crystal, which also shows alteration of the coordination polyhedraon around the (Ca, Gd) site, suggesting the formation of vacancies at an oxygen site.

  14. Soot oxidation and NO{sub x} reduction over BaAl{sub 2}O{sub 4} catalyst

    SciTech Connect

    Lin, He; Li, Yingjie; Shangguan, Wenfeng; Huang, Zhen

    2009-11-15

    This study addresses soot oxidation and NO{sub x} reduction over a BaAl{sub 2}O{sub 4} catalyst. By XRD analysis, the catalyst was shown to be of spinel structure. Temperature Programmed Oxidation (TPO) and Constant Temperature Oxidation (CTO) at 673 K show that the presence of O{sub 2} decreases the ignition temperature of soot, and it enhances the conversion of NO{sub x} to N{sub 2} and N{sub 2}O. The kinetic features of soot oxidation in the TPO test are similar to that in the TG-DTA analysis. Analysis by Diffuse Reflectance Fourier Infrared Transform Spectroscopy (DRIFTS) indicates that the nitrates formed from NO{sub x} adsorption and the C(O) intermediates from soot oxidation are the key precursors of the redox process between soot and NO{sub x} over surfaces of the BaAl{sub 2}O{sub 4} catalyst. Moreover, DRIFTS tests suggest that nitrates act as the principal oxidants for C(O) oxidation, through which nitrates are reduced to N{sub 2} and N{sub 2}O. The O{sub 2} in the gas mixture presents a positive effect on the conversion of NO{sub x} to N{sub 2} and N{sub 2}O by promoting the oxidation of nitrites into nitrates species. (author)

  15. Thermal transformation of quaternary compounds in NaF-CaF{sub 2}-AlF{sub 3} system

    SciTech Connect

    Zaitseva, Julia N.; Yakimov, Igor S.; Kirik, Sergei D.

    2009-08-15

    Details of quaternary compounds formation in the system NaF-CaF{sub 2}-AlF{sub 3} are specified. To achieve this aim, the samples of phases NaCaAlF{sub 6} and Na{sub 2}Ca{sub 3}Al{sub 2}F{sub 14} have been obtained by high-temperature solid-phase synthesis. Their thermal behavior when heated up to 800 deg. C has been studied using the methods of high-temperature X-ray diffraction (XRD) and thermal analysis (TA). The system under consideration can be regarded as a quasibinary section CaF{sub 2}-NaAlF{sub 4}, where at T=745-750 deg. C invariant equilibrium is implemented with the phases CaF{sub 2}-NaCaAlF{sub 6}-Na{sub 2}Ca{sub 3}Al{sub 2}F{sub 14}-(liquid melt)-(NaAlF{sub 4}). The peculiarity of the equilibrium is NaAlF{sub 4} metastability at normal pressure. Below the equilibrium temperature the quaternary phase Na{sub 2}Ca{sub 3}Al{sub 2}F{sub 14} is stable and NaCaAlF{sub 6} above this temperature. The phase NaCaAlF{sub 6} fixed by rapid quenching from high temperatures and when heated up to 640 deg. C decomposes, yielding Na{sub 2}Ca{sub 3}Al{sub 2}F{sub 14}. Further heating in vacuum at temperature up to 740 deg. C results in decomposition of Na{sub 2}Ca{sub 3}Al{sub 2}F{sub 14} into CaF{sub 2} and Na{sub 3}AlF{sub 6}. The expected reverse transformation of Na{sub 2}Ca{sub 3}Al{sub 2}F{sub 14} into NaCaAlF{sub 6} has not been observed under experimental conditions. Transformations in bulk samples reveal direct and reverse transformation of quaternary phases. Synopsis: Thermal transformation of the quaternary compounds in system (NaF-CaF{sub 2}-AlF{sub 3}) was investigated using high-temperature X-ray diffraction (XRD) and thermal analysis (TA). In the system the invariant equilibrium is implemented with the phases CaF{sub 2}-NaCaAlF{sub 6}-Na{sub 2}Ca{sub 3}Al{sub 2}F{sub 14}-(liquid melt)-(NaAlF{sub 4}) at T=745-750 deg. C. - Graphical Abstract: The paper concerns of a small piece of the ternary system (NaF-CaF{sub 2}-AlF{sub 3}) which is very important for

  16. Photoluminescence and cathodoluminescence properties of Eu{sup 3+} ions activated AMoO{sub 4} (A = Mg, Ca, Sr, Ba) phosphors

    SciTech Connect

    Du, Peng; Yu, Jae Su

    2015-10-15

    Highlights: • Under 393 nm excitation, strong red emission located at 615 nm was observed in all the samples. • The Eu{sup 3+}-activated CaMoO{sub 4} phosphor exhibited the strongest PL properties. • The CIE chromaticity coordinate of Eu{sup 3+}-activated CaMoO{sub 4} phosphor was (0.647,0.352). • The color purity of Eu{sup 3+}-activated CaMoO{sub 4} phosphor was 92.8%. • Strong CL properties were observed in the Eu{sup 3+}-activated CaMoO{sub 4} phosphor. - Abstract: Eu{sup 3+}-activated AMoO{sub 4} (A = Mg, Ca, Sr, Ba) phosphors were synthesized by a solid-state reaction method. Photoluminescence and cathodoluminescence (CL) spectra as well as X-ray diffraction patterns were measured to characterize the fabricated samples. Under 393 nm excitation, strong red emissions located at ∼615 nm corresponding to the {sup 5}D{sub 0} → {sup 7}F{sub 2} transition of Eu{sup 3+} ions were observed in all the samples. Compared with other Eu{sup 3+} ions activated AMoO{sub 4} (A = Mg, Sr, Ba) phosphors, Eu{sup 3+}-activated CaMoO{sub 4} phosphor exhibited the strongest red emission intensity with better Commission Internationale de L’Eclairage chromaticity coordinate and higher color purity. Furthermore, the CL results indicated that the Eu{sup 3+}-activated CaMoO{sub 4} phosphor had excellent luminescence properties.

  17. Multiband orange-red photoluminescence of Eu{sup 3+} ions in new '114' LnBaZn{sub 3}GaO{sub 7} and LnBaZn{sub 3}AlO{sub 7} oxides

    SciTech Connect

    Saradhi, M.P.; Raveau, B.; Caignaert, V.; Varadaraju, U.V.

    2010-02-15

    A new series of gallozincates LnBaZn{sub 3}GaO{sub 7} (Ln=La, Nd, Sm, Eu, Gd, Dy, Y) and new aluminozincates LnBaZn{sub 3}AlO{sub 7} (Ln=Y, Eu, Dy) have been synthesized. Their structure refinements show that these phases belong to the '114' series, with hexagonal P6{sub 3}mc space group previously described for SmBaZn{sub 3}AlO{sub 7}. The photoluminescence study of these oxides shows that the Eu{sup 3+} activated LnBaZn{sub 3}MO{sub 7} oxides with Ln=Y, La, Gd; and M=Al, Ga exhibit strong magnetic and electric dipole transitions (multiband emission) which is of interest for white light production. These results also confirm that the site occupied by Eu{sup 3+} is not strictly centrosymmetric. The electric dipole transition intensity is the highest in GdBaZn{sub 3}MO{sub 7} [M=Al, Ga]: 0.05Eu{sup 3+} as compared with other Eu{sup 3+} activated compositions. This is due to the layer distortion around GdO{sub 6} octahedra when compared with YO{sub 6} and LaO{sub 6} octahedra. - Graphical abstract: The projected structure consists of alternate stacked layers of Kagome and Triangular type with statistical distribution of Zn and Ga atoms between two tetrahedral sites. Ba{sup 2+} present in anticuboctahedron coordinating with 12 oxygen atoms. The Eu{sup 3+} present in octahedral coordination with 3-fold rotational symmetry.

  18. Electrical properties and crystal structures of the homologous series of oxides Nd 2Ba 2Ca mCe nTi 2-δCu 2+δO 11+ m+2 n ( m, n = 0 or 1)

    NASA Astrophysics Data System (ADS)

    Den, T.; Kobayashi, T.; Izumi, F.; Kamiyama, T.; Shimakawa, Y.; Jorgensen, J. D.; Rotella, F. J.; Hitterman, R. L.

    1995-02-01

    Four oxides belonging to the homologous series with the general formula Nd 2Ba 2Ca mCe nTi 2-δCu 2+δO 11+ m+2 n, were prepared for m, n = 0 or 1. Although all of these oxides have two-dimensional CuO 2 planes, they do not show any superconductivity, only a normal paramagnetic behavior. Their crystal structures were analyzed by TOF neutron powder diffraction. Nd 2Ba 2Ti 1.908Cu 2.092O 11 ( m=0, n=0 and δ=0.09) is isomorphous with Gd 2Ba 2Ti 2Cu 2O 11. The structures of the other three oxides can be derived from that of Nd 2Ba 2Ti 1.908Cu 2.092O 11. The structure of Nd 2Ba 2Ti 1.92Cu 2.08O 12 ( m=1, n=0 and δ=0.08) is obtained by the substitution of rock-salt-type (Ca,Nd,Ba)O(Ca,Nd,Ba)O layers for the (Nd,Ba)O layer. The structure of Nd 2Ba 2CeTi 2Cu 2O 13 ( m=0, n=1 and δ=0) is characterized by the insertion of fluorite-type (Nd,Ce)O 2(Nd,Ce) layers in the place of the Nd layer. Nd 2Ba 2CaCeTi 2Cu 2O 14 ( m=1, n=1, and δ=0) results from the alternate substitutions of rock-salt-type and fluorite-type layers for the (Nd,Ba)O and Nd layers, respectively.

  19. Origin of Ca-Al-rich inclusions. II - Sputtering and collisions in the three-ph8se interstellar medium

    NASA Technical Reports Server (NTRS)

    Clayton, D. D.

    1981-01-01

    The theory put forward by Clayton (1977) for the formation of the Ca-Al-rich inclusions within C3 meteorites is extended to an evolutionary history in a three-phase interstellar medium. Widespread supersonic turbulence in the hot interstellar medium is maintained by supernova shock waves, giving rise to heavy sputtering of the refractory dust. Subsequent reaccumulation with varying dust/gas ratios or varying particle sizes produces isotopically fractionated Ca-Al-rich accumulates. It is thought that the Ca-Al-rich inclusions themselves are formed by the following sequence in the solar system: (1) cold accumulation of larger-than-average Ca-Al-rich particles containing supernova condensate cores into macroscopic (approximately 1 cm) Ca-Al-rich agglomerates, probably by sedimentation; and (2) fusion of the supernova condensates into macroscopic minerals by exothermic chemical reactions that begin when the accumulate has been warmed, thereby releasing energy from the unequilibrated forms accumulated from the interstellar medium.

  20. Eu(2+)-Activated Alkaline-Earth Halophosphates, M5(PO4)3X:Eu(2+) (M = Ca, Sr, Ba; X = F, Cl, Br) for NUV-LEDs: Site-Selective Crystal Field Effect.

    PubMed

    Kim, Donghyeon; Kim, Sung-Chul; Bae, Jong-Seong; Kim, Sungyun; Kim, Seung-Joo; Park, Jung-Chul

    2016-09-01

    Eu(2+)-activated M5(PO4)3X (M = Ca, Sr, Ba; X = F, Cl, Br) compounds providing different alkaline-earth metal and halide ions were successfully synthesized and characterized. The emission peak maxima of the M5(PO4)3Cl:Eu(2+) (M = Ca, Sr, Ba) compounds were blue-shifted from Ca to Ba (454 nm for Ca, 444 nm for Sr, and 434 nm for Ba), and those of the Sr5(PO4)3X:Eu(2+) (X = F, Cl, Br) compounds were red-shifted along the series of halides, F → Cl → Br (437 nm for F, 444 nm for Cl, and 448 nm for Br). The site selectivity and occupancy of the activator ions (Eu(2+)) in the M5(PO4)3X:Eu(2+) (M = Ca, Sr, Ba; X = F, Cl, Br) crystal lattices were estimated based on theoretical calculation of the 5d → 4f transition energies of Eu(2+) using LCAO. In combination with the photoluminescence measurements and theoretical calculation, it was elucidated that the Eu(2+) ions preferably enter the fully oxygen-coordinated sites in the M5(PO4)3X:Eu(2+) (M = Ca, Sr, Ba; X = F, Cl, Br) compounds. This trend can be well explained by "Pauling's rules". These compounds may provide a platform for modeling a new phosphor and application in the solid-state lighting field. PMID:27494550

  1. Observations of the Minor Species Al, Fe and Ca(+) in Mercury's Exosphere

    NASA Technical Reports Server (NTRS)

    Bida, Thomas A.; Killen, Rosemary M.

    2011-01-01

    We report the first detections of Al and Fe, and strict upper limits for Ca(+) in the exosphere of Mercury, using the HIRES spectrometer at the Keck I telescope. We report observed 4-sigma tangent columns of 1.5x10(exp 7) Al atoms per square centimeter at an altitude of 1220 km (1.5 Mercury radii (R(sub M)) from planet center), and that for Fe of 1.6 x 10 per square centimeter at an altitude of 950 km (1.4 R(sub M)). The observed 3-sigma Ca(+) column was 3.9x10(exp 6) ions per square centimeter at an altitude of 1630 km (1.67 R(sub M). A simple model for zenith column abundances of the neutral species were 9.5 x 10(exp 7) Al per square centimeter, and 3.0 x 10(exp 8) Fe per square centimeter. The observations appear to be consistent with production of these species by impact vaporization with a large fraction of the ejecta in molecular form. The scale height of the Al gas is consistent with a kinetic temperature of 3000 - 9000 K while that of Fe is 10500 K. The apparent high temperature of the Fe gas would suggest that it may be produced by dissociation of molecules. A large traction of both Al and Fe appear to condense in a vapor cloud at low altitudes.

  2. ABiO2X (A = Cd, Ca, Sr, Ba, Pb; X = halogen) Sillen X1 Series: Polymorphism Versus Optical Properties.

    PubMed

    Olchowka, Jacob; Kabbour, Houria; Colmont, Marie; Adlung, Matthias; Wickleder, Claudia; Mentré, Olivier

    2016-08-01

    The Sillen X1 series of Bi(3+)A(2+)O2X (A = Cd, Ca, Sr, Ba, Pb; X = Cl, Br, I) compounds is composed of three main crystallographic types, namely, the tetragonal form (space group (S.G.) I4/mmm), the orthorhombic form (S.G. Cmcm), and the monoclinic form (S.G. P21/m). Because of Bi(3+)/A(2+) disorder the Bi(3+) based photoluminescence (PL) of the tetragonal polytypes is quenched at room temperature (RT). In the two other ordered forms, the Bi-O-Bi connectivity is different but limited, such that bluish/greenish emission occurs at RT in the monoclinic CdBiO2Cl and CaBiO2Cl and orthorhombic SrBiO2Cl and BaBiO2Cl phases. The crystal structure of BaBiO2Br was refined in the orthorhombic Cmcm space group and also shows RT emission. Focusing on the RT luminescent activity as a key parameter, the PL active compounds were investigated by means of density functional theory calculations and UV-visible reflectance spectroscopy. The influence of A and X ions on the excitation energy is discussed by analyzing the A-O-Bi and Bi-X bonding schemes and gives some insights for rational tuning of both the excitation and emission energies. PMID:27414069

  3. Improvement of critical current density in thallium-based (Tl,Bi)Sr{sub 1.6}Ba{sub 0.4}Ca{sub 2}Cu{sub 3}O{sub x} superconductors

    SciTech Connect

    Ren, Z.F.; Wang, C.A.; Wang, J.H.

    1994-12-31

    Epitaxial (Tl,Bi)Sr{sub 1.6}Ba{sub 0.4}Ca{sub 2}Cu{sub 3}O{sub x} (Tl,Bi)-1223 thin films on (100) single crystal LaAlO{sub 3} substrates were synthesized by a two-step procedure. Phase development, microstructure, and relationships between film and substrate were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Resistance versus temperature, zero-field-cooled and field-cooled magnetization, and transport critical current density (J{sub c}) were measured. The zero-resistance temperature was 105-111 K. J{sub c} at 77 K and zero field was > 2 x 10{sup 6} A/cm{sup 2}. The films exhibited good flux pinning properties.

  4. High Tc superconductivity in the triple-perovskite La-rare earth or alkali metal-Ba-Ca-Mg or Cd-Cu-oxide system. Technical report, January-December 1996

    SciTech Connect

    Tauber, A.; Tidrow, S.C.; Pierce, D.; Eckart, D.W.

    1997-03-01

    Bulk targets of compounds in the system La(3{minus}z)Me(z)Ba3Ca(1{minus}v)Nc{sub v}Cu7O(16+v) where Me=rare earth or Na and Nc=Mg or Cd were prepared by solid state reactions. They were employed to deposit by pulse laser deposition thin films of the superconductor on single crystal substrates of LaAlO3, LSAT, and GGG. Phase relationships and orientation relationships were obtained from diffractometer scans. All compounds exhibited a (001) relationship with all substrates. Lattice parameters, transition temperatures and widths are reported for each superconducting compound. All substituted compounds were superconducting but no increase in Tc was observed for any. All thin films heated to 750 deg C desorbed little oxygen compared to YBCO.

  5. Sr isotopic fractionation in Ca-Al inclusions from the Allende meteorite

    USGS Publications Warehouse

    Patchett, P.J.

    1980-01-01

    True relative Sr isotopic compositions, determined by double spiking on Ca-Al inclusions from the Allende meteorite show up to 1.5??? per mass unit mass fractionation relative to the Earth and bulk chondrites. All abnormal inclusions are light-isotope enriched. A lack of isotopically heavy Sr in inclusions would place constraints on the time, place and mechanism of origin of these objects. ?? 1980 Nature Publishing Group.

  6. Rapid synthesis and characterization of (Ca 1- xBa x) 3Co 4O 9 thin films using combinatorial methods

    NASA Astrophysics Data System (ADS)

    Minami, H.; Itaka, K.; Kawaji, H.; Wang, Q. J.; Koinuma, H.; Lippmaa, M.

    2002-09-01

    We have successfully fabricated high-quality thin film of Ca 3Co 4O 9, an oxide with superior thermoelectric properties, on a lattice matched TiO 2 (1 0 0) substrate using PLD. In order to investigate the effect of elemental substitution on thermoelectric properties, we fabricated a composition-spread library of (Ca 1- xBa x) 3Co 4O 9 (0≤ x≤0.2), having linear compositional variation x along one direction of the substrate surface. A pin-probe type multi-channel measurement system was developed to quickly measure the thermoelectric properties (Seebeck coefficient and electric conductivity) of the library for the rapid characterization. The good correspondence of the data for Ca 3Co 4O 9 film with those for bulk sample verifies that we can accelerate the exploration of thermoelectric oxides at least 10 times faster than the conventional one-by-one approach.

  7. Crystal growth, polarized spectra, and laser performance of Yb:CaGdAlO4 crystal

    NASA Astrophysics Data System (ADS)

    Di, J. Q.; Xu, X. D.; Xia, C. T.; Zheng, L. H.; Aka, G.; Yu, H. H.; Sai, Q. L.; Guo, X. Y.; Zhu, L.

    2016-04-01

    In this paper, the crystal growth, polarized spectra, and laser performance of Yb:CaGdAlO4 crystal were reported. The segregation coefficient of Yb3+ ions was calculated to be 0.47. The cell parameters were determined to be a  =  b  =  0.3658 nm, c  =  1.1985 nm. The peak absorption cross-section was calculated to be 2.65  ×  10-20 cm2 at 979 nm and the peak stimulated emission cross-section was 2.23  ×  10-20 cm2 at 980 nm for the π polarization. The continuous-wave (CW) laser operations of uncoated Yb:CaGdAlO4 crystals with 5  ×  5  ×  3 mm3 in size were demonstrated. A maximum output power of 1.6 W at 1048 nm was obtained with a slope efficiency of 28%. The results show that Yb:CaGdAlO4 crystal is a promising laser medium.

  8. Hibonite, Ca2/Al, Ti/24O38, from the Leoville and Allende chondritic meteorites.

    NASA Technical Reports Server (NTRS)

    Keil, K.; Fuchs, L. H.

    1971-01-01

    Hibonite was discovered in light-colored, Ca-Al-Ti-rich and Si-Fe-poor, achondritic inclusions of the Leoville and Allende HL-group chondrites. Two varieties of hibonite occur: one emits a bright red-orange luminescence under electron bombardment and has high amounts of Al2O3 (87.7; 87.9) and low amounts of MgO (0.65; 0.8) and TiO2 (0.68; 0.8). The other emits a bright blue luminescence and is low in Al2O3 (78.7; 79.2) and high in MgO (3.3; 3.7) and TiO2 (6.5; 7.9) (in wt. %). The oxide CaO is about the same in both varieties. It is suggested that the change in the color of the visible luminescence results from changes in composition. The origin of hibonite which occurs in complex mineral assemblages together with anorthite, gelhenite, wollastonite, aluminous diopside, andradite, Ca-pyroxene, perovskite, spinel, taenite, chromite, and pentlandite, and in close proximity to nodules containing calcite, whewellite, forsterite and many of the aforementioned phases, is discussed. The proposition that hibonite and associated phases originated by contact metamorphism and metasomatism of calcite-dolomite bearing assemblages cannot, at this time, be completely ruled out.

  9. Polymer Coated CaAl-Layered Double Hydroxide Nanomaterials for Potential Calcium Supplement

    PubMed Central

    Kim, Tae-Hyun; Lee, Jeong-A; Choi, Soo-Jin; Oh, Jae-Min

    2014-01-01

    We have successfully prepared layered double hydroxide (LDH) nanomaterials containing calcium and aluminum ions in the framework (CaAl-LDH). The surface of CaAl-LDH was coated with enteric polymer, Eudragit®L 100 in order to protect nanomaterials from fast dissolution under gastric condition of pH 1.2. The X-ray diffraction patterns, Fourier transform infrared spectroscopy, scanning electron and transmission electron microscopy revealed that the pristine LDH was well prepared having hydrocalumite structure, and that the polymer effectively coated the surface of LDH without disturbing structure. From thermal analysis, it was determined that only a small amount (less than 1%) of polymer was coated on the LDH surface. Metal dissolution from LDH nanomaterials was significantly reduced upon Eudragit®L 100 coating at pH 1.2, 6.8 and 7.4, which simulates gastric, enteric and plasma conditions, respectively, and the dissolution effect was the most suppressed at pH 1.2. The LDH nanomaterials did not exhibit any significant cytotoxicity up to 1000 μg/mL and intracellular calcium concentration significantly increased in LDH-treated human intestinal cells. Pharmacokinetic study demonstrated absorption efficiency of Eudragit®L 100 coated LDH following oral administration to rats. Moreover, the LDH nanomaterials did not cause acute toxic effect in vivo. All the results suggest the great potential of CaAl-LDH nanomaterials as a calcium supplement. PMID:25490138

  10. Luminous characteristics and thermal stability of BaMgAl 10O 17:Eu 2+ phosphor for white light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Shen, Changyu; Yang, Yi; Jin, Shangzhong; Ming, Jiangzhou

    2010-02-01

    A blue-emitting phosphor, BaMgAl 10O 17:Eu 2+ (BAM) was prepared by the solid-state reaction and X-ray powder diffraction (XRD) analysis confirmed the formation of BAM. Photoluminescence (PL) results showed that the phosphor can be efficiently excited by the light from near ultraviolet (NUV) to visible, and exhibited bright blue emission. The effect of the doped-Eu 2+ in BAM on the PL was investigated. To improve the BAM's thermal stability, BAM doped with additional Mg 2+ was studied. The experiment results showed that additional 0.05 mol Mg 2+-doped BAM had the highest emission intensity and thermal stability. By combining with NUV LED chip (GaN-based 380 nm emitting), a novel intense white LED was fabricated based on the blue phosphor BAM and a red phosphor Ca(La 0.5Eu 0.5) 4Si 3O 13. The white LED has the characteristics of color-rendering index of 87, CIE chromaticity coordinates ( x, y) of (0.3225, 0.3187), color temperature Tc of 5680 K, and light output of 51.7 lm/W under the forward-bias current of 20 mA. As the current increases, the relative intensity increases, the correlated color temperature Tc increases from 4000 to 7900 K and the color-rendering index Ra increases from 83 to 91 simultaneously.

  11. Effect of Eu substitution on superconductivity in Ba{sub 8−x}Eu{sub x}Al{sub 6}Si{sub 40} clathrates

    SciTech Connect

    Liu, Lihua; Bi, Shanli; Peng, Bailu; Li, Yang

    2015-05-07

    The silicon clathrate superconductor is uncommon as its structure is dominated by strong Si-Si covalent bonds, rather than the metallic bond, that are more typical of traditional superconductors. To understand the influence of large magnetic moment of Eu on superconductivity for type-I clathrates, a series of samples with the chemical formula Ba{sub 8−x}Eu{sub x}Al{sub 6}Si{sub 40} (x = 0, 0.5, 1, and 2) were synthesised in which Eu occupied Ba sites in cage center. With the increase of Eu content, the cubic lattice parameter decreases monotonically signifying continuous shrinkage of the constituting (Ba/Eu)@Si{sub 20} and (Ba/Eu)@Si{sub 24} cages. The temperature dependence of magnetization at low temperature revealed that Ba{sub 8}Al{sub 6}Si{sub 40} is superconductive with transition temperature at T{sub C} = 5.6 K. The substitution of Eu for Ba results in a strong superconductivity suppression; Eu-doping largely decreases the superconducting volume and transition temperature T{sub C}. Eu atoms enter the clathrate lattice and their magnetic moments break paired electrons. The Curie-Weiss temperatures were observed at 3.9, 6.6, and 10.9 K, respectively, for samples with x = 0.5, 1.0, and 2.0. Such ferromagnetic interaction of Eu can destroy superconductivity.

  12. A double substitution induced Ca(Mg0.8, Al0.2)(Si1.8, Al0.2)O6:Eu(2+) phosphor for w-LEDs: synthesis, structure, and luminescence properties.

    PubMed

    Li, Yang; Liu, Wenjing; Wang, Xicheng; Zhu, Ge; Wang, Chuang; Wang, Yuhua

    2015-08-01

    A double substitution induced blue-emitting phosphor Ca(Mg0.8, Al0.2)(Si1.8, Al0.2)O6:Eu(2+) (CMAS:Eu(2+)) was successfully synthesized by a solid-state reaction process, and its structure and luminescence properties were investigated in detail. The crystal structure and chemical composition of the CMAS matrix were analyzed and determined based on Rietveld refinements and Energy Dispersive Spectroscopy (EDS). The composition-optimized CMAS:Eu(2+) exhibited a strong blue light, centered at 446 nm upon excitation at 365 nm with the Commission Internationale de L'Eclairage (CIE) coordinates of (0.144, 0.113). Under 380 nm excitation, the PL emission intensity area of the optimized phosphor was found to be 46.95% of that of the commercial BaMgAl10O17:Eu(2+) (BAM:Eu(2+)) phosphor and the quantum efficiency of the phosphor is 41.32%. The temperature-dependent PL studies have been investigated which show the thermal stability of the CMAS:Eu(2+) phosphor compared with that of the CaMgSi2O6:Eu(2+) (CMS:Eu(2+)) phosphor. PMID:26115078

  13. A double substitution induced Ca(Mg0.8, Al0.2)(Si1.8, Al0.2)O6:Eu(2+) phosphor for w-LEDs: synthesis, structure, and luminescence properties.

    PubMed

    Li, Yang; Liu, Wenjing; Wang, Xicheng; Zhu, Ge; Wang, Chuang; Wang, Yuhua

    2015-08-01

    A double substitution induced blue-emitting phosphor Ca(Mg0.8, Al0.2)(Si1.8, Al0.2)O6:Eu(2+) (CMAS:Eu(2+)) was successfully synthesized by a solid-state reaction process, and its structure and luminescence properties were investigated in detail. The crystal structure and chemical composition of the CMAS matrix were analyzed and determined based on Rietveld refinements and Energy Dispersive Spectroscopy (EDS). The composition-optimized CMAS:Eu(2+) exhibited a strong blue light, centered at 446 nm upon excitation at 365 nm with the Commission Internationale de L'Eclairage (CIE) coordinates of (0.144, 0.113). Under 380 nm excitation, the PL emission intensity area of the optimized phosphor was found to be 46.95% of that of the commercial BaMgAl10O17:Eu(2+) (BAM:Eu(2+)) phosphor and the quantum efficiency of the phosphor is 41.32%. The temperature-dependent PL studies have been investigated which show the thermal stability of the CMAS:Eu(2+) phosphor compared with that of the CaMgSi2O6:Eu(2+) (CMS:Eu(2+)) phosphor.

  14. Tetragonal To Collapsed Tetragonal Phase Transition In BaFe{sub 2}As{sub 2} and CaFe{sub 2}As{sub 2}

    SciTech Connect

    Mittal, R.; Mishra, S. K.; Chaplot, S. L.; Ovsyannikov, S. V.; Trots, D. M.; Dubrovinsky, L.; Greenberg, E.; Su, Y.; Brueckel, Th.; Matsuishi, S.; Hosono, H.; Garbarino, G.

    2010-12-01

    Superconductivity in MFe{sub 2}As{sub 2} (M = Ba, Ca) compounds appears either at a critical doping level at ambient pressure or in the parent compound itself by application of pressure above a critical value. We report high pressure powder x-ray diffractions studies for these compounds at 300 K up to about 56 GPa using membrane diamond anvil cells. The measurements for BaFe{sub 2}As{sub 2} show a new tetragonal to collapsed tetragonal phase transition at about 22 GPa that remains stable upto 56 GPa. CaFe{sub 2}As{sub 2} is already known to transform to collapsed phase at 1.7 GPa at 300 K. Our measurements on CaFe{sub 2}As{sub 2} do not show any post collapsed phase transition on increase of pressure 50 GPa at 300 K. It is important to note that the transition in both compounds occurs when they are compressed to almost the same value of the unit cell volume and attain similar c{sub t}/a{sub t} ratios. We present a detailed analysis of the pressure dependence and structure phase transitions as well as equation of state in these important FeAs compounds that should be useful in the context of possible superconductivity in the collapsed phase.

  15. μSR study of charge neutrally doped Y 1-2xCa xTh xBa 2Cu 3O 7- δ system covering the

    NASA Astrophysics Data System (ADS)

    Hartmann, O.; Karlsson, E.; Lidström, E.; Wäppling, R.; Lundqvist, P.; Hegedüs, Z.; Rapp, Ö.

    1994-12-01

    Muon spin relaxation measurements were performed on the Y 1-2xCa xTh xBa 2Cu 3O 7- δ solubility range for doping in the orthorhombic phase. The low temperature relaxation rate was found to decrease with CaTh concentration in the dilute range and to be constant for high doping levels.

  16. Characteristics of TlBa[sub 2]Ca[sub 2]Cu[sub 3]O[sub 9+][sub [delta

    SciTech Connect

    Kung, P.J.; Maley, M.P.; Wahlbeck, P.G.; Peterson, D.E. )

    1993-04-01

    Crystal structure and superconductivity of the Tl--Ba--Ca--Cu--O powder prepared by a solid-state reaction were studied. The results of x-ray diffraction, scanning electron microscopy, and transmission electron microscopy analyses indicate that the powder of a major single 1223 phase was synthesized with a cauliflower-like morphology; by grinding, the powder was partially transformed to an amorphous phase. The measurement of magnetic hysteresis was also performed in the temperature range of 7--75 K up to 5 T from which the weak field-dependent behavior of critical current density was observed. The as-synthesized powder, with [ital T][sub [ital c

  17. Complex Formation Between Ca(II), Mg(II), Al(III) Ions and Salicylglycine

    PubMed Central

    Kilyén, Melinda; Labádi, lmre; Tombácz, Etelka; Kiss, Tamás

    2003-01-01

    For modelling the interactions of proteins/peptides with hard metal ions the complex formation of salicylglycine (SalGly) with Ca(II), Mg(ll) and AI(III) ions was studied in aqueous solution using pHpotentiometric and UV-vis spectroscopic techniques. Al(lll) ion was found to form more stable complexes with SalGiy than Ca(ll) or Mg(ll) ions. While AI(III) ion forms various 1:1 complexes of different protonation states in the pH range 2-7, Ca(ll), Mg(ll) ions seem to interact with SalGly only in the basic pH range and form mixed hydroxo species MLH-1 at pH ~ 8. According to the UV-vis spectroscopic measurements in the species MLH-1 the carboxylate-O- atom and the phenolate-O- coordinate to the metal ions. SaIGiy is able to keep Al(lll) in solution through inner and outer sphere coordination to metastable amorphous AI(OH)3 particles. Deprotonation of the peptide amide Nil does not occur in these systems. PMID:18365063

  18. Network topology for the formation of solvated electrons in binary CaO-Al2O3 composition glasses.

    PubMed

    Akola, Jaakko; Kohara, Shinji; Ohara, Koji; Fujiwara, Akihiko; Watanabe, Yasuhiro; Masuno, Atsunobu; Usuki, Takeshi; Kubo, Takashi; Nakahira, Atsushi; Nitta, Kiyofumi; Uruga, Tomoya; Weber, J K Richard; Benmore, Chris J

    2013-06-18

    Glass formation in the CaO-Al2O3 system represents an important phenomenon because it does not contain typical network-forming cations. We have produced structural models of CaO-Al2O3 glasses using combined density functional theory-reverse Monte Carlo simulations and obtained structures that reproduce experiments (X-ray and neutron diffraction, extended X-ray absorption fine structure) and result in cohesive energies close to the crystalline ground states. The O-Ca and O-Al coordination numbers are similar in the eutectic 64 mol % CaO (64CaO) glass [comparable to 12CaO·7Al2O3 (C12A7)], and the glass structure comprises a topologically disordered cage network with large-sized rings. This topologically disordered network is the signature of the high glass-forming ability of 64CaO glass and high viscosity in the melt. Analysis of the electronic structure reveals that the atomic charges for Al are comparable to those for Ca, and the bond strength of Al-O is stronger than that of Ca-O, indicating that oxygen is more weakly bound by cations in CaO-rich glass. The analysis shows that the lowest unoccupied molecular orbitals occurs in cavity sites, suggesting that the C12A7 electride glass [Kim SW, Shimoyama T, Hosono H (2011) Science 333(6038):71-74] synthesized from a strongly reduced high-temperature melt can host solvated electrons and bipolarons. Calculations of 64CaO glass structures with few subtracted oxygen atoms (additional electrons) confirm this observation. The comparable atomic charges and coordination of the cations promote more efficient elemental mixing, and this is the origin of the extended cage structure and hosted solvated (trapped) electrons in the C12A7 glass.

  19. Geoenvironmental weathering/deterioration of landfilled MSWI-BA glass.

    PubMed

    Wei, Yunmei; Saffarzadeh, Amirhomayoun; Shimaoka, Takayuki; Zhao, Chun; Peng, Xuya; Gao, Junmin

    2014-08-15

    Municipal solid waste incineration bottom ash (MSWI-BA) glass serves as a matrix of assorted bottom ash (BA) compounds. Deterioration of the BA glass phases is quite important as they regulate the distribution of a series of toxic elements. This paper studied landfilled MSWI-BA samples from the mineralogical and geochemical viewpoint to understand the deterioration behavior of the BA glass phases as well as mechanisms involved. Bulk analysis by PXRD as well as micro-scale analysis by optical microscopy and SEM/EDX was conducted for such purposes. The results revealed that dissolution of the BA glass phases has resulted in a deterioration layer of 10(0)-10(2)μm thickness after years of disposal. This rapid weathering process is highly relevant to the specific glass characteristics and solution pH. The BA glass phases with more embedded compounds and cracks/fissures tend to be more vulnerable. Moreover, the generally alkaline pH in ash deposit favors a rapid disruption of the glass phase. The weathering products are mainly gel phases (including Al-Si gel, Ca-Al-Si gel, Fe-Al-Si gel etc.) with iron oxide/hydroxide as accessory products. Breakdown of the BA glass phases triggers chemical evolution of the embedded compounds. Based on all the findings above, a model is proposed to illustrate a general evolution trend for the landfilled MSWI-BA glass phases.

  20. Low-temperature heat capacities of CaAl2SiO6 glass and pyroxene and thermal expansion of CaAl2SiO6 pyroxene.

    USGS Publications Warehouse

    Haselton, H.T.; Hemingway, B.S.; Robie, R.A.

    1984-01-01

    Low-T heat capacities (5-380 K) have been measured by adiabatic calorimetry for synthetic CaAl2SiO6 glass and pyroxene. High-T unit cell parameters were measured for CaAl2SiO6 pyroxene by means of a Nonius Guinier-Lenne powder camera in order to determine the mean coefficient of thermal expansion in the T range 25-1200oC. -J.A.Z.

  1. Nqrs Data for AlCa2ClH10O8 [AlCa2ClO3·5(H2O)] (Subst. No. 0020)

    NASA Astrophysics Data System (ADS)

    Chihara, H.; Nakamura, N.

    This document is part of Subvolume A `Substances Containing Ag … C10H15' of Volume 48 `Nuclear Quadrupole Resonance Spectroscopy Data' of Landolt-Börnstein - Group III `Condensed Matter'. It contains an extract of Section `3.2 Data tables' of the Chapter `3 Nuclear quadrupole resonance data' providing the NQRS data for AlCa2ClH10O8 [AlCa2ClO3·5(H2O)] (Subst. No. 0020)

  2. Method of forming a dielectric thin film having low loss composition of Ba.sub.x Sr.sub.y Ca.sub.1-x-y TiO.sub.3 : Ba.sub.0.12-0.25 Sr.sub.0.35-0.47 Ca.sub.0.32-0.53 TiO.sub.3

    DOEpatents

    Xiang, Xiao-Dong; Chang, Hauyee; Takeuchi, Ichiro

    2000-01-01

    A dielectric thin-film material for microwave applications, including use as a capacitor, the thin-film comprising a composition of barium strontium calcium and titanium of perovskite type (Ba.sub.x Sr.sub.y Ca.sub.1-x-y)TiO.sub.3. Also provided is a method for making a dielectric thin film of that formula over a wide compositional range through a single deposition process.

  3. Low Loss Composition of BA{sub X}SR{sub Y}CA{sub 1-X-Y}TIO{sub 3}:BA{sub 0.12-0.25}SR{sub 0.35-0.47}CA{sub 0.32-0.53}TIO{sub 3}

    SciTech Connect

    Xiang, Xiao-Dong; Chang, Hauyee; Takeuchi, Ichiro

    1999-10-19

    A dielectric thin-film material for microwave applications, including use as a capacitor, the thin-film comprising a composition of barium strontium calcium and titanium of perovskite type (Ba{sub x}Sr{sub y}Ca{sub 1-x-y})TiO{sub 3}. Also provided is a method for making a dielectric thin film of that formula over a wide compositional range through a single deposition process.

  4. Surface micromorphology of dental composites [CE-TZP]-[Al2O3] with Ca(+2) modifier.

    PubMed

    Berezina, Sofia; Il'icheva, Alla Alexandrovna; Podzorova, Lyudmila Ivanovna; Ţălu, Ştefan

    2015-09-01

    The objective of this study was to characterize the three-dimensional (3D) surface micromorphology of the ceramics produced from nanoparticles of alumina and tetragonal zirconia (t-ZrO2) with addition of Ca(+2) for sintering improvement. The 3D surface roughness of samples was studied by atomic force microscopy (AFM), fractal analysis of the 3D AFM-images, and statistical analysis of surface roughness parameters. Cube counting method, based on the linear interpolation type, applied for AFM data was used for fractal analysis. The morphology of non-modified ceramic sample was characterized by the rather big (1-2 μm) grains of α-Al2O3 phase with a habit close to hexagonal drowned in solid solution of t-ZrO2 with smooth surface. The pattern surfaces of modified composite content a little amount of elongated prismatic grains with composition close to the phase of СаСеAl3О7 as well as hexahedral α-Al2O3-grains. Fractal dimension, D, as well as height values distribution have been determined for the surfaces of the samples with and without modifying. It can be concluded that the smoothest surface is of the modified samples with Ca(+2) modifier but the most regular one is of the non-modified samples. A connection was observed between the surface morphology and the physical properties as assessed in previous works. PMID:26190812

  5. CaMn2Al10: Itinerant Mn magnetism on the verge of magnetic order

    DOE PAGES

    Steinke, L.; Simonson, J. W.; Yin, W. -G.; Smith, G. J.; Kistner-Morris, J. J.; Zellman, S.; Puri, A.; Aronson, M. C.

    2015-07-24

    We report the discovery of CaMn2Al10, a metal with strong magnetic anisotropy and moderate electronic correlations. Magnetization measurements find a Curie-Weiss moment of 0.83μB/Mn, significantly reduced from the Hund's rule value, and the magnetic entropy obtained from specific heat measurements is correspondingly small, only ≈ 9% of Rln2. These results imply that the Mn magnetism is highly itinerant, a conclusion supported by density functional theory calculations that find strong Mn-Al hybridization. Consistent with the layered nature of the crystal structure, the magnetic susceptibility χ is anisotropic below 20 K, with a maximum ratio of χ[010]/χ[001] ≈ 3.5. A strong power-lawmore » divergence χ(T) ~ T–1.2 below 20 K implies incipient ferromagnetic order, an Arrott plot analysis of the magnetization suggests a vanishing low Curie temperature TC ~ 0. Our experiments indicate that CaMn2Al10 is a rare example of a system where the weak and itinerant Mn-based magnetism is poised on the verge of order.« less

  6. Interfacial Reactions Between BaAl2Si2O8 and Molten Al Alloy at 1423 K and 1523 K (1150 °C and 1250 °C)

    NASA Astrophysics Data System (ADS)

    Adabifiroozjaei, E.; Koshy, P.; Pardehkhorram, R.; Rastkerdar, E.; Hart, J.; Sorrell, C. C.

    2016-06-01

    This work investigates the interfacial interactions of Al7075 alloy with BaAl2Si2O8 at high temperatures [1423 K and 1523 K (1150 °C and 1250 °C)]. X-ray diffraction, electron probe microanalysis, and scanning electron microscopy coupled with energy dispersive spectroscopy were used to identify the mineralogical and microstructural changes at the interfaces. The vaporization, migration, and subsequent oxidation of alloying constituents (Mg and Zn) in contact with BaAl2Si2O8 caused intense interfacial phase transformations, forming spinel solid solution, magnesia solid solution, celsian-based solid solution, and barium magnesium silicate solid solution. The driving force for these phase transformations at the reaction front is the interdiffusion processes between Al (or Mg/Zn)-Si and Mg (or Zn)-Ba that occurs owing to the relative elemental gradients. The rate-limiting step of corrosion kinetics was identified to be Ba substitution in the MgO structure. The corrosion mechanism (extensive phase transformation of Ba-celsian by interdiffusion processes) at high temperatures was found to be different from that observed at lower temperatures [1123 K (850 °C)].

  7. Chemical zoning and diffusion of Ca, Al, Mn, and Cr in olivine of springwater pallasite

    NASA Technical Reports Server (NTRS)

    Zhou, Y.; Steele, Ian M.

    1993-01-01

    The pallasites, consisting mainly of Fe-Ni metal and olivine, are thought to represent the interior of a planetary body which slowly cooled from high temperature. Although the olivines are nearly homogeneous, ion microprobe studies revealed variations of Ca, Ti, Co, Cr, and Ni near grain edges. These variations were thought to represent diffusion in response to falling temperature of the parent body. Pallasite cooling rates have been estimated based on kamacite taenite textures but results differ by x100. In principle elemental profiles in olivine can allow estimates of cooling rate if diffusion coefficients are known; in addition, given a cooling rate, diffusion coefficients could be derived. Data are presented which show that apparent diffusion profiles can be measured for Al, Ca, Cr, and Mn which qualitatively agree with expected diffusion rates and have the potential of providing independent estimates of pallasite cooling rates.

  8. New oxyfluoride glass with high fluorine content and laser patterning of nonlinear optical BaAlBO{sub 3}F{sub 2} single crystal line

    SciTech Connect

    Shionozaki, K.; Honma, T.; Komatsu, T.

    2012-11-01

    A new oxyfluoride glass of 50BaF{sub 2}-25Al{sub 2}O{sub 3}-25B{sub 2}O{sub 3} (mol. %) with a large fraction of fluorine, i.e., F/(F + O) = 0.4, was prepared using a conventional melt-quenching method in order to synthesize new glass-ceramics containing nonlinear optical oxyfluoride crystals. The refractive index at 632.8 nm and ultra-violet cutoff wavelength of the glass were 1.564 and {approx}200 nm, respectively. Eu{sup 3+} ions in the glass showed a high quantum yield of 88% in the photoluminescence spectrum in the visible region. BaAlBO{sub 3}F{sub 2} crystals (size: 50-100 nm) showing second harmonic generations were formed through the crystallization of the glass. Lines consisting of BaAlBO{sub 3}F{sub 2} crystals were patterned successfully on the glass surface by laser irradiations (Yb:YVO{sub 4} laser with a wavelength of 1080 nm, laser power of 1.1 W, scanning speed of 8 {mu}m/s). High resolution transmission electron microscope observations combined with a focused ion beam technique indicate that BaAlBO{sub 3}F{sub 2} crystals are highly oriented just like a single crystal. The present study proposes that the new oxyfluoride glass and glass-ceramics prepared have a high potential for optical device applications.

  9. Electronic Properties of Lead-Free (Ba0.95Ca0.05)(Ti0.92Sn0.08)O3 Piezoceramic Nanofibers by Electrospinning

    NASA Astrophysics Data System (ADS)

    Sahoo, Benudhar; Panda, Prasanta Kumar

    2015-11-01

    Lead-free (Ba0.95Ca0.05)(Ti0.92Sn0.08)O3, (BCTS) piezoceramic nanofibers were prepared by electrospinning acetate precursor solutions in polyvinyl pyrrolidone, followed by calcining at 1150ºC for 2 h. X-ray diffraction of calcined nanofibers confirmed the formation of the BCTS phase and energy dispersive x-ray analysis confirmed the presence of Ca and Sn ions. The scanning electron microscope studies showed cylindrical fibers with a diameter in the range 80-275 nm. The dielectric constant and piezoelectric charge constant ( d 33) were 3485 at 100 Hz, RT and 398 pC/N, respectively.

  10. Dielectric properties of CaNdAlO sub 4 at microwave frequencies

    SciTech Connect

    Konopka, J.; Wolff, I. ); Lewandowski, S.J. )

    1992-07-01

    Dielectric properties of CaNdAlO{sub 4} monocrystals, a prospective substrate material for the deposition of high-{ital T}{sub {ital c}} superconductors, were measured with high accuracy at microwave frequencies from 8 to 40 GHz in the temperature range from 10 to 300 K by measuring the resonant frequencies of a completely filled resonant cavity. The material was found to be highly anisotropic. At 300 K it exhibits the dielectric constant along {ital c} axis {epsilon}{sup {prime}}{sub {ital c}} = 17.68, while the dielectric constant in the {ital a}-{ital b} plane is {epsilon}{prime}=19.62, and loss tangent tan {delta}{sub {ital c}} {congruent} tan {delta} {congruent} 5.1{times} 10{sup {minus}4}. Both {epsilon}{sup {prime}}{sub {ital c}} and {epsilon}{prime} depend strongly on temperature and their thermal coefficients have opposite signs, apparently a unique property of CaNdAlO{sub 4}. Below 160 K microwave losses caused by electric field perpendicular to the optical {ital c} axis increase with decreasing temperature, exhibiting a maximum near 65 K followed by a minimum at 30 K. It is suggested that neodymium ions in CaNdAlO{sub 4} at lower temperatures become magnetically ordered, causing an increase of magnetic permeability {mu}{sup {prime}}{sub {ital c}} {gt} 1 and a significant increase of magnetic losses at microwave frequencies. A crystallographic phase transition below 60 K cannot also be excluded.

  11. Partition coefficients for Al, Ca, Ti, Cr, and Ni in olivine obtained by melting experiment on an LL6 chondrite

    NASA Technical Reports Server (NTRS)

    Miyamoto, M.; Mikouchi, T.; Mckay, G. A.

    1994-01-01

    We report the partition coefficients for Ca, Al, Ti, Cr, and Ni in olivine obtained through a series of melting experiments on an LL6 chondrite under varying conditions of temperature and oxygen fugacity. It is necessary to examine the variation of partition coefficients up to extremely reducing conditions in order to study meteoritic olivines. For Ca, Al, and Cr, the partition coefficients tend to decrease as temperature increases, but do not change even under extremely reducing conditions.

  12. Water-Induced Morphology Changes in BaO/gamma-Al2O3 NOx Storage Materials: an FTIR, TPD, and Time-Resolved Synchrotron XRD Study

    SciTech Connect

    Szanyi,J.; Kwak, J.; Kim, D.; Wang, X.; Chimentao, R.; Hanson, J.; Epling, W.; Peden, C.

    2007-01-01

    The effect of water on the morphology of BaO/Al{sub 2}O{sub 3}-based NO{sub x} storage materials was investigated using Fourier transform infrared spectroscopy, temperature programmed desorption, and time-resolved synchrotron X-ray diffraction techniques. The results of this multispectroscopy study reveal that in the presence of water surface Ba-nitrates convert to bulk nitrates and water facilitates the formation of large Ba(NO{sub 3}){sub 2} particles. The conversion of surface to bulk Ba-nitrates is completely reversible (i.e., after the removal of water from the storage material a significant fraction of the bulk nitrates reconverts to surface nitrates). NO{sub 2} exposure of a H{sub 2}O-containing (wet) BaO/Al{sub 2}O{sub 3} sample results in the formation of nitrites and bulk nitrates exclusively (i.e., no surface nitrates form). After further exposure to NO{sub 2}, the nitrites completely convert to bulk nitrates. The amount of NO{sub x} taken up by the storage material, however, is essentially unaffected by the presence of water regardless of whether the water was dosed prior to or after NO{sub 2} exposure. On the basis of the results of this study, we are now able to explain most of the observations reported in the literature on the effect of water on NO{sub x} uptake on similar storage materials.

  13. Acid precipitation and food quality: Effects of dietary Al, Ca and P on bone and liver characteristics in American black ducks and mallards

    USGS Publications Warehouse

    Sparling, D.W.

    1991-01-01

    American black ducks (Anas rubripes) and mallards (A. platyrhynchos) were fed diets varying in concentrations of aluminum (Al). calcium (Ca), and phosphorus (P) for 10 weeks to identify toxic effects of Al under conditions representative of areas with acid precipitation. Femur and liver tissues were analyzed for Al. Ca, and P concentrations and structural characteristics. At two weeks of age, both species demonstrated pronounced differences in femur Al and P concentrations and femur mass from dietary Al and interaction between Ca:P regimen and Al:Low Ca:Low P enhanced Al storage and decreased P and mass in femurs. Femur Ca was lowest in the Low Ca:Low P regimen but was not affected by dietary Al. At 10 weeks, femur and liver Al continued to vary with dietary Al. Elevated Al and reduced Ca lowered modulus of elasticity. Femur P increased with elevated dietary P in black ducks. Elevated dietary P negated some of the effects of dietary A! on femur mass in black ducks. Reduced Ca concentrations weakened bones of both species and lowered both Ca and P. An array of clinical signs including lameness, discoloration of the upper mandible, complete and greenstick fractures, and death were responses to elevated Al and Ca:P regimen. Black ducks seemed to display these signs over a wider range of diets than mallards. Diets of 1,000 mg/kg Al had toxic effects on both species, particularly when combined with diets low in Ca and P.

  14. The first-principle study of the electronic, optical and thermoelectric properties of XTiO3 (X = Ca, Sr and Ba) compounds

    NASA Astrophysics Data System (ADS)

    Mubarak, A. A.

    2016-07-01

    The FP-LAPW method is utilized to investigate the elastic, optoelectronic and thermoelectric properties of XTiO3 (X = Ca, Sr and Ba) within the GGA. The calculated lattice constants and bulk modulus are found in agreement with previous studies. The present oxide-perovskite compounds are characterized as elastically stable and anisotropic. CaTiO3 and SrTiO3 are categorized as ductile compounds, whereas the BaTiO3 compound is in the critical region between ductile and brittle. The DOS and the band structure calculations reveal indirect (M-Γ) energy bandgap for the present compounds. The hydrostatic pressure increases the energy bandgap and the width of the valence band. The character of the band structure does not change due to this pressure. The optical parameters are calculated in different radiation regions. Beneficial optics applications are predicted as revealed from the optical spectra. The transport properties are applied as a function of the variable temperatures or carrier concentration. It is found that the compounds under study are classified as a p-type semiconductor. The majority charge carriers responsible for conduction in these calculated compounds are holes rather than electrons.

  15. Synthesis, spectroscopic characterization, thermal analysis and electrical conductivity studies of Mg(II), Ca(II), Sr(II) and Ba(II) vitamin B2 complexes

    NASA Astrophysics Data System (ADS)

    Refat, Moamen S.; Moussa, Mohamed A. A.; Mohamed, Soha F.

    2011-05-01

    Riboflavin (RF) complexes of Mg(II), Ca(II), Sr(II) and Ba(II) were successfully synthesized. Structures of metal complexes obtained were confirmed and characterized by elemental analysis, molar conductance, and infrared spectra. DC electrical conductivity measurements indicated that the alkaline earth metal (II) complexes of RF ligand are non-electrolytes. Elemental analysis of chelates suggest that the metal(II) ligand ratio is 1:2 with structure formula as [M(RF) 2( X) 2]· nH 2O. Infrared assignments clearly show that RF ligand coordinated as a bidentate feature through azomethine nitrogen of pyrazine ring and C dbnd O of pyrimidine-2,4-dione. Thermal analyses of Mg(II), Ca(II), Sr(II) and Ba(II) complexes were investigated using (TG/DSC) under atmospheric nitrogen between 30 and 800 °C. The surface morphology of the complexes was studied by SEM. The electrical conductivities of RF and its metal complexes were also measured with DC electrical conductivity in the temperature range from room to 483 K.

  16. Structural studies of the rhombohedral and orthorhombic monouranates: CaUO4, α-SrUO4, β-SrUO4 and BaUO4

    NASA Astrophysics Data System (ADS)

    Murphy, Gabriel; Kennedy, Brendan J.; Johannessen, Bernt; Kimpton, Justin A.; Avdeev, Maxim; Griffith, Christopher S.; Thorogood, Gordon J.; Zhang, Zhaoming

    2016-05-01

    The structures of some AUO4 (A=Ca, Sr, or Ba) oxides have been determined using a combination of neutron and synchrotron X-ray diffraction, supported by X-ray absorption spectroscopic measurements at the U L3-edge. The smaller Ca cation favours a rhombohedral AUO4 structure with 8-coordinate UO8 moieties whilst an orthorhombic structure based on UO6 groups is found for BaUO4. Both the rhombohedral and orthorhombic structures can be stabilised for SrUO4. The structural studies suggest that the bonding requirements of the A site cation play a significant role in determining which structure is favoured. In the rhombohedral structure, Bond Valence Sums demonstrate the A site is invariably overbonded, which, in the case of rhombohedral α-SrUO4, is compensated for by the formation of vacancies in the oxygen sub-lattice. The uranium cation, with its flexible oxidation state, is able to accommodate this by inducing vacancies along its equatorial coordination site as demonstrated by neutron powder diffraction.

  17. Thermoluminescence of Ba 0.97Ca 0.03SO 4:Eu irradiated with 48 MeV 7Li ion beam

    NASA Astrophysics Data System (ADS)

    Lochab, S. P.; Salah, Numan; Sahare, P. D.; Chauhan, R. S.; Ranjan, Ranju

    2007-01-01

    Thermoluminescence (TL) of Ba0.97Ca0.03SO4:Eu phosphor, irradiated with 48 MeV 7Li ions at different fluences in the range 1 × 109-1 × 1012 ions/cm2, has been studied. The phosphor was prepared by the chemical co-precipitation technique. Its pellets were irradiated using a 16 MV Tandem Van de-Graff type Electrostatic Pelletron Accelerator at Inter-University Accelerator Centre, New Delhi, India. The samples from the same batch were also irradiated with γ-rays from a Cs137 source for comparative studies. It has been found that the TL glow peak at 460 K, seen prominently in γ-irradiated sample, appeared as a small shoulder at around 465 K in 7Li3+ ion irradiated sample, while that observed as a shoulder in the former at 430 K, dominantly appeared in the latter at around 435 K. Trapping parameters of both, ion beam and γ-irradiated materials, were also obtained after the deconvolution of the glow curves and discussed in the paper. The TL response curve of the ion beam irradiated samples has a linear ion beam fluence response over the range 1 × 109-1 × 1010 ions/cm2. This property along with its low fading and simple glow curve structure makes Ba0.97Ca0.03SO4:Eu phosphor a suitable dosimeter for heavy charged particles (HCP).

  18. Crystal structure and luminescence properties of a novel red-emitting phosphor BaAlBO{sub 3}F{sub 2}:Eu{sup 3+}

    SciTech Connect

    Chen, Wanping Zhou, Ahong; Liu, Yan; Dai, Xiaoyan; Yang, Xin

    2014-12-15

    A series of novel red-emitting phosphors BaAlBO{sub 3}F{sub 2}:xEu{sup 3+} (0.001≤x≤0.08) were first synthesized via a high temperature solid-state reaction. X-ray diffraction and photoluminescence spectroscopy were used to characterize the crystal structure and photoluminescence properties of the phosphor, respectively. The phosphor can be effectively excited with a 395 nm light, and shows a dominant {sup 5}D{sub 0}−{sup 7}F{sub 2} emission with chromatic coordination of 0.628 and 0.372. The optimal doping concentration is about 0.04. Rietveld refinement results and the luminescence behavior of Eu{sup 3+} indicate that the Eu{sup 3+} ion occupies a C{sub 3} symmetry site, and the host BaAlBO{sub 3}F{sub 2} has a hexagonal structure with P-6 space group. In addition, the phosphor could be a potential candidate as red-emitting phosphor for application in white light-emitting diode. - Graphical abstract: The luminescence behavior and Rietveld refinement of BaAlBO{sub 3}F{sub 2}:Eu{sup 3+} indicate that the red-emitting phosphor has potential application in white LED and the host has a hexagonal structure with P-6 space group. - Highlights: • A novel red-emitting phosphor BaAlBO{sub 3}F{sub 2}:Eu{sup 3+} is first synthesized. • The crystal structure of BaAlBO{sub 3}F{sub 2} is confirmed. • The phosphor shows potential application in white LED.

  19. Nanoscale polarisation switching and leakage currents in (Ba0.955Ca0.045)(Zr0.17Ti0.83)O3 epitaxial thin films

    NASA Astrophysics Data System (ADS)

    Sreenivas Puli, Venkata; Pradhan, Dhiren K.; Adireddy, Shiva; Martínez, R.; Silwal, Punam; Scott, J. F.; Ramana, C. V.; Chrisey, Douglas B.; Katiyar, Ram S.

    2015-09-01

    This paper investigates the crystal structure, ferroelectric, temperature-dependent leakage current conduction mechanism and the piezoresponse force microscopy (PFM) behaviours of (Ba0.955Ca0.045) (Zr0.17Ti0.83)O3-BZT-BCT (x=0.15 ) films at the vicinity of the morphotropic phase boundary (MPB) of the [(1  -  x) BaZr0.20Ti0.80O3-xBa0.70Ca0.30TiO3] (x=0.50 ) composition. Epitaxial BZT-BCT thin films were grown on conductive La0.5Sr0.5CoO3 (LSCO) layers coated onto MgO (1 0 0) single-crystal substrates by pulsed laser deposition (PLD). High resolution x-ray diffraction (HR-XRD) reciprocal space maps (RSMs) confirmed the epitaxy with in-plane tetragonal symmetry (c  <  a), and Raman spectra also revealed a tetragonal perovskite crystalline lattice structure. Polarisation studies demonstrate that BZT-BCT films exhibit a high saturation polarisation of 148 µC cm-2 and a high recoverable (discharged) energy-storage density of 39.11 J cm-3 at 2.08 MV cm-1. Temperature-dependent P-E hysteresis loops resulted in a decrease in polarisation. Temperature-dependent leakage current behaviour was obtained and possible conduction mechanism is discussed. PPFM images revealed switchable ferroelectric piezoelectric contrasts after the application of a  ±9 V dc voltage on the conductive tip of the piezoresponse force microscope.

  20. Biochemical responses of the mycorrhizae in Pinus massoniana to combined effects of Al, Ca and low pH.

    PubMed

    Kong, F X; Liu, Y; Hu, W; Shen, P P; Zhou, C L; Wang, L S

    2000-02-01

    Biochemical responses of Pinus massoniana, with and without the inoculation mycorrhizal fungus Pisolithus tinctorius at the root, to artificial acid rain (pH 2.0) and various Ca/Al ratios were investigated. Some enzymes associated with the nutritive metabolism, such as acid phosphatase, alkaline phosphatase, nitrate reductase, mannitol dehydrogenase and trehalase, in the roots, stems and leaves of plant were obviously inhibited by the artificial acid rain and Al. After treatment with pH 2.0 + Ca/Al (0/1 or 1/10) artificial acid rain, the protein content in the organs was decreased. However, the activities of superoxide dismutase (SOD) and peroxidase (POD) and glutathione (GSH) concentrations were induced. It demonstrated that acid rain and Al could induce oxygen radicals in plant. Compared with the treatments with lower pH or Al, respectively, the combination of lower pH and Al concentration was more toxic to P. massoniana. Al toxicity could be ameliorated by the addition of Ca and the amelioration was the most when the ratio was 1/1 among the various Ca/Al ratio. Infection with mycorrhizal fungus P. tinctorius at the root of P. massoniana increased the ability of the plant to resist the toxicity of artificial acid rain and Al stress.

  1. Network topology for the formation of solvated electrons in binary CaO–Al2O3 composition glasses

    PubMed Central

    Akola, Jaakko; Kohara, Shinji; Ohara, Koji; Fujiwara, Akihiko; Watanabe, Yasuhiro; Masuno, Atsunobu; Usuki, Takeshi; Kubo, Takashi; Nakahira, Atsushi; Nitta, Kiyofumi; Uruga, Tomoya; Weber, J. K. Richard; Benmore, Chris J.

    2013-01-01

    Glass formation in the CaO–Al2O3 system represents an important phenomenon because it does not contain typical network-forming cations. We have produced structural models of CaO–Al2O3 glasses using combined density functional theory–reverse Monte Carlo simulations and obtained structures that reproduce experiments (X-ray and neutron diffraction, extended X-ray absorption fine structure) and result in cohesive energies close to the crystalline ground states. The O–Ca and O–Al coordination numbers are similar in the eutectic 64 mol % CaO (64CaO) glass [comparable to 12CaO·7Al2O3 (C12A7)], and the glass structure comprises a topologically disordered cage network with large-sized rings. This topologically disordered network is the signature of the high glass-forming ability of 64CaO glass and high viscosity in the melt. Analysis of the electronic structure reveals that the atomic charges for Al are comparable to those for Ca, and the bond strength of Al–O is stronger than that of Ca–O, indicating that oxygen is more weakly bound by cations in CaO-rich glass. The analysis shows that the lowest unoccupied molecular orbitals occurs in cavity sites, suggesting that the C12A7 electride glass [Kim SW, Shimoyama T, Hosono H (2011) Science 333(6038):71–74] synthesized from a strongly reduced high-temperature melt can host solvated electrons and bipolarons. Calculations of 64CaO glass structures with few subtracted oxygen atoms (additional electrons) confirm this observation. The comparable atomic charges and coordination of the cations promote more efficient elemental mixing, and this is the origin of the extended cage structure and hosted solvated (trapped) electrons in the C12A7 glass. PMID:23723350

  2. Dissolution Behavior of Indium in CaO-SiO2-Al2O3 Slag

    NASA Astrophysics Data System (ADS)

    Ko, Kyu Yeol; Park, Joo Hyun

    2011-12-01

    The solubility of indium in a molten CaO-SiO2-Al2O3 system was measured at 1773 K (1500 °C) to establish the dissolution mechanism of indium under a highly reducing atmosphere. The solubility of indium increases with increasing oxygen potential, whereas it decreases with increased activity of basic oxide. Therefore, a dissolution mechanism of indium can be constructed according to the following equation: {{In}}({{s}}) + 1/4{{O}}2 ({{g}}) = ({{In}}^{ + } ) + 1/2({{O}}^{2 - } ) The relationship between indium capacity and sulfide capacity shows a good correlation that is consistent with theoretical expectations. The enthalpy change of the indium dissolution reaction is negative, which indicates that the dissolution is an exothermic reaction. The heat of dissolution into high-silica melts is greater than that into low-silica melts. The solubility of indium is strongly dependent on the silica content. The activity coefficient, and thus the excess free energy of In2O, decreases linearly with increasing silica content, indicating that the In2O is believed to behave as a weak basic oxide in the current CaO-SiO2-Al2O3 ternary system under reducing conditions.

  3. Magnesium doping on brownmillerite Ca{sub 2}FeAlO{sub 5}

    SciTech Connect

    Malveiro, J.; Ramos, T.; Ferreira, L.P.; Waerenborgh, J.C.

    2007-06-15

    Ca{sub 2}FeAl{sub 1-} {sub x} Mg {sub x} O{sub 5} (x=0, 0.05 and 0.1) compounds adopting the brownmillerite-type structure were prepared by a self-combustion route using two different fuels. Characterisation was performed using X-ray powder diffraction, Moessbauer spectroscopy, magnetisation measurements, chemical analysis, scanning electron microscopy and 4-point dc conductivity measurements. Global results indicate that the solubility limit was reached for x=0.1. An antiferromagnetic behaviour was detected for all studied compositions, with magnetic ordering temperatures of 340 and 290 K for x=0 and 0.05, respectively. Mg doping increases the number of iron cations in tetrahedral sites, which induces magnetisation enhancement at low temperatures through the coupling between octahedral iron cations in different octahedral planes. The compounds exhibit semiconductor behaviour and Mg{sup 2+} doping yields a significant enhancement of the total conductivity, which can be essentially attributed to the presence of Fe{sup 4+} ions. - Graphical abstract: Ca{sub 2}FeAl{sub 1-} {sub x} Mg {sub x} O{sub 5} (x=0, 0.05, 0.1) compounds with the brownmillerite structure were prepared and characterised. The paramagnetic Moessbauer spectra presented were obtained at T=363 K (x=0); T=297 K (x=0.05) and T=353 K (x=0.1)

  4. Periodicity Dependence of the Built-in Electric Field in (Ba0.7Ca0.3)TiO3/Ba(Zr0.2Ti0.8)O3 Ferroelectric Superlattices.

    PubMed

    Lin, Qianru; Wang, Danyang; Chen, Zhigang; Liu, Wenfeng; Lim, Sean; Li, Sean

    2015-12-01

    Symmetric ferroelectric superlattices consisting of (Ba0.7Ca0.3)TiO3 (BCT) and Ba(Zr0.2Ti0.8)O3 (BZT) layers were successfully grown on La0.7Sr0.3MnO3 electroded (001)-oriented SrTiO3 substrates by laser molecular beam epitaxy. With the monitor of reflective high-energy electron diffraction, the growth mode and rate were precisely controlled to realize the desired superlattice periodicity as confirmed by both X-ray diffraction and transmission electron microscopy results. The microscopic piezoelectric response and macroscopic ferroelectric properties were investigated as a function of periodicity of the BCTm/BZTm (m = 3, 5, 10, and 15 unit cells) superlattices. The existence of a built-in electric field was confirmed in all the superlattices and its strength was highly dependent on the periodicity. The excellent tunability of built-in electric field opens a path for designing microelectronic devices with various functionalities based on BCTm/BZTm superlattices.

  5. Phase coexistence and ferroelastic texture in high strain (1-x)Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 piezoceramics

    NASA Astrophysics Data System (ADS)

    Ehmke, Matthias C.; Ehrlich, Steven N.; Blendell, John E.; Bowman, Keith J.

    2012-06-01

    Dielectric permittivity and x-ray diffraction measurements were used to identify a region of phase coexistence between the rhombohedral and tetragonal phases near the morphotropic phase boundary in (1-x)Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 (BZT-BCT). This phase coexistence prevails over a considerable composition and temperature range and is bounded by single rhombohedral or tetragonal phases. The maximum piezoelectric response measured in terms of maximum strain divided by maximum electric field, Smax/Emax, is extraordinarily high, with the largest value of 1310 pm/V for x = 0.45. Electrical poling induces ferroelastic domain textures in both the rhombohedral and tetragonal phases simultaneously, which increases the piezoelectric performance significantly. The stability of that ferroelastic texture is limited by the phase transition at the morphotropic phase boundary, suggesting coupling between both coexisting phases and limiting potential applications. The results were confirmed using in situ temperature dependent synchrotron x-ray diffraction. The findings indicate that the BZT-BCT system is considerably more complex than discussed in initial reports and that this complexity is likely related to the impressive properties that have been previously reported.

  6. Lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 nanowires for energy harvesting

    NASA Astrophysics Data System (ADS)

    Zhou, Zhi; Bowland, Christopher C.; Malakooti, Mohammad H.; Tang, Haixiong; Sodano, Henry A.

    2016-02-01

    Lead-free piezoelectric nanowires (NWs) show strong potential in sensing and energy harvesting applications due to their flexibility and ability to convert mechanical energy to electric energy. Currently, most lead-free piezoelectric NWs are produced through low yield synthesis methods and result in low electromechanical coupling, which limit their efficiency as energy harvesters. In order to alleviate these issues, a scalable method is developed to synthesize perovskite type 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 (BZT-BCT) NWs with high piezoelectric coupling coefficient. The piezoelectric coupling coefficient of the BZT-BCT NWs is measured by a refined piezoresponse force microscopy (PFM) testing method and shows the highest reported coupling coefficient for lead-free piezoelectric nanowires of 90 +/- 5 pm V-1. Flexible nanocomposites utilizing dispersed BZT-BCT NWs are fabricated to demonstrate an energy harvesting application with an open circuit voltage of up to 6.25 V and a power density of up to 2.25 μW cm-3. The high electromechanical coupling coefficient and high power density demonstrated with these lead-free NWs produced via a scalable synthesis method shows the potential for high performance NW-based devices.

  7. High pyroelectricity in lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 ceramics

    NASA Astrophysics Data System (ADS)

    Yao, Shanshan; Ren, Wei; Ji, Hongfen; Wu, Xiaoqing; Shi, Peng; Xue, Dezhen; Ren, Xiaobing; Ye, Zuo-Guang

    2012-05-01

    We report high pyroelectricity in lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 (BZT-50BCT) ceramics which were previously reported to exhibit high piezoelectricity. The pyroelectric coefficient measured by the Byer-Roundy method upon heating for dc-poled samples shows a high value of 5.84 × 10-4 C m-2 K-1 at 300 K, comparable to those of PZT-based ceramics and significantly higher than many other lead-free pyroelectric materials. The pyroelectric coefficient calculated from the remanent polarization versus temperature relationship obtained during a cooling process is 17.17 × 10-4 C m-2 K-1 at 300 K, which is considerably larger than the value obtained by the Byer-Roundy method. This difference is attributed to the thermal hysteresis of the rhombohedral-tetragonal phase transition between the heating and cooling processes.

  8. Wide Compositional Range In Situ Electric Field Investigations on Lead-Free Ba (Zr0.2Ti0.8)O3-x (Ba0.7Ca0.3)TiO3 Piezoceramic

    NASA Astrophysics Data System (ADS)

    Zakhozheva, M.; Schmitt, L. A.; Acosta, M.; Guo, H.; Jo, W.; Schierholz, R.; Kleebe, H.-J.; Tan, X.

    2015-06-01

    The evolution of ferroelectric domains in the lead-free Ba (Zr0.2Ti0.8)O3-x (Ba0.7Ca0.3)TiO3 (abbreviated as BZT -x BCT ) piezoelectric ceramic is investigated in situ under an applied electric field using transmission electron microscopy (TEM). Poling-induced, reversible, transformation from a multidomain to a single-domain state is monitored for a large variety of compositions. For all studied materials, this transformation occurs with the appearance of an intermediate nanodomain state at moderate poling fields. According to our results, under high poling fields, a single-domain state vanishes and multiple domains reappear within the grains. Upon further cycling, switching between two different multidomain states occurs. For all BZT -x BCT compositions that we investigate, no sign of the electric-field-induced structural changes is detected using the selected area electron-diffraction (SAED) patterns, which are devoid of the reflection splitting or any detectable changes during electrical poling. The extrinsic contribution to the piezoelectric properties is found to dominate in the BZT -x BCT piezoceramic.

  9. Lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 nanowires for energy harvesting.

    PubMed

    Zhou, Zhi; Bowland, Christopher C; Malakooti, Mohammad H; Tang, Haixiong; Sodano, Henry A

    2016-03-01

    Lead-free piezoelectric nanowires (NWs) show strong potential in sensing and energy harvesting applications due to their flexibility and ability to convert mechanical energy to electric energy. Currently, most lead-free piezoelectric NWs are produced through low yield synthesis methods and result in low electromechanical coupling, which limit their efficiency as energy harvesters. In order to alleviate these issues, a scalable method is developed to synthesize perovskite type 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 (BZT-BCT) NWs with high piezoelectric coupling coefficient. The piezoelectric coupling coefficient of the BZT-BCT NWs is measured by a refined piezoresponse force microscopy (PFM) testing method and shows the highest reported coupling coefficient for lead-free piezoelectric nanowires of 90 ± 5 pm V(-1). Flexible nanocomposites utilizing dispersed BZT-BCT NWs are fabricated to demonstrate an energy harvesting application with an open circuit voltage of up to 6.25 V and a power density of up to 2.25 μW cm(-3). The high electromechanical coupling coefficient and high power density demonstrated with these lead-free NWs produced via a scalable synthesis method shows the potential for high performance NW-based devices. PMID:26868967

  10. Phase transition behaviours near the triple point for Pb-free (1 - x)Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 piezoceramics

    NASA Astrophysics Data System (ADS)

    Gao, Jinghui; Dai, Ye; Hu, Xinghao; Ke, Xiaoqin; Zhong, Lisheng; Li, Shengtao; Zhang, Lixue; Wang, Yu; Wang, Dong; Wang, Yan; Liu, Yongbin; Xiao, Hu; Ren, Xiaobing

    2016-08-01

    The reason for the large electromechanical response in Pb-free piezoceramic Ba(Zr0.2Ti0.8)O3-(Ba0.7Ca0.3)TiO3 (BZT-BCT) still remains controversial, and a central issue is whether or not the multi-phase-coexisting point (triple point) in the phase diagram is a thermodynamic tricritical point. In this letter, we study the phase transition behaviour for the ferro-para transitions of BZT-BCT specimens in the vicinity of a triple point. Our results show that latent heat and thermal hysteresis approach zero, while the permittivity peak value is maximized close to the triple-point composition, which suggests that the triple point exhibits nearly tricritical transition behaviours in the BZT-BCT system. Further, the TEM result shows that the domain width is minimized with composition approaching the triple point, which indicates a reduction of the domain wall energy possibly relevant to the tricriticality of the triple point. A sixth-order Landau energy modeling shows that the triple tricritical point provides a free-energy state of near-vanishing polarization anisotropy and thus enhances the piezoelectric response for such a material system.

  11. Lead-free 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 nanowires for energy harvesting.

    PubMed

    Zhou, Zhi; Bowland, Christopher C; Malakooti, Mohammad H; Tang, Haixiong; Sodano, Henry A

    2016-03-01

    Lead-free piezoelectric nanowires (NWs) show strong potential in sensing and energy harvesting applications due to their flexibility and ability to convert mechanical energy to electric energy. Currently, most lead-free piezoelectric NWs are produced through low yield synthesis methods and result in low electromechanical coupling, which limit their efficiency as energy harvesters. In order to alleviate these issues, a scalable method is developed to synthesize perovskite type 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 (BZT-BCT) NWs with high piezoelectric coupling coefficient. The piezoelectric coupling coefficient of the BZT-BCT NWs is measured by a refined piezoresponse force microscopy (PFM) testing method and shows the highest reported coupling coefficient for lead-free piezoelectric nanowires of 90 ± 5 pm V(-1). Flexible nanocomposites utilizing dispersed BZT-BCT NWs are fabricated to demonstrate an energy harvesting application with an open circuit voltage of up to 6.25 V and a power density of up to 2.25 μW cm(-3). The high electromechanical coupling coefficient and high power density demonstrated with these lead-free NWs produced via a scalable synthesis method shows the potential for high performance NW-based devices.

  12. Resistive switching in ferroelectric lead-free 0.5Ba (Zr0.2Ti0.8)O3–0.5(Ba0.7Ca0.3)TiO3 thin films

    NASA Astrophysics Data System (ADS)

    Silva, J. P. B.; Kamakshi, K.; Sekhar, K. C.; Queirós, E. C.; Agostinho Moreira, J.; Almeida, A.; Pereira, M.; Tavares, P. B.; Gomes, M. J. M.

    2016-08-01

    In this work, resistive switching in pulsed laser deposited ferroelectric lead-free 0.5Ba(Zr0.2Ti0.8)O3–0.5(Ba0.7Ca0.3)TiO3 (0.5BZT–0.5BCT) thin films was investigated. This study reveals that films grown at 5.5 J cm‑2 have shown optimal ferroelectric and resistive switching response, which are attributed to high tetragonality, large grain size and less defect concentration. Au/0.5BZT–0.5BCT/Pt capacitors show the electroforming free resistive switching that is explained based on the polarization modulation of the Schottky-like barrier at the 0.5BZT–0.5BCT/Au interface. The polarization induced resistive switching is evidenced by its disappearance as the temperature increases to the Curie temperature. The capacitor based on film grown at 5.5 J cm‑2 shows resistive switching characterized by high switching ratio of 106 at a low set/reset voltage  ≈1 V, and by a stable memory window, which are highly required for memory applications.

  13. Sequence of phase transitions induced by chemical composition and high temperature in [Ba2CaWO6](1-x)[Sr2CaWO6]x double perovskite tungsten oxides

    NASA Astrophysics Data System (ADS)

    Mirinioui, F.; Manoun, Bouchaib; Tamraoui, Y.; Lazor, P.

    2015-12-01

    [Ba2CaWO6]1-x[Sr2CaWO6]x (0≤x≤1) materials were synthesized by the high temperature solid state reaction and firing methods, and characterized using techniques of X-ray diffraction and Raman spectroscopy. The crystal structures were determined by Rietveld refinements on the laboratory X-ray powder diffraction data. As a function of composition, upon increasing the strontium content, the samples exhibit a sequence of three phase transitions: from cubic (Fm 3 ̅m) to tetragonal (I4/m) to monoclinic structural phases (I2/m, P21/n). These transitions have been confirmed by Raman studies Fm 3 bar m x = 0 → I 4 / m 0.1 ≤ x ≤ 0.2 → I 2 / m 0.3 ≤ x ≤ 0.5 → P21 / n 0.6 ≤ x ≤ 1 Furthermore, increasing the temperature for the compositions [Ba2CaWO6]1-x[Sr2CaWO6]x (0.1≤x<1), manifests the P21/n to I2/m, the I2/m to I4/m and the I4/m to Fm 3 ̅m phase transitions. For the compositions (0.1≤x≤0.2) the tetragonal to cubic phase transition is well illustrated. For the room temperature I2/m monoclinic compositions, two phase transitions were observed for all the compositions with x ranging from 0.3 to 0.5: from the monoclinic (I2/m) to tetragonal (I4/m), and from I4/m to Fm 3 ̅m structures. Finally, for the room temperature P21/n monoclinic compositions, only two phase transitions are observed in the temperature range probed by Raman spectroscopy, the temperature was not high enough to reach the tetragonal-to-cubic phase transition.

  14. Growth of (Y1-x Ca x )Ba2Cu4O8 in ambient pressure and its tri-axial magnetic alignment

    NASA Astrophysics Data System (ADS)

    Horii, S.; Yamaki, M.; Shimoyama, J.; Kishio, K.; Doi, T.

    2015-10-01

    We report the growth of single crystals in ambient pressure and tri-axial orientation under modulated rotation magnetic fields (MRFs) for (Y1-x Ca x )Ba2Cu4O8 [(Y1-x Ca x )124] with x ≤ 0.1. Rectangular (Y1-x Ca x )124 crystals approximately 50 μm in size have been successfully grown for x ≤ 0.1 in a growth temperature region from 650 °C to 750 °C. Their critical temperatures increased with x and exhibited approximately 91 K for x = 0.1. By applying an MRF of 10 T, pulverised powders of (Y1-x Ca x )124 were tri-axially aligned in epoxy resin at room temperature in a whole x region below x = 0.1. The magnitude relationship of the magnetic susceptibilities (χ) along crystallographic directions for (Y1-x Ca x )124 was χ c > χ a > χ b at room temperature and was unchanged with a change in x. From changes in the degrees of the c-axis and the in-plane orientation (Δω) for the (Y1-x Ca x )124 powder samples aligned under three different MRF conditions, it was found that MRFs above at least 1 T were required to achieve almost complete tri-axial alignment with Δω < 5°. Irreversibility lines for H//c were successfully determined even from the powder samples by the introduction of magnetic alignment without using single crystalline samples. The present study indicates that magnetic alignment is a useful process for the fabrication of quasi-single-crystals from the perspective of solid-state physics and the production of cuprate superconducting materials.

  15. Self-reactivated mesostructured Ca-Al-O composite for enhanced high-temperature CO2 capture and carbonation/calcination cycles performance.

    PubMed

    Chang, Po-Hsueh; Huang, Wei-Chen; Lee, Tai-Jung; Chang, Yen-Po; Chen, San-Yuan

    2015-03-25

    In this study, highly efficient high-temperature CO2 sorbents of calcium aluminate (Ca-Al-O) mesostructured composite were synthesized using presynthesized mesoporous alumina (MA) as a porous matrix to react with calcium nitrate through a microwave-assisted process. Upon annealing at 600 °C, a highly stable mesoporous structure composed of poorly crystalline Ca12Al14O33 phase and the CaO matrix was obtained. The Ca-Al-O mesostructured sorbents with a Ca(2+)/Al(3+) ratio of 5:1 exhibit an enhanced increasing CO2 absorption kinetics in the CO2 capture capacity from 37.2 wt % to 48.3 wt % without apparent degradation with increasing carbonation/calcination cycling up to 50 at 700 °C due to the strong self-reactivation effect of the mesoporous Ca-Al-O microstructure. Remarkable improvements in the CaO-CaCO3 conversion attained from the mesostructured Ca-Al-O composite can be explained using the concept combined with available mesoporous structure and Ca12Al14O33 phase content. However, a high Ca(2+)/Al(3+) =8:1 Ca-Al-O composite causes degradation because the pores become blocked and partial sintering induces CaO agglomeration. PMID:25730384

  16. Atomistic and Ab initio modeling of CaAl2O4 high-pressure polymorphs under Earth's mantle conditions

    NASA Astrophysics Data System (ADS)

    Eremin, N. N.; Grechanovsky, A. E.; Marchenko, E. I.

    2016-05-01

    Semi-empirical and ab initio theoretical investigation of crystal structure geometry, interatomic distances, phase densities and elastic properties for some CaAl2O4 phases under pressures up to 200 GPa was performed. Two independent simulation methods predicted the appearance of a still unknown super-dense CaAl2O4 modification. In this structure, the Al coordination polyhedron might be described as distorted one with seven vertices. Ca atoms were situated inside polyhedra with ten vertices and Ca-O distances from 1.96 to 2.49 Å. It became the densest modification under pressures of 170 GPa (density functional theory prediction) or 150 GPa (semi-empirical prediction). Both approaches indicated that this super-dense CaAl2O4 modification with a "stuffed α-PbO2" type structure could be a probable candidate for mutual accumulation of Ca and Al in the lower mantle. The existence of this phase can be verified experimentally using high pressure techniques.

  17. Synthesis, structural characterization and properties of SrAl{sub 4−x}Ge{sub x}, BaAl{sub 4−x}Ge{sub x}, and EuAl{sub 4−x}Ge{sub x} (x≈0.3–0.4)—Rare examples of electron-rich phases with the BaAl{sub 4} structure type

    SciTech Connect

    Zhang, Jiliang; Bobev, Svilen

    2013-09-15

    Three solid solutions with the general formula AEAl{sub 4−x}Ge{sub x} (AE=Eu, Sr, Ba; 0.32(1)≤x≤0.41(1)) have been synthesized via the aluminum self-flux method, and their crystal structures have been established from powder and single-crystal X-ray diffraction. They are isotypic and crystallize with the well-known BaAl{sub 4} structure type, adopted by the three AEAl{sub 4} end members. In all structures, Ge substitutes Al only at the 4e Wyckoff site. Results from X-rays photoelectron spectroscopy on EuAl{sub 4−x}Ge{sub x} and EuAl{sub 4} indicate that the interactions between the Eu{sup 2+} cations and the polyanionic framework are enhanced in the Ge-doped structure, despite the slightly elevated Fermi level. Magnetic susceptibility measurements confirm the local moment magnetism, expected for the [Xe]4f{sup 7} electronic configuration of Eu{sup 2+} and suggest strong ferromagnetic interactions at cryogenic temperatures. Resistivity data from single-crystalline samples show differences between the title compounds, implying different bonding characteristics despite the close Debye temperatures. A brief discussion on the observed electron count and homogeneity ranges for AEAl{sub 4−x}Ge{sub x} (AE=Eu, Sr, Ba) is also presented. - Graphical abstract: AEAl{sub 4−x}Ge{sub x} (AE=Eu, Sr, Ba; 0.32(1)≤x≤0.41(1)), three “electron-rich” phases with BaAl{sub 4} structure type have been synthesized and characterized. Display Omitted - Highlights: • Three BaAl{sub 4}-type ternary aluminum germanides have been synthesized with Eu, Sr and Ba. • Eu, Sr and Ba cations have no apparent influence on the solubility of Ge. • The Ge atoms substitute Al on one of two framework sites, thereby strengthening the interactions between the cations and the polyanionic framework.

  18. Alkaline Earth Metal Zirconate Perovskites MZrO3 (M=Ba(2+), Sr(2+), Ca(2+)) Derived from Molecular Precursors and Doped with Eu(3+) Ions.

    PubMed

    Drąg-Jarząbek, Anna; John, Łukasz; Petrus, Rafał; Kosińska-Klähn, Magdalena; Sobota, Piotr

    2016-03-24

    The effect of alkaline earth metal alkoxides on the protonation of zirconocene dichloride was investigated. This approach enabled the design of compounds with preset molecular structures for generating high-purity binary metal oxide perovskites MZrO3 (M=Ba(2+), Sr(2+), Ca(2+)). Single-source molecular precursors [Ba4 Zr2 (μ6 -O)(μ3 ,η(2)-OR)8 (OR)2(η(2) -HOR)2 (HOR)2 Cl4], [Sr4 Zr2 (μ6 -O)(μ3 ,η(2)-OR)8 (OR)2 (HOR)4 Cl4], [Ca4 Zr2 (μ6-O)(μ3 ,η(2)-OR)8 (OR)2 Cl4], and [Ca6 Zr2 (μ2 ,η(2)-OR)12 (μ-Cl)2 (η(2) -HOR)4 Cl6 ]⋅8 CH2 Cl2 were prepared via elimination of the cyclopentadienyl ring from Cp2 ZrCl2 as CpH in the presence of M(OR)2 and alcohol ROH (ROH=CH3OCH2 CH2OH) as a source of protons. The resulting complexes were characterized by elemental analysis, IR and NMR spectroscopy, and single-crystal X-ray diffraction. The compounds were then thermally decomposed to MCl2 /MZrO3 mixtures. Leaching of MCl2 from the raw powder with deionized water produced highly pure perovskite-like oxide particles of 40-80 nm in size. Luminescence studies on Eu(3+)-doped MZrO3 revealed that the perovskites are attractive host lattices for potential applications in display technology. PMID:26891039

  19. Fluorine sites in glasses and transparent glass-ceramics of the system Na{sub 2}O/K{sub 2}O/Al{sub 2}O{sub 3}/SiO{sub 2}/BaF{sub 2}

    SciTech Connect

    Bocker, Christian; Munoz, Francisco; Duran, Alicia; Ruessel, Christian

    2011-02-15

    The transparent glass-ceramics obtained in the silicate system Na{sub 2}O/K{sub 2}O/SiO{sub 2}/BaF{sub 2} show homogeneously dispersed BaF{sub 2} nano crystals with a narrow size distribution. The X-ray diffraction and the nuclear magnetic resonance spectroscopy were applied to glasses and the respective glass-ceramics in order to clarify the crystallization mechanism and the role of fluorine during crystallization. With an increasing annealing time, the concentration and also the number of crystals remain approximately constant. With an increasing annealing temperature, the crystalline fraction increases until a saturation limit is reached, while the number of crystals decreases and the size of the crystals increases. Fluoride in the glassy network occurs as Al-F-Ba, Al-F-Na and also as Ba-F structures. The latter are transformed into crystalline BaF{sub 2} and fluoride is removed from the Al-F-Ba/Na bonds. However, some fluorine is still present in the glassy phase after the crystallization. -- Graphical abstract: The X-ray diffraction and the nuclear magnetic resonance spectroscopy were applied to glasses in the silicate system Na{sub 2}O/K{sub 2}O/SiO{sub 2}/BaF{sub 2} and the respective glass-ceramics with BaF{sub 2} nano crystals in order to clarify the crystallization mechanism and the role of fluorine during crystallization. Display Omitted Research highlights: {yields} BaF{sub 2} nano crystals are precipitated from a silicate glass system. {yields} Ostwald ripening during the late stage of crystallization does not occur. {yields} Fluorine in the glass is coordinated with Ba as well as Al together with Ba or Na.{yields} In the glass-ceramics, the residual fluorine is coordinated as Al-F-Ba/Na.

  20. Biocompatible nanogenerators through high piezoelectric coefficient 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 nanowires for in-vivo applications.

    PubMed

    Yuan, Miaomiao; Cheng, Li; Xu, Qi; Wu, Weiwei; Bai, Suo; Gu, Long; Wang, Zhe; Lu, Jun; Li, Huanping; Qin, Yong; Jing, Tao; Wang, Zhong Lin

    2014-11-26

    Lead-free BZT-BCT (0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3) nanowires with a high piezoelectric coefficient are synthesized and nanogenerators (NGs) composed of them are successfully developed. The studied in vitro and in vivo biocompatibility of the NGs shows great potential for their application as in vivo power sources.

  1. Major soil element (Ca, Mg, K, Na, Al, Fe) distribution along the Qinghai-Tibet Railway

    NASA Astrophysics Data System (ADS)

    Wang, Z.; Zhang, Y.; Zhang, H.; Ding, M.; Lin, X.

    2011-12-01

    The Tibetan Plateau (TP), which has been called the third polar region, is the highest plateau in the world. There are a series of special soils present in the TP, which are extremely important in soil sciences for their particularities. Soil chemical composition is one of the necessary indices of soil characteristics. The major element content of the soil, such as Ca, Mg, K, Na, not only can affect the soil pH value and soil fertility but also are the main drivers of soil geochemical processes. It is helpful to understand the TP environmental characteristics, to study the major soil element content.The Qinghai-Tibet Railway (QTR) is the highest-elevation and the longest highland railway on earth. There are nearly all types of TP soil along the QTR. Most of the areas along the QTR are in fairly pristine condition. This offers a good platform to study the natural environmental characteristics of the soil. This study selected 240 soil samples from 28 sample areas along the Qinghai-Tibet Railway, and the aluminum, iron, calcium, sodium, potassium and magnesium content in the soil were measured with ICP-AES. The results indicated: (1) Compared with the national soil background values, the Ca content in soil was higher along the QTR and Al was lower; but the Fe, Mg, K and Na contents were similar. (2) Along the whole QTR, the soil Al, Fe and Mg content showed a decreasing trend from Xining to Lhasa, the changes in K and Na values were relatively complex, and the distribution of Ca could be divided three sections. (3) The soil element contents varied with different soil types and parent materials. Most of the six elements content was minimum in soil, which derived from debris materials for ice and water, and the elements content was maximum in soil, which evolved from debris for flood, and the content of soil Ca developed from debris for lake was maximum. The amount of each element present in the Hapli-Cryic Aridosols and Calci-Cryic Aridosols was relatively higher than

  2. A simple method for the normal pressure synthesis of Cu 1- xTl xBa 2Ca 3Cu 4O 12- δ superconductor

    NASA Astrophysics Data System (ADS)

    Khan, Nawazish A.; Khurram, A. A.; Javed, Asim

    2005-05-01

    A very simple method for the direct synthesis of Cu 1- xTl xBa 2Ca 3Cu 4O 12- δ (Cu 1- xTl x-1234) superconductor is reported. A predominant single phase Cu 1- xTl x-1234 is achieved by the solid state reaction of Ba(NO 3) 2, CaCO 3 and Cu(CN) at first stage and with appropriate amount of Tl 2O 3 at the second stage. These materials were fired twice for 24 h at 880 °C followed by intermediate grinding. Thoroughly ground and fired material was mixed with Tl 2O 3 in appropriate amount and pellets were made by applying a pressure of 5 tons. Pellets were wrapped in an aluminum foil and sintered at 880 °C for 3-30 min. A predominantly single phase of Cu 1- xTl xBa 2Ca 3Cu 4O 12- δ was achieved with an inclusion of unknown impurity. The resistivity measurements established the onset temperature of superconductivity [ Tc (onset)] at 120 K and zero resistivity critical temperature [ Tc( R = 0)] at 106 K. Bulk superconductivity was also confirmed by ac-magnetic susceptibility measurements. The surface of the samples was analyzed by electron microscopy and their composition by energy dispersive X-ray spectroscopy (EDX) measurements. For optimizing the carriers in the final compound, post-annealing experiments were carried out in the flowing nitrogen atmosphere. For the study of the doping mechanisms, in the post-annealed samples, the phonon modes of Cu 1- xTl x-1234 were investigated by infrared absorption measurements. The absorption mode of O δ [O3] atoms decreased in intensity after the post-annealing and the apical oxygen modes were softened to lower wave numbers. The softening of these phonon modes suggested the reduction of thallium from Tl 3+ to Tl 1+; which resulted in an increase of [ Tc( R = 0)] of the material.

  3. Time-Dependent Negative Capacitance Effects in Al2O3/BaTiO3 Bilayers.

    PubMed

    Kim, Yu Jin; Yamada, Hiroyuki; Moon, Taehwan; Kwon, Young Jae; An, Cheol Hyun; Kim, Han Joon; Kim, Keum Do; Lee, Young Hwan; Hyun, Seung Dam; Park, Min Hyuk; Hwang, Cheol Seong

    2016-07-13

    The negative capacitance (NC) effects in ferroelectric materials have emerged as the possible solution to low-power transistor devices and high-charge-density capacitors. Although the steep switching characteristic (subthreshold swing < sub-60 mV/dec) has been demonstrated in various devices combining the conventional transistors with ferroelectric gates, the actual applications of the NC effects are still some way off owing to the inherent hysteresis problem. This work reinterpreted the hysteretic properties of the NC effects within the time domain and demonstrated that capacitance (charge) boosting could be achieved without the hysteresis from the Al2O3/BaTiO3 bilayer capacitors through short-pulse charging. This work revealed that the hysteresis phenomenon in NC devices originated from the dielectric leakage of the dielectric layer. The suppression of charge injection via the dielectric leakage, which usually takes time, inhibits complete ferroelectric polarization switching during a short pulse time. It was demonstrated that a nonhysteretic NC effect can be achieved only within certain limited time and voltage ranges, but that these are sufficient for critical device applications. PMID:27231754

  4. Crystallization behavior and properties of BaO-Al2O3-2SiO2 glass matrices

    NASA Technical Reports Server (NTRS)

    Drummond, Charles H., III; Bansal, Narottam P.

    1990-01-01

    Glass of stoichiometric celsian composition, BaO-Al2O3-2SiO2, is a potential glass-ceramic matrix for high-temperature composites. The glass has a density of 3.39 g/cu cm, thermal expansion coefficient of 6.6 x 10(exp -6)/deg C glass transition temperature of 910 C, and dilatometric softening point of 925 C. On heat treatment, only hexacelsian crystallized out on the surface, but both celsian and hexacelsian were present in the bulk. Effects of cold isostatic pressing (CIP), sintering, and hot pressing, in the presence and absence of an additive, on the formation of the celsian phase in the glass were studied. CIP'ed samples, after appropriate heat treatments, always crystallized out as celsian whereas the presence of 5 to 10 weight percent of an additive was necessary for formation of celsian in sintered as well as hot pressed specimens. Green density increased with CIP'ing pressure but had no effect on sintered density. Hot pressing resulted in fully dense samples.

  5. Two competing soft modes and an unusual phase transition in the stuffed tridymite-type oxide BaAl2O4

    NASA Astrophysics Data System (ADS)

    Ishii, Y.; Mori, S.; Nakahira, Y.; Moriyoshi, C.; Park, J.; Kim, B. G.; Moriwake, H.; Taniguchi, H.; Kuroiwa, Y.

    2016-04-01

    We investigated the structural phase transition of BaAl2O4 , which has a network structure with corner-sharing AlO4 tetrahedra, via synchrotron x-ray thermal diffuse scattering measurements and first-principles calculations. BaAl2O4 shows the structural phase transition at TC=451.4 K from the P 6322 parent crystal structure to the low-temperature superstructure with a cell volume of 2 a ×2 b ×c . This phase transition is unusual, in which two energetically competing phonon modes at M and K points soften simultaneously. When approaching TC from above, the K -point mode appears first. However, this K -point mode is overcome by the later-developed M -point mode. The thermal diffuse scattering intensities from both modes increase sharply at TC; therefore, both modes soften simultaneously. The first-principles calculations demonstrate that the M -point mode is electrostatically more preferable than the K -point mode and determines the eventual low-temperature structure, although these two modes are competing energetically. This competition is characteristic of BaAl2O4 , which is ascribed to the structurally flexible network structure of this compound.

  6. Hole-doping effect on the Verwey-type transition and magnetoresistivity of Ba(Sm,Ca)Fe 2O 5+ δ

    NASA Astrophysics Data System (ADS)

    Nakamura, J.; Lindén, J.; Yamauchi, H.; Karppinen, M.

    2002-02-01

    Two series of samples of the oxygen-deficient double-perovskite phase, Ba(Sm,Ca)Fe 2O 5+ δ were synthesized employing a sample encapsulation technique that utilizes Fe metal as an oxygen getter. The hole-doping level on the FeO 2 plane was controlled by varying the amount of excess oxygen or the Ca concentration at the Sm site. Earlier it had been found that at room temperature five-coordinated Fe 2+ and Fe 3+ species form pairs by sharing a d electron, leading to the formation of a Fe 2.5+ fluctuating valence state [Phys. Rev. B 60 (1999) 15,251]. At TV, a Verwey-type transition occurred, signifying the charge separation of the Fe 2.5+ fluctuating valence state into high-spin Fe 2+ and Fe 3+. Moreover, related to the Verwey-type transition a negative magnetoresistance peak with a magnitude of a few percent was observed [Appl. Phys. Lett. 77 (2000) 1683]. The position of the peak was found to correspond to the jumps seen in the susceptibility and resistivity vs. temperature curves. For the present samples, it is found that the value of TV is severely decreased upon increasing the Ca concentration, as seen by susceptibility and magnetoresistivity measurements. Introduction of excess oxygen leads to a less severe decrease of the transition temperature. The observed behavior of TV was reproduced by a simple model based on combinatorial-entropy calculations.

  7. Water-induced morphology changes in BaO/γ-Al2O3 NOx storage materials: an FTIR, TPD, and time-resolved synchrotron XRD study

    SciTech Connect

    Szanyi, Janos; Kwak, Ja Hun; Kim, Do Heui; Wang, Xianqin; Chimentao, Ricardo J.; Hanson, Jonathan; Epling, William S.; Peden, Charles HF

    2007-03-29

    The effect of water on the morphology of BaO/Al2O3-based NOx storage materials was investigated using Fourier transform infrared spectroscopy, temperature programmed desorption, and time-resolved synchrotron X-ray diffraction techniques. The results of this multi-spectroscopy study reveal that, in the presence of water, surface Ba-nitrates convert to bulk nitrates, and water facilitates the formation of large Ba(NO3)2 particles. This process is completely reversible, i.e. after the removal of water from the storage material a significant fraction of the bulk nitrates re-convert to surface nitrates. NO2 exposure of a H2O-containing (wet) BaO/Al2O3 sample results in the formation of nitrites and bulk nitrates exclusively, i.e. no surface nitrates form. After further exposure to NO2, the nitrites completely convert to bulk nitrates. The amount of NOx taken up by the storage material is, however, essentially unaffected by the presence of water, regardless of whether the water was dosed prior to or after NO2 exposure. Based on the results of this study we are now able to explain most of the observations reported in the literature on the effect of water on NOx uptake on similar storage materials.

  8. Refinement of Eutectic Si in High Purity Al-5Si Alloys with Combined Ca and P Additions

    NASA Astrophysics Data System (ADS)

    Ludwig, Thomas Hartmut; Li, Jiehua; Schaffer, Paul Louis; Schumacher, Peter; Arnberg, Lars

    2015-01-01

    The effects of combined additions of Ca and P on the eutectic Si in a series of high purity Al-5 wt pct Si alloys have been investigated with the entrained droplet technique and complementary sets of conventional castings. Differential scanning calorimetry (DSC) and thermal analysis were used to investigate the eutectic droplet undercooling and the recalescence undercooling, respectively. Optical microscopy, SEM, EPMA, and TEM were employed to characterize the resultant microstructures. It was found that 250 ppm Ca addition to Al-5Si wt pct alloys with higher P contents leads to a significant increase of the eutectic droplet undercooling. For low or moderate cooling rates, the TEM results underline that Ca additions do not promote Si twinning. Thus, a higher twin density cannot be expected in Ca containing Al-Si alloys after, e.g., sand casting. Consequently, a refinement of the eutectic Si from coarse flake-like to fine plate-like structure, rather than a modification of the eutectic Si to a fibrous morphology, was achieved. This strongly indicates that the main purpose of Ca additions is to counteract the coarsening effect of the eutectic Si imposed by higher P concentrations. Significant multiple Si twinning was observed in melt-spun condition; however, this can be attributed to the higher cooling rate. After DSC heating (slow cooling), most of Si twins disappeared. Thus, the well-accepted impurity-induced twinning mechanism may be not valid in the case of Ca addition. The possible refinement mechanisms were discussed in terms of nucleation and growth of eutectic Si. We propose that the pre-eutectic Al2Si2Ca phase and preferential formation of Ca3P2 deactivate impurity particles, most likely AlP, poisoning the nucleation sites for eutectic Si.

  9. Interaction of an aluminum atom with an alkaline earth atom: Spectroscopic and ab initio investigations of AlCa

    NASA Astrophysics Data System (ADS)

    Behm, Jane M.; Morse, Michael D.; Boldyrev, Alexander I.; Simons, Jack

    1994-10-01

    A spectroscopic analysis of diatomic AlCa generated by laser vaporization of a 2:1 Al:Ca metal alloy followed by supersonic expansion has been completed using resonant two-photon ionization spectroscopy. Four excited electronic states have been identified and investigated in the energy region from 13 500 to 17 900 cm-1. These are the [13.5] 2Πr, the [15.8] 2Σ, the [17.0] 2Δ3/2(?), and the [17.6] 2Δ3/2 states. From rotational analysis excited state bond lengths have been measured for three of the four excited states, and the ground state has been unambiguously determined as a 2Πr state with a weighted least squares value of the ground state bond length of r0` = 3.1479± 0.0010 Å. The ionization energy of the molecule has also been directly determined as 5.072±0.028 eV. Ab initio calculations for the potential energy curves of seven low-lying states of AlCa [X 2Πr, 2Σ+, 4Σ-, 4Πr, 2Πr(2), 2Δ, and 2Σ-] and for the X 1Σ+ ground electronic state of AlCa+ have been carried out. In agreement with experiment, 2Πr is calculated to be the ground electronic state of the neutral molecule. The dissociation energies of AlCa (X 2Πr) into Al(3s23p1,2P0)+Ca(4s2,1S) and for AlCa+ (X 1Σ+) into Al+(3s2,1S)+Ca(4s2,1S) are calculated to be 0.47 and 1.50 eV, respectively. The excited 2Σ+, 4Σ-, 4Πr, 2Πr(2), 2Δ, and 2Σ- states are calculated to lie 0.2, 0.7, 0.7, 1.1, 1.1, and 1.1 eV above X 2Πr, respectively, and the vertical and adiabatic ionization energies of AlCa have been calculated to be 5.03 and 4.97 eV, respectively.

  10. Roles of Pt and BaO in the Sulfation of Pt/BaO/Al2O3 Lean NOx Trap Materials: Sulfur K-edge XANES and Pt LIII XAFS Studies

    SciTech Connect

    Kim, Do Heui; Kwak, Ja Hun; Szanyi, Janos; Cho, Sung June; Peden, Charles HF

    2008-02-28

    The roles of barium oxide and platinum during the sulfation of Pt-BaO/Al2O3 lean NOx trap catalysts were investigated by S K edge XANES (X-ray absorption near-edge spectroscopy) and Pt LIII XAFS (X-ray absorption fine structure). All of the samples studied (Al2O3, BaO/Al2O3, Pt/Al2O3 and Pt-BaO/Al2O3) were pre-sulfated prior to the X-ray absorption measurements. It was found that barium oxide itself has the ability to directly form barium sulfate even in the absence of Pt and gas phase oxygen. In the platinum-containing samples, the presence of Pt-O species plays an important role in the formation of sulfate species. Even if barium and aluminum sites are available for SO2 to form sulfate, for the case of the BaO(8)/Al2O3 sample, where the barium coverage is about 0.26 ML, S XANES spectroscopy results show that barium sulfates are preferentially produced over aluminum sulfates . When oxygen is absent from the gas phase, the sulfation route that involves Pt-O is eliminated after the initially present Pt-O species are completely consumed. In this case, formation of sulfates is suppressed unless barium oxide is also present. Pt LIII XAFS results show that the first coordination sphere around the Pt atoms in the Pt particles is dependent upon the redox nature of the gas mixture used during the sulfation process. Sulfation under reducing environments (e.g. SO2+H2) leads to formation of Pt-S bonds, while oxidizing conditions (e.g. SO2+O2) continue to show the presence of Pt-O bonds. In addition, the former condition was found to give rise to a higher degree of Pt sintering than the latter one. This result explains why samples sulfated under reducing conditions had lower NOx uptakes than those sulfated under oxidizing conditions. Therefore, our results provide needed information for the development of optimum practical operation conditions (e.g. sulfation or desulfation) for lean NOx trap catalysts that minimize deactivation by sulfur.

  11. Enthalpies of formation of CaAl sub 4 O sub 7 and CaAl sub 12 O sub 19 (hibonite) by high temperature, alkali borate solution calorimetry

    SciTech Connect

    Geiger, C.A.; Kleppa, O.J.; Mysen, B.O.; Lattimer, J.M.; Grossman, L. )

    1988-06-01

    The enthalpies of formation of CaAl{sub 4}O{sub 7} and CaAl{sub 12}O{sub 19} (hibonite), by alkali borate solution calorimetry at 1063 K are discussed. Using these experimental enthalpy data for CaAl{sub 4}O{sub 7} and estimated values for CaAl{sub 12}O{sub 19}, the standard enthalpies of formation of these compounds from the elements at 298 K are derived. Comparison with high-temperature galvanic cell data for the Gibbs energy of formation of CaAl{sub 12}O{sub 19} allows a calculation of the standard entropy of hibonite. This value is only about 2% larger than the oxide sum. Hence it is inferred that the standard entropy of hibonite at 298 K is probably only slightly larger than oxide sum value of 343.7 J/K g.f.w. The present data were used to extrapolate Kumar and Kay's (1985) data for the Gibbs energies of formation of hibonite and CaAl{sub 4}O{sub 7} to the temperature range 1500-1700 K. These data were then used in equilibrium thermodynamic calculations of the condensation of a gas of solar composition. Contrary to calculations of Kornacki and Fegley (1984), who used thermodynamic data of Allibert et al. (1981) for calcium aluminates, the authors results show no stability field for CaAl{sub 4}O{sub 7} in a gas of solar composition at 10{sup {minus}3} to 10{sup {minus}5} atm total pressure. At 10{sup {minus}3} atm pressure, hibonite forms by reaction of corundum with the gas at 1725 K, begins to react with the gas to form gehlenite at 1607 K and disappears completely in a reaction to form spinel at 1494 K. The absence of CaAl{sub 4}O{sub 7}, from hibonite-, spinel-rich inclusions in carbonaceous chondrites cannot be used as an argument against a condensation origin for these objects.

  12. Growth and spectral characters of Nd:CaGdAlO4 crystal

    NASA Astrophysics Data System (ADS)

    Di, Juqing; Sun, Xiaohui; Xu, Xiaodong; Xia, Changtai; Sai, Qinglin; Yu, Haohai; Wang, Yicheng; Zhu, Liu; Gao, Yuan; Guo, Xueyi

    2016-04-01

    In this paper, crystal growth and polarized spectra of Nd:CaGdAlO4 (Nd:CALGO) crystal were reported. The maximal absorption cross-sections are 6.8 and 7.5 × 10-20 cm2 for π-polarization and σ-polarization, and the emission cross-sections are 12.5 × 10-20 cm2 with full width at half maximum (FWHM) of 18 and 11 nm, respectively. The Judd-Ofelt (JO) theory was used to calculate the spectral parameters and the effective intensity parameters Ω2, Ω4 and Ω6 were 0.8 × 10-20 cm2, 7.5 × 10-20 cm2 and 5.8 × 10-20 cm2, respectively. The lifetime was 123 μs. The results show that Nd:CALGO crystal is a promising medium for laser output.

  13. Photoluminescence and thermoluminescence studies of CaAl2O4:Dy(3+) phosphor.

    PubMed

    Ziyauddin, Mohammad; Tigga, Shalinta; Brahme, Nameeta; Bisen, D P

    2016-02-01

    Calcium aluminate phosphors activated by Dy(3+) have been prepared by a combustion method at a temperature of 600°C. Photoluminescence (PL) and thermoluminescence (TL) properties of gamma-irradiated Dy-doped calcium aluminate were investigated. The PL spectrum shows a broad peak around 488 nm and 573 nm, under 347 nm excitation. Thermoluminescence studies were performed for different concentrations of Dy. Optimum intensity of photoluminescence was found for 0.02 mol% concentration of Dy. It was found that initially the peak TL intensity increases with increasing concentration of Dy in the CaAl2O4 host, attains a maximum value for 0.05 mol% concentration and decreases with further increase in the doping concentration due to concentration quenching.

  14. Average and local structure of the Pb-free ferroelectric perovskites (Sr,Sn)TiO3 and (Ba,Ca,Sn)TiO3

    DOE PAGES

    Laurita, Geneva; Page, Katharine; Suzuki, Shoichiro; Seshadri, Ram

    2015-12-16

    The characteristic structural off -centering of Pb2+ in oxides, associated with its 6s2 lone pair, allows it to play a dominant role in polar materials, and makes it a somewhat ubiquitous component of ferroelectrics. In this work, we examine the compounds Sr0.9Sn0.1TiO3 and Ba0.79Ca0.16Sn0.05TiO3 using neutron total scattering techniques with data acquired at di erent temperatures. In these compounds, previously reported as ferroelectrics, Sn2+ appears to display some of the characteristics of Pb2+. We compare the local and long-range structures of the Sn2+-substituted compositions to the unsubstituted parent compounds SrTiO3 and BaTiO3. Lastly, we find that even at these smallmore » substitution levels, the Sn2+ lone pairs drive the local ordering behavior, with the local structure of both compounds more similar to the structure of PbTiO3 rather than the parent compounds.« less

  15. Development of very high Jc in Ba(Fe1-xCox)2As2 thin films grown on CaF2

    PubMed Central

    Tarantini, C.; Kametani, F.; Lee, S.; Jiang, J.; Weiss, J. D.; Jaroszynski, J.; Hellstrom, E. E.; Eom, C. B.; Larbalestier, D. C.

    2014-01-01

    Ba(Fe1-xCox)2As2 is the most tunable of the Fe-based superconductors (FBS) in terms of acceptance of high densities of self-assembled and artificially introduced pinning centres which are effective in significantly increasing the critical current density, Jc. Moreover, FBS are very sensitive to strain, which induces an important enhancement in critical temperature, Tc, of the material. In this paper we demonstrate that strain induced by the substrate can further improve Jc of both single and multilayer films by more than that expected simply due to the increase in Tc. The multilayer deposition of Ba(Fe1-xCox)2As2 on CaF2 increases the pinning force density (Fp = Jc × µ0H) by more than 60% compared to a single layer film, reaching a maximum of 84 GN/m3 at 22.5 T and 4.2 K, the highest value ever reported in any 122 phase. PMID:25467177

  16. Density and symmetry of unoccupied electronic states of Tl sub 2 Ba sub 2 CaCu sub 2 O sub 8

    SciTech Connect

    Romberg, H.; Nuecker, N.; Alexander, M.; Fink, J. ); Hahn, D.; Zetterer, T.; Otto, H.H.; Renk, K.F. )

    1990-02-01

    The local density and symmetry of unoccupied electronic states at the O and Cu sites in Tl{sub 2}Ba{sub 2}CaCu{sub 2}O{sub 8} single crystals has been investigated by measuring O 1{ital s} and Cu 2{ital p} absorption edges. High-energy electron-energy-loss spectroscopy in transmission has been used. There are O 2{ital p}{sub {ital x},{ital y}} states at the Fermi level from the CuO{sub 2} planes and O 2{ital p}{sub {ital z}} states from the BaO and TlO layers. The empty Cu 3{ital d} states have predominantly 3{ital d}{sub {ital x}{sup 2}{minus}{ital y}{sup 2}} symmetry. There is an admixture of about 10% probably with 3{ital d}{sub 3{ital z}{sup 2}{minus}{ital r}{sup 2}} character.

  17. Isovalent Ca and Ba substitutions in thermoelectric layer-structured oxyselenide Sr2CoO2Cu2Se2

    NASA Astrophysics Data System (ADS)

    Chou, T. L.; Mustonen, O.; Tripathi, T. S.; Karppinen, M.

    2016-01-01

    Multilayered compounds typically present exotic functionalities, and some of them have been suggested as potential materials for thermoelectric conversion owing to their unique capability to decouple electronic and heat transport. Here we report new [CoO2] and [Cu2Se2] layered A 2CoO2Cu2Se2 compounds in which Sr at the intervening alkaline-earth A site is partially replaced with Ca or Ba. The parent Sr2CoO2Cu2Se2 phase is a direct gap p-type semiconductor, and density functional theory (DFT) calculations indicate its topmost valence band consists of Cu 3d-Se 4p states. Upon the isovalent cation substitution the lattice modification in the ab plane is constrained by the stiff [CoO2] layer such that the lattice shrinkage/expansion mainly happens along the c axis. Substitution of Sr with the heavier and larger Ba significantly enhances the thermopower but more hole states would be required to optimize the thermoelectric performance. Thermal stability is related to the inter-oxide-selenide-layer interaction, and our thermogravimetric measurement data reveal that the A 2CoO2Cu2Se2 materials could operate in the intermediate temperature region.

  18. Development of very high Jc in Ba(Fe1-xCox)2As2 thin films grown on CaF2

    DOE PAGES

    Tarantini, C.; Kametani, F.; Lee, S.; Jiang, J.; Weiss, J. D.; Jaroszynski, J.; Hellstrom, E. E.; Eom, C. B.; Larbalestier, D. C.

    2014-12-03

    Ba(Fe1-xCox)2As2 is the most tunable of the Fe-based superconductors (FBS) in terms of acceptance of high densities of self-assembled and artificially introduced pinning centres which are effective in significantly increasing the critical current density, Jc. Moreover, FBS are very sensitive to strain, which induces an important enhancement in critical temperature,Tc, of the material. In this study we demonstrate that strain induced by the substrate can further improve Jc of both single and multilayer films by more than that expected simply due to the increase in Tc. The multilayer deposition of Ba(Fe1-xCox)2As2 on CaF2 increases the pinning force density (Fp=Jc xmore » μ₀H) by more than 60% compared to a single layer film, reaching a maximum of 84 GN/m3 at 22.5 T and 4.2 K, the highest value ever reported in any 122 phase.« less

  19. Growth and properties of Ca{sub 0.28}Ba{sub 0.72}Nb{sub 2}O{sub 6} single crystals

    SciTech Connect

    Song Hualong; Zhang Huaijin . E-mail: hjzhang@icm.sdu.edu.cn; Xu Xiangang; Hu Xiaobo; Cheng Xiufeng; Wang Jiyang; Jiang Minhua

    2005-04-20

    Calcium barium niobate Ca{sub 0.28}Ba{sub 0.72}Nb{sub 2}O{sub 6} (CBN-28) crystals were successfully grown by the Czochralski method. X-ray powder diffraction experiments indicated that CBN single crystals are tetragonal with a 12.432({+-}0.002) A and c = 3.957({+-}0.001) A, which have almost the same structure as the Sr{sub 0.50}Ba{sub 0.50}Nb{sub 2}O{sub 6} (SBN-50) crystal. The thermal expansion coefficient perpendicular to Z-direction had been measured to be 1.25 x 10{sup -5} K{sup -1} between 293.15 and 572.15 K, and along Z-axis was negative between 298.15 and 543.15 K. The specific heat of the crystal had been measured by the differential scanning calorimetric experiments. The transmittance spectra from 200 to 3200 nm were also measured. The measured temperature dependence of dielectric constants showed that the Curie temperature of the CBN-28 crystals is 260 deg. C, which is about 200 deg. C higher than that of the (SBN) crystal.

  20. Interplay between spin-orbit coupling and strong correlation effects: Comparison of the three osmate double perovskites Ba2A OsO6 (A =Na , Ca, Y)

    NASA Astrophysics Data System (ADS)

    Gangopadhyay, Shruba; Pickett, Warren E.

    2016-04-01

    High formal valence Os-based double perovskites are a focus of current interest because they display strong interplay of large spin-orbit coupling and strong electronic correlation. Here we present the electronic and magnetic characteristics of a sequence of three cubic Os based double perovskites Ba2A OsO6 (A =Na , Ca, Y), with formal valences of Os +7(d1) ,Os +6(d2) , and Os +5(d3) . For these first principles based calculations we apply an "exact exchange for correlated electrons" functional, with exact exchange applied in a hybrid fashion solely to the Os (5 d ) states. While Ba2NaOsO6 is a reported ferromagnetic Dirac-Mott insulator studied previously, the other two show antiferromagnetic ordering while all retain the undistorted cubic structure. For comparison purposes we have investigated only the ferromagnetic ordered phase. A metal-insulator transition is predicted to occur upon rotating the direction of magnetization in all three materials, reflecting the central role of spin-orbit coupling in these small gap osmates. Surprises arising from comparing formal charge states with the radial charge densities are discussed. Chemical shielding factors and orbital susceptibilities are provided for comparison with future nuclear magnetic resonance data.

  1. Millimeter wave inducing subharmonic steps in the Tl2Ba2CaCu2O8 thin film bicrystal Josephson junction

    NASA Astrophysics Data System (ADS)

    Liu, X.; Hu, L.; Xie, W.; Wang, P.; Ma, L. J.; Zhao, X. J.; He, M.; Zhang, X.; Ji, L.

    2015-04-01

    The bicrystal Josephson junction (BJJ) was fabricated by patterning microbridge into Tl2Ba2CaCu2O8 (Tl-2212) thin film grown epitaxially on the bicrystal SrTiO3 (STO) substrate. The millimeter wave responses of BJJ were researched by experiment and numerical simulation. Shapiro steps and subharmonic steps were both observed in the current-voltage (I-V) curve at the liquid nitrogen temperature. In the resistive-capacitive-inductive shunted junction (RCLSJ) model, both of the Shapiro steps and subharmonic steps were reproduced with varying capacitances and inductances. The result of simulation has a good agreement with the experiment. The relative large capacitance and inductance correspond to distinct subharmonic steps.

  2. μSR study on multi-layered HgBa 2Ca 4Cu 5O y (Hg-1245) superconductor

    NASA Astrophysics Data System (ADS)

    Tokiwa, K.; Ito, S.; Okumoto, H.; Higemoto, W.; Nishiyama, K.; Iyo, A.; Tanaka, Y.; Watanabe, T.

    2003-05-01

    We have carried out zero-field muon spin relaxation (ZF-μSR) measurements in multi-layered HgBa2Ca4Cu5Oy (Hg-1245) superconductor with Tc of 108 K. The variation of ZF-μSR time spectra from Gaussian-type to exponential-type behavior was observed with decreasing temperature below 60 K and the muon precessions were also observed below 45 K. These results indicate the appearance of a static magnetic order of Cu moments at muon sites below Tc. Compared with the results of NMR measurements, they suggest that this magnetic order is caused in three under-doped inner planes of five CuO2 planes in Hg-1245.

  3. Model of deep and shallow traps for the crystal Ba0.77Ca0.23TiO3

    NASA Astrophysics Data System (ADS)

    Matusevich, V.; Kiessling, A.; Kowarschik, R.

    A model of deep and shallow traps has been applied in order to explain the temporal development of the signal wave amplification as well as the pump wave depletion in two-wave-mixing experiments in the crystal Ba0.23Ca0.77TiO3 (BCT). The intensities of the outgoing waves have been studied at different intensities of the incident waves during the first 500 s before the beams have reached their stable states. On the basis of the obtained temporal dependences of the intensities, some material parameters of the crystal have been estimated, like excitation cross sections from the deep and shallow traps (valence levels) into the conduction band, recombination rates from the conduction band into the valence levels, absolute and redistributed charge densities of the deep and shallow traps, and modulations of the absorption and refractive indices.

  4. Unconventional High-Energy-State Contribution to the Cooper Pairing in the Underdoped Copper-Oxide Superconductor HgBa_{2}Ca_{2}Cu_{3}O_{8+δ}.

    PubMed

    Loret, B; Sakai, S; Gallais, Y; Cazayous, M; Méasson, M-A; Forget, A; Colson, D; Civelli, M; Sacuto, A

    2016-05-13

    We study the temperature-dependent electronic B_{1g} Raman response of a slightly underdoped single crystal HgBa_{2}Ca_{2}Cu_{3}O_{8+δ} with a superconducting critical temperature T_{c}=122  K. Our main finding is that the superconducting pair-breaking peak is associated with a dip on its higher-energy side, disappearing together at T_{c}. This result reveals a key aspect of the unconventional pairing mechanism: spectral weight lost in the dip is transferred to the pair-breaking peak at lower energies. This conclusion is supported by cellular dynamical mean-field theory on the Hubbard model, which is able to reproduce all the main features of the B_{1g} Raman response and explain the peak-dip behavior in terms of a nontrivial relationship between the superconducting gap and the pseudogap. PMID:27232035

  5. Crystal Structures of the Trifluoromethyl Sulfonates M(SO3CF3)2 (M = Mg, Ca, Ba, Zn, Cu) from Synchrotron X-ray Powder Diffraction Data

    SciTech Connect

    Dinnebier,R.; Sofina, N.; Hildebrandt, L.; Jansen, M.

    2006-01-01

    The crystal structures of divalent metal salts of trifluoromethyl sulfonic acid ('trifluoromethyl sulfonates') M(SO{sub 3}CF{sub 3}){sub 2} (M = Mg, Ca, Ba, Zn, Cu) were determined from high-resolution X-ray powder diffraction data. Magnesium, calcium and zinc trifluoromethyl sulfonate crystallize in the rhombohedral space group R{bar 3}. Barium trifluoromethyl sulfonate crystallizes in the monoclinic space group I2/a(C2/c) and copper trifluoromethyl sulfonate crystallizes in the triclinic group P{bar 1}. Within the crystal structures the trifluoromethyl sulfonate anions are arranged in double layers with the apolar CF{sub 3} groups pointing towards each other. The cations are located next to the SO{sub 3} groups. The symmetry relations between the different crystal structures have been analyzed.

  6. Multiple caloric effects in (Ba0.865Ca0.135Zr0.1089Ti0.8811Fe0.01)O3 ferroelectric ceramic

    NASA Astrophysics Data System (ADS)

    Patel, Satyanarayan; Chauhan, Aditya; Vaish, Rahul

    2015-07-01

    Multiple caloric effects have been investigated for Fe-doped bulk (Ba0.865Ca0.135Zr0.1089Ti0.8811Fe0.01)O3 (BCZTO-Fe) ferroelectric ceramic. Indirect predictions were made using Maxwell's relations in conjunction with data from experimental observations. It was revealed that bulk BCZTO-Fe has huge untapped potential for solid-state refrigeration. A peak electrocaloric effect of 0.45 K (347 K) was predicted for 0-3 kV.mm-1 electric field, significantly higher than other BCZTO based materials. A maximum elastocaloric cooling of 1.4 K (298 K) was achieved for applied stress of 0-200 MPa. Finally, an unforeseen component of electric field driven caloric effect has been reported as inverse piezocaloric effect, with a maximum temperature change of 0.28 K (298 K).

  7. High piezoelectricity due to multiphase coexistence in low-temperature sintered (Ba,Ca)(Ti,Sn)O3-CuOx ceramics

    NASA Astrophysics Data System (ADS)

    Zhou, Peng-Fei; Zhang, Bo-Ping; Zhao, Lei; Zhao, Xiao-Kun; Zhu, Li-Feng; Cheng, Li-Qian; Li, Jing-Feng

    2013-10-01

    Ultrahigh piezoelectric constant (d33 = 683 pC/N) and converse piezoelectric coefficient (dS/dE = 1257 pm/V) were observed in CuO-doped lead-free (Ba,Ca)(Ti,Sn)O3 ceramics at an optimal composition fabricated by a conventional sintering method at a low temperature 1250 °C. Since all samples showed a pure perovskite structure with coexisting multiphases including cubic, tetragonal, orthorhombic, and rhombohedral phases around two converged triple points, a good compositional stability of high piezoelectricity along with a high d33 and dS/dE over 600 pC/N and 1000 pm/V was achieved within a wide compositional region (1.0 ≤ x ≤ 3.0) regardless of the CuO content (x).

  8. Measurements of heat capacity associated with the magnetic transition in La_0.7A_0.3MnO3 (A = Ca, Sr, Ba)

    NASA Astrophysics Data System (ADS)

    Jeong, Yoon Hee; Moon, I. K.; Ju, H. L.

    2001-03-01

    It is well known that the transition temperature of the paramagnetic insulator-magnetic metal transition in the perovskite manganites La_1-xA_xMnO3 (x = 0.3, A = divalent metal) depends sensitively on the average size of A-site cations. In order to elucidate the physical reason for this behavior, we have carried out high-resolution measurements of heat capacity of samples with A = Ca, Sr, Ba. By critically comparing these results as well as magnetization measurements, we were able to draw a conclusion: as the average size of the A-site cation gets smaller than a certain value, the two-phase coexistence sets in and the transition temperature abruptly decreases.

  9. Diminishing sign anomaly and scaling behavior of the mixed-state Hall resistivity in Tl2Ba2Ca2Cu3O10 films containing columnar defects

    NASA Technical Reports Server (NTRS)

    Budhani, R. C.; Liou, S. H.; Cai, Z. X.

    1993-01-01

    The issues of sign reversal of the Hall voltage and scaling between longitudinal (rho(xx)) and Hall (rho(xy)) resistivities are studied in Tl2Ba2Ca2Cu3O10 films in which the vortex dynamics is drastically changed by flux pinning at heavy-ion-irradiation-induced linear defects. While the sign anomaly diminishes with increasing defect concentration, the power law rho(xy) is approximately equal to rho(xx) exp beta, beta = 1.85 +/- 0.1, holds even after irradiation. This result shows that the scaling is a universal feature of the mixed state in this system. The sign anomaly, on the other hand, is not consistent with a model that invokes pinning-induced backflow in the vortex core as the mechanism for this effect.

  10. Crossovers in the out-of-plane resistivity of superconducting Tl2Ba2CaCu2O8 single crystals

    NASA Astrophysics Data System (ADS)

    Salvetat, J.-P.; Berger, H.; Halbritter, A.; Mihály, G.; Pavuna, D.; Forró, L.

    2000-12-01

    We report the in-plane (ρab) and out-of-plane (ρc) resistivities in the 4 800 K range on single crystals of Tl2Ba2CaCu2O8 high-Tc cuprate with Tc = 111 K (ρc/ρab approx 1000). ρab(T) exhibits "usual" linear behavior and ρc(T) follows generally metallic-like, positive slope in the 150 400 K temperature range. There is a clear crossover to semiconductor-like behavior close to Tc. However, for the first time in a chainless high-Tc cuprate we observe a crossover above 500 K due to hopping conduction. Under high pressures ( < 15 kbar) the magnitude of ρc strongly decreases, yet the ρc(T) slope does not change. This suggests that the out-of-plane charge transport is governed by the interplane tunneling rate.

  11. Optical waveguide properties of Ca0.4Ba0.6Nb2O6 crystal formed by oxygen ion irradiation

    NASA Astrophysics Data System (ADS)

    Wang, Tie-Jun; Zhou, Yu-Fan; Yu, Xiao-Fei; Liu, Tao; Zhang, Lian; Song, Hong-Lian; Qiao, Mei; Wang, Xue-Lin

    2015-07-01

    We report the fabrication of a planar optical waveguide in a Ca0.4Ba0.6Nb2O6 crystal by irradiation with 6.0 MeV oxygen ions. We measured the guiding mode by the prism-coupling method at 633 nm and 1539 nm. The near-field intensity distributions were measured by the end-face coupling setup at a wavelength of 633 nm. The reflectivity calculation method (RCM) was used for reconstructing refractive index profiles. SRIM was used to simulate the electronic and nuclear stopping power caused by oxygen ion irradiation, and the finite-difference beam propagation method (FD-BPM) was used to simulate the near-field intensity distributions. Micro-Raman spectra were measured at room temperature in air to study the differences between the substrate and waveguide region.

  12. Effect of pr and ca Doping on the Superconducting Properties of Dy1-2xPrxCaxBa2Cu3O7-δ HTSCs

    NASA Astrophysics Data System (ADS)

    Charoenthai, N.; Udomkan, N.

    The structure changes and the suppression of superconductivity in the Dy-123 high-temperature superconductors (HTSCs) due to equal substitution of Pr and Ca are studied. The onset temperatures (Tc's) of the co-doped Dy1-2xPrxCaxBa2Cu3O7-δ HTSC's are measured by AC susceptibility measurements. The Tc's and rates of decrease of dTc/dx due to Pr substitution for both series exhibit rare earth size effects. It is found that the lattice distortion defined by D = (b-a)/(b+a), where a and b are the lattice parameters in the basal plane, decreases systematically as the doping is increased. A hole-filling and pair-breaking model is used to explain the behaviors of both the Tc's and the rates of decrease of dTc/dx as Pr4+ ions are doped into two "123" HTSCs.

  13. Excess conductivity in Y 1-2xCa xTb xBa 2Cu 3O 7-δ

    NASA Astrophysics Data System (ADS)

    Han, Shun-Hui; Lundqvist, P.; Rapp, Ö.

    1997-08-01

    Superconducting fluctuations have been studied in zero magnetic field in sintered samples of Y 1-2xCa xTb xBa 2Cu 3O 7-δ by electrical resistivity measurements for x=0, 0.025, and 0.05. The excess conductivity Δσ was analysed as a function of reduced temperature ɛ=ln(T/T c) in the range -5 < ln ɛ < -1.5. With decreasing temperature, characteristic cross-overs were found in all samples from 2D to 3D behavior, and at a lower temperature to a critical regime, with characteristic exponents in Δσ∝ ɛα of α1=-1, α2=-0.5 and α3 ≈ -0.4 respectively.

  14. Flux Pinning by Cr Nanoparticles in Cu_{0.5}Tl_{0.5}Ba2Ca2Cu3O_{10-δ } Superconductor

    NASA Astrophysics Data System (ADS)

    Waqee-ur-Rehman, M.; Mumtaz, M.; Qasim, Irfan; Nadeem, K.

    2016-09-01

    Increase in flux pinning strength of Cu_{0.5}Tl_{0.5}Ba2Ca2Cu3O_{10-δ }(CuTl-1223) superconductor has been observed after addition of Cr nanoparticles. We have thoroughly investigated the infield response of Cr nanoparticles-added CuTl-1223 superconductor in an external applied magnetic field in the range of 0-7 T. Solid-state reaction technique has been employed to synthesize (Cr)x-CuTl-1223; x = 0-1.00 wt% nanoparticle-superconductor composites. The flux pinning mechanism has been analyzed on the basis of thermally activated flux flow model in the presence of a small current (10 μ A). The increase in activation energy and decrease in transition width of CuTl-1223 superconducting phase show the enhancement in its flux pinning strength upon the addition of Cr nanoparticles.

  15. Unconventional High-Energy-State Contribution to the Cooper Pairing in the Underdoped Copper-Oxide Superconductor HgBa2 Ca2 Cu3 O8 +δ

    NASA Astrophysics Data System (ADS)

    Loret, B.; Sakai, S.; Gallais, Y.; Cazayous, M.; Méasson, M.-A.; Forget, A.; Colson, D.; Civelli, M.; Sacuto, A.

    2016-05-01

    We study the temperature-dependent electronic B1 g Raman response of a slightly underdoped single crystal HgBa2 Ca2 Cu3 O8 +δ with a superconducting critical temperature Tc=122 K . Our main finding is that the superconducting pair-breaking peak is associated with a dip on its higher-energy side, disappearing together at Tc. This result reveals a key aspect of the unconventional pairing mechanism: spectral weight lost in the dip is transferred to the pair-breaking peak at lower energies. This conclusion is supported by cellular dynamical mean-field theory on the Hubbard model, which is able to reproduce all the main features of the B1 g Raman response and explain the peak-dip behavior in terms of a nontrivial relationship between the superconducting gap and the pseudogap.

  16. The features of structural transformations in lanthanum manganites La{sub 1−x}A{sub x}MnO{sub 3+δ} (A = Ca, Sr, Ba)

    SciTech Connect

    Sedykh, Vera D.

    2014-10-27

    In this work, the effect of the ionic radius and concentration of a doping element on the features of the structural transformations in polycrystalline lanthanum manganites, La{sub 1−x}A{sub x}MnO{sub 3+δ} (A = Ca, Sr, Ba), has been studied by Mössbauer spectroscopy and X-ray diffraction analysis. For Mössbauer investigations, a small amount of {sup 57}Fe (2 at%) Mössbauer isotope was introduced into the samples. It follows from the analysis of the obtained data that both common features of the structural transformations and differences between them exist in lanthanum manganites depending on ionic radius and concentration of a doping element.

  17. Luminescence properties of M2Si5N8:Ce3+ (M = Ca, Sr, Ba) mixed nitrides prepared by metal hydrides as starting materials

    NASA Astrophysics Data System (ADS)

    Kuramoto, Daiki; Kim, Hyo Sung; Horikawa, Takashi; Itoh, Masahiro; Machida, Ken-ichi

    2012-08-01

    Mixed metal nitrides, M2Si5N8:Ce3+ (M = Ca, Sr, Ba), were synthesized from M2-yCeySi5 or an appropriate mixture of MSiHx, Si3N4 and CeF3, by a direct nitriding process in N2 gas: 2 MSiHx + Si3N4 + CeF3 → M2Si5N8:Ce3+. Also, charge-compensated materials, M2AlzSi5-zN8:Ce3+ were prepared (from an appropriate mixture of MSiHx, MAlSiHx, Si3N4 and CeF3) and the luminescence properties were characterized. The resultant phosphors showed green emission suitable for LED illumination by optimizing the mixing ratio of metal elements.

  18. (Ba0.85Ca0.15)(Zr0.1Ti0.9)O3 Ceramics Synthesized by a Gel-Casting Method

    NASA Astrophysics Data System (ADS)

    Xiong, Wei

    2016-08-01

    (Ba0.85Ca0.15)(Zr0.1Ti0.9)O3 (BCZT) powder was synthesized by a solid-state reaction method, then the ceramics were fabricated by gel-casting and die-pressing routes, respectively. Piezoelectric coefficient ( d 33 ) was measured by the d 33 m; Planar mode electromechanical coupling coefficient ( k p ), dielectric loss ( tanδ) and relative permittivity ( ɛ r ) were measured by the impedance analyzer. Results of measurements showed that in the range of tested sintering temperature (1300-1500°C), gel-casting samples showed better piezoelectric and electromechanical coupling coefficients ( d 33 = 395 pC/N, k p = 0.44) compared with die-pressing samples, and comparable dielectric properties were also observed. ( tanδ = 0.037, ɛ r = 3267).

  19. Unconventional High-Energy-State Contribution to the Cooper Pairing in the Underdoped Copper-Oxide Superconductor HgBa_{2}Ca_{2}Cu_{3}O_{8+δ}.

    PubMed

    Loret, B; Sakai, S; Gallais, Y; Cazayous, M; Méasson, M-A; Forget, A; Colson, D; Civelli, M; Sacuto, A

    2016-05-13

    We study the temperature-dependent electronic B_{1g} Raman response of a slightly underdoped single crystal HgBa_{2}Ca_{2}Cu_{3}O_{8+δ} with a superconducting critical temperature T_{c}=122  K. Our main finding is that the superconducting pair-breaking peak is associated with a dip on its higher-energy side, disappearing together at T_{c}. This result reveals a key aspect of the unconventional pairing mechanism: spectral weight lost in the dip is transferred to the pair-breaking peak at lower energies. This conclusion is supported by cellular dynamical mean-field theory on the Hubbard model, which is able to reproduce all the main features of the B_{1g} Raman response and explain the peak-dip behavior in terms of a nontrivial relationship between the superconducting gap and the pseudogap.

  20. A tale of three double perovskites: Ba2XOsO6 (X =Na,Ca,Y)

    NASA Astrophysics Data System (ADS)

    Gangopadhyay, Shruba; Pickett, Warren

    2015-03-01

    High valent Os based double perovskites are one center of current interest because they display extreme interplay of large spin orbit coupling and strong electronic correlation. We present electronic and magnetic structures of three cubic Os based double perovskites with Os+7 (d1) , Os+6(d2) , Os+5(d3) . For these first principles based calculation we used an onsite hybrid exchange only on Os(5d), as implemented in Wien2k. While Ba2NaOsO6 is a ferromagnetic Mott insulator, the other two show antiferromagnetic ordering. For comparison purposes we have investigated only the ferromagnetic ordered phase of these three materials. A metal-insulator transition by changing spin orbit coupling direction is found in all three materials, however each double perovskite is metallic for different magnetic directions. Surprises from looking at the radial charge densities will be discussed. We provide a resolution to the riddle: why, despite d1 configuration, does Ba2NaOsO6 remain cubic. This material introduces a new class of J = 3/2 Mott insulator. DOE Stockpile Stewardship Academic Alliance Program.

  1. Inelastic neutron scattering studies of phonon spectra, and simulations of pressure-induced amorphization in tungstates A W O4 (A =Ba ,Sr ,Ca , and Pb )

    NASA Astrophysics Data System (ADS)

    Goel, Prabhatasree; Gupta, M. K.; Mittal, R.; Rols, S.; Achary, S. N.; Tyagi, A. K.; Chaplot, S. L.

    2015-03-01

    Lattice dynamics and high-pressure phase transitions in A W O4 (A =Ba ,Sr ,Ca , and Pb ) have been investigated using inelastic neutron scattering experiments, ab initio density functional theory calculations, and extensive molecular dynamics simulations. The vibrational modes that are internal to W O4 tetrahedra occur at the highest energies consistent with the relative stability of W O4 tetrahedra. The neutron data and the ab initio calculations are found to be in excellent agreement. The neutron and structural data are used to develop and validate an interatomic potential model. The model is used for classical molecular dynamics simulations to study their response to high pressure. We have calculated the enthalpies of the scheelite and fergusonite phases as a function of pressure, which confirms that the scheelite to fergusonite transition is second order in nature. With increase in pressure, there is a gradual change in the A O8 polyhedra, while there is no apparent change in the W O4 tetrahedra. We found that all the four tungstates amorphize at high pressure. This is in good agreement with available experimental observations which show amorphization at around 45 GPa in BaW O4 and 40 GPa in CaW O4 . Further molecular dynamics simulations at high pressure and high temperature indicate that application of pressure at higher temperature hastens the process of amorphization. On amorphization, there is an abrupt increase in the coordination of the W atom while the bisdisphenoids around the A atom are considerably distorted. The pair-correlation functions of the various atom pairs corroborate these observations. Our observations aid in predicting the pressure of amorphization in SrW O4 and PbW O4 .

  2. Ultrasonically-enhanced mechanochemical synthesis of CaAl-layered double hydroxides intercalated by a variety of inorganic anions.

    PubMed

    Szabados, Márton; Mészáros, Rebeka; Erdei, Szabolcs; Kónya, Zoltán; Kukovecz, Ákos; Sipos, Pál; Pálinkó, István

    2016-07-01

    CaAl-layered double hydroxides (CaAl-LDHs) were synthesised with various interlayer anions (CO3(2-), F(-), Cl(-), Br(-) and I(-)) by mechanochemical pre-treatment followed by ultrasonic irradiation in aqueous media. The parameters of the syntheses (duration of pre-milling and sonication, quality of the aqueous media, temperature) were altered in order to optimise the procedure and to understand the formation of LDH and other secondary products. The products were characterised by X-ray diffractometry (XRD) and scanning electron microscopy (SEM). The optimisation resulted in close-to-phase-pure CaAl-LDHs, not only with carbonate and chloride interlayer anions, but the hard-to-intercalate bromide and iodide as well.

  3. High electrostrictive coefficient Q33 in lead-free Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 piezoelectric ceramics

    NASA Astrophysics Data System (ADS)

    Li, Fei; Jin, Li; Guo, Runping

    2014-12-01

    In this study, the electrostrictive effect in Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 (BZT-xBCT, x = 0.4, 0.5, and 0.6) ceramics was investigated to gain understanding of their high piezoelectric activity. The electrostrictive coefficient Q33 of the BZT-xBCT ceramics was observed to be around 0.04 m4/C2, twice that reported for Pb(Zr,Ti)O3-based ceramics. The Q33 was found to be quite stable with respect to temperature and composition for the BZT-xBCT ceramics. The addition of Fe3+ dopant to the ceramics greatly decreased their Curie temperature without affecting their Q33, which remained 0.04 m4/C2. Moreover, a high and hysteresis-free electric-field-induced strain was obtained for 2 at. % Fe-doped BZT-0.5BCT ceramics at room temperature, caused by their high Q33 coefficient and lower-than-room-temperature Curie temperature. The small-signal M33 coefficient of 2 at. % Fe-doped BZT-0.5BCT ceramics was found to be 1.5 × 10-16 m2/V2 (0.32 × 10-16 m2/V2 for undoped counterpart). These results indicate that 2 at. % Fe-doped BZT-0.5BCT ceramics have great potential as alternatives for hard Pb(Zr,Ti)O3 ceramics in actuator applications, where reproducible and non-hysteretic deformation responses are required.

  4. Three-dimensional superconducting behavior and thermodynamic parameters of HgBa{sub 2}Ca{sub 0.86}Sr{sub 0.14}Cu{sub 2}O{sub 6{minus}{delta}}

    SciTech Connect

    Kim, M. |; Lee, S.; Yu, S.; Hur, N.H.

    1996-04-01

    This study measures the temperature dependence of reversible magnetization of grain-aligned HgBa{sub 2}Ca{sub 0.86}Sr{sub 0.14}Cu{sub 2}O{sub 6{minus}{delta}} high-{ital T}{sub {ital c}} superconductor with external magnetic fields parallel to the {ital c} axis. The magnetization is field independent at {ital T}{sup {asterisk}} = 114.5 K, which indicates strong thermal vortex fluctuations. From the vortex fluctuation model, the lower limit of coherence length along the {ital c} axis {xi}{sub {ital c}}(0){approx_equal} 2 and the anisotropy ratio {gamma}{le} 7.7 has been obtained, which implies that this sample is anisotropic three-dimensional (3D) superconductor as Y{sub 1}Ba{sub 2}Cu{sub 3}O{sub 7{minus}{delta}}. These results are supported by good 3D scaling behavior of high-field magnetization around {ital T}{sub {ital c}}({ital H}) as a function of [{ital T}{minus}{ital T}{sub {ital c}}({ital H})]/({ital TH}){sup 2/3}. The thermodynamic critical field {ital H}{sub {ital c}}({ital T}) and the Ginzburg-Landau parameter {kappa} = 114.8 were extracted from the model of Hao {ital et} {ital al}. Also, the various thermodynamic parameters were obtained: the penetration depth {lambda}{sub {ital ab}}(0) = 1913 A, coherence length {xi}{sub {ital ab}}(0) = 13.9 A, and the zero temperature upper critical field {ital H}{sub {ital c}2}(0) = 170.4 T. {copyright} {ital 1996 The American Physical Society.}

  5. Infrared study of the vibrational behavior of CrO 42- guest ions matrix-isolated in metal (II) sulfates (Me=Ca, Sr, Ba, Pb)

    NASA Astrophysics Data System (ADS)

    Stoilova, D.; Georgiev, M.; Marinova, D.

    2005-03-01

    Infrared spectra of matrix-isolated CrO 42- guest ions in host sulfate matrices - CaSO 4·2H 2O, SrSO 4, BaSO 4 and PbSO 4 are reported and discussed with respect to the Cr-O stretching and O-Cr-O bending modes. An adequate measure for the CrO 42- guest ion distortion is the site group splitting Δ νas and Δ νmax (the difference between the highest and the lowest wavenumbered components of the stretching and bending modes). When the smaller SO 42- ions are replaced by the larger CrO 42- ions the mean frequencies of the asymmetric stretching and bending modes ( ν and ν) as well as the frequencies of ν1 of the CrO 42- guest ions are shifted to higher wavenumbers as compared to those in the respective neat chromates due to the larger repulsion potential at the host lattice sites (smaller values of the unit-cell volumes of the neat sulfates than those of the neat chromates). The CrO 42- guest ions exhibit three bands corresponding to the ν3 modes as deduced from the site group analysis ( C2 site symmetry in CaSO 4·2H 2O and Cs site symmetry in SrSO 4, BaSO 4 and PbSO 4). However, the bending modes ν4 and ν2 of the CrO 42- guest ions in SrSO 4, BaSO 4 and PbSO 4 show an effectively higher local symmetry than the 'rigorous' crystallographic one (two bands for ν4 and one band for ν2 instead of a triplet and a doublet expected, respectively). Such different apparent site symmetries observed in various spectral regions may be attributed to the different influence of energetic and geometrical distortions of the polyatomic entities at particular site on various modes.

  6. High mobility field effect transistor based on BaSnO{sub 3} with Al{sub 2}O{sub 3} gate oxide

    SciTech Connect

    Park, Chulkwon; Kim, Useong; Ju, Chan Jong; Park, Ji Sung; Kim, Young Mo; Char, Kookrin

    2014-11-17

    We fabricated an n-type accumulation-mode field effect transistor based on BaSnO{sub 3} transparent perovskite semiconductor, taking advantage of its high mobility and oxygen stability. We used the conventional metal-insulator-semiconductor structures: (In,Sn){sub 2}O{sub 3} as the source, drain, and gate electrodes, Al{sub 2}O{sub 3} as the gate insulator, and La-doped BaSnO{sub 3} as the semiconducting channel. The Al{sub 2}O{sub 3} gate oxide was deposited by atomic layer deposition technique. At room temperature, we achieved the field effect mobility value of 17.8 cm{sup 2}/Vs and the I{sub on}/I{sub off} ratio value higher than 10{sup 5} for V{sub DS} = 1 V. These values are higher than those previously reported on other perovskite oxides, in spite of the large density of threading dislocations in the BaSnO{sub 3} on SrTiO{sub 3} substrates. However, a relatively large subthreshold swing value was found, which we attribute to the large density of charge traps in the Al{sub 2}O{sub 3} as well as the threading dislocations.

  7. Kasatkinite, Ba2Ca8B5Si8O32(OH)3 · 6H2O6, a new mineral from the Bazhenovskoe deposit, the Central Urals, Russia

    NASA Astrophysics Data System (ADS)

    Pekov, I. V.; Chukanov, N. V.; Filinchuk, Ya. E.; Zadov, A. E.; Kononkova, N. N.; Epanchintsev, S. G.; Kaden, P.; Kutzer, A.; Göttlicher, J.

    2013-12-01

    A new mineral, kasatkinite, Ba2Ca8B5Si8O32(OH)3 · 6H2O, has been found at the Bazhenovskoe chrysotile asbestos deposit, the Central Urals, Russia in the cavities in rhodingite as a member of two assemblages: (l) on prehnite, with pectolite, calcite, and clinochlore; and (2) on grossular, with diopside and pectolite. Kasatkinite occurs as spherulites or bunches up to 3 mm in size, occasionally combined into crusts. Its individuals are acicular to hair-like, typically split, with a polygonal cross section, up to 0.5 mm (rarely, to 6 mm) in length and to 20 μm in thickness. They consist of numerous misoriented needle-shaped subindividuals up to several dozen μm long and no more than 1 μm thick. Kasatkinite individuals are transparent and colorless; its aggregates are snow white. The luster is vitreous or silky. No cleavage was observed; the fracture is uneven or splintery for aggregates. Individuals are flexible and elastic. The Mohs' hardness is 4-4.5. D meas = 2.95(5), D calc = 2.89 g/cm3. Kasatkinite is optically biaxial (+), α = 1.600(5), β = 1.603(2), γ = 1.626(2), 2 V meas = 30(20)°, 2 V calc = 40°. The IR spectrum is given. The 11B MAS NMR spectrum shows the presence of BO4 in the absence of BO3 groups. The chemical composition of kasatkinite (wt %; electron microprobe, H2O by gas chromatography) is as follows: 0.23 Na2O, 0.57 K2O, 28.94 CaO, 16.79 BaO, 11.57 B2O3, 0.28 Al2O3, 31.63 SiO2, 0.05 F, 9.05 H2O, -0.02 -O=F2; the total is 99.09. The empirical formula (calculated on the basis of O + F = 41 apfu, taking into account the TGA data) is: Na0.11K0.18Ba1.66Ca7.84B5.05Al0.08Si8.00O31.80(OH)3.06F0.04 · 6.10H2O. Kasatkinite is monoclinic, space group P21/ c, P2/ c, or Pc; the unit-cell dimensions are a = 5.745(3), b = 7.238(2), c = 20.79 (1) Å, β = 90.82(5)°, V = 864(1) Å3, Z = 1. The strongest reflections ( d Å- I[ hkl]) in the X-ray powder diffractions pattern are: 5.89-24[012], 3.48-2.1[006], 3.36-24[114]; 3.009-100[, 121, ], 2

  8. Binary, ternary and quaternary silicates of CaO, BaO and ZnO in high thermal expansion seals for solid oxide fuel cells studied by high-temperature X-ray diffraction (HT-XRD)

    SciTech Connect

    Kerstan, Marita; Mueller, Matthias; Ruessel, Christian

    2011-12-15

    Highlights: Black-Right-Pointing-Pointer We examined the thermal expansion of various silicates of CaO, BaO and ZnO. Black-Right-Pointing-Pointer Thermal expansions were determined by dilatometry and high-temperature X-ray diffraction. Black-Right-Pointing-Pointer High-temperature X-ray diffraction enabled to determine anisotropic thermal expansion. Black-Right-Pointing-Pointer CaSiO{sub 3}, Ca{sub 3}Si{sub 2}O{sub 7} and BaCa{sub 2}Si{sub 3}O{sub 9} exhibit the highest thermal expansion. Black-Right-Pointing-Pointer CaSiO{sub 3}, Ca{sub 3}Si{sub 2}O{sub 7} and BaCa{sub 2}Si{sub 3}O{sub 9} are suitable as components in high temperature seals. -- Abstract: Gas-tight seals based on glasses suitable for joining of materials with high thermal expansion coefficients are for example required for solid-oxide fuel cells. If these seals are to be used at high temperatures, they can only be fabricated from glasses which enable the crystallization of phases with high thermal expansion coefficients. This paper reports on some components from systems suitable for high thermal expansion seals: binary calcium silicates, CaSiO{sub 3}, Ca{sub 3}Si{sub 2}O{sub 7} and Ca{sub 2}SiO{sub 4} zinc silicates, Zn{sub 2}SiO{sub 4}, ternary silicates of BaO, CaO and ZnO, BaCa{sub 2}Si{sub 3}O{sub 9}, Ca{sub 2}ZnSi{sub 2}O{sub 7}, and one quaternary silicate, Ba{sub 2}CaZn{sub 2}Si{sub 6}O{sub 17,} studied by high-temperature X-ray diffraction. Only CaSiO{sub 3}, Ca{sub 3}Si{sub 2}O{sub 7} and BaCa{sub 2}Si{sub 3}O{sub 9} exhibit thermal expansion coefficients in the range suitable for high thermal expansion seals of 11.2-11.8 Multiplication-Sign 10{sup -6} K{sup -1} (100-800 Degree-Sign C). The thermal expansions strongly depend on the respective crystallographic axis. The coefficient of thermal expansion of a sealing glass is not only affected by the thermal expansions of the crystalline phases, but also by that of the residual glassy phase as well as by the elastic properties. The phase

  9. Microwave dielectric properties of CaCu3Ti4O12-Al2O3 composite

    NASA Astrophysics Data System (ADS)

    Rahman, Mohd Fariz Ab; Abu, Mohamad Johari; Karim, Saniah Ab; Zaman, Rosyaini Afindi; Ain, Mohd Fadzil; Ahmad, Zainal Arifin; Mohamed, Julie Juliewatty

    2016-07-01

    (1-x)CaCu3Ti4O12 + (x)Al2O3 composite (0 ≤ x ≤0.25) was prepared via conventional solid-state reaction method. The fabrication of sample was started with synthesizing stoichiometric CCTO from CaCO3, CuO and TiO2 powders, then wet-mixed in deionized water for 24 h. The process was continued with calcined CCTO powder at 900 °C for 12 h before sintered at 1040 °C for 10 h. Next, the calcined CCTO powder with different amount of Al2O3 were mixed for 24 h, then palletized and sintered at 1040 °C for 10. X-ray diffraction analysis on the sintered samples showed that CCTO powder was in a single phase, meanwhile the trace of secondary peaks which belong to CaAl2O4 and Corundum (Al2O3) could be observed in the other samples Scanning electron microscopy analysis showed that the grain size of the sample is firstly increased with addition of Al2O3 (x = 0.01), then become smaller with the x > 0.01. Microwave dielectric properties showed that the addition of Al2O3 (x = 0.01) was remarkably reduced the dielectric loss while slightly increased the dielectric permittivity. However, further addition of Al2O3 was reduced both dielectric loss and permittivity at least for an order of magnitude.

  10. Free-electron-like Hall effect and deviations from free-electron behavior in Ca-Al amorphous alloys

    NASA Astrophysics Data System (ADS)

    Mayeya, F. M.; Hickey, B. J.; Howson, M. A.

    1995-06-01

    The Hall coefficients of Ca-Al amorphous alloys have been measured at 4.2 K over a wide range of compositions. It is shown that the magnitude of the Hall coefficients are close to the nearly-free-electron (NFE) prediction for low Ca concentrations but deviate significantly from the NFE values for Ca concentration greater than 45 at. %. The deviations from the free-electron values have previously been attributed to the effects of s-d hybridization, while a reduction in magnitude by Au doping has been argued to result from the side-jump effect.

  11. Phase separation enhanced magneto-electric coupling in La0.7Ca0.3MnO3/BaTiO3 ultra-thin films.

    PubMed

    Alberca, A; Munuera, C; Azpeitia, J; Kirby, B; Nemes, N M; Perez-Muñoz, A M; Tornos, J; Mompean, F J; Leon, C; Santamaria, J; Garcia-Hernandez, M

    2015-12-09

    We study the origin of the magnetoelectric coupling in manganite films on ferroelectric substrates. We find large magnetoelectric coupling in La0.7Ca0.3MnO3/BaTiO3 ultra-thin films in experiments based on the converse magnetoelectric effect. The magnetization changes by around 30-40% upon applying electric fields on the order of 1 kV/cm to the BaTiO3 substrate, corresponding to magnetoelectric coupling constants on the order of α = (2-5) · 10(-7) s/m. Magnetic anisotropy is also affected by the electric field induced strain, resulting in a considerable reduction of coercive fields. We compare the magnetoelectric effect in pre-poled and unpoled BaTiO3 substrates. Polarized neutron reflectometry reveals a two-layer behavior with a depressed magnetic layer of around 30 Å at the interface. Magnetic force microscopy (MFM) shows a granular magnetic structure of the La0.7Ca0.3MnO3. The magnetic granularity of the La0.7Ca0.3MnO3 film and the robust magnetoelastic coupling at the La0.7Ca0.3MnO3/BaTiO3 interface are at the origin of the large magnetoelectric coupling, which is enhanced by phase separation in the manganite.

  12. Phase separation enhanced magneto-electric coupling in La0.7Ca0.3MnO3/BaTiO3 ultra-thin films.

    PubMed

    Alberca, A; Munuera, C; Azpeitia, J; Kirby, B; Nemes, N M; Perez-Muñoz, A M; Tornos, J; Mompean, F J; Leon, C; Santamaria, J; Garcia-Hernandez, M

    2015-01-01

    We study the origin of the magnetoelectric coupling in manganite films on ferroelectric substrates. We find large magnetoelectric coupling in La0.7Ca0.3MnO3/BaTiO3 ultra-thin films in experiments based on the converse magnetoelectric effect. The magnetization changes by around 30-40% upon applying electric fields on the order of 1 kV/cm to the BaTiO3 substrate, corresponding to magnetoelectric coupling constants on the order of α = (2-5) · 10(-7) s/m. Magnetic anisotropy is also affected by the electric field induced strain, resulting in a considerable reduction of coercive fields. We compare the magnetoelectric effect in pre-poled and unpoled BaTiO3 substrates. Polarized neutron reflectometry reveals a two-layer behavior with a depressed magnetic layer of around 30 Å at the interface. Magnetic force microscopy (MFM) shows a granular magnetic structure of the La0.7Ca0.3MnO3. The magnetic granularity of the La0.7Ca0.3MnO3 film and the robust magnetoelastic coupling at the La0.7Ca0.3MnO3/BaTiO3 interface are at the origin of the large magnetoelectric coupling, which is enhanced by phase separation in the manganite. PMID:26648002

  13. Phase separation enhanced magneto-electric coupling in La0.7Ca0.3MnO3/BaTiO3 ultra-thin films

    PubMed Central

    Alberca, A.; Munuera, C.; Azpeitia, J.; Kirby, B.; Nemes, N. M.; Perez-Muñoz, A. M.; Tornos, J.; Mompean, F. J.; Leon, C.; Santamaria, J.; Garcia-Hernandez, M.

    2015-01-01

    We study the origin of the magnetoelectric coupling in manganite films on ferroelectric substrates. We find large magnetoelectric coupling in La0.7Ca0.3MnO3/BaTiO3 ultra-thin films in experiments based on the converse magnetoelectric effect. The magnetization changes by around 30–40% upon applying electric fields on the order of 1 kV/cm to the BaTiO3 substrate, corresponding to magnetoelectric coupling constants on the order of α = (2–5)·10−7 s/m. Magnetic anisotropy is also affected by the electric field induced strain, resulting in a considerable reduction of coercive fields. We compare the magnetoelectric effect in pre-poled and unpoled BaTiO3 substrates. Polarized neutron reflectometry reveals a two-layer behavior with a depressed magnetic layer of around 30 Å at the interface. Magnetic force microscopy (MFM) shows a granular magnetic structure of the La0.7Ca0.3MnO3. The magnetic granularity of the La0.7Ca0.3MnO3 film and the robust magnetoelastic coupling at the La0.7Ca0.3MnO3/BaTiO3 interface are at the origin of the large magnetoelectric coupling, which is enhanced by phase separation in the manganite. PMID:26648002

  14. Biotic and geochemical (δ18O, δ13C, Mg/Ca, Ba/Ca) responses of Globigerinoides ruber morphotypes to upper water column variations during the last deglaciation, Gulf of Mexico

    NASA Astrophysics Data System (ADS)

    Antonarakou, A.; Kontakiotis, G.; Mortyn, P. G.; Drinia, H.; Sprovieri, M.; Besiou, E.; Tripsanas, E.

    2015-12-01

    Within the Gulf of Mexico (GOM), the Bryant Canyon is exceptional in that rapid sedimentation sustained by high rates of terrigenous sediment delivery and surface marine productivity make this basin an excellent recorder of paleoenvironmental and paleoclimatic conditions. We present a new 21-kyr record of sea surface temperature (SST) and local salinity changes from the NW GOM (core JPC-26) approximated from combined Globigerinoides ruber morphotype-specific δ18O and Mg/Ca, as well as Ba/Ca, which reflect the subtropical GOM hydrographic dynamics and their relationship to both Mississippi River discharges and climate evolution during the last deglaciation. Overall, the reconstructed SST and SSS-related patterns reveal notable variations in amplitude between the analyzed morphotypes, adding valuable insights to previously published G. ruber (w, mixed) GOM records. Especially during the deglaciation, Bryant Canyon meltwater flooding events (BCDFs) and associated sea surface freshening seem to be more pronounced than the SST reduction. Our Mg/Ca-derived SST records of both morphotypes (G. ruber sensu stricto (s.s.) and G. ruber sensu lato (s.l.)) show comparable general trends, but with important SST differences (ΔT). We interpret down-core ΔT as a record of changing upper water column hydrography, with particular influence from the deglacial meltwater (BCDFs) or Holocene (BCHFs) flooding events. During the warm intervals, the deeper, thicker and probably more seasonally persistent mixed layer led to more uniform thermal conditions for both G. ruber morphotypes and therefore to a minimum ΔT. On the contrary, during the cold and low salinity periods, the shallower mixed layer favored more habitat divergence, and caused a maximum thermal gradient in the well-stratified upper water column. Overall, this supports the notion that G. ruber s.s. is consistently calcifying in warmer waters than G. ruber s.l., either due to a shallower depth habitat or to a more summer

  15. Evaluating controlling factors to Al(i)/(Ca + Mg) molar ratio in acidic soil water, southern and southwestern China: multivariate approach.

    PubMed

    Guo, Jing-Heng; Zhang, Xiao-Shan; Vogt, Rolf D; Xiao, Jin-Song; Zhao, Da-Wei; Xiang, Ren-Jun; Luo, Jia-Hai

    2007-06-01

    Al(i)/(Ca + Mg) molar ratio in soil water has been used as an indicator to the effects of acid deposition on terrestrial ecosystems. However, the main factors controlling this ratio have not been well documented in southern and southwestern China. In this study, we presented the variation in inorganic aluminum (Al(i)) and Al(i)/(Ca + Mg) molar ratio in different sites and soil horizons based on two to three years monitoring data, and evaluated the main factors controlling Al(i)/(Ca + Mg) molar ratio using principle component analysis (PCA) and partial least square (PLS) regression. Monitoring data showed although Al(i)/(Ca + Mg) molar ratios in most soil water were lower than assumed critical 1.0, higher molar ratios were found in some soil water at TSP and LXH site. Besides acid loading, both soil properties and soil water chemistry affected the value of Al(i)/(Ca + Mg) molar ratio in soil water. Partial least square (PLS) indicated that they had different relative importance in different soil horizons. In A-horizon, soil aluminum saturation (AlS) had higher influence on Al(i)/(Ca + Mg) molar ratio than soil water chemistry did; higher soil aluminum saturation (AlS) led to higher Al(i)/(Ca + Mg) molar ratio in soil water. In the deeper horizons (i.e., B(1)-, B(2)- and BC-horizon), inorganic aluminum (Al(i)) in soil water had more and more important role in regulating Al(i)/(Ca + Mg) molar ratio. On regional scale, soil aluminum saturation (AlS) as well as cation exchange capacity (CEC) was the dominant factor controlling Al(i)/(Ca + Mg) molar ratio. This should be paid enough attention on when making regional acid rain control policy in China.

  16. Evaluating controlling factors to Al(i)/(Ca + Mg) molar ratio in acidic soil water, southern and southwestern China: multivariate approach.

    PubMed

    Guo, Jing-Heng; Zhang, Xiao-Shan; Vogt, Rolf D; Xiao, Jin-Song; Zhao, Da-Wei; Xiang, Ren-Jun; Luo, Jia-Hai

    2007-06-01

    Al(i)/(Ca + Mg) molar ratio in soil water has been used as an indicator to the effects of acid deposition on terrestrial ecosystems. However, the main factors controlling this ratio have not been well documented in southern and southwestern China. In this study, we presented the variation in inorganic aluminum (Al(i)) and Al(i)/(Ca + Mg) molar ratio in different sites and soil horizons based on two to three years monitoring data, and evaluated the main factors controlling Al(i)/(Ca + Mg) molar ratio using principle component analysis (PCA) and partial least square (PLS) regression. Monitoring data showed although Al(i)/(Ca + Mg) molar ratios in most soil water were lower than assumed critical 1.0, higher molar ratios were found in some soil water at TSP and LXH site. Besides acid loading, both soil properties and soil water chemistry affected the value of Al(i)/(Ca + Mg) molar ratio in soil water. Partial least square (PLS) indicated that they had different relative importance in different soil horizons. In A-horizon, soil aluminum saturation (AlS) had higher influence on Al(i)/(Ca + Mg) molar ratio than soil water chemistry did; higher soil aluminum saturation (AlS) led to higher Al(i)/(Ca + Mg) molar ratio in soil water. In the deeper horizons (i.e., B(1)-, B(2)- and BC-horizon), inorganic aluminum (Al(i)) in soil water had more and more important role in regulating Al(i)/(Ca + Mg) molar ratio. On regional scale, soil aluminum saturation (AlS) as well as cation exchange capacity (CEC) was the dominant factor controlling Al(i)/(Ca + Mg) molar ratio. This should be paid enough attention on when making regional acid rain control policy in China. PMID:17057971

  17. High Permittivity (1 - x)Ba(Zr(0.2)Ti(0.8))O3 - x(Ba(0.7)Ca(0.3))TiO3 (x = 0.45) Epitaxial Thin Films with Nanoscale Phase Fluctuations.

    PubMed

    Scarisoreanu, Nicu D; Craciun, Floriana; Moldovan, Antoniu; Ion, Valentin; Birjega, Ruxandra; Ghica, Corneliu; Negrea, Raluca F; Dinescu, Maria

    2015-11-01

    Epitaxial (1 - x)Ba(Ti0.8Zr0.2)TiO3 - x(Ba0.7Ca0.3)TiO3, x = 0.45 (BCZT 45), thin films have been deposited on (001) SrTiO3 (STO) and (001/100) SrLaAlO4 (SLAO) substrates by pulsed laser deposition. X-ray diffraction and high-resolution transmission electron microscopy (HRTEM) confirmed the epitaxial growth of the films. A high structural quality has been evidenced for the BCZT/STO films. Geometric phase analysis (GPA) associated with the HRTEM enabled us to obtain microstrain analysis and the in-plane and out-of-plane lattice parameter variation on different areas. Tetragonality ratio fluctuations at nanoscale level which are relevant for the existence of nanodomains have been evidenced on the BCZT/STO films. The in-plane dielectric constant has been measured on interdigital electrodes deposited by lift-off technique on the top of the films. High values of dielectric permittivity (>3000) combined with low dielectric loss (<0.01) are obtained for BCZT 45 film deposited on STO substrate, showing nearly constant values between 1 kHz and 10 MHz. The high dielectric permittivity of BCZT thin films was attributed to their high structural quality and to the loss of rotation stability of the polarization associated with the presence of nanodomains. This results into a divergence of fluctuations of polarization direction and a peak of dielectric susceptibility. The enhanced switching of such nanodomain configuration was probed by piezoforce microscopy, by writing and reading domains during topography scanning. PMID:26488203

  18. Characteristics of Y-Ba-Cu-O superconductor films on GaAs with an Al sub 2 O sub 3 or AlGaO sub 3 buffer layer

    SciTech Connect

    Shewchun, J.; Chen, Y.; Hoelder, J.S.; Uher, C. )

    1991-06-10

    By depositing a buffer layer of Al{sub 2}O{sub 3} on GaAs, we have been able to laser ablate a superconducting film of Y{sub 1}Ba{sub 2}Cu{sub 3}O{sub 7{minus}{ital x}} overtop. The onset of superconductivity is 92 K and zero resistance is observed at 80 K in a structure with a suitably annealed Al{sub 2}O{sub 3} film which is converted to AlGaO{sub 3}. Both the Al{sub 2}O{sub 3}-GaAs and the Al{sub 2}O{sub 3}-Y{sub 1}Ba{sub 2}Cu{sub 3}O{sub 7{minus}{ital x}} interfaces are remarkably well preserved with virtually no interdiffusion or interaction. The Al{sub 2}O{sub 3} or homolog AlGaO{sub 3} film also prevents decomposition of the GaAs at the deposition temperature of 730 {degree}C.

  19. Electronic structure and properties of isoelectronically substituted compounds Y{sub 1}Ba{sub 2-m}M{sub m}Cu{sub 3}O{sub 7} and Y{sub 1}Ba{sub 2-m}M{sub m}Cu{sub 4}O{sub 8} (M = Be, Mg, Ca, Sr, Ba, Ra)

    SciTech Connect

    Ermakov, A.I.; Zharikova, E.A.; Markushin, N.A.

    1994-09-01

    According to cluster calculations, the electronic structures of compounds based on Y{sub 1}Ba{sub 2}Cu{sub 3}O{sub 7} and Y{sub 1}Ba{sub 2}Cu{sub 4}O{sub 8} with isoelectronically substituted barium have some qualitative distinctions. These compounds behave differently upon barium substitution by other elements due to differences in the character of their highest occupied and lowest unoccupied molecular orbitals. Substitution of barium by radium is expected to lead to an increase in oxygen stability without a significant decrease in the critical temperature of superconduction transition T{sub s}. In order to raise T{sub s}, it is of interest to study the systems YBa{sub 2-m}(Be or Mg){sub m}Cu{sub 3}O{sub x} and YBa{sub 2-m}(Ca, Sr){sub m}Cu{sub 3}O{sub x}. On partial substitution of barium by calcium in YBa{sub 2}Cu{sub 4}O{sub 8}, the mechanism of T{sub s} elevation may involve contraction of the forbidden band due to oxygen sublattice distortions in the vicinity of Ba centers.

  20. Structural and large magnetocaloric properties of La0.67-xYxBa0.23Ca0.1MnO3 perovskites (0≤x≤0.15)

    NASA Astrophysics Data System (ADS)

    Abassi, Mounira; Dhahri, N.; Dhahri, J.; HLIL, E. K.

    2014-09-01

    La0.67Ba0.23Ca0.1MnO3 doped with different amounts of yttrium (Y) result in the series La0.67-xYxBa0.23Ca0.1MnO3 (LYBCMO) (x=0.00, 0.05, 0.10 and 0.15) which was synthesized by conventional solid state ceramics route. All samples show a rhombohedral structure (space group R3 barc) at room temperature. A transition from a paramagnetic to a ferromagnetic phase is observed at Curie temperature, TC. It has been found that the substitution of Y on the La site causes a reduction in TC. Analyses of crystallographic data suggested a strong correlation between structural properties and magnetism. As an example, a relationship between the distortion of MnO6 octahedron and the reduction in Curie temperature. The magnetic entropy change (-ΔS)m was estimated from isothermal magnetization curves. It decreases from 4.91 J/kg K at 350 k (x=0.00) to 4.14 J/kg K at 289 K (x=0.15) with the increase of Y content under μ0H=5 T. The relative cooling power (RCP) is found to be 365 J/kg for La0.67Ba0.23Ca0.1MnO3 and 288 J/kg for La0.52Y0.15Ba0.23Ca0.1MnO3 in the magnetic field change of 5 T. From these results, La0.67-xYxBa0.23Ca0.1MnO3 materials are strongly suggested for use as active refrigerants in magnetic refrigeration technology at near room temperature.

  1. Uniaxial-strain mechanical detwinning of CaFe[subscript 2]As[subscript 2] and BaFe[subscript 2]As[subscript 2] crystals: Optical and transport study

    SciTech Connect

    Tanatar, M.A.; Blomberg, E.C.; Kreyssig, A.; Kim, M.G.; Ni, N.; Thaler, A.; Bud’ko, S.L.; Canfield, P.C.; Goldman, A.I.; Mazin, I.I.; Prozorov, R.

    2010-10-22

    The parent compounds of iron-arsenide superconductors, AFe{sub 2}As{sub 2} (A=Ca, Sr, Ba), undergo a tetragonal to orthorhombic structural transition at a temperature T{sub TO} in the range 135-205 K depending on the alkaline-earth element. Below T{sub TO} the free standing crystals split into equally populated structural domains, which mask intrinsic, in-plane, anisotropic properties of the materials. Here we demonstrate a way of mechanically detwinning CaFe{sub 2}As{sub 2} and BaFe{sub 2}As{sub 2}. The detwinning is nearly complete, as demonstrated by polarized light imaging and synchrotron x-ray measurements, and reversible, with twin pattern restored after strain release. Electrical resistivity measurements in the twinned and detwinned states show that resistivity, {rho}, decreases along the orthorhombic a{sub o} axis but increases along the orthorhombic b{sub o} axis in both compounds. Immediately below T{sub TO} the ratio {rho}{sub bo}/{rho}{sub ao} = 1.2 and 1.5 for Ca and Ba compounds, respectively. Contrary to CaFe{sub 2}As{sub 2}, BaFe{sub 2}As{sub 2} reveals an anisotropy in the nominally tetragonal phase, suggesting that either fluctuations play a larger role above T{sub TO} in BaFe{sub 2}As{sub 2} than in CaFe{sub 2}As{sub 2} or that there is a higher temperature crossover or phase transition.

  2. Tululite, Ca14(Fe3+,Al)(Al,Zn,Fe3+,Si,P,Mn,Mg)15O36: a new Ca zincate-aluminate from combustion metamorphic marbles, central Jordan

    NASA Astrophysics Data System (ADS)

    Khoury, Hani N.; Sokol, Ella V.; Kokh, Svetlana N.; Seryotkin, Yurii V.; Nigmatulina, Elena N.; Goryainov, Sergei V.; Belogub, Elena V.; Clark, Ian D.

    2016-02-01

    Tululite (Ca14(Fe3+,Al)(Al,Zn,Fe3+,Si,P,Mn,Mg)15O36 (the hypothetical end-member formula Ca14{Fe3+O6}[SiO4][Zn5Al9]O26) (IMA2014-065) is a new natural Ca zincate-aluminate, identified in medium-temperature (800-850 °C) combustion metamorphic (CM) spurrite-fluorellestadite marbles from central Jordan. The type locality (Tulul Al Hammam area) is situated in the northern part of the Siwaqa complex, the largest area of the "Mottled Zone" Formation in the Dead Sea region. The marbles originated from bitumen-rich chalky marine sediments of the Maastrichtian-Paleogene Muwaqqar Chalk Marl Formation, which have low clay content (and, consequently, low Al) and high Zn, Cd, and U enrichments. The bulk CM rocks derived from the low-Al protolith have unusually high (Zn + Cd)/Al ratios ( 0.2) and, as a result, a mineralogy with negligibly small percentages of Ca aluminates having low Ca:Al molar ratios (minerals of mayenite supergroup, Ca:Al = 6:7) common to most of calcareous CM rocks in the Mottled Zone. Instead, the mineral assemblage of the Zn-rich marbles contains tululite, with high Ca:Al = 2.55 molar ratios and Zn substituting for a large portion of Al (Zn:Al = 1.1). Tululite occurs in thin clusters as irregular grains with indented outlines (20-100 μm in size), having typical open-work textures associated with rock-forming calcite, fluorellestadite, spurrite, and accessory Zn-rich periclase, lime-monteponite solid solutions, calcium uranates, and zincite. Marbles also bear brownmillerite, dorrite, fluormayenite, high-fluorine Ca aluminate, and lakargiite. Secondary phases are brucite, gel-like calcium silicate hydrates and calcium silicate aluminate hydrates, including Zn- and U-bearing and Cd-rich compounds, Si-bearing hydrated compounds after calcium uranates, and basic Cd chlorides. The empirical formula of the holotype tululite (a mean of 32 analyses) is (Ca13.29Cd0.75)Σ14.04(Al5.46Zn5.20Fe3+ 2.23Si0.95Mn3+ 1.01Mg0.78P0.41)Σ16.04O36. Tululite is cubic, space

  3. Thermoluminescence and synchrotron radiation studies on the persistent luminescence of BaAl{sub 2}O{sub 4}:Eu{sup 2+},Dy{sup 3+}

    SciTech Connect

    Rodrigues, L.C.V.; Stefani, R.; Brito, H.F.; Felinto, M.C.F.C.; Hoelsae, J.; Lastusaari, M.; Laamanen, T.; Malkamaeki, M.

    2010-10-15

    The persistent luminescence materials, barium aluminates doped with Eu{sup 2+} and Dy{sup 3+} (BaAl{sub 2}O{sub 4}:Eu{sup 2+},Dy{sup 3+}), were prepared with the combustion synthesis at temperatures between 400 and 600 {sup o}C as well as with the solid state reaction at 1500 {sup o}C. The concentrations of Eu{sup 2+}/Dy{sup 3+} (in mol% of the Ba amount) ranged from 0.1/0.1 to 1.0/3.0. The electronic and defect energy level structures were studied with thermoluminescence (TL) and synchrotron radiation (SR) spectroscopies: UV-VUV excitation and emission, as well as with X-ray absorption near-edge structure (XANES) methods. Theoretical calculations using the density functional theory (DFT) were carried out in order to compare with the experimental data. - Graphical abstract: BaAl{sub 2}O{sub 4}:Eu{sup 2+},Dy{sup 3+} phosphors: Thermoluminescence glow curve and synchrotron radiation spectra. Persistent luminescence photographs obtained after ceased UV irradiation.

  4. Progress in the material development of LiCaAlF sub 6 :Cr sup 3+ laser crystals

    SciTech Connect

    Michelle D. Shinn.; Chase, L.L.; Caird, J.A.; Payne, S.A.; Atherton, L.J.; Kway, W.L.

    1990-03-01

    High Cr{sup 3+} doping levels, up to 8 mole percent, and low losses have been obtained with the tunable solid-state laser material LiCaAlF{sub 6}:Cr{sup 3+} (Cr:LiCAF). Measurements and calculations show that high pumping and extraction efficiencies are possible with the improved material. 13 refs., 4 figs., 1 tab.

  5. Photoelectron velocity-map imaging and theoretical studies of heteronuclear metal carbonyls MNi(CO)3- (M = Mg, Ca, Al)

    NASA Astrophysics Data System (ADS)

    Xie, Hua; Zou, Jinghan; Yuan, Qinqin; Fan, Hongjun; Tang, Zichao; Jiang, Ling

    2016-03-01

    The heteronuclear metal carbonyl anions MNi(CO)3- (M = Mg, Ca, Al) have been investigated using photoelectron velocity-map imaging spectroscopy. Electron affinities of neutral MNi(CO)3 (M = Mg, Ca, Al) are measured from the photoelectron spectra to be 1.064 ± 0.063, 1.050 ± 0.064, and 1.541 ± 0.040 eV, respectively. The C-O stretching mode in these three clusters is observed and the vibrational frequency is determined to be 2049, 2000, and 2041 cm-1 for MgNi(CO)3, CaNi(CO)3, and AlNi(CO)3, respectively. Density functional theory calculations are carried out to elucidate the geometric and electronic structures and to aid the experimental assignments. It has been found that three terminal carbonyls are preferentially bonded to the nickel atom in these heterobinuclear nickel carbonyls MNi(CO)3-1/0, resulting in the formation of the Ni(CO)3 motif. Ni remains the 18-electron configuration for MgNi(CO)3 and CaNi(CO)3 neutrals, but not for AlNi(CO)3. This is different from the homobinuclear nickel carbonyl Ni-Ni(CO)3 with the involvement of three bridging ligands. Present findings would be helpful for understanding CO adsorption on alloy surfaces.

  6. High-resolution X-ray absorption near edge structure studies of monophasic Tl 2Ba 2Ca 2Cu 3O 10-δ (Tl-2223) superconductor

    NASA Astrophysics Data System (ADS)

    Chen, J. M.; Chung, S. C.; Liu, R. S.

    1996-08-01

    High-resolution O K-edge and Cu L 23-edge X-ray-absorption near-edge-structure (XANES) spectra of a monophasic high-T c Tl 2Ba 2Ca 2Cu 3O 10-δ (Tl-2223) superconductor in powder form were measured using the total-electron yield (TEY) and total-X-ray-fluorescence yield (TFY) techniques. Near the O 1s edge, three distinct pre-edge peaks with maxima at 528.3, 529.6, and 530.8 eV are revealed in the TFY spectrum. On the contrary, these pre-edge peaks have almost diminished in the TEY spectrum. The observed differences between the TFY and TEY spectra can be explained by the presence of an oxygen depletion layer. We ascribe these pre-edge peaks to the core-level excitations of O 1s electrons to O 2p holes located in the CuO 2 planes, in the BaO planes, and in the TlO planes, respectively. This assignment is supported by the local-density approximation (LDA) band-structure calculations. Moreover, based on the Cu L 23-edge TFY spectrum, the high-energy structures at ˜ 932.8 and 953.0 eV are attributed to the transitions from the Cu(2p {3}/{2}, {1}/{2})3d 9L ground states to the Cu(2p {3}/{2}, {1}/{2}) -13d 10L excited states, where L denotes the O 2p ligand hole.

  7. Positron annihilation studies of the Al-Ca-Zn superplastic alloy: thermal and thermomechanical contribution

    SciTech Connect

    Ayciriex, M.D. ); Romero, R.; Somoza, A. ); Silvetti, S.P.; Villagra, O. )

    1993-06-15

    Positron annihilation spectroscopy (PAS) is an established method for the study of electronic structure and defect properties in metals and alloys. The application of this technique to the study of positron trapping in grain boundaries and related phenomena, however, is relatively scarce. The physical basis for the application of PAS to the study of grain boundaries is the fact that grain boundaries are regions of low atomic density which result in attractive sites to the trap positions. The superplastic alloys are particularly suitable materials to be studied with PAS; they have a fine-grained structure, and therefore a high density of grain boundaries. Moreover, in the annealed condition, they have a low density of other types of defects capable of trapping positrons, such as dislocations. This type of polycrystalline material can undergo extremely high deformations (up to hundreds and thousands percent) in a certain temperature-strain rate range without macroscopic failure. This paper is part of a whole study of the thermal and thermomechanical effects on the positron lifetime parameters and their relation with microstructural changes and the phenomenon of structural superplasticity in a Al-Ca-Zn alloy.

  8. Experimentally Produced Spinel Rims on Ca-Al-Rich Inclusion Bulk Compositions

    NASA Technical Reports Server (NTRS)

    Paque, Julie M.; Le, L.; Lofgren, G. E.

    1998-01-01

    Most Ca-Al-rich inclusions (CAls) from Allende are surrounded by a series of mineralogically distinct rim layers. Proposed modes of formation for these layers include flash heating, evaporation, and condensation. The innermost of these rim layers is generally spinel (SP), in some cases intergrown with perovskite (PV), and commonly containing varying amounts of secondary iron increasing towards the edge of the CAI. The SP or SP+PV rim is not always contiguous with the other rim layers, indicating that it is probably the result of a separate event. We have produced continuous SP rims on synthetic analogs representing Type A/B1, average Type B, and Type B2 bulk compositions by reheating a solid glass experimental charge to subliquidus crystallization temperatures. This experimental result is consistent with the formation of chondrules; and CAIs by more than one sequence of heating and cooling. Previous work indicated that prior crystallization events produced observable effects in the texture and chemistry of the final run product. Information on the nature of the heating/cooling cycles experienced by CAls and chondrules is important in modeling the environment of their formation. Additional information is contained in the original extended abstract.

  9. Characterization of ZrO2 buffer layers for sequentially evaporated Y-Ba-CuO on Si and Al2O3 substrates

    NASA Technical Reports Server (NTRS)

    Valco, George J.; Rohrer, Norman J.; Pouch, John J.; Warner, Joseph D.; Bhasin, Kul B.

    1988-01-01

    Thin film high temperature superconductors have the potential to change the microwave technology for space communications systems. For such applications it is desirable that the films be formed on substrates such as Al2O3 which have good microwave properties. The use of ZrO2 buffer layers between Y-Ba-Cu-O and the substrate has been investigated. These superconducting films have been formed by multilayer sequential electron beam evaporation of Cu, BaF2 and Y with subsequent annealing. The three layer sequence of Y/BaF2/Cu is repeated four times for a total of twelve layers. Such a multilayer film, approximately 1 micron thick, deposited directly on SrTiO3 and annealed at 900 C for 45 min produces a film with a superconducting onset of 93 K and critical temperature of 85 K. Auger electron spectroscopy in conjunction with argon ion sputtering was used to obtain the distribution of each element as a function of depth for an unannealed film, the annealed film on SrTiO3 and annealed films on ZrO2 buffer layers. The individual layers were apparent. After annealing, the bulk of the film on SrTiO3 is observed to be fairly uniform while films on the substrates with buffer layers are less uniform. The Y-Ba-Cu-O/ZrO2 interface is broad with a long Ba tail into the ZrO2, suggesting interaction between the film and the buffer layer. The underlying ZrO2/Si interface is sharper. The detailed Auger results are presented and compared with samples annealed at different temperatures and durations.

  10. Discharge properties of Mg-Al-Mn-Ca and Mg-Al-Mn alloys as anode materials for primary magnesium-air batteries

    NASA Astrophysics Data System (ADS)

    Yuasa, Motohiro; Huang, Xinsheng; Suzuki, Kazutaka; Mabuchi, Mamoru; Chino, Yasumasa

    2015-11-01

    The discharge behaviors of rolled Mg-6 mass%Al-0.3 mass%Mn-2 mass%Ca (AMX602) and Mg-6 mass%Al-0.3 mass%Mn (AM60) alloys used as anodes for Magnesium-air batteries were investigated. The AMX602 alloy exhibited superior discharge properties compared to the AM60 alloy, especially at low current density. The discharge products of the AMX602 alloy were dense and thin, and many cracks were observed at all current densities. In addition, the discharge products were detached at some sites. These sites often corresponded to the positions of Al2Ca particles. The comparison of the discharge and corrosion tests indicated that the dense and thin discharge products of AMX602 were easily cracked by dissolution of the Mg matrix around Al2Ca particles, and the cracks promoted the penetration of the electrolyte into the discharge products, retaining the discharge activity. In contrast, concerning the AM60 alloy, thick discharge products were formed on the surface during discharge, and cracking of the discharge products hardly occurred, degrading the discharge properties. Localized and deeply corroded pits that could result from the detachment of metal pieces from the anode during discharge were partly observed in the AM60 alloy. It is suggested that these detached metal pieces are another reason for the low discharge properties of the AM60 alloy.

  11. Evolution of the magnetic properties during the thermal treatment of nanosize BaMFe 11O 19 (M=Fe, Co, Ni and Al) obtained through aerosol route

    NASA Astrophysics Data System (ADS)

    Singhal, Sonal; Garg, A. N.; Chandra, Kailash

    2005-01-01

    Nanosize pure and metal substituted barium hexaferrites BaMFe11O19 (M=Fe, Co, Ni and Al) were prepared through aerosol route. The particle size of as-obtained samples were found to be ∼15 nm through TEM, which increases up to 100-130 nm after annealing at 1000 °C. The saturation magnetization for all the samples after annealing at 1000 °C lies in the range 45.7-59.8 emu/g. In case of Co substituted barium hexaferrite, the saturation magnetization is maximum and coercivity is minimum. Room temperature Mössbauer spectra of BaFe12O19 exhibited a doublet suggesting super paramagnetic nature, however, after annealing at 1000 °C this doublet gets converted into four magnetic sextets, which are typical of bulk barium hexaferrite.

  12. Core-shell-shell heterostructures of α-NaLuF4:Yb/Er@NaLuF4:Yb@MF2 (M = Ca, Sr, Ba) with remarkably enhanced upconversion luminescence.

    PubMed

    Su, Yue; Liu, Xiuling; Lei, Pengpeng; Xu, Xia; Dong, Lile; Guo, Xianmin; Yan, Xingxu; Wang, Peng; Song, Shuyan; Feng, Jing; Zhang, Hongjie

    2016-07-01

    Core-shell-shell heterostructures of α-NaLuF4:Yb/Er@NaLuF4:Yb@MF2 (M = Ca, Sr, Ba) have been successfully fabricated via the thermal decomposition method. Upconversion nanoparticles (UCNPs) were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), upconversion luminescence (UCL) spectroscopy, etc. Under 980 nm excitation, the emission intensities of the UCNPs are remarkably enhanced after coating the MF2 (M = Ca, Sr, and Ba) shell. Among these samples, CaF2 coated UCNPs show the strongest overall emission, while BaF2 coated UCNPs exhibit the longest lifetime. These results demonstrate that alkaline earth metal fluorides are ideal materials to improve the UCL properties. Meanwhile, although the lattice mismatch between the ternary NaREF4 core and the binary MF2 (M = Sr and Ba) shell is relatively large, the successfully synthesized NaLuF4:Yb/Er@NaLuF4:Yb@MF2 indicates a new outlook on the fabrication of heterostructural core-shell UCNPs. PMID:27327414

  13. Sintering aids for producing BaO-Al2O3-2SiO2 and SrO-Al2O3-2SiO2 ceramic materials

    SciTech Connect

    Talmy, I.G.; Zaykoski, J.A.

    1995-07-26

    Accordingly, an object of this invention is to provide a new lower temperature process for preparing dense monoclinic BaO.Al2O3.2SiO2 (BAS; celsian) monoclinic SrO.Al2O3.2SiO2 (SAS), or monoclinic BAS/SAS solid solution ceramic materials. Another object of this invention is to provide new sintering aids suitable for producing high strength, low dielectric ceramic materials from BAS, SAS, or mixtures thereof. These and other objects of this invention are accomplished by providing a sintering aid that is a homogenous glass containing (1) from 14 10 45 mole percent of an alkaline earth oxide that is BaO. SrO. or mixtures of BaO and SrO (2) from 8 to 16 weight percent of Al2O3 and (3) The remainder of the glass being SiO2. The homogeneous glass when mixed as a powder with monoclinic BAS powder, monoclinic SAS powder. or mixture of monoclinic BAS and SAS powders reduces the firing temperature required to produce a fully densified ceramic material.

  14. Microstructure and Fatigue Behavior of Friction Stir-welded Noncombustive Mg-9Al-Zn-Ca Magnesium Alloy

    NASA Astrophysics Data System (ADS)

    Zhou, L.; Li, Z. Y.; Nakata, K.; Feng, J. C.; Huang, Y. X.; Liao, J. S.

    2016-06-01

    Microstructure and fatigue behavior of friction stir-welded noncombustive Mg-9Al-Zn-Ca magnesium alloy were investigated. The as-received hot-extruded material consisted of equiaxed α-Mg grains with β-Mg17Al12 and Al2Ca compounds distributed along the grain boundaries. Friction stir welding produced much refined α-Mg grains accompanied by the dissolution of the eutectic β-Mg17Al12 phase, while Al2Ca phase was dispersed homogenously into the Mg matrix. Friction stir welding produced slightly increased hardness and tensile strength in the defect-free welds compared with the base material due to microstructural refinement and uniform distribution of intermetallic compounds. The load-controlled uniaxial tensile high-cycle fatigue tests indicated that fatigue strength of 90 MPa was obtained for the friction stir-welded joint with fatigue crack initiated basically near the specimen's surface and at the retreating side of the joint. Crack propagation was characterized by cleavage and fatigue striations.

  15. Constraints on Titanite Acitvity in the System CaTiSiO4O-CaAlSiO4F: Implications for Thermobarometry in Metamorphic Rocks

    NASA Astrophysics Data System (ADS)

    Tropper, P.; Manning, C. E.; Essene, E. J.

    2006-12-01

    Titanite is a common accessory mineral that could be used reliably in phase equilibrium calculations, if activity-composition relations in Al-F titanites were known. Troitzsch and Ellis (2001, CMP, 142, 543) and Tropper et al. (2002, JPet., 43, 1787) gave non-ideal mixing models along the join CaTiSiO4O- CaAlSiO4F. Tropper et al. (2002) derived a negative interaction parameter W, whereas Troitzsch and Ellis (2001) derived a regular model with both positive and negative W, but favored positive values. These differences strongly influence calculated CaTiSiO4O activity (attn). Although more experiments are needed, our result that γttn<1 at high T indicates a large degree of non-ideal behavior, even at >900°C, which in turn will affect thermobarometry. Comparing available activity models shows that at these T, attn is substantially underestimated by the fully ionic model used by Manning and Bohlen (1991, CMP, 109, 1), in which attn = XCaXTiXSi(XO)5. This model assumes independent mixing of Al for Ti and random mixing of F and O on all O sites. However, F substitutes only in one O site (O1; Oberti et al., 1991, EJM, 3, 777). A fully ionic model should therefore be recast as attn = XCaXTiXSiXO, where XO indicates the mole fraction of O on the (O1) site. The substitution of F on the O1 site is coupled with Al, so it is called the ideal coupled model. Unlike the regular model, the prefered ionic model departs strongly from ideality at ≤600°C, consistent with independent constraints. However, experimentally determined attn is approximated by an ideal molecular model (XTi) at ≥900°C, so this model is recommended for thermobarometry in high- T metamorphic rocks until more data are available. Recalculation of the P recorded by the three eclogites from Manning and Bohlen (1991) using the different activity models discussed here yields differences that may be as high as 2.0 GPa.

  16. Structural and dielectric properties of A(Fe{sub 1/2}Ta{sub 1/2})O{sub 3} [A = Ba, Sr, Ca

    SciTech Connect

    Dutta, Alo

    2011-04-15

    Graphical abstract: FTIR spectra of BFT, SFT and CFT at room temperature. Research highlights: {yields} The structural and dielectric properties of BaFe{sub 1/2}Ta{sub 1/2}O{sub 3}, SrFe{sub 1/2}Ta{sub 1/2}O{sub 3} and CaFe{sub 1/2}Ta{sub 1/2}O{sub 3}. {yields} Fourier transform infrared spectra show two primary phonon modes of the samples at around 450 cm{sup -1} and 620 cm{sup -1}. {yields} The compounds show significant frequency dispersion in its dielectric properties. {yields} The relaxation mechanism of the samples is modelled by Cole-Cole equation. -- Abstract: The complex perovskite oxide barium iron tantalate (BFT), BaFe{sub 1/2}Ta{sub 1/2}O{sub 3}, strontium iron tantalate (SFT), SrFe{sub 1/2}Ta{sub 1/2}O{sub 3} and calcium iron tantalate (CFT), CaFe{sub 1/2}Ta{sub 1/2}O{sub 3} are synthesized by a solid-state reaction technique. Rietveld refinement of the X-ray diffraction data of the samples shows that BFT and SFT crystallize in cubic structure, with lattice parameter a = 4.06 A for BFT and 3.959 A for SFT, whereas CFT crystallizes in orthorhombic structure having lattice parameters a = 5.443 A, b = 5.542 A and c = 7.757 A. Fourier transform infrared spectra show two primary phonon modes of the samples at around 450 cm{sup -1} and 620 cm{sup -1}. The compounds show significant frequency dispersion in its dielectric properties. The complex impedance plane plots of the samples show that the relaxation (conduction) mechanism in these materials is purely a bulk effect arising from the semiconductive grains. The relaxation mechanism of the samples is modelled by Cole-Cole equation. The frequency dependent conductivity spectra are found to follow the power law.

  17. Nanocrystalline Ba{sub 0.97}Ca{sub 0.03}SO{sub 4}:Eu for ion beams dosimetry

    SciTech Connect

    Lochab, S. P.; Kanjilal, D.; Salah, Numan; Habib, Sami S.; Lochab, Jyoti; Ranjan, Ranju; Aleynikov, V. E.; Rupasov, A. A.; Pandey, A.

    2008-08-01

    Nanoparticles of Ba{sub 0.97}Ca{sub 0.03}SO{sub 4}:Eu have been irradiated by 48 MeV Li{sup 3+}, 75 MeV C{sup 6+}, and 90 MeV O{sup 7+} ion beams with a fluence range of 1x10{sup 9}-1x10{sup 13} ion/cm{sup 2}. The thermoluminescence (TL) glow curves along with the response curves of this nanophosphor have been investigated and compared with those of the corresponding microcrystalline samples. TL glow curve of the nanophosphor exposed to {gamma}-rays has also been included in the letter with the aim of reporting some of the comparative measurements. The glow curves of the ion-beam irradiated nanomaterials are similar in their shapes to those induced by gamma rays, with a shift in the peak positions to the higher temperature side by around 30 K. The TL intensity of the ion-beam irradiated nanomaterials is found to decrease, while going from low to high atomic number (Z) ions (i.e., Li{sup 3+}{yields}O{sup 7+}). Similar trend was also observed in the linearity of the TL response curves. The response curve of Li ion irradiated nanomaterials is sublinear in the whole range of studied fluences. C ion has also a more or less similar response, while the O ion has a sublinear response over a shorter range of 1x10{sup 9}-1x10{sup 12} ion/cm{sup 2}, and above this range the response saturates. These results for the nanomaterials are much better than that of the corresponding microcrystalline sample irradiated by Li{sup 3+} ions. The curve was sublinear up to the fluence 1x10{sup 10} ion/cm{sup 2} and then saturates at higher fluences. The wider sublinear TL response of the nanocrystalline Ba{sub 0.97}Ca{sub 0.03}SO{sub 4}:Eu makes it superior to its corresponding microform and thus makes it a suitable candidate as a dosimeter to be used for detecting the doses of ions, especially the Li and C ions for their application in cancer radiotherapy and radiation biology.

  18. Antiferromagnetism in CaAl2Si2-type CaMn2As2 and SrMn2As2 single crystals

    NASA Astrophysics Data System (ADS)

    Sangeetha, N. S.; Pandey, Abhishek; Benson, Zackery A.; Johnston, D. C.

    Magnetic susceptibility versus temperature χ (T) measurements of CaMn2As2 and SrMn2As2 crystals show clear antiferromagnetic (AFM) transitions at TN ~ 65 K and 120 K,1 respectively. The anisotropic behaviors in χ (T <=TN) suggest that both compounds are noncollinear antiferromagnets which may result either from an intrinsic noncollinear structure or from multiple collinear AFM domains that are not aligned collinearly.2 The χ (T) data at T >TN reveal that both compounds exhibit strong short-range AFM ordering, evidently associated with quasi-two-dimensional spin lattices. The electrical resistivities show insulating ground states with activation energies of ~ 63 meV in CaMn2As2 and 44 meV in SrMn2As2 . The experimental results thus reveal that both (Ca , Sr) Mn2As2 materials are AFM insulators at low temperatures and in analogy with the high Tc cuprates, may be potential parent compounds for CaAl2Si2-type superconductors. Work was supported by the USDOE under Contract No. DE-AC02-07CH11358.

  19. Distribution of Al atoms in the clathrate-I phase Ba8AlxSi46-x at x = 6.9.

    PubMed

    Bobnar, Matej; Böhme, Bodo; Wedel, Michael; Burkhardt, Ulrich; Ormeci, Alim; Prots, Yurii; Drathen, Christina; Liang, Ying; Nguyen, Hong Duong; Baitinger, Michael; Grin, Yuri

    2015-07-28

    The clathrate-I phase Ba8AlxSi46-x has been structurally characterized at the composition x = 6.9 (space group Pm3[combining macron]n, no. 223, a = 10.4645(2) Å). A crystal structure model comprising the distribution of aluminium and silicon atoms in the clathrate framework was established: 5.7 Al atoms and 0.3 Si atoms occupy the crystallographic site 6c, while 1.2 Al atoms and 22.8 Si atoms occupy site 24k. The atomic distribution was established based on a combination of (27)Al and (29)Si NMR experiments, X-ray single-crystal diffraction and wavelength-dispersive X-ray spectroscopy.

  20. Distribution of Al atoms in the clathrate-I phase Ba8AlxSi46-x at x = 6.9.

    PubMed

    Bobnar, Matej; Böhme, Bodo; Wedel, Michael; Burkhardt, Ulrich; Ormeci, Alim; Prots, Yurii; Drathen, Christina; Liang, Ying; Nguyen, Hong Duong; Baitinger, Michael; Grin, Yuri

    2015-07-28

    The clathrate-I phase Ba8AlxSi46-x has been structurally characterized at the composition x = 6.9 (space group Pm3[combining macron]n, no. 223, a = 10.4645(2) Å). A crystal structure model comprising the distribution of aluminium and silicon atoms in the clathrate framework was established: 5.7 Al atoms and 0.3 Si atoms occupy the crystallographic site 6c, while 1.2 Al atoms and 22.8 Si atoms occupy site 24k. The atomic distribution was established based on a combination of (27)Al and (29)Si NMR experiments, X-ray single-crystal diffraction and wavelength-dispersive X-ray spectroscopy. PMID:26085288

  1. Phase equilibria and elements partitioning in zirconolite-rich region of Ca-Zr-Ti-Al-Gd-Si-O system

    SciTech Connect

    Knyazev, O.A.; Stefanovsky, S.V.; Ioudintsev, S.V.; Nikonov, B.S.; Omelianenko, B.I.; Mokhov, A.V.; Yakushev, A.I.

    1997-12-31

    Zirconolite-rich ceramics were produced by the cold crucible melting technique in an air atmosphere, at 1550 {+-} 50 C and 1 atm. Four samples with overall composition (in wt.%): 4.9-14.3 CaO; 19.0-41.3 ZrO{sub 2}; 24.1-42.6 TiO{sub 2}; 1.3-11.3 Al{sub 2}O{sub 3}; 6.8-30.0 Gd{sub 2}O{sub 3}; and 1.1-8.5 SiO{sub 2} have been studied. Total phases in the ceramics consist of major zirconolite and minor rutile, perovskite, zirconia, aluminium titanate, and glass. The Gd{sub 2}O{sub 3} content in zirconolite reaches up to 31.4 wt.% corresponding to the formula: (Ca{sub 0.4},Gd{sub 0.7})Zr{sub 1.0}(Ti{sub 1.4},Al{sub 0.5})O{sub 7.0}. The data on the phase composition agree well with coupled Gd incorporation into the mineral structure: Ca(II) + Ti(IV) = Gd(III) + Al(III), and 2Gd(III) = Ca(II) + Zr(IV). The highest Gd contents observed in the other phases are 25.4% for zirconia, 12.6% in glass, 8.8% in perovskite, and 1.4% for rutile. The rest of the elements` distribution in the samples are analyzed.

  2. Primary fragmentation pathways of gas phase [M(uracil-H)(uracil)]+ complexes (M=Zn, Cu, Ni, Co, Fe, Mn, Cd, Pd , Mg, Ca, Sr, Ba, and Pb): loss of uracil versus HNCO.

    PubMed

    Ali, Osama Y; Randell, Nicholas M; Fridgen, Travis D

    2012-04-23

    Complexes formed between metal dications, the conjugate base of uracil, and uracil are investigated by sustained off-resonance irradiation collision-induced dissociation (SORI-CID) in a Fourier transform ion cyclotron resonance (FTICR) mass spectrometer. Positive-ion electrospray spectra show that [M(Ura-H)(Ura)](+) (M=Zn, Cu, Ni, Co, Fe, Mn, Cd, Pd, Mg, Ca, Sr, Ba, or Pb) is the most abundant ion even at low concentrations of uracil. SORI-CID experiments show that the main primary decomposition pathway for all [M(Ura-H)(Ura)](+) , except where M=Ca, Sr, Ba, or Pb, is the loss of HNCO. Under the same SORI-CID conditions, when M is Ca, Sr, Ba, or Pb, [M(Ura-H)(Ura)](+) are shown to lose a molecule of uracil. Similar results were observed under infrared multiple-photon dissociation excitation conditions, except that [Ca(Ura-H)(Ura)](+) was found to lose HNCO as the primary fragmentation product. The binding energies between neutral uracil and [M(Ura-H)](+) (M=Zn, Cu, Ni, Fe, Cd, Pd ,Mg, Ca, Sr Ba, or Pb) are calculated by means of electronic-structure calculations. The differences in the uracil binding energies between complexes which lose uracil and those which lose HNCO are consistent with the experimentally observed differences in fragmentation pathways. A size dependence in the binding energies suggests that the interaction between uracil and [M(Ura-H)](+) is ion-dipole complexation and the experimental evidence presented supports this. PMID:22447672

  3. Crystal structure and X-ray photoemission spectroscopic study of A{sub 2}LaMO{sub 6} [A=Ba, Ca; M=Nb, Ta

    SciTech Connect

    Dutta, Alo; Saha, Sujoy; Sinha, T.P.

    2015-09-15

    The X-ray photoemission spectroscopic (XPS) study of the double perovskite oxides A{sub 2}LaMO{sub 6} [A=Ba, Ca; M=Nb, Ta] synthesized by the solid-state reaction technique has been carried out to investigate the nature of the chemical state of the constituent ions and the bonding between them. The Rietveld refinement of the X-ray diffraction patterns suggests the monoclinic crystal structure of all the materials at room temperature. The negative and positive chemical shifts of the core level XPS spectrum of O-1s and Nb-3d{sub 3/2}/Ta-4f{sub 5/2} respectively suggest the covalent bonding between Nb/Ta cations and O ion. The change of the bonding strength between the anion and the cations from one material to another has been analyzed. The vibrational property of the materials is investigated using the room temperature Raman spectra. A large covalency of Ta-based compound than Nb compound is confirmed from the relative shifting of the Raman modes of the materials. - Graphical abstract: Crystal structure of two perovskite oxides CLN and CLT is investigated. XPS study confirms the two different co-ordination environments of Ca and covalent bonding between B-site cations and O-ion. - Highlights: • Ordered perovskite structure obtained by Rietveld refinement of XRD patterns. • Study of nature of chemical bonding by X-ray photoemission spectroscopy. • Opposite chemical shift of d-states of Nb/Ta with respect to O. • Covalent bonding between d-states of Nb/Ta and O. • Relative Raman shifts of CLN and CLT substantiate the more covalent character of Ta than Nb.

  4. LiCaAlF6 scintillators in neutron and gamma radiation fields

    NASA Astrophysics Data System (ADS)

    Viererbl, L.; Klupák, V.; Vinš, M.; Koleška, M.; Šoltés, J.; Yoshikawa, A.; Nikl, M.

    2016-09-01

    Intentionally doped LiCaAlF6 (LiCAF) single crystals are prospective scintillators, especially for thermal neutron detection through the 6Li(n,t)4He nuclear reaction. Four different LiCAF scintillator samples were tested in various neutron and gamma fields. Two of the tested samples were LiCAF:Eu and LiCAF:Eu,Na single crystals, and another two samples were made of LiCAF:Eu micro crystals dispersed in transparent rubber, with different rubber dimensions. All LiCAF samples contain lithium enriched to6Li. A plutonium-beryllium source was used as a neutron source. The neutron spectrum was modified by moderator and filter to get different ratios between thermal, epithermal and fast neutron fluence rates. The MCNP code was used for calculations of the fluence rates for different configurations. Radionuclides 137Cs and 60Co were applied as gamma radiation sources. The light signal from the scintillator was evaluated with a photomultiplier and a multichannel analyzer. The purpose of this work was to study the characteristics of LiCAF scintillators, especially the ability to discriminate signals from neutron and gamma radiation, which is the basic scintillator condition for neutron detection in mixed neutron-gamma radiation fields. Generally, the discrimination can be done by the pulse height and/or the pulse shape of the evaluated signals. Both methods can be used for a LiCAF scintillator. However, only the pulse height discrimination method is discussed in this paper. The possibility of fast neutron detection with LiCAF scintillators was also tested.

  5. Critical magnetic fields of superconducting aluminum-substituted Ba{sub 8}Si{sub 42}Al{sub 4} clathrate

    SciTech Connect

    Li, Yang Garcia, Jose; Lu, Kejie; Shafiq, Basir; Franco, Giovanni; Lu, Junqiang; Rong, Bo; Chen, Ning; Liu, Yang; Liu, Lihua; Song, Bensheng; Wei, Yuping; Johnson, Shardai S.; Luo, Zhiping; Feng, Zhaosheng

    2015-06-07

    In recent years, efforts have been made to explore the superconductivity of clathrates containing crystalline frameworks of group-IV elements. The superconducting silicon clathrate is unusual in that the structure is dominated by strong sp{sup 3} covalent bonds between silicon atoms, rather than the metallic bonding that is more typical of traditional superconductors. This paper reports on critical magnetic fields of superconducting Al-substituted silicon clathrates, which were investigated by transport, ac susceptibility, and dc magnetization measurements in magnetic fields up to 90 kOe. For the sample Ba{sub 8}Si{sub 42}Al{sub 4}, the critical magnetic fields were measured to be H{sub C1} = 40.2 Oe and H{sub C2} = 66.4 kOe. The London penetration depth of 4360 Å and the coherence length 70 Å were obtained, whereas the estimated Ginzburg–Landau parameter of κ = 62 revealed that Ba{sub 8}Si{sub 42}Al{sub 4} is a strong type-II superconductor.

  6. Coexisting charge and magnetic orders in the dimer-chain iridate Ba5AlIr2O11

    SciTech Connect

    Terzic, J.; Wang, J. C.; Ye, Feng; Song, W. H.; Yuan, S. J.; Aswartham, S.; DeLong, L. E.; Streltsov, S. V.; Khomskii, Daniel I.; Cao, G.

    2015-06-29

    In this paper, we have synthesized and studied single-crystal Ba5AlIr2O11 that features dimer chains of two inequivalent octahedra occupied by tetravalent Ir4+(5d5) and pentavalent Ir5+(5d4) ions, respectively. Ba5AlIr2O11 is a Mott insulator that undergoes a subtle structural phase transition near TS=210K and a magnetic transition at TM=4.5K; the latter transition is surprisingly resistant to applied magnetic fields μoH≤12T but more sensitive to modest applied pressure (dTM/dp ≈ +0.61K/GPa). All results indicate that the phase transition at TS signals an enhanced charge order that induces electrical dipoles and strong dielectric response near TS. It is clear that the strong covalency and spin-orbit interaction (SOI) suppress double exchange in Ir dimers and stabilize a novel magnetic state that is neither S=3/2 nor J=1/2, but rather lies in an “intermediate” regime between these two states. Finally, the novel behavior of Ba5AlIr2O11 therefore provides unique insights into the physics of SOI along with strong covalency in competition with double-exchange interactions of comparable strength.

  7. Crustal structure of and boundary between the AlCaPa and Tisza terrains in the Pannonian basin

    NASA Astrophysics Data System (ADS)

    Hetényi, György; Ren, Yong; Dando, Ben; Stuart, Graham W.; Houseman, Gregory A.

    2014-05-01

    The evolution of the Pannonian Basin is strongly linked to that of the surrounding Alpine, Carpathian and Dinaric orogens. The eastward extrusion of Alpine-type basement that accompanied lithospheric thinning must have been accompanied by mantle downwelling and/or subduction along the Carpathians but the motive forces for these movements are debated. The internal structure of the crust within the basin is mostly covered by relatively recent sedimentary infill whose variable thickness further complicates seismic imaging. Palaeomagnetic and geological data have, however, shown that two tectonic terrains of distinct origin: AlCaPa and Tisza, occupy the basin's NW and SE part respectively. The two units have undergone different amounts of extension during opposite orientation rotations (counter-clockwise and clockwise, respectively). The boundary between these two units, known as the Mid-Hungarian Zone, is recognized as a major sinistral shear zone, geophysically clearly marked across the basin by a trough in Bouguer gravity. The Carpathian Basins Project deployed 49 broadband seismological stations perpendicular to the boundary between the AlCaPa and Tisza units. A NW-SE oriented swath of three lines covers a 450 km long and 75 km wide area. We use these and 4 permanent stations to image the crustal structure of and the boundary between AlCaPa and Tisza using the receiver function technique. The measured Moho depths show no significant change in crustal thickness between the two terrains, but the Moho is not or very weakly imaged along a ca. 40 km wide strip centred on the MHZ. Our Moho depths elsewhere in the basin agree with earlier controlled-source seismic results and recent shear-wave velocity models deduced from ambient noise analysis. The lack of a sharp Moho image beneath the MHZ implies that the crust-mantle boundary between AlCaPa and Tisza is not a sharp transition but rather a gradual increase in velocity with depth. The distinct low in gravity anomalies

  8. Teaching the Modes of Ca[superscript 2+] Transport between the Plasma Membrane and Endoplasmic Reticulum Using a Classic Paper by Kwan et al.

    ERIC Educational Resources Information Center

    Liang, Willmann

    2009-01-01

    This teaching article uses the report by Kwan et al., "Effects of methacholine, thapsigargin, and La[superscript 3+] on plasmalemmal and intracellular Ca[superscript 2+] transport in lacrimal acinar cells," where the effects of Ca[superscript 2+]-mobilizing agents in regulating Ca[superscript 2+] fluxes were examined under various conditions.…

  9. Piezoelectric properties of 0.5(Ba0.7Ca0.3TiO3) - 0.5[Ba(Zr0.2Ti0.8)O3] ferroelectric lead-free laser deposited thin films

    NASA Astrophysics Data System (ADS)

    Piorra, A.; Petraru, A.; Kohlstedt, H.; Wuttig, M.; Quandt, E.

    2011-05-01

    Ferroelectric lead-free thin films of 0.5(Ba0.7Ca0.3TiO3) - 0.5[Ba(Zr0.2Ti0.8)O3] (BCZT) were successfully deposited by pulsed laser deposition on Pt/TiO2/SiO2/Si substrates using a ceramic BCZT target prepared by conventional solid state reaction. The in (111) direction orientated 600 nm thick films shows a clamped piezoelectric response of approximately d33,f = 80 pm/V and a dielectric coefficient of about ɛr = 1010; these are close to values obtained for lead zirconate titanate (PZT) films.

  10. Probing the role of encapsulated alkaline earth metal atoms in endohedral metallofullerenes M@C76 (M = Ca, Sr, and Ba) by first-principles calculations.

    PubMed

    Yang, Tao; Zhao, Xiang; Xu, Qian; Zheng, Hong; Wang, Wei-Wei; Li, Sheng-Tao

    2012-05-01

    By means of density functional theory and statistical mechanics, we investigate the geometric and electronic structures, thermodynamic stability and infrared (IR) vibrational frequencies of alkaline earth metal endohedral fullerenes, M@C(76) (M = Ca, Sr, and Ba). The results reveal that M@C(1)(17,459)-C(76) possesses the lowest energy followed by M@C(2v)(19,138)-C(76) with a very small energy difference. Both the structures have a pair of adjacent pentagons and are related by a single Stone-Wales transformation. Equilibrium statistical thermodynamic analyses based on Gibbs energy treatments suggest that M@C(1)(17,459)-C(76) has a prominent thermodynamic stability at higher temperatures, in contrast with M@C(2v)(19,138)-C(76) whose thermodynamic stability is affected by the encapsulated metal atom. The encapsulated metallic atoms as well as cage structures significantly influence the electronic properties of endohedral fullerenes such as electron affinities and ionization potentials. On the other hand, the singlet-triplet splitting energy ΔE(S-T) depends on the cage structures. In addition, IR spectra and chemical shifts of these compounds have been computed to assist further experimental characterization.

  11. Magnetic relaxation in Tl2Ba2CaCu2O8 single crystals by SQUID magnetometer and micro-Hall sensor

    NASA Astrophysics Data System (ADS)

    Chowdhury, P.; Kim, Heon-Jung; Kang, W. N.; Zang, Dong-Jin; Lee, Sung-Ik; Kim, D. H.

    2003-10-01

    Measurements of the isothermal magnetization hysteresis loops M(H) and the magnetic relaxation for a Tl2Ba2CaCu2O8 single crystal were carried out by using a superconducting quantum interference device magnetometer and a micro-Hall sensor. In the temperature window from 30 to 60 K, the measurements for M(H) show a second anomalous peak at a field Hsp and an onset field of Hon. From these relaxation data measured by two different techniques, the activation barrier U0 and the creep exponent μ were separately calculated as functions of H based on the weak collective pinning theory. The variation of the normalized creep rate, S=(|d ln M/d ln t|), with H is also presented. The results at T=35 K indicate that at a characteristic field H* lying between Hon and Hsp, a minimum is observed in S(H) whereas a maximum is observed in U0(H). These analyses also show that below H*, the creep phenomenon is controlled by an elastic process. However, above Hsp a negative power law, U0(H)∝Hν with ν˜-0.9, is observed suggesting the existence of plastic creep. At a low temperature of T=20 K, where no second peak is observed, both S(H) and U0(H) behave differently. A comparative study of the different creep parameters obtained from the two different measurement techniques is also discussed.

  12. Effect of Mg(2+), Ca(2+), Sr(2+) and Ba(2+) metal ions on the antifungal activity of ZnO nanoparticles tested against Candida albicans.

    PubMed

    Haja Hameed, Abdulrahman Syedahamed; Karthikeyan, Chandrasekaran; Senthil Kumar, Venugopal; Kumaresan, Subramanian; Sasikumar, Seemaisamy

    2015-01-01

    The antifungal ability of pure and alkaline metal ion (Mg(2+), Ca(2+), Sr(2+) and Ba(2+)) doped ZnO nanoparticles (NPs) prepared by the co-precipitation method was tested against the pathogenic yeast, Candida albicans (C. albicans), and the results showed that the Mg-doped ZnO NPs possessed greater effect than the other alkaline metal ion doped ZnO NPs. The impact of the concentration of Mg doped ZnO sample on the growth of C. albicans was also studied. The Minimal Fungicidal Concentration (MFC) of the Mg doped ZnO NPs was found to be 2000 μg/ml for which the growth of C. albicans was completely inhibited. The ZnO:Mg sample (1.5mg/ml) with various concentrations of histidine reduced the fungicidal effect of the nanoparticles against C. albicans, which was deliberately explained by the role of ROS. The ZnO:Mg sample added with 5mM of histidine scavenged the ample amount of generated ROS effectively. The binding of the NPs with fungi was observed by their FESEM images and their electrostatic attraction is confirmed by the zeta potential measurement. PMID:25953555

  13. Observation of superconductivity at 30~46 K in A(x)Fe₂Se₂(A = Li, Na, Ba, Sr, Ca, Yb, and Eu).

    PubMed

    Ying, T P; Chen, X L; Wang, G; Jin, S F; Zhou, T T; Lai, X F; Zhang, H; Wang, W Y

    2012-01-01

    New iron selenide superconductors by intercalating smaller-sized alkali metals (Li, Na) and alkaline earths using high-temperature routes have been pursued ever since the discovery of superconductivity at about 30 K in KFe₂Se₂, but all have failed so far. Here we demonstrate that a series of superconductors with enhanced T(c) = 30∼46 K can be obtained by intercalating metals, Li, Na, Ba, Sr, Ca, Yb, and Eu in between FeSe layers by the ammonothermal method at room temperature. Analysis on their powder X-ray diffraction patterns reveals that all the main phases can be indexed based on body-centered tetragonal lattices with a∼3.755-3.831 Å while c∼15.99-20.54 Å. Resistivities show the corresponding sharp transitions at 45 K and 39 K for NaFe₂Se₂ and Ba₀.₈Fe₂Se₂, respectively, confirming their bulk superconductivity. These findings provide a new starting point for studying the properties of these superconductors and an effective synthetic route for the exploration of new superconductors as well. PMID:22645642

  14. Structural analysis, optical and dielectric function of [Ba0.9Ca0.1](Ti0.9Zr0.1)O3 nanocrystals

    NASA Astrophysics Data System (ADS)

    Herrera-Pérez, G.; Morales, D.; Paraguay-Delgado, F.; Borja-Urby, R.; Reyes-Rojas, A.; Fuentes-Cobas, L. E.

    2016-09-01

    This work presents the identification of inter-band transitions in the imaginary part of the dielectric function (ɛ2) derived from the Kramers-Kronig analysis for [Ba0.9Ca0.1](Ti0.9Zr0.1)O3 (BCZT) nanocrystals synthesized by the modified Pechini method. The analysis started with the chemical identification of the atoms that conform BCZT in the valence loss energy region of a high energy-resolution of electron energy loss spectroscopy. The indirect band energy (Eg) was determined in the dielectric response function. This result is in agreement with the UV-Vis technique, and it obtained an optical band gap of 3.16 eV. The surface and volume plasmon peaks were observed at 13.1 eV and 26.2 eV, respectively. The X-ray diffraction pattern and the Rietveld refinement data of powders heat treated at 700 °C for 1 h suggest a tetragonal structure with a space group (P4 mm) with the average crystal size of 35 nm. The average particle size was determined by transmission electron microscopy.

  15. Investigation about relationships between the symmetries of ferroelectric crystal Ca0.28Ba0.72Nb2O6 and second-harmonic patterns

    NASA Astrophysics Data System (ADS)

    Xu, Tianxiang; Yu, Haohai; Zhang, Huaijin; Wang, Jiyang

    2015-08-01

    The broadband quasi-phase matching (QPM) process in a uniaxial ferroelectric crystal Ca0.28Ba0.72Nb2O6 (CBN-28) was demonstrated with the second-harmonic wavelength range from 450 nm to 650 nm, and the relationship between the symmetries of CBN-28 and the second-harmonic patterns was experimentally and theoretically investigated based on the random anti-parallel domains in the crystal and QPM conditions. The dependences of frequency-doubled patterns on the wavelength and anisotropy of the nonlinear crystal were also studied, and the frequency-doubled photons were found to be trapped on circles. By analyzing the light-matter interacting Hamiltonians, the trapping force for second-harmonic photons was found to be centripetal and tunable by the fundamental lasers, and the variation tendencies of the rotational velocity of second-harmonic generation photons could also be predicated. The results indicate that the CBN-28 ferroelectric crystal is a promising nonlinear optical material for the generation of broadband frequency-doubled waves, and the analysis on centripetal force based on the interaction Hamiltonians may provide a novel recognition for the investigation of QPM process to be further studied.

  16. AuBa 2(Y 1- x, Ca x)Cu 2O 7: a new superconducting gold cuprate with Tc above 80 K

    NASA Astrophysics Data System (ADS)

    Bordet, P.; LeFloch, S.; Chaillout, C.; Duc, F.; Gorius, M. F.; Perroux, M.; Capponi, J. J.; Toulemonde, P.; Tholence, J. L.

    1997-02-01

    We have synthesised by the high pressure-high temperature technique a new layered gold cuprate of chemical formula AuBa 2(Y 1- x,Ca x)Cu 2O 7 (0 ≤ × ≤ 0.4) (hereafter denoted as Au-1212). The structural properties of this compound are investigated by means of electron microscopy and powder X-ray diffraction. The average structure (orthorhombic Pmmm, a = 3.8298(5) Å, b = 3.8420(5) Å, c = 12.111(1) Å for nominal composition x = 0.4) is very similar to that of YBa 2Cu 3O 7, with Au 3+ cations in square planar coordination sharing corners to form chains running along the b axis. Electron microscopy reveals the presence of a superstructure with double b parameter, which is attributed to a long range ordered zig-zag conformation of the square chains. For x = 0, the formal copper valence is 2 + and the compound is insulating. Doping of the conducting CuO 2 planes is achieved by the partial substitution of yttrium by calcium, up to x ≈ 0.4. Upon substitution, the compound becomes superconducting with a maximum Tc at ∼ 82 K for x ≈ 0.4.

  17. Direct imaging of the structural domains in the iron pnictides AFe[subscript 2]As[subscript 2] (A=Ca, Sr, Ba)

    SciTech Connect

    Tanatar, M.A.; Kreyssig, A.; Nandi, S.; Ni, N.; Bud'ko, S.L.; Canfield, P.C.; Goldman, A.I.; Prozorov, R.

    2009-06-29

    The parent compounds of recently discovered iron-arsenide superconductors, AFe{sub 2}As{sub 2} with alkaline earth A=Ca,Sr,Ba, undergo simultaneous structural and magnetic phase transitions at a temperature T{sub SM}. Using a combination of polarized light microscopy and spatially resolved high-energy synchrotron x-ray diffraction we show that the orthorhombic distortion leads to the formation of 45{sup o}-type structural domains in all parent compounds. Domains penetrate through the sample thickness in the c direction and are not affected by crystal imperfections such as growth terraces. The domains form regular stripe patterns in the plane with a characteristic dimension of 10--50 {mu}m. The direction of the stripes is fixed with respect to the tetragonal (100) and (010) directions but can change by 90{sup o} on thermal cycling through the transition. This domain pattern may have profound implications for intrinsic disorder and anisotropy of iron arsenides.

  18. Effects of Cr2O3 doping on the microstructure and electrical properties of (Ba,Ca)(Zr,Ti)O3 lead-free ceramics

    NASA Astrophysics Data System (ADS)

    Xia, Xiang; Jiang, Xiangping; Chen, Chao; Jiang, Xingan; Tu, Na; Chen, Yunjing

    2016-06-01

    Lead-free ceramics (Ba0.85Ca0.15)(Zr0.1Ti0.9)O3- x wt.%Cr2O3 (BCZT- xCr) were prepared via the conventional solid-state reaction method. The microstructure and electrical properties of BCZT- xCr samples were systematically studied. XRD and Raman results showed that all samples possessed a single phased perovskite structure and were close to the morphotropic phase boundary (MPB). With the increase of the Cr content, the rhombohedral-tetragonal phase transition temperature ( T R-T) increases slightly, and the Curie temperature ( T C) shifts towards the low temperature side. XPS analysis reveals that Cr3+ and Cr5 + ions co-existed in Cr-doped BCZT ceramics, indicating the different impact on the electrical properties from Cr ions as "acceptor" or "donor". For the x = 0.1 sample, relative high piezoelectric constants d 33 (˜316 pC/N) as well as high Q m (˜554) and low tanδ (˜0.8%) were obtained. In addition, the AC conductivity was also investigated. Hopping charge was considered as the main conduction mechanism at low temperature. As the temperature increases, small polarons and oxygen vacancies conduction played important roles.

  19. Spin dynamics, short range order and spin freezing in Y0.5Ca0.5BaCo4O7

    SciTech Connect

    Stewart, John Ross; Ehlers, Georg; Fouquet, Peter; Mutka, Hannu; Payen, Christophe; Lortz, Rolf

    2011-01-01

    Y0.5Ca0.5BaCo4O7 was recently introduced as a possible candidate for capturing some of the predicted classical spin kagome ground-state features. Stimulated by this conjecture, we have taken up a more complete study of the spin correlations in this compound with neutron scattering methods on a powder sample characterized with high-resolution neutron diffraction and the temperature dependence of magnetic susceptibility and specific heat. We have found that the frustrated near-neighbor magnetic correlations involve not only the kagome planes but concern the full Co sublattice, as evidenced by the analysis of the wave-vector dependence of the short-range order. We conclude from our results that the magnetic moments are located on the Co sublattice as a whole and that correlations extend beyond the two-dimensional kagome planes. We identify intriguing dynamical properties, observing high-frequency fluctuations with a Lorentzian linewidth G?20 meV at ambient temperature. On cooling a low-frequency ({approx}1 meV) dynamical component develops alongside the high-frequency fluctuations, which eventually becomes static at temperatures below T {approx} 50 K. The high-frequency response with an overall linewidth of {approx}10 meV prevails at T?2 K, coincident with a fully elastic short-range-ordered contribution.

  20. Millimeter wave characteristics of intrinsic Josephson junctions with planar equiangular spiral antenna in misaligned Tl2Ba2CaCu2O8 thin film

    NASA Astrophysics Data System (ADS)

    Liu, X.; Wang, P.; Xie, W.; Ma, L. J.; Zhao, X. J.; He, M.; Ji, L.; Zhang, X.

    2015-12-01

    An intrinsic Josephson junctions (IJJs) microbridge with planar equiangular spiral antenna (PESA) is proposed and studied by simulation and experiment. This IJJs circuit is simulated firstly to obtain the minimum of reflection coefficient and pattern. Secondly, IJJs with PESA are fabricated on misaligned Tl2Ba2CaCu2O8 superconducting film. The millimeter wave characteristics are investigated by a Febry-Pérot resonator, which consists of a spherical mirror antenna and a plane mirror. At 37.4 GHz, the IJJs and the millimeter wave show an optimum coupling, which deviate from the simulation for only 0.004 GHz. In addition, the extent of the coupling between IJJs and the resonator is discussed at different angle for the polarization direction of the spherical mirror antenna with the microbridge. The result shows that the strongest coupling is obtained at 0-30° angle. Good conformance of measurements and simulations illustrate the effectiveness of our design in strong coupling between sample and resonator.

  1. The Effect of Nanosized Pb Liquid Phase on the Damping Behavior in Aluminum Matrix Composite Based on the 2024Al-BaPbO3 System

    NASA Astrophysics Data System (ADS)

    Fan, G. H.; Geng, L.; Wu, H.; Zheng, Z. Z.; Meng, Q. C.

    2016-03-01

    An aluminum matrix composite containing nanosized Pb particles was fabricated by a powder metallurgy technique based on the 2024Al-BaPbO3 system. The composite exhibited a high and broad damping peak at the melting temperature range of nanosized Pb particles. The increase in value and breadth of the damping peak was attributed to the dislocation damping of the interfacial matrix close to the nanosized Pb liquid phase. The damping peak is expected to be enhanced by further refining the Pb particle size.

  2. Investigation of the degradation mechanisms in BaMgAl10O17:Eu2+ phosphor: on the influence of thermal process on operational durability

    NASA Astrophysics Data System (ADS)

    Kim, Y.; Kang, S.

    2010-02-01

    The thermal and operational degradation in optical property of a europium-doped barium magnesium aluminate (BaMgAl10O17:Eu2+, BAM) phosphor was studied. BAM was heat-treated at 500°C under various conditions to determine the mechanism of thermal degradation. Operational degradation tests were then performed under a discharging Xe/Ne mixed gas to study the influence of thermal history on operational degradation. It was found that the atmosphere during thermal processing was the major factor affecting not only the thermal degradation, but also the operational degradation. The sample heat-treated under a reducing atmosphere showed enhanced stability during operation.

  3. Synthesis, characterization and TL response of Ce{sup 3+} activated BaMgAl{sub 10}O{sub 17} phosphor

    SciTech Connect

    Selot, Anupam; Aynyas, Mahendra; Tiwari, Manoj; Dev, Kapil

    2015-06-24

    Phosphor material BaMgAl{sub 10}O{sub 17} with varying concentration of rare earth Ce{sup 3+} synthesis by combustion method at 500°C. The synthesized phosphor material characterized for their crystallinity and nature by XRD measurements. The thermoluminescecne response of phosphor exhibit TL spectra at 204°c and detailed analysis of kinetic parameter by de convoluted curve. These results show that concentration quenching occur at 5mol% of Ce dopant. The results suggest the possibility of utilizing as a phosphor may be in UV dosimeter and solid state lighting.

  4. 266  nm ultraviolet light generation in Ga-doped BaAlBO3F2 crystals.

    PubMed

    Yang, Lei; Yue, Yinchao; Yang, Feng; Hu, Zhanggui; Xu, Zuyan

    2016-04-01

    BaAlBO3F2 (BABF) crystals are a recently developed and promising nonlinear optical material, notably for the third harmonic generation of ultraviolet (UV) light at 355 nm. However, the fourth harmonic generation of UV light at 266 nm has never been obtained by using a BABF crystal due to its relatively small birefringence. We demonstrate that the birefringence of BABF can be effectively increased by doping it with Ga3+. The fourth harmonic generation of UV light at 266 nm was achieved for the first time in a Ga-doped BABF crystal. PMID:27192296

  5. Hillesheimite, (K,Ca,□)2(Mg,Fe,Ca,□)2[(Si,Al)13O23(OH)6](OH) · 8H2O, a new phyllosilicate mineral of the Günterblassite group

    NASA Astrophysics Data System (ADS)

    Chukanov, N. V.; Zubkova, N. V.; Pekov, I. V.; Belakovskiy, D. I.; Schüller, W.; Ternes, B.; Blass, G.; Pushcharovsky, D. Yu.

    2013-12-01

    A new mineral, hillesheimite, has been found in the Graulai basaltic quarry, near the town of Hillesheim, the Eifel Mountains, Rhineland-Palatinate (Rheinland-Pfalz), Germany. It occurs in the late assemblage comprising nepheline, augite, fluorapatite, magnetite, perovskite, priderite, götzenite, lamprophyllite-group minerals, and åkermanite. Colorless flattened crystals of hillesheimite reaching 0.2 × 1 × 1.5 mm in size and aggregates of the crystals occur in miarolitic cavities in alkali basalt. The mineral is brittle, with Mohs' hard-ness 4. Cleavage is perfect parallel to (010) and distinct on (100) and (001). D calc = 2.174 g/cm3, D meas = 2.16(1) g/cm3. IR spectrum is given. Hillesheimite is biaxial (-), α = 1.496(2), β = 1.498(2), γ = 1.499(2), 2 V meas = 80°. The chemical composition (electron microprobe, mean of 4 point analyses, H2O determined from structural data, wt %) is as follows: 0.24 Na2O, 4.15 K2O, 2.14 MgO, 2.90 CaO, 2.20 BaO, 2.41 FeO, 15.54 Al2O3, 52.94 SiO2, 19.14 H2O, total is 101.65. The empirical formula is: K0.96Na0.08Ba0.16Ca0.56Mg0.58Fe{0.37/2+}[Si9.62Al3.32O23(OH)6][(OH)0.82(H2O)0.18] · 8H2O. The crystal structure has been determined from X-ray single-crystal diffraction data, R = 0.1735. Hillesheimite is orthorhombic, space group Pmmn, the unit-cell dimensions are: a = 6.979(11), b = 37.1815(18), c = 6.5296(15) Å; V=1694(3) Å3, Z = 2. The crystal structure is based on the block [(Si,Al)13O25(OH)4] consisting of three single tetrahedral layers linked via common vertices and is topologically identical to the triple layers in günterblassite and umbrianite. The strong reflections [ d Å ( I %)] in the X-ray powder diffraction pattern are: 6.857(58), 6.545(100), 6.284(53), 4.787(96), 4.499(59), 3.065(86), 2.958(62), 2.767(62). The mineral was named after its type locality. Type specimens are deposited in the Fersman Mineralogical Museum, Russian Academy of Sciences, Moscow, registration number 4174/1.

  6. On the photo-luminescence properties of sol–gel derived undoped and Dy{sup 3+} ion doped nanocrystalline Scheelite type AMoO{sub 4} (A = Ca, Sr and Ba)

    SciTech Connect

    Jena, Paramananda; Gupta, Santosh K.; Natarajan, V.; Padmaraj, O.; Satyanarayana, N.; Venkateswarlu, M.

    2015-04-15

    Nanocrystalline Scheelite type Dy doped AMoO{sub 4} [where A = Ba, Sr and Ca] samples were prepared by acrylamide assisted sol–gel process and characterized by XRD, FT-Raman, FTIR, SEM and photoluminescence (PL). PL of undoped sample shows blue/green emission in CaMoO{sub 4} and SrMoO{sub 4} but multicolour visible emission leading to near white light in BaMoO{sub 4} nanoparticles; the origin of which is explained. It was observed that on doping 0.5 mol% of Dy{sup 3+} in molybdate samples complete energy transfer takes place in case of SrMoO{sub 4} and BaMoO{sub 4}, but host contributed substantially in Dy doped BaMoO{sub 4} sample, resulting in biexponential decay. It was also observed that symmetry around Dy{sup 3+} decreases as the size of alkaline earth ion increases. Due to combined blue, yellow and red colour emission in dysprosium doped sample; all samples showed near white light emission under UV and near UV excitation.

  7. Study of new sheep bone and Zn/Ca ratio around TiAlV screw: PIXE RBS analysis

    NASA Astrophysics Data System (ADS)

    Guibert, G.; Munnik, F.; Langhoff, J. D.; Von Rechenberg, B.; Buffat, Ph. A.; Laub, D.; Faber, L.; Ducret, F.; Gerber, I.; Mikhailov, S.

    2008-03-01

    This study reports on in vivo particle induced X-ray emission (PIXE) measurements combined with Rutherford backscattering spectroscopy (RBS) analyses of new remodeled sheep bone formed around TiAlV screws. The implants (screws) were anodized by a modified TiMax™ process. The interface between the implant and the bone was carefully investigated. [Zn]/[Ca] in-depth composition profiles as well as Ca, Fe elemental maps were recorded. The thickness of new bone formed around the screw reached 300-400 μm. Osteon and Osteoid phases were identified in the new bone. A higher [Zn]/[Ca] ratio was observed in the new bone as compared to the mature bone. Blood vessels were observed in the bone in close contact with the screw. This study shows the potential of ion beam analysis for biological and biomedical characterization.

  8. A new series of oxycarbonate superconductors (Cu(0.5)C(0.5))(m)Ba(m+1)Ca(n-1)Cu(n)O2(m+n)+1

    NASA Technical Reports Server (NTRS)

    Takayama-Muromachi, E.; Kawashima, T.; Matsui, Y.

    1995-01-01

    We found a new series of oxycarbonate superconductors in the Ba-CaCu-C-O system under high pressure of 5 GPa. Their ideal formula is (Cu(0.5)C(0.5)(m)Ba(m+1)Ca(n-1)Cu(n)O2)((m+n)+1) ((Cu,C)-m(m+1)(n-1)n). Thus far, n = 3, 4 members of the m = 1 series, (Cu,C)-1223 and (Cu,C)-1234, have been prepared in bulk while n = 4, 5 members, (Cu,C)-2334 and (Cu,C)-2345, have been prepared for the m = 2 series. (Cu,C)-1223 shows superconductivity below 67 K while T(sub c)'s of other compounds are above 110 K. In particular, (Cu,C)-1234 has the highest T(sub c) of 117 K.

  9. Crystal structure of Na 2MMgP 2O 8 ( M: Ba, Sr, Ca) orthophosphates and their luminescence properties activated by Eu 2+; analogous structural behaviors of glaserite-type phosphates and silicates

    NASA Astrophysics Data System (ADS)

    Yonesaki, Yoshinori; Matsuda, Chihiro

    2011-12-01

    Rietveld refinements of X-ray powder diffraction data and vibrational spectroscopy have confirmed the crystal structure of Na 2MMgP 2O 8 ( M: Ba, Sr, Ca) prepared by a standard solid state reaction. They have glaserite-type layered structure. Na 2MMgP 2O 8 has a trigonal P3¯ form for M=Ba, and monoclinic P2 1/ c forms for M=Sr and Ca. The observed structural transition is analogous to the corresponding layered orthosilicate M3MgSi 2O 8. Eu 2+-doped Na 2MMgP 2O 8 exhibits an intense blue to violet emission under ultraviolet excitation, based on 5 d-4 f electron transition of Eu 2+ ions. The emission character is very sensitive to the structural transition induced by M2+ and the subsequent site symmetry changes.

  10. LARGE PIEZOELECTRIC EFFECT IN LOW-TEMPERATURE-SINTERED LEAD-FREE (Ba0.85Ca0.15)(Zr0.1Ti0.9)O3 THICK FILMS

    NASA Astrophysics Data System (ADS)

    Feng, Zuyong; Shi, Dongqi; Dou, Shixue; Hu, Yihua; Tang, Xingui

    2012-09-01

    High-quality piezoelectric (Ba0.85Ca0.15)(Zr0.1Ti0.9)O3 thick films with dense and homogenous microstructures were fabricated at a low sintering temperature (900°C) using a CuBi2O4 sintering aid. The 10 μm thick film exhibited a high longitudinal piezoelectric constant d33,eff of 210 pC/N with estimated unconstrained d33 value of 560 pC/N very close to that in the corresponding bulks. Such excellent piezoelectric effect in the low-temperature sintered (Ba0.85Ca0.15)(Zr0.1Ti0.9)O3 thick films is comparable to the case of lead-based PZT thick films, and may be a promising application in lead-free microdevices such as piezoelectric microelectromechanical systems (MEMS).

  11. Structural investigations of {beta}-CaAlF{sub 5} by coupling powder XRD, NMR, EPR and spectroscopic parameter calculations

    SciTech Connect

    Body, M. . E-mail: monique.body@univ-lemans.fr; Silly, G.; Legein, C.; Buzare, J.-Y.; Calvayrac, F.; Blaha, P.

    2005-12-15

    {beta}-CaAlF{sub 5} was synthesized by solid-state reaction. The precise structure was refined from X-ray powder diffraction data in the monoclinic space group P2{sub 1}/c with lattice constants a=5.3361A, b=9.8298A, c=7.3271A, and {beta}=109.91{sup o} (Z=4). The structure exhibits isolated chains of AlF{sub 6}{sup 3-} octahedra sharing opposite corners.{sup 19}F and {sup 27}Al solid state NMR spectra were recorded using MAS and SATRAS techniques. An EPR spectrum was recorded for {beta}-CaAlF{sub 5}:Cr{sup 3+}. The experimental spectra were simulated in order to extract the NMR and EPR parameter values. Five fluorine sites and one low symmetry aluminium site were found in agreement with the refined structure. These parameters were calculated using empirical and ab-initio methods. The agreement obtained between the calculated {sup 19}F chemical shift values, {sup 27}Al quadrupolar parameters, Cr{sup 3+} EPR fine structure parameters and the experimental results demonstrates the complementarity of XRD, magnetic resonance experiments and theoretical methodologies.

  12. Synthesis and hydration behavior of calcium zirconium aluminate (Ca{sub 7}ZrAl{sub 6}O{sub 18}) cement

    SciTech Connect

    Kang, Eun-Hee; Yoo, Jun-Sang; Kim, Bo-Hye; Choi, Sung-Woo; Hong, Seong-Hyeon

    2014-02-15

    Calcium zirconium aluminate (Ca{sub 7}ZrAl{sub 6}O{sub 18}) cements were prepared by solid state reaction and polymeric precursor methods, and their phase evolution, morphology, and hydration behavior were investigated. In polymeric precursor method, a nearly single phase Ca{sub 7}ZrAl{sub 6}O{sub 18} was obtained at relatively lower temperature (1200 °C) whereas in solid state reaction, a small amount of CaZrO{sub 3} coexisted with Ca{sub 7}ZrAl{sub 6}O{sub 18} even at higher temperature (1400 °C). Unexpectedly, Ca{sub 7}ZrAl{sub 6}O{sub 18} synthesized by polymeric precursor process was the large-sized and rough-shaped powder. The planetary ball milling was employed to control the particle size and shape. The hydration behavior of Ca{sub 7}ZrAl{sub 6}O{sub 18} was similar to that of Ca{sub 3}Al{sub 2}O{sub 6} (C3A), but the hydration products were Ca{sub 3}Al{sub 2}O{sub 6}·6H{sub 2}O (C3AH6) and several intermediate products. Thus, Zr (or ZrO{sub 2}) stabilized the intermediate hydration products of C3A.

  13. Trace element (Al, As, B, Ba, Cr, Mo, Ni, Se, Sr, Tl, U and V) distribution and seasonality in compartments of the seagrass Cymodocea nodosa.

    PubMed

    Malea, Paraskevi; Kevrekidis, Theodoros

    2013-10-01

    Novel information on the biological fate of trace elements in seagrass ecosystems is provided. Al, As, B, Ba, Cr, Mo, Ni, Se, Sr, Tl, U and V concentrations in five compartments (blades, sheaths, vertical rhizomes, main axis plus additional branches, roots) of the seagrass Cymodocea nodosa, as well as in seawater and sediments from the Thessaloniki Gulf, Greece were determined monthly. Uni- and multivariate data analyses were applied. Leaf compartments and roots displayed higher Al, Mo, Ni and Se annual mean concentrations than rhizomes, B was highly accumulated in blades and Cr in sheaths; As, Ba, Sr and Tl contents did not significantly vary among plant compartments. A review summarizing reported element concentrations in seagrasses has revealed that C. nodosa sheaths display a high Cr accumulation capacity. Most element concentrations in blades increased in early mid-summer and early autumn with blade size and age, while those in sheaths peaked in late spring-early summer and autumn when sheath size was the lowest; elevated element concentrations in seawater in late spring and early-mid autumn, possibly as a result of elevated rainfall and associated run-off from the land, may have also contributed to the observed variability. Element concentrations in rhizomes and roots generally displayed a temporary increase in late autumn, which was concurrent with high rainfall, low wind speed associated with reduced hydrodynamism, and elevated sediment element levels. The bioaccumulation factor based on element concentrations in seagrass compartments and sediments was lower than 1 except for B, Ba, Mo, Se and Sr in all compartments, Cr in sheaths and U in roots. Blade V concentration positively correlated with sediment V concentration, suggesting that C. nodosa could be regarded as a bioindicator for V. Our findings can contribute to the design of biomonitoring programs and the development of predictive models for rational management of seagrass meadows. PMID:23838054

  14. The Relative Nature of Perception: A Response to Cañal-Bruland and van der Kamp (2015)

    PubMed Central

    2015-01-01

    Cañal-Bruland and van der Kamp present an argument about the incommensurate relationship between affordance perception and spatial perception in a criticism of Proffitt and Linkenauger’s phenotypic approach to perception. Many of their criticisms are based on a difference in the interpretation of the core ideas underlying the phenotypic approach. The most important of these differences in interpretations concern fundamental assumptions about the nature of the perceptions of size and distance themselves. Extent perception must be relative to the organism; therefore, there can be no veridical perception of space. Also, we argue in the phenotypic approach that space perception is an emergent property of affordance perception; they are not different types of perceptions as Cañal-Bruland and van der Kamp presume. Third, affordance perception need not be perfectly accurate, just good enough. Additionally, affordance perception need not be dichotomous; this presumption likely originates in the methodology typically employed to study affordance perception. Finally, I agree with Cañal-Bruland and van der Kamp that joint research efforts will clarify and improve our understanding of these issues. PMID:27648215

  15. The Relative Nature of Perception: A Response to Cañal-Bruland and van der Kamp (2015)

    PubMed Central

    2015-01-01

    Cañal-Bruland and van der Kamp present an argument about the incommensurate relationship between affordance perception and spatial perception in a criticism of Proffitt and Linkenauger’s phenotypic approach to perception. Many of their criticisms are based on a difference in the interpretation of the core ideas underlying the phenotypic approach. The most important of these differences in interpretations concern fundamental assumptions about the nature of the perceptions of size and distance themselves. Extent perception must be relative to the organism; therefore, there can be no veridical perception of space. Also, we argue in the phenotypic approach that space perception is an emergent property of affordance perception; they are not different types of perceptions as Cañal-Bruland and van der Kamp presume. Third, affordance perception need not be perfectly accurate, just good enough. Additionally, affordance perception need not be dichotomous; this presumption likely originates in the methodology typically employed to study affordance perception. Finally, I agree with Cañal-Bruland and van der Kamp that joint research efforts will clarify and improve our understanding of these issues.

  16. The Relative Nature of Perception: A Response to Cañal-Bruland and van der Kamp (2015).

    PubMed

    Linkenauger, Sally A

    2015-10-01

    Cañal-Bruland and van der Kamp present an argument about the incommensurate relationship between affordance perception and spatial perception in a criticism of Proffitt and Linkenauger's phenotypic approach to perception. Many of their criticisms are based on a difference in the interpretation of the core ideas underlying the phenotypic approach. The most important of these differences in interpretations concern fundamental assumptions about the nature of the perceptions of size and distance themselves. Extent perception must be relative to the organism; therefore, there can be no veridical perception of space. Also, we argue in the phenotypic approach that space perception is an emergent property of affordance perception; they are not different types of perceptions as Cañal-Bruland and van der Kamp presume. Third, affordance perception need not be perfectly accurate, just good enough. Additionally, affordance perception need not be dichotomous; this presumption likely originates in the methodology typically employed to study affordance perception. Finally, I agree with Cañal-Bruland and van der Kamp that joint research efforts will clarify and improve our understanding of these issues. PMID:27648215

  17. Crystallinity and in-field characterization of high-Tc YBa2Cu408 and Y0.9Ca0.1Ba2Cu4O8 epitaxial films fabricated by low temperature flux method

    NASA Astrophysics Data System (ADS)

    Funaki, S.; Yamada, Y.; Nakayama, F.

    2014-05-01

    REBa2Cu4O8 superconductor has an important advantage that the critical temperature (Tc) is improved by Ca substitution for RE site. We fabricated the YBa2Cu4O8 (Y124) and Y0.9Ca0.1Ba2Cu4O8 (YCa124) films by molten hydroxide method in ambient atmosphere and investigated the crystallinity and in-field characterization. Obtained samples show that the film alignment is biaxial orientation and the grain size is larger than 50 μm, and the irreversibility field of YCa124 film is superior to that of Y124 in all the measured magnetic fields

  18. Structure, thermodynamic and transport properties of CaAl 2Si 2O 8 liquid. Part I: Molecular dynamics simulations

    NASA Astrophysics Data System (ADS)

    Spera, Frank J.; Nevins, Dean; Ghiorso, Mark; Cutler, Ian

    2009-11-01

    Molecular dynamics simulations for liquid CaAl 2Si 2O 8 have been carried out at 72 state points spanning ranges in density ( ρ: 2398-4327 kg/m 3), temperature ( T: 3490-6100 K) and pressure ( P: 0.84-120 GPa) relevant to geosystems. The atomic scale structure of the melt is determined by analysis of nearest neighbor coordination statistics as a function of T and P. Dramatic structural change occurs as pressure increases especially for 0 < P <20 GPa at all temperatures. Changes in structure are encapsulated by examining the coordination of Si, Al, Ca and O around oxygen and vice versa. Si and Al change from predominantly fourfold at low- P to dominantly sixfold for P >˜ 20 GPa. Pentahedrally coordinated Si and Al in distorted trigonal bipyramids attain abundance maxima corresponding to ˜60% of total (Si, Al)O n at 3-5 GPa and weakly depend on T. The coordination of Ca by oxygen increases from 7 to 10 for 0 < P < 20 GPa and changes slowly for P > 20 GPa at 3500 K. Similar behavior is seen at 6000 K except that the interval of rapid changes occurs at higher pressure. Oxygen with only one nearest Si or Al neighbor (i.e., non-bridging oxygen, NBO) decreases whereas oxygen with two or three nearest neighbors of Si, Al or Ca increases as pressure increases. Changes in melt structure are reflected in the variation of thermodynamic and transport properties of the liquid. Values of the self-diffusivities of Ca, Al, Si and O are fit to a modified Arrhenian expression and compare well to limited laboratory data. Self-diffusivities are best fit using 'low P' and 'high- P' expressions, identical in form but with different parameters, with activation energies and activation volumes in the range 150-200 kJ/mol and +5 to -1 cm 3/mol, respectively. Green-Kubo calculations for liquid shear viscosity are presented and compare well with limited laboratory results. Application of the Eyring model to determine the characteristic size and number of atoms in the activated cluster based

  19. Structural, morphological and optical investigations on BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} elaborated by a microwave induced solution combustion synthesis

    SciTech Connect

    Pradal, Nathalie; Potdevin, Audrey; Chadeyron, Genevieve; Mahiou, Rachid

    2011-04-15

    Graphical abstract: Graphical abstract (with Research highlights). This is a paragraph for graphical abstract. Research highlights: {yields} Synthesis of BAM:Eu{sup 2+} by MISCS using different fuel to oxidizer molar ratios. {yields} Both blue and red phosphors were obtained. {yields} Majority of blue phosphors was obtained for fuel-rich synthesis. {yields} A specific morphology was observed for each contribution. -- Abstract: Blue-emitting Eu{sup 2+}-doped barium magnesium aluminate (BaMgAl{sub 10}O{sub 17}:Eu{sup 2+}) for advanced displays and lighting devices was prepared by a microwave induced solution combustion synthesis using urea as combustion fuel and nitrates as oxidizer. Purity control of as-synthesized blue phosphor particles was undertaken by modifying the fuel to oxidizer molar ratio. X-ray diffraction, scanning electron microscopy and photoluminescence were used to investigate powders crystallinity, particles size, morphology and luminescent properties, respectively. Fuel-rich urea reactions preferentially lead to pure phases compared to the powders synthesized with a stoichiometric fuel to oxidizer ratio. In both cases, we produce a nearly pure well-crystallized and nanostructured BaMgAl{sub 10}O{sub 17}:Eu{sup 2+}. Photoluminescence measurements exhibit the characteristic blue emission of Eu{sup 2+} under UV light excitation however a weak red emission associated to Eu{sup 3+} is also detected.

  20. On BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphor degradation mechanism by vacuum-ultraviolet excitation

    SciTech Connect

    Bizarri, G.; Moine, B.

    2005-12-01

    Additional to a correct color and a high efficiency, phosphors for plasma display panels must maintain their light output for thousands of hours. Often the degradation is the restricting factor in using phosphors. In this article, the mechanism of luminance decrease in blue-emitting BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphor during the operation of the PDPs has been studied. It is shown experimentally that the aging process is mainly due to the vacuum-ultraviolet excitation (VUV). It is demonstrated that the degradation mechanism can be accelerated by using a 193 nm laser excitation. Based on excitation, reflectance, thermoluminescence spectra, and aging or annealing processes by laser excitation, the main causes of the degradation are demonstrated. The aging process can be separated in two different processes according to the temperature: a first one, at low temperature, corresponding to the autoionization of luminescent centers (Eu{sup 2+}{yields}Eu{sup 3+}); and a second one, at high temperature, linked to the formation of traps in the phosphor. These traps induce a perturbation of the energy migration in the phosphor. In addition, the relevant parameters of trap formation are highlighted: density of the VUV excitation, temperature, and atmosphere/pressure surrounding the phosphor. A model of BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphor degradation mechanism is proposed.

  1. Study of Eu{sup 3+} → Eu{sup 2+} reduction in BaAl{sub 2}O{sub 4}:Eu prepared in different gas atmospheres

    SciTech Connect

    Rezende, Marcos V. dos S.; Valerio, Mário E.G.; Jackson, Robert A.

    2015-01-15

    Highlights: • The effect of different gas atmospheres on the Eu reduction process was studied. • The Eu reduction was monitored analyzing XANES region at the Eu L{sub III}-edge. • Hydrogen reducing agent are the most appropriate gas for Eu{sup 2+} stabilization. • Only a part of the Eu ions can be stabilized in the divalent state. • A model of Eu reduction process is proposed. - Abstract: The effect of different gas atmospheres such as H{sub 2}(g), synthetic air, carbon monoxide (CO) and nitrogen (N{sub 2}) on the Eu{sup 3+} → Eu{sup 2+} reduction process during the synthesis of Eu-doped BaAl{sub 2}O{sub 4} was studied using synchrotron radiation. The Eu{sup 3+} → Eu{sup 2+} reduction was monitored analyzing XANES region when the sample are excited at the Eu L{sub III}-edge. The results show that the hydrogen reducing agent are the most appropriate gas for Eu{sup 2+} stabilization in BaAl{sub 2}O{sub 4} and that only a part of the Eu ions can be stabilized in the divalent state. A model of Eu reduction process, based on the incorporation of charge compensation defects, is proposed.

  2. Comparison of Ba sub 2 YCu sub 3 O sub 7 minus. delta. films on NdGaO sub 3 and LaAlO sub 3

    SciTech Connect

    Phillips, J.M.; Siegal, M.P.; Perry, C.L.; Marshall, J.H. )

    1991-03-01

    This paper studies the properties of 100 nm films of Ba{sub 2}YCu{sub 3}O{sub 7{minus}{delta}} (BYCO) grown on LaAlO{sub 3}(100) and NdGaO{sub 3}(100) by co- evaporation of Cy, Y, and BaF{sub 2} followed by a two-stage anneal ex situ. The authors find that the structural properties of the films on both substrates are optimized when the maximum temperature of the anneal is 900{degrees} C, while the superconducting properties are slightly better if the maximum temperature does not exceed 875{degrees} C. Films on LaAlO{sub 3} can tolerate a longer time at the maximum annealing temperature than can films on NdGaP{sub 3}. The authors postulate that this is due to a reaction between Ga in the NdGaO{sub 3} and at least one of the constituents of the BYCO film (probably Y).

  3. Ferroelectric, and piezoelectric properties of BaTi{sub 1−x}Al{sub x}O{sub 3}, 0 ≤ x ≤ 0.015

    SciTech Connect

    Ali, Ahmed I.; Hassen, A.; Khang, Nguyen Cao; Kim, Y. S.

    2015-09-15

    Single phase polycrystalline samples of BaTi{sub 1−x}Al{sub x}O{sub 3}, 0 ≤ x ≤ 0.015, have been prepared by a conventional powder processing method. The Rietveld refinements of X- ray powder diffraction patterns at room temperature indicate that the samples crystallize in tetragonal structure with group symmetry P4mm. Because of the oxygen vacancies, the volume of the unit cell increases with increasing x. Field emission scanning electron microscopy revealed that the particle size of pure BTO ceramics was affected by the Al content. Dielectric, ferroelectric and piezoelectric properties of pure BTO as well as Al-doped BTO were studied. It was found that the dielectric permittivity (ε′) increases significantly with increasing x while the transition from ferroelectric phase to a paraelectric phase changes slightly. The Curie-Weiss law is verified over a wide temperature range. Both ferroelectric and piezoelectric properties of BTO are enhanced by the substitution of Ti{sup 4+} by Al{sup 3+} ions. Piezoelectric strains of Al-doped BTO showed a suitable behavior for application compared with that of pure BTO compound. Finally, the results obtained in this work are discussed and compared with those for similar materials.

  4. High-pressure phase relations and thermodynamic properties of CaAl 4Si 2O 11 CAS phase

    NASA Astrophysics Data System (ADS)

    Akaogi, M.; Haraguchi, M.; Yaguchi, M.; Kojitani, H.

    2009-03-01

    Phase relations in CaAl4Si2O11 were examined at 12-23 GPa and 1000-1800 °C by multianvil experiments. A three-phase mixture of grossular, kyanite and corundum is stable below about 13 GPa at 1000-1800 °C. At higher pressure and at temperature below about 1200 °C, a mixture of grossular, stishovite and corundum is stable, indicating the decomposition of kyanite. Above about 1200 °C, CaAl4Si2O11 CAS phase is stable at pressure higher than about 13 GPa. The triple point is placed at 14.7 GPa and 1280 °C. The equilibrium boundary of formation of CAS phase from the mixture of grossular, kyanite and corundum has a small negative slope, and that from the mixture of grossular, stishovite and corundum has a strongly negative slope, while the decomposition boundary of kyanite has a small positive slope. Enthalpies of the transitions were measured by high-temperature drop-solution calorimetry. The enthalpy of formation of CaAl4Si2O11 CAS phase from the mixture of grossular, kyanite and corundum was 139.5 ± 15.6 kJ/mol, and that from the mixture of grossular, stishovite and corundum was 94.2 ± 15.4 kJ/mol. The transition boundaries calculated using the measured enthalpy data were consistent with those determined by the high-pressure experiments. The boundaries in this study are placed about 3 GPa higher in pressure and about 200 °C lower in temperature than those by Zhai and Ito [Zhai, S., Ito, E., 2008. Phase relations of CaAl4Si2O11 at high-pressure and high-temperature with implications for subducted continental crust into the deep mantle. Phys. Earth Planet. Inter. 167, 161-167]. Combining the thermodynamic data measured in this study with those in the literature, dissociation boundary of CAS phase into a mixture of Ca-perovskite, corundum and stishovite and that of grossular into Ca-perovskite plus corundum were calculated to further constrain the stability field of CAS phase. The result suggests that the stability of CAS phase would be limited at the bottom of

  5. Pulsed laser deposition and characterization of highly tunable (1-x)Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 thin films grown on LaNiO3/Si substrate

    NASA Astrophysics Data System (ADS)

    Bhardwaj, Chandan; Daniel, B. S. S.; Kaur, Davinder

    2013-01-01

    The structural and electric properties of Ba(Zr0.2Ti0.8)O3 {BZT}, (Ba0.7Ca0.3)TiO3 {BCT} and 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 {BCZT50} thin films grown on LaNiO3 coated Si(1 0 0) substrate by pulsed laser deposition (PLD) were thoroughly investigated. XRD results revealed relatively higher (1 0 0) preferred orientation and higher crystallinity for BCZT50 film in comparison to BZT and BCT thin films. FESEM showed that the average grain size of BCZT50 thin film is larger than that of BZT and BCT thin films. The optimal composition BCZT50 also exhibited maximum spontaneous polarization (Pm), maximum remanant polarization (Pr), minimum coercive field (Ec), maximum dielectric constant ɛr(0) and maximum tunability (nr). The increase in nr, ɛr(0) and polarization P(E) for BCZT50 thin film is attributed to (1 0 0) preferred orientation, microstructural homogeneity, large grain growth and most importantly to its proximity to the morphotropic phase boundary (MPB) causing very low energy barrier for polarization rotation and lattice distortion. It is also observed that BCZT50 thin film exhibits low leakage current density and good fatigue endurance as compared to BZT and BCT thin films.

  6. The normal state Hall effect in Nd 1-2 xCa xM xBa 2Cu 3O 7- δ (M = Pr, Th): Evidence for hole localization by disorder

    NASA Astrophysics Data System (ADS)

    Ghorbani, S. R.; Andersson, M.; Rapp, Ö.

    2005-08-01

    The transport properties of sintered samples of Nd1-2xCaxMxBa2Cu3O7-δ (M = Pr, Th) with 0 ⩽ x ⩽ 0.10 have been studied in the normal state by Hall effect measurements. The Hall coefficient at high temperature was almost constant for Ca-Pr while it increased with increasing Ca-Th doping concentration. The results for the Hall coefficient as a function of temperature and doping concentration were analyzed within two different models. A good agreement between models and data was obtained. On the basis of these models, it was inferred that Ca-Pr and Ca-Th doping introduce electronic disorder in the CuO2 planes. The localization tendency is driven by electronic disorder. This is the main reason for strong depression of the superconducting critical temperature in both alloys. It was found that the Hall angle is proportional to T2 in the whole measured temperature range in Ca-Pr doped samples while there are deviations at high temperature in the Ca-Th doped series. In a phenomenological narrow band model, the conduction band was asymmetric for the pure sample and this asymmetry decreased with increasing Ca-Th doping while it was almost constant for Ca-Pr doped samples.

  7. The influence of Ca-Mg-Al hydrotalcite synthesized from brine water on thermal and mechanical properties of HTlc-EVA composite

    NASA Astrophysics Data System (ADS)

    Karina, Wiwiek; Heraldy, Eddy; Pramono, Edi; Heriyanto, Astuti, Shanti

    2016-02-01

    Ca-Mg-Al hydrotalcite-like compound (Ca-Mg-Al HTlc) was prepared by co-precipitation method using brine water that is well known as the desalination process waste water. The structure of Ca-Mg-Al HTlc was determined by X-Ray Diffraction (XRD) and Fourier Transform Infrared (FTIR) analysis. Ca-Mg-Al HTlc was studied as a non-halogenated filler in ethylene vinyl acetate (EVA) matrix. Composites with different filler concentrations were prepared to evaluate the influence of Ca-Mg-Al HTlc on thermal and mechanical properties of EVA.The presence of Ca-Mg-Al HTlc in the composite has been confirmed by FTIR analysis. Thermal properties of composites show significant reduction of degradation temperature as well as the loading of HTlc in EVA. However, the total enthalpies combustion of composites with 1% and 5% HTlc loadings higher compared to neat EVA. Further, mechanical properties were determined by tensile test. The result shows that tensile strength and elongation at break of composites decrease relatively by Ca-Mg-Al HTlc addition.

  8. Double-sided Tl{sub 2}Ba{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10} thin films based high temperature superconducting filter operating above 100 K

    SciTech Connect

    Xie, Wei; Wang, Pei; He, Ming Qiao, Ren; Du, Jia-Nan; Gao, Xiao-Xin; Liu, Xin; Zhang, Xu; Ji, Lu; Chen, Hai-Hua; Zhao, Xin-Jie

    2014-09-01

    A high temperature superconducting (HTS) filter on double-sided Tl{sub 2}Ba{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10} (Tl-2223) thin films is designed in this letter. High-quality double-sided Tl-2223 thin films are prepared on 10 × 10 × 0.5 mm{sup 3} LaAlO{sub 3} (001) substrate. The critical temperatures T{sub c} of the films are 120 ± 1 K and the critical current densities J{sub c} are 3–4 MA/cm{sup 2} at 77 K for both sides. X-ray diffraction θ-2θ scans and rotational ϕ-scans prove that the films are strongly textured with the c axis perpendicular to the substrate surface. A 3-pole band-pass filter is then fabricated on the Tl-2223 thin films with 4% relative bandwidth and a center frequency of 4.0 GHz. At 77 K, 100 K, and 102 K, the insertion loss in the passband is 0.088 dB, 0.21 dB, and 0.27 dB, respectively. These performances show that the proposed HTS filter is satisfying even when the operating temperature is above 100 K, which makes it possible to work in outer space without cryogenic systems.

  9. Dependence of acoustic property on Al substitution for Ca3Ta(Ga1‑ x Al x )3Si2O14 single crystals

    NASA Astrophysics Data System (ADS)

    Ohashi, Yuji; Arakawa, Mototaka; Kudo, Tetsuo; Yokota, Yuui; Shoji, Yasuhiro; Kurosawa, Shunsuke; Kamada, Kei; Kushibiki, Jun-ichi; Yoshikawa, Akira

    2016-07-01

    The acoustic properties of Ca3Ta(Ga1‑ x Al x )3Si2O14 (CTGASx) were experimentally studied as a function of the Al substitution content x in the ranges from x = 0 to 0.50. Five specimens, X-, Y-, Z-, 35°Y-, and 140°Y-cut, were prepared from each crystal of CTGASx (x = 0, 0.25, and 0.50) grown by the Czochralski technique. Longitudinal wave and shear wave velocities for CTGASx linearly increase with Al content for all propagation directions. Dielectric constants and density were measured and then elastic and piezoelectric constants were determined from the measured velocities for each crystal. The results revealed that all of the constants change linearly with Al content. From the relationship, the constants for CTAS (x = 1) were estimated. Calculations of the velocities using the determined constants also suggested that the maximum electromechanical coupling factor k 2 for the slow shear wave mode propagating along the rotated Y-axis direction of CTAS was improved to 4.42% compared with 3.83% for CTGS, owing to the Al substitution effect.

  10. Ca,Al-rich inclusions, amoeboid olivine aggregates, and Al-rich chondrules from the unique carbonaceous chondrite Acfer 094: I. mineralogy and petrology

    NASA Astrophysics Data System (ADS)

    Krot, Alexander N.; Fagan, Timothy J.; Keil, Klaus; McKeegan, Kevin D.; Sahijpal, Sandeep; Hutcheon, Ian D.; Petaev, Mikhail I.; Yurimoto, Hisayoshi

    2004-05-01

    Based on their mineralogy and petrography, ˜200 refractory inclusions studied in the unique carbonaceous chondrite, Acfer 094, can be divided into corundum-rich (0.5%), hibonite-rich (1.1%), grossite-rich (8.5%), compact and fluffy Type A (spinel-melilite-rich, 50.3%), pyroxene-anorthite-rich (7.4%), and Type C (pyroxene-anorthite-rich with igneous textures, 1.6%) Ca,Al-rich inclusions (CAIs), pyroxene-hibonite spherules (0.5%), and amoeboid olivine aggregates (AOAs, 30.2%). Melilite in some CAIs is replaced by spinel and Al-diopside and/or by anorthite, whereas spinel-pyroxene assemblages in CAIs and AOAs appear to be replaced by anorthite. Forsterite grains in several AOAs are replaced by low-Ca pyroxene. None of the CAIs or AOAs show evidence for Fe-alkali metasomatic or aqueous alteration. The mineralogy, textures, and bulk chemistry of most Acfer 094 refractory inclusions are consistent with their origin by gas-solid condensation and may reflect continuous interaction with SiO and Mg of the cooling nebula gas. It appears that only a few CAIs experienced subsequent melting. The Al-rich chondrules (ARCs; >10 wt% bulk Al 2O 3) consist of forsteritic olivine and low-Ca pyroxene phenocrysts, pigeonite, augite, anorthitic plagioclase, ± spinel, FeNi-metal, and crystalline mesostasis composed of plagioclase, augite and a silica phase. Most ARCs are spherical and mineralogically uniform, but some are irregular in shape and heterogeneous in mineralogy, with distinct ferromagnesian and aluminous domains. The ferromagnesian domains tend to form chondrule mantles, and are dominated by low-Ca pyroxene and forsteritic olivine, anorthitic mesostasis, and Fe,Ni-metal nodules. The aluminous domains are dominated by anorthite, high-Ca pyroxene and spinel, occasionally with inclusions of perovskite; have no or little FeNi-metal; and tend to form cores of the heterogeneous chondrules. The cores are enriched in bulk Ca and Al, and apparently formed from melting of CAI

  11. Critical current density and irreversibility line of CuBa{sub 2}Ca{sub 3}Cu{sub 4}O{sub y}

    SciTech Connect

    Iyo, A.; Tokumoto, M.; Ihara, H.

    1997-06-01

    The critical current density and irreversibility line of the single-phase polycrystalline sample of CuBa{sub 2}Ca{sub 3}Cu{sub 4}O{sub y} with T{sub c}= 117 K have been estimated from measurements of magnetic hysteresis loops assuming Bean critical state model. Simple power law relations, J{sub c}{proportional_to}H{sup {minus}m}, are observed in the magnetic field dependence of the intragrain J{sub c}. Values of the intragrain J{sub c} in a magnetic field of 1 T are about 10{sup 6} and 10{sup 4} A/cm{sup 2} at temperatures of 5 and 77 K, respectively. An exponential decay of the J{sub c} with increasing temperature, J{sub c}{proportional_to}exp({minus}T/T{sub 0}), is observed below 60 K. The characteristic temperature T{sub 0} of Cu-1234 is T{sub 0}= 16.1 K in a magnetic field of 1.0 T. The dependence of the J{sub c} on temperature is relatively small among the oxide superconductors. Simple power law relations, J{sub c}{proportional_to}(1{minus}T/T{sub c}){sup n}, are found in whole ranges of the temperature and magnetic field. The value of n is 5.24 for a magnetic field of 1.0 T. The irreversibility fields at 70 and 77 K are estimated to be 9.5 and 3.7 T, respectively. The temperature dependence of the H{sub irr} is fitted by H{sub irr}=a(1{minus}T/T{sub c}){sup n} with a=2130 and n=5.91.

  12. On the magnetization relaxation of ring-shaped Tl 2Ba 2CaCu 2O 8 thin films as determined by superconducting quantum interference device measurements

    NASA Astrophysics Data System (ADS)

    Wen, Hai-hu; Ziemann, Paul; Radovan, Henri A.; Herzog, Thomas

    1998-09-01

    By using a superconducting quantum interference device (SQUID), the temporal relaxation of the magnetization was determined for ring-shaped Tl 2Ba 2CaCu 2O 8 thin films at various temperatures between 10 K and 80 K in magnetic fields ranging from 2 mT to 0.3 T. Based on these data, a detailed analysis has been performed related to the following methods or models: (1) Fitting the data to the thermally activated flux motion and collective pinning model; (2) Applying the Generalized Inversion Scheme to extract the temperature dependence of the unrelaxed critical current density jc( T) and pinning potential Uc( T); (3) Testing a modified Maley's method to obtain the current dependent activation energy for flux motion; (4) 2D vortex glass scaling. It is found that, for low fields (2 mT, 10 mT, 40 mT) the experimental data can be described by an elastic flux motion, most probably due to 3D single vortex creep. At higher fields (0.1 T, 0.2 T, 0.3 T), the observed behavior can be interpreted in terms of plastic flux motion which is probably governed by dislocation mediated flux creep. These high field data can also be consistently described by the 2D vortex glass scaling with scaling parameters ν2D, T0 and p being consistent with those derived from corresponding transport measurement. Also, results are presented demonstrating the importance of optimizing the scan length of the sample in a moving sample SQUID magnetometer to avoid artifacts.

  13. The impedance spectroscopic study and dielectric relaxation in A(Ni1/3Ta2/3)O3 [A=Ba, Ca and Sr

    NASA Astrophysics Data System (ADS)

    Hoque, Md M.; Dutta, A.; Kumar, S.; Sinha, T. P.

    2012-09-01

    We present the results of impedance spectroscopic study with its analytical interpretations in the framework of electric modulus formalism for Barium Nickel Tantalate Ba(Ni1/3Ta2/3)O3 (BNT), Calcium Nickel Tantalate Ca(Ni1/3Ta2/3)O3 (CNT) and Strontium Nickel Tantalate Sr(Ni1/3Ta2/3)O3 (SNT) synthesized by the solid-state reaction technique. The results of powder X-ray diffraction study reveal that BNT and SNT crystallize in cubic structure with lattice parameter a=4.07 Å and 3.98 Å respectively, whereas CNT crystallizes in monoclinic structure having lattice parameters, a=5.71 Å, b=13.45 Å and c=5.47 Å with β=118.3°. The logarithmic angular frequency dependence of the real part of complex dielectric permittivity and loss tangent as a function of temperature indicate significant dielectric relaxation in the samples, which have been explained by the Debye theory. The frequency dependence of the loss peak and the imaginary part of electrical modulus are found to obey the Arrhenius law. The relaxation mechanism of these samples is modeled by the Cole-Cole equation. This confirms that the polarization mechanism in BNT, CNT and SNT is due to the bulk effect arising in semiconductive grains. The scaling behavior of imaginary part of electric modulus M″ suggests that the relaxation describes the same mechanism at various temperatures but relaxation frequency is strongly temperature dependent. The normalized peak positions of tan δ/tan δm and M″/M″m versus log ω for BNT, CNT and SNT do not overlap completely and are very close to each other. These indicate the presence of both long-range and localized relaxation. Due to their high dielectric constant and low loss tangent, these materials may find several technological applications such as in capacitors, resonators, filters and integrated circuits.

  14. Unimolecular and hydrolysis channels for the detachment of water from microsolvated alkaline earth dication (Mg2+, Ca2+, Sr2+, Ba2+) clusters

    SciTech Connect

    Miliordos, Evangelos; Xantheas, Sotiris S.

    2014-02-07

    We examine theoretically the three channels that are associated with the detachment of a single water molecule from the aqueous clusters of the alkaline earth dications, [M(H2O)n]2+, M = Mg, Ca, Sr, Ba, n ≤ 6. These are the unimolecular water loss (M2+(H2O)n-1 + H2O) and the two hydrolysis channels resulting to the loss of hydronium ([MOH(H2O)n-2]+ + H3O+) and Zundel ([MOH(H2O)n-3]+ + H3O+(H2O)) cations. The Potential Energy Curves (PECs) corresponding to those three channels were constructed at the Møller-Plesset second order perturbation (MP2) level of theory with basis sets of double- and triple-ζ quality. We furthermore investigated the water and hydronium loss channels from the mono-hydroxide water clusters with up to four water molecules, [MOH(H2O)n]+, 1 ≤ n ≤ 4. Our results indicate the preference of the hydronium loss and possibly the Zundel cation loss channels for the smallest size clusters, whereas the unimolecular water loss channel is preferred for the larger ones as well as the mono-hydroxide clusters. Although the charge separation (hydronium and Zundel cation loss) channels produce more stable products when compared to the ones for the unimolecular water loss, they also require the surmounting of high energy barriers, a fact that makes the experimental observation of fragments related to these hydrolysis channels difficult.

  15. Nonlinear optical properties and glass structure for MO-Nb 2O 5-TeO 2 (M = Zn, Mg, Ca, Sr, Ba) glasses

    NASA Astrophysics Data System (ADS)

    Hayakawa, Tomokatsu; Hayakawa, Masahiko; Nogami, Masayuki; Thomas, Philippe

    2010-01-01

    The third-order nonlinear optical susceptibilities χ(3) of tellurite(TeO 2)-based ternary glasses of MO-Nb 2O 5-TeO 2 (M = Zn, Mg, Ca, Sr, Ba) were investigated by Z-scan measurement using Ti:Sapphire femtosecond laser pulses. The relationship between the nonlinear optical properties and the glass structures estimated by Raman spectroscopy was discussed. The nonlinear susceptibilities χ(3) of these tellurite glasses increased as the stretching Raman band of Te IV-O ax in TeO 4 (trigonal bipyramids (tbp), the roman superscript denotes the coordination number) increased, while the stretching band of Te III-O in TeO 3 (trigonal pyramid (tp)) decreased. This indicates that the amount of TeO 4 (tbp) units was deeply related to the value of χ(3), which was consistent with the theoretical calculation of higher hyperpolarizabilities of TeO 4 than TeO 3 unit. It was also found that higher χ(3) was obtained with decreasing Te IV- eqO ax-Te IV Raman band, indicating that when divalent cations (M 2+) was doped in Nb 2O 5-TeO 2 binary network system the cleavage of Te IV- eqO ax-Te IV chain structure necessarily occurred but the terminations of -Te IV- eqO - M 2+-O-Nb VI-O ax-Te IV-, which importantly stabilized TeO 4 units even in the presence of the network modifier M 2+, were more preferentially induced with an assist of NbO 6 octahedron than -Te IV- eqO - M 2+ O = Te III-O-.

  16. Superconductivity in Zn-doped tetragonal LaBaCaCu{sub 3}O{sub 7{minus}{delta}} systems

    SciTech Connect

    Singh, R.; Lal, R.; Upreti, U.C.; Suri, D.K.; Narlikar, A.V.; Awana, V.P.; Albino Aguiar, J.; Shahabuddin, M.

    1997-01-01

    Resistivity and ac susceptibility of Zn-doped samples of the LaBaCaCu{sub 3}O{sub 7{minus}{delta}} (LBCCO) system have been measured for Zn content of 0.5{percent}, 1.0{percent}, 1.5{percent}, 2.0{percent}, 2.5{percent}, and 3.0{percent} at.wt. X-ray diffraction has been used to find the lattice parameters of the samples. The samples remain tetragonal for all the considered concentrations of Zn. Idometry and thermogravimetric analyses have been done to estimate the oxygen content of different samples. Analyzing the resistivity and ac susceptibility data, the following conclusions are drawn about the role of Zn in the LBCCO samples. (1) The conduction mechanism of electrons appears to follow a crossover from the purely metallic regime to the localization regime due to either weak localization or electron-electron interaction effects after about 1.5{percent} Zn. (2) The superconducting transition as revealed by the resistivity vs temperature curves or susceptibility vs temperature curves becomes sharper with Zn increasing content of Zn up to 1.0{percent}. After 1.5{percent} the resistive and ac susceptibility transitions become broader with increasing Zn. (3) T{sub c} depression up to Zn content of 1.0{percent} seems due to direct suppression of the effective pairing interaction, while at and above 2.5{percent} Zn T{sub c} depression is expected to be due to disorder effects such as reduction of density of states at the Fermi energy. {copyright} {ital 1997} {ital The American Physical Society}

  17. Super Smooth Modification of Al2O3 Ceramic Substrate by High Temperature Glaze of CaO-Al2O3-SiO2 System

    NASA Astrophysics Data System (ADS)

    Zhang, Jihua; Zhen, Shanxue; Yang, Lijun; Lou, Feizhi; Chen, Hongwei; Yang, Chuanren

    2011-01-01

    The rough surface of ceramic substrate is an obstacle for the scale down of line-width for thin film passive integrated devices (PID). In this paper, a modification method for Al2O3 ceramic substrate with super smooth in surface was proposed. Coating a layer of CaO-Al2O3-SiO2 (CAS) glass was performed to flat the rough surface of alumina substrate by sol-gel method. It was found that addition of 0.06% V2O5 can inhibit the recrystallization of the glaze. The root-mean-square (RMS) roughness of the glazed substrates reached a surprising flatness as small as 0.5 nm, and its melting temperature is higher than 1300 °C. This substrate with super flatness and high temperature endurance may be promising for high performance thin film devices.

  18. The Influence of Na2O on the Solidification and Crystallization Behavior of CaO-SiO2-Al2O3-Based Mold Flux

    NASA Astrophysics Data System (ADS)

    Gao, Jinxing; Wen, Guanghua; Sun, Qihao; Tang, Ping; Liu, Qiang

    2015-08-01

    The reaction between [Al] and SiO2 sharply increased the Al2O3 and decreased SiO2 contents in mold flux during the continuous casting of high-Al steels. These changes converted original CaO-SiO2-based flux into CaO-SiO2-Al2O3-based flux, promoting the crystallization and deteriorating the mold lubrication. Therefore, study on the solidification and crystallization behavior of CaO-SiO2-Al2O3-based mold flux, with the applicable fluidizers, is of importance. The effect of Na2O, predominantly used as the fluidizer in mold flux, on the solidification and crystallization behavior of CaO-SiO2-Al2O3-based mold flux needs to be investigated. In this study, a CaO-SiO2-Al2O3-based mold flux containing 6.5 wt pct Li2O was designed; the effect of Na2O on the solidification and crystallization behavior of these mold fluxes was investigated using the single hot thermocouple technique (SHTT) and the double hot thermocouple technique (DHTT). Moreover, the slag film obtained by a heat flux simulator was analyzed using X-ray diffraction (XRD). The results indicate that the solid fraction of molten slag (Fs) and the crystalline fraction of solid slag (Fc) in the mold slag films decrease with increasing Na2O content from 0 to 2 wt pct. However, Fs and Fc increased when the Na2O content increased from 2 to 6 wt pct. The critical cooling rates initially decreases and then increases with increasing Na2O content. The XRD analysis results show that LiAlO2 and CaF2 were the basic crystals for all the mold fluxes. Increasing the Na2O content both inhibits the Ca2Al2SiO7 formation and promotes the production of Ca12Al14O33, indicating that the mold lubrication deteriorated because of the high melting-point phase formation of Ca2Al2SiO7 in the CaO-SiO2-Al2O3-based mold flux containing 6.5 wt pct Li2O, without Na2O. The strong crystallization tendency also deteriorated the mold lubrication for the mold flux with a higher Na2O content. Therefore, the addition of Na2O was less than 2 wt pct in

  19. Crystal characterization and optical spectroscopy of Ti{sup 3+}-doped CaGdAlO{sub 4} crystals

    SciTech Connect

    Kodama, N.; Yamaga, M.

    1998-01-01

    CaGdAlO{sub 4} crystals doped with Ti ions were grown using the Czochralski technique in a reducing atmosphere in order to convert the valence of Ti to trivalence. The fluorescence of the {sup 2}E{r_arrow}{sup 2}T{sub 2} transition of Ti{sup 3+} in the crystals shows a broad band with a peak at 535 nm excited with the light of 410 nm in the optical absorption band at room temperature because of a strong electron-phonon coupling of the {sup 2}E excited state. The Ti{sup 3+} fluorescence is influenced in intensity by O{sup 2{minus}} vacancies at the ligands of the Ti{sup 3+} octahedra along the c axis, which are easily produced in a reducing atmosphere. The x-ray crystal analyses and the polarization of the optical absorption and fluorescence spectra deduce the energy levels and wave functions of the ground and excited states of Ti{sup 3+} in CaGdAlO{sub 4}. The peak energy of the fluorescence band shifts to higher energy as increasing excitation energy in the absorption band. The linear dependence of the fluorescence-peak energy on the excitation energy shows that the fluorescence is inhomogeneously broadened by a random distribution of Ca{sup 2+} and Gd{sup 3+} ions in the disordered lattice.

  20. Thermodynamics and Structure of CaO-Al2O3-3 Mass Pct B2O3 Slag at 1773 K (1500 °C)

    NASA Astrophysics Data System (ADS)

    Shu, Qifeng; Li, Pengfei; Zhang, Xiang; Chou, Kuochih

    2016-08-01

    Activity values of Al2O3 in CaO-Al2O3-B2O3 systems at 1773 K (1500 °C) were determined experimentally using a gas-copper-slag equilibrium technique. The oxygen partial pressure was controlled by C/CO equilibrium. A negative deviation from ideality was found in measured activity of Al2O3. The activity coefficient of Al2O3 decreases with the increase of CaO/Al2O3 ratio. To interpret the variation of Al2O3 activity with composition, structures of CaO-Al2O3-B2O3 glassy slag were investigated by using Raman spectroscopy. It was found that the number of bridging oxygen decreases with increasing CaO/Al2O3 ratio. With increase of CaO content, the aluminate network was gradually depolymerized, which corresponds to the decrease of the activity coefficient of Al2O3.

  1. Fuel mixture approach for solution combustion synthesis of Ca{sub 3}Al{sub 2}O{sub 6} powders

    SciTech Connect

    Ianos, Robert Lazau, Ioan; Pacurariu, Cornelia; Barvinschi, Paul

    2009-07-15

    Single-phase 3CaO.Al{sub 2}O{sub 3} powders were prepared via solution combustion synthesis using a fuel mixture of urea and {beta}-alanine. The concept of using this fuel mixture comes from the individual reactivity of calcium nitrate and aluminum nitrate with respect to urea and {beta}-alanine. It was proved that urea is the optimum fuel for Al(NO{sub 3}){sub 3} whereas {beta}-alanine is the most suitable fuel for Ca(NO{sub 3}){sub 2}. X-ray diffraction and thermal analysis investigations revealed that heating at 300 deg. C the precursor mixture containing the desired metal nitrates, urea and {beta}-alanine triggers a vigorous combustion reaction, which yields single-phase nanocrystalline 3CaO.Al{sub 2}O{sub 3} powder (33.3 nm). In this case additional annealing was no longer required. The use of a single fuel failed to ensure the formation of 3CaO.Al{sub 2}O{sub 3} directly from the combustion reaction. After annealing at 900 deg. C for 1 h, the powders obtained by using a single fuel (urea or {beta}-alanine) developed a phase composition comprising of 3CaO.Al{sub 2}O{sub 3}, 12CaO.7Al{sub 2}O{sub 3} and CaO.

  2. CaMn2Al10: Itinerant Mn magnetism on the verge of magnetic order

    SciTech Connect

    Steinke, L.; Simonson, J. W.; Yin, W. -G.; Smith, G. J.; Kistner-Morris, J. J.; Zellman, S.; Puri, A.; Aronson, M. C.

    2015-07-24

    We report the discovery of CaMn2Al10, a metal with strong magnetic anisotropy and moderate electronic correlations. Magnetization measurements find a Curie-Weiss moment of 0.83μB/Mn, significantly reduced from the Hund's rule value, and the magnetic entropy obtained from specific heat measurements is correspondingly small, only ≈ 9% of Rln2. These results imply that the Mn magnetism is highly itinerant, a conclusion supported by density functional theory calculations that find strong Mn-Al hybridization. Consistent with the layered nature of the crystal structure, the magnetic susceptibility χ is anisotropic below 20 K, with a maximum ratio of χ[010][001] ≈ 3.5. A strong power-law divergence χ(T) ~ T–1.2 below 20 K implies incipient ferromagnetic order, an Arrott plot analysis of the magnetization suggests a vanishing low Curie temperature TC ~ 0. Our experiments indicate that CaMn2Al10 is a rare example of a system where the weak and itinerant Mn-based magnetism is poised on the verge of order.

  3. Enhanced magnetic response in single-phase Bi0.80La0.15A0.05FeO3-δ (A=Ca, Sr, Ba) ceramics

    NASA Astrophysics Data System (ADS)

    Sharma, Poorva; Kumar, Ashwini; Varshney, Dinesh

    2015-10-01

    Single phase Bi0.80La0.15A0.05FeO3-δ (A=Ca, Sr, Ba) dense ceramics were synthesized via solid state reaction method. Structural studies through X-ray diffraction shows that all prepared ceramics crystallized in a rhombohedrally (R 3 barC)distorted BiFeO3 structure with compressive lattice distortion induced by the rare earth (La3+) ion and divalent co-doping at the Bi-site for the Raman study. Scanning electron micrograph of the compounds showed the uniform distribution of grains on the sample surface with high density. A large ferromagnetic hysteresis loop is observed for La/Ba co-doped BiFeO3 as compared with BiFeO3 prepared under similar conditions, with saturation magnetization of 6.85 emu/g and remnant magnetization of 2.72 emu/ g at 300 K. Clear ferromagnetic ground state was observed in Bi0.80La0.15Ba0.05FeO3 and weak ferromagnetism in BLCFO and BLSFO samples. Dielectric constant and dielectric loss were found to decrease with increase in frequency for all the compounds. These improved properties of La/Ba co-doped BFO demonstrate the possibility of enhancing the magnetic applicability and makes very promising for industrial applications such as new devices in information storage.

  4. Conduction phenomenon of Al3+ modified lead free (Na0.5Bi0.5)0.92Ba0.08TiO3 electroceramics

    NASA Astrophysics Data System (ADS)

    Borkar, Hitesh; Kumar, Ashok

    2016-05-01

    Choice of proper dopants at A or B-site of ABO3 perovskite structure can modify the morphotropic phase boundary (MPB), and hence functional properties of polar systems. The chemical nature of donor or acceptor will significantly influence the fundamental properties. Lead-free ferroelectrics have vast potential to replace the lead-based ceramics. The (Na0.5Bi0.5)1-xBaxTiO3 (NBT-BT) (at x=0.08) near MPB with small substitution of trivalent cations (Al3+) has been synthesized by solid state reaction route. The aim to choose the trivalent cations (Al3+) was its relatively smaller radii than that of Bi3+ cations to develop the antipolar phases in the ferroelectric ceramic. Structural, morphological and elemental compositional analyses were studied by X-ray diffraction (XRD), Secondary electron microscope (SEM) and Energy-dispersive X-ray spectroscopy (EDAX), respectively. Ferroelectric studies were carried out on various compositions of (Na0.46Bi0.46-xAlxBa0.08)TiO3 (NBAT-BT) (x=0, 0.05, 0.07, 0.10) electroceramics. It was observed that with increase in concentration of Al the ferroelectricity state changes from soft to hard. Temperature dependent dielectric spectroscopy shows broad dielectric dispersion. The Al doping diminishes the relaxor behavior of NBT-BT ceramics. Impedance spectroscopy shows that electrical resistivity and relaxation frequency decreases with increase in Al-concentration. Modulus spectra indicate that Al significantly change the bulk capacitance of NBT-BT.

  5. Structural and magnetic properties of SiO2-CaO-Na2O-P2O5 containing BaO-Fe2O3 glass-ceramics

    NASA Astrophysics Data System (ADS)

    Leenakul, W.; Kantha, P.; Pisitpipathsin, N.; Rujijanagul, G.; Eitssayeam, S.; Pengpat, K.

    2013-01-01

    The incorporation method was employed to produce bioactive glass-ceramics from the BaFe12O19-SiO2-CaO-Na2O-P2O5 glass system. The ferrimagnetic BaFe12O19 was first prepared using a simple mixed oxide method, where the oxide precursors of 45S5 bioglass were initially mixed and then melted to form glass. The devitrification of Na3Ca6(PO4)5 and Fe3O4 was observed in all of the quenched glass samples. The glass samples were then subjected to a heat treatment schedule for further crystallization. It was found that the small traces of BaFe12O19 phases started to crystallize in high BF content samples of 20 and 40 wt%. These samples also exhibited good magnetic properties comparable to that of other magnetic glass-ceramics. The bioactivity of the BF glass-ceramics improved with increasing BF content as was evident by the formation of bone-like apatite layers on the surface of all of the glass-ceramics after soaking in SBF for 14 days. The results support the use of these bioactive glass-ceramics for hyperthermia treatment within the human body.

  6. Anomalous shifts of oxygen-mode frequencies in La sub 2 minus x Sr sub x CuO sub 4 , YBa sub 2 Cu sub 3 O sub 7 minus. delta. and Tl sub 2 Ba sub 2 Ca sub 1 minus x Gd sub x Cu sub 2 O sub 8

    SciTech Connect

    Mihailovic, D. J. Stefan Institute, Jamova 39, Ljubljana, ); Foster, C.M.; Voss, K.F. ); Mertelj, T.; Poberaj, I. ); Herron, N. )

    1991-07-01

    Comparison of photoinduced local modes (PILM's) of insulating YBa{sub 2}Cu{sub 3}O{sub 6.3} and Tl{sub 2}Ba{sub 2}Ca{sub 1{minus}{ital x}}Gd{sub {ital x}}Cu{sub 2}O{sub 8} with Raman spectra of their metallic counterparts suggests that carrier injection anomalously increases the frequencies of phonons involving {ital z}-axis apex-oxygen motion in both the dilute (insulator) and concentrated (metallic) limit. In La{sub 2}CuO{sub 4}, we observe PILM's whose frequencies suggest a correspondence with the ghost modes'' observed in neutron scattering (Rietschel {ital et} {ital al}., Physica C 162--164, 1705 (1989)). These data, together with Raman data on apex-oxygen anharmonicity, enable us to discuss the vibronic mode couplings involved in polaron formation in the three materials.

  7. Spectroscopic properties of UV active medium Ce3+:LiSr0.8Ca0.2AlF6

    NASA Astrophysics Data System (ADS)

    Nizamutdinov, A. S.; Shavelev, A. A.; Marisov, M. A.; Semashko, V. V.

    2016-02-01

    The aim of this work is phase composition and near UV spectroscopic studies of UV active media in fluoride crystals with colquiriite structure, such as Ce3+:LiSr0.8Ca0.2AlF6. Colquiriite structure mixed crystals show higher segregation coefficient of Ce3+ activator ions than common LiCaAlF6 hosts. An important result is based on the fact that this enhancement was achieved for two types of Ce3+ centers in a multisite Ce:LiSr0.8Ca0.2AlF6 system. Thus, it provides a higher gain coefficient for the 5d-4f transitions of Ce3+ ions and it spans a wider continuous wavelength tuning range between 280 and 320 nm for tunable Ce:LiSr0.8Ca0.2AlF6 laser systems.

  8. Cross sections for He and Ne isotopes in natural Mg, Al, and Si, He isotopes in CaF2, Ar isotopes in natural Ca, and radionuclides in natural Al, Si, Ti, Cr, and stainless steel induced by 12- to 45-MeV protons

    NASA Technical Reports Server (NTRS)

    Walton, J. R.; Heymann, D.; Yaniv, A.; Edgerley, D.; Rowe, M. W.

    1976-01-01

    Stacks of thin Mg, Al, Si, Ca, CaF2, Ti, and stainless steel foils were bombarded in twelve irradiations by a variable energy cyclotron. Cross sections are reported for He and Ne in natural Mg, Al, and Si, and for He in CaF2, and for Ar in natural Ca, as determined from mass spectrometer analysis of the inert gases. In addition, cross sections of Na-22 in natural Al and Si, of V-48 in natural Ti, and of Cr-51, Mn-52, and Co-57 in stainless steel are reported. From these were deduced Cr-51 and Mn-52 cross sections in natural Cr.

  9. New acoustic velocity measurements on CaO-MgO-Al2O3-SiO2 liquids: Reevaluation of the volume and compressibility of CaMgSi2O6-CaAl2Si2O8 liquids to 25 GPa

    NASA Astrophysics Data System (ADS)

    Ai, Yuhui; Lange, Rebecca A.

    2008-04-01

    Relaxed sound speed measurements on 12 liquids in the CaO-MgO-Al2O3-SiO2 (CMAS) system have been performed from 1410 to 1620°C at 1 bar with a frequency sweep acoustic interferometer. In all liquids, the sound speeds either decrease or remain constant with increasing temperature. These data are combined with those in the literature to calibrate models for βT and (∂V/∂P)T as a function of composition and temperature for CMAS liquids. CaO is the only oxide component that contributes to the temperature dependence of compressibility. The new compressibility models permit the bulk modulus (KT,0) of CaMgSi2O6 (Di), CaAl2Si2O8 (An), and the Di64-An36 eutectic liquid to be directly obtained. These results are used to uniquely constrain values for the pressure dependence of the bulk modulus (K0' = dK0/dP) in a third-order Birch-Murnaghan equation of state (EOS) for these three liquids from shock wave data in the literature. The revised K0' value is 6.8 (versus 6.9) for CaMgSi2O6 liquid, 4.7 (versus 5.3) for CaAl2Si2O8 liquid, and 5.6 (versus 4.85) for Di64-An36 liquid. Information on both KT,0 and K0' allows the density and compressibility for each of these three liquids to be calculated as a function of pressure to 25 GPa. Both the molar volume and isothermal compressibility of CaMgSi2O6-CaAl2Si2O8 liquids mix ideally between 0 and 25 GPa. The dominant mechanism of compression at low pressure (0-5 GPa) for all three liquids (CaMgSi2O6, CaAl2Si2O8, and the Di64-An36 eutectic) is topological, whereas gradual Al/Si coordination change plays an increasingly important role at higher pressure as topological mechanisms of compression are diminished.

  10. Efficient Yb³⁺:CaGdAlO₄ bulk and femtosecond-laser-written waveguide lasers.

    PubMed

    Hasse, Kore; Calmano, Thomas; Deppe, Bastian; Liebald, Christoph; Kränkel, Christian

    2015-08-01

    We report on, to the best of our knowledge, the first fs-laser-written waveguide laser in Yb3+:CaGdAlO4 (Yb:CALGO). With Yb:CALGO crystals grown in our labs, we obtained a slope efficiency of 69% and up to 2.4 W of continuous wave (cw) output power in a waveguide-laser configuration. Moreover, bulk laser experiments with Yb:CALGO were performed, and slope efficiencies up to 73%, optical-to-optical efficiencies of 65%, and maximum cw output powers of 3.3 W were reached. These are the highest efficiencies in the laser configuration with Yb:CALGO.

  11. Vibrational spectroscopic characterization of the phosphate mineral kulanite Ba(Fe2+,Mn2+,Mg)2(Al,Fe3+)2(PO4)3(OH)3

    NASA Astrophysics Data System (ADS)

    Frost, Ray L.; López, Andrés; Xi, Yunfei; Granja, Amanda; Scholz, Ricardo

    2013-11-01

    The mineral kulanite BaFe2Al2(PO4)3(OH)3, a barium iron aluminum phosphate, has been studied by using a combination of electron microscopy and vibrational spectroscopy. Scanning electron microscopy with EDX shows the mineral is homogenous with no other phases present. The Raman spectrum is dominated by an intense band at 1022 cm-1 assigned to the PO43-ν1 symmetric stretching mode. Low intensity Raman bands at 1076, 1110, 1146, 1182 cm-1 are attributed to the PO43-ν3 antisymmetric stretching vibrations. The infrared spectrum shows a complex spectral profile with overlapping bands. Multiple phosphate bending vibrations supports the concept of a reduction in symmetry of the phosphate anion. Raman spectrum at 3211, 3513 and 3533 cm-1 are assigned to the stretching vibrations of the OH units. Vibrational spectroscopy enables aspects on the molecular structure of kulanite to be assessed.

  12. Synthesis of a novel green fluorescent material Ca3Al2O6:Tb3+ based on a layered double hydroxide precursor

    NASA Astrophysics Data System (ADS)

    Gao, Xiaorui; Jiang, Kangle; Hao, Yongjing; Chang, Tao; Yin, Yaobing

    2015-08-01

    A novel green light emitting material, Ca3Al2O6:Tb3+ was synthesized by calcination of a terbium doped Ca/Al layered double hydroxide precursor at 1350°C. The precursor was prepared by coprecipitation from metal nitrates with sodium hydroxide. The material shows characteristic green emission at 543 nm when excited with 266 nm UV source. The photoluminescence intensity reaches its maximum at Tb3+ concentration of 0.5 mol %.

  13. Syntheses and luminescent properties of CaAl2Si2O8:Eu2+, Mn2+ phosphors for white LED

    NASA Astrophysics Data System (ADS)

    Kwon, Sook Hyun; Moon, Byung Kee; Choi, Byung Chun; Jeong, Jung Hyun; Kim, Jung Hwan

    2016-01-01

    Aluminosilicate-based luminescent materials, a series of CaAl2Si2O8:Eu2+ samples were prepared by using a solid-state reaction method. The X-ray diffraction patterns of the samples confirmed their triclinic structure after annealing at 1100 °C. The excitation spectra of CaAl2Si2O8:Eu2+ exhibited a broad band ranging between 220 to 420 nm with a point peak at a longer wavelength. Moreover, a shift in the broad band was also recorded with increasing Eu2+ concentration. The emission spectrum of CaAl2Si2O8:Eu2+ consists of a broad band from 390 to 550 nm with a maximum intensity at about 438 nm, which can be ascribed to the electric-dipole-allowed 4f65d1-8S7/2(4f7) transition of the Eu2+ ions. A series of Eu2+ and Mn2+ co-activated CaAl2Si2O8 samples were synthesized at 1400 °C. The CaAl2Si2O8:Eu2+, Mn2+ samples had a wide emission band ranging from blue to yellow and peaking at 438 and 550 nm under an excitation wavelength of 352 nm. The PL spectrum of the CaAl2Si2O8:Eu2+, Mn2+ samples reveal an effective energy transfer from Eu2+ to Mn2+ in CaAl2Si2O8. By utilizing the principle of energy transfer, we also demonstrated that with appropriate tuning of the activator content, CaAl2Si2O8:Eu2+, Mn2+ phosphors exhibit great potential as a phosphor for white-light-emitting diodes.

  14. Substitution effects of barium and calcium on magnetic properties of AxSr1-x(Fe0.5Ru0.5)O3 double perovskites (x =0.05, A =Ba,Ca)

    NASA Astrophysics Data System (ADS)

    Nomura, K.; Zboril, R.; Tucek, J.; Kosaka, W.; Ohkoshi, S.; Felner, I.

    2007-07-01

    AxSr1-x(Fe0.5Ru0.5)O3 double perovskites (x =0.05 and A =Ba,Ca) were prepared by a sol-gel method and an effect of the cation substitution at the A site of the crystal structure of SrFe0.5Ru0.5O3 on their magnetic properties was monitored by x-ray diffraction (XRD), magnetic measurements, transmission electron microscopy (TEM), scanning electron microscopy (SEM), and temperature-dependent and in-field Fe57 Mössbauer spectroscopy. Both Ca- and Ba-substituted samples reveal the orthorhombic structure similar to the undoped perovskite; however, the cell volume changes with the substituting ion radius. TEM and SEM micrographs manifest agglomerated nanocrystalline samples with particle sizes of about 20-60, 15-50, and 40-70nm for the undoped, Ba-doped, and Ca-doped perovskites, respectively. Generally, the magnetic regime of both substituted and undoped perovskites can be described by a spin-glass behavior caused by a spin frustration. Among other factors, this is manifested by a nonsaturation of the hysteresis loops even at a high field of 50kOe, by a low-temperature divergence of the zero-field-cooled and field-cooled magnetization curves, and by a cusp in the zero-field-cooled magnetization curve. The low-temperature spin-glass state is also supported by the in-field Mössbauer spectra, recorded on these systems. The isomer shift parameters, extracted from the Mössbauer spectra, confirm a high-spin iron(III) state with S =5/2. In contrast to the undoped and Ba-doped samples, the narrower distribution of the hyperfine magnetic fields, observed in the Ca-doped perovskite can be ascribed to the larger particles. Compared to the undoped sample, the field of maximum probability is higher in the Ca-substituted perovskite while it is reduced in the Ba-doped sample because of the effects of the chemical compression and expansion, respectively. In addition, the Ca-doped sample exhibits more negative Weiss temperature (Θ=-105K) than that found for the Ba

  15. An analysis of temperature-dependent absorption and photocurrent spectra in BaAl{sub 2}Se{sub 4} layers

    SciTech Connect

    Hong, K. J.; Jeong, T. S.; Youn, C. J.; Moon, J. D.

    2015-04-28

    The temperature-dependent photoresponse behavior of BaAl{sub 2}Se{sub 4} layers has been investigated through the analysis of optical absorption and photocurrent (PC) spectra. Based on these results, the optical band gap was well expressed by E{sub g}(T) = E{sub g}(0) − 4.39 × 10{sup −4}T{sup 2}/(T + 250), where E{sub g}(0) is estimated to be 3.4205, 3.6234, and 3.8388 eV for the transitions corresponding to the valence band states Γ{sub 3}(A), Γ{sub 4}(B), and Γ{sub 5}(C), respectively. From the PC measurement, three peaks A, B, and C corresponded with the intrinsic transitions from the valence band states of Γ{sub 3}(A), Γ{sub 4}(B), and Γ{sub 5}(C) to the conduction band state of Γ{sub 1}, respectively. According to the selection rule, the crystal field and spin orbit splitting were found to be 0.2029 and 0.2154 eV, respectively, through the direct use of PC spectroscopy. However, the PC intensities decreased with lowering temperature. In the log J{sub ph} versus 1/T plot, the dominant trap level at the high-temperature region was observed and its value was 12.7 meV. This level corresponds to the activation energy for the electronic transition from the shallow donor levels to the edge of the conduction band. It is estimated that the decrease in the PC intensity is caused by trapping centers related to native defects in the BaAl{sub 2}Se{sub 4} layers. Consequently, this trap level limited the PC intensity with decreasing temperature.

  16. Structural, electrical, and magnetic properties of Ba0.9Ca0.1Ti0.97Fe0.03O3 and the effect of oxygen vacancies

    NASA Astrophysics Data System (ADS)

    Chakraborty, Tanushree; Meneghini, Carlo; Aquilanti, Giuliana; Ray, Sugata

    2013-12-01

    Detailed experimental studies have been carried out on a new possible dilute magnetic insulator Ba0.9Ca0.1Ti0.97Fe0.03O3-δ and its oxygen deficient counterpart. Both the samples stabilize in overall tetragonal BaTiO3 structure at room temperature as indicated by x-ray diffraction and do exhibit room temperature magnetic order with obvious dependencies on δ. Apart from this, the as-grown sample also retains ferroelectricity at room temperature, which could potentially open up a possibility of achieving multifunctionality at room temperature. However, even though the magnetism is positively influenced by oxygen vacancies, the microscopic phase and ferroelectricity get adversely affected. Finally, using local structural probes, existence of diffused phases has been found, which successfully explains all the observed physical properties.

  17. Structurally modulated magnetic properties in the A(3)MnRu(2)O(9) phases (A = Ba, Ca): the role of metal-metal bonding in perovskite-related oxides.

    PubMed

    Gönen, Z S; Gopalakrishnan, J; Eichhorn, B W; Greene, R L

    2001-09-10

    Ca(3)MnRu(2)O(9) and Ba(3)MnRu(2)O(9) were synthesized from transition metal dioxides and alkaline earth metal carbonates at 1100-1300 degrees C. Ca(3)MnRu(2)O(9) adopts the prototypical GdFeO(3)-type perovskite structure with Mn and Ru statistically disordered over the single metal atom site. The susceptibility shows Curie-Weiss behavior above 240 K with mu(eff) = 3.14 micro(B)/metal atom, which is in excellent agreement with the expected spin-only moment of 3.20 micro(B). Below 150 K, the compound shows spin-glass-like short-range ferrimagnetic correlations. The high-temperature region of the electrical resistivity reveals a small activation energy of 17(1) meV whereas the low-temperature region is nonlinear and does not fit a variable range hopping model. Ba(3)MnRu(2)O(9) crystallizes in the 9-layer BaRuO(3)-type structure containing M(3)O(12) face-shared trioctahedral clusters in which Mn and Ru are statistically disordered. Ba(3)MnRu(2)O(9) shows nonlinear reciprocal susceptibility at all temperatures and is described by a variable-spin cluster model with an S = (1)/(2) ground state with thermally populated excited states. The low spin value of this system (S = (1)/(2)) is attributed to direct metal-metal bonding. Below 30 K, the compound shows short-range magnetic correlations and spin-glass-like behavior. The high-temperature region of the electrical resistivity indicates a small activation energy of 8.8(1) meV whereas the low-temperature region is nonlinear. The importance of metal-metal bonding and the relationships to other related compounds are discussed.

  18. The atomic structure of lead-free Ba(Zr{sub 0.2}Ti{sub 0.8})O{sub 3}-(Ba{sub 0.7}Ca{sub 0.3})TiO{sub 3} by using neutron total scattering analysis

    SciTech Connect

    Jeong, I.-K.; Ahn, J. S.

    2012-12-10

    We conducted neutron total scattering measurements on lead-free Ba(Zr{sub 0.2}Ti{sub 0.8})O{sub 3}-0.5(Ba{sub 0.7}Ca{sub 0.3})TiO{sub 3} (BZT-0.5BCT) ceramic at 300 K and 150 K, and studied both long-range and local structures near the morphotropic phase boundary. Despite the long-range phase transition from tetragonal to rhombohedral structures, we found that local atomic structure of BZT-0.5BCT barely changes between 300 K and 150 K. To incorporate both long-range and local structures in a consistent way, we performed reverse Monte Carlo modeling. In BZT-0.5BCT, we found that the Ca substitution on Ba sites causes little impact on the local displacement of Ti ion but enhances octahedral tilting of ZrO{sub 6}, resulting in nonuniform lattice distortion.

  19. The Jahn-Teller effect in the excitation and emission spectra of Ba/sub 6/Y/sub 2/Al/sub 4/O/sub 15/:Sn/sup 2+/ and Ba/sub 2/YAlO/sub 5/:Sn/sup 2+/

    SciTech Connect

    Smets, B.M.J.; Verlijsdonk, J.G.; Rutten, J. )

    1989-04-01

    Luminescence measurements are presented for Sn/sup 2+/ doped Ba/sub 6/Y/sub 2/Al/sub 4/O/sub 15/ and Ba/sub 2/YAlO/sub 5/. In these compounds several crystallographic sites are available for Sn/sup 2+/. The luminescence properties of Sn/sup 2+/ in one of these sites can be accounted for by assuming that the Jahn-Teller effect is acting on the /sup 3/P/sub 1/ excited state of the Sn/sup 2+/ ion. The vibronic interaction results in the occurrence of two emission bands in the case of Ba/sub 6/Y/sub 2/Al/sub 4/O/sub 15/:Sn/sup 2+/.

  20. Crustal structure of the Pannonian Basin: The AlCaPa and Tisza Terrains and the Mid-Hungarian Zone

    NASA Astrophysics Data System (ADS)

    Hetényi, György; Ren, Yong; Dando, Ben; Stuart, Graham W.; Hegedűs, Endre; Kovács, Attila Csaba; Houseman, Gregory A.

    2015-04-01

    The Pannonian Basin of Central Europe is one of the key examples of Miocene continental extension that is easily accessible to surface seismological investigation. It comprises two major crustal blocks: AlCaPa and Tisza which abut along a poorly understood structure referred to as the Mid-Hungarian Zone (MHZ), the whole being surrounded by the arc of the Carpathian Mountains, the Alps and the Dinarides. Using data from the CBP (Carpathian Basins Project) temporary broadband seismic array of 46 stations deployed across the western Pannonian Basin in 2006-2007, we calculated receiver functions that constrain the variation of crustal thickness across the basin and derive a map of Moho depth across a NW-SE oriented swath about 450 km long and 75 km wide. The measured Moho depths show no significant change in crustal thickness between AlCaPa and Tisza terrains, but the Moho is not or very weakly imaged along a ca. 40 km wide strip centred on the MHZ. Moho depths within the Pannonian Basin are typically in the range 25-30 km, and increase toward the periphery of the basin. Our measurements are generally consistent with earlier VP models from controlled-source seismic surveys and recent VS models determined by tomographic analysis of ambient noise signals. The lack of a sharp Moho image beneath the MHZ suggests that the crust-mantle boundary in that zone may consist of a gradual increase in velocity with depth. The relatively constant crustal thickness across the two domains of the Pannonian Basin suggests that thinning to the same final state is controlled thermally. This structural characteristic seems to be governed by a large-scale balance of gravitational potential energy that is insensitive to the separate prior histories of the two regions.

  1. Phase transitions and the piezoelectricity around morphotropic phase boundary in Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 lead-free solid solution

    NASA Astrophysics Data System (ADS)

    Zhang, Le; Zhang, Ming; Wang, Liang; Zhou, Chao; Zhang, Zhen; Yao, Yonggang; Zhang, Lixue; Xue, Dezhen; Lou, Xiaojie; Ren, Xiaobing

    2014-10-01

    In this paper, two displacive phase transitions around the morphotropic phase boundary (MPB) in Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 (BZT-xBCT) ceramics were detected by inspecting two anomalies of the Raman Ti4+-O2- longitudinal optical mode (˜725 cm-1). Further, permittivity and X-ray diffraction results demonstrated these two phase transitions originate from tetragonal (T) to rhombohedral (R) through an intermediate orthorhombic (O) phase. Importantly, we found that the maximum piezoelectric response (d33 = 545pC/N) was achieved at the boundary between the T and O phase, indicating that the giant piezoelectricity of BZT-xBCT may mainly stem from the T-O phase boundary due to easier polarization rotation and larger lattice softening.

  2. In-situ observation of nanomechanical behavior arising from critical-temperature-induced phase transformation in Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 thin film

    NASA Astrophysics Data System (ADS)

    Wang, Z. M.; Cai, Zh. L.; Zhao, K.; Guo, X. L.; Chen, J.; Sun, W.; Cheng, Zh. X.; Kimura, H.; Li, B. W.; Yuan, G. L.; Yin, J.; Liu, Zh. G.

    2013-08-01

    In this Letter, we use the nanoindentation technique and vary the testing temperature to above and below critical values to study the nanomechanical features of a strong Pb-free piezoelectric Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 (BZT-0.5BCT) thin film across its piezoelectric-optimal morphotropic phase boundary. The mechanisms responsible for the Young's modulus and hardness evolution are then discussed. An X-ray diffraction method that can detect the d(110) variation associated with the change in the inclination angle ψ of the (110) plane was developed to quantify the residual stress in the BZT-0.5BCT films.

  3. Dielectric relaxor behaviors and tunability of (1- x)Ba(Zr0.2Ti0.8)O3- x(Ba0.7Ca0.3)TiO3 thin films fabricated by sol-gel method

    NASA Astrophysics Data System (ADS)

    Lin, Yanting; Qin, Ni; Wu, Guangheng; Sa, Tongliang; Bao, Dinghua

    2012-11-01

    Temperature dependence of dielectric properties of (1- x)Ba(Zr0.2Ti0.8)O3- x(Ba0.7Ca0.3)TiO3 ( x=0.15, 0.30, and 0.50) (BZT- xBCT) thin films prepared by a sol-gel method has been investigated. The results show that there is a broad dielectric maximum near T m and the diffuse parameter γ is close to 2, indicating a nearly complete diffuse phase transition in BZT- xBCT thin films. The dielectric relaxor behaviors of the thin films well follow Vogel-Fulcher relation. The thin films show a high dielectric tunability up to 65 %, with a small variation in the temperature range from 248.15 to 373.15 K. This study indicates that the thin films, especially for x=0.50, are promising candidates for tunable device applications with good temperature stability.

  4. Symmetry determination on Pb-free piezoceramic 0.5Ba(Zr0.2Ti0.8)O3-0.5(Ba0.7Ca0.3)TiO3 using convergent beam electron diffraction method

    NASA Astrophysics Data System (ADS)

    Gao, Jinghui; Zhang, Lixue; Xue, Dezhen; Kimoto, Takayoshi; Song, Minghui; Zhong, Lisheng; Ren, Xiaobing

    2014-02-01

    (1-x)(Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 (BZT-xBCT) Pb-free piezoceramic has been reported showing ultrahigh piezoelectric performance in its morphotropic phase boundary (MPB) region. However, the crystal structure characteristic for the MPB composition of BZT-xBCT is still under debate—between single orthorhombic phase and tetragonal + rhombohedral two phase mixture. In the present study, we perform the local symmetry determination on the MPB composition x = 0.5 using convergent beam electron diffraction analysis (CBED). Our CBED results from multiple zone axes suggest that there are two coexisting phases with the point group symmetries of 4 mm (tetragonal) and 3 m (rhombohedral) respectively, which agree with two phase mixture model. The strong piezoelectricity can thus be understood by considering the polarization rotation between tetragonal and rhombohedral phases by external field.

  5. Local texture and strongly linked conduction in spray-pyrolyzed TlBa{sub 2}Ca{sub 2}Cu{sub 3}O{sub 8+x} deposits

    SciTech Connect

    Kroeger, D.M.; Goyal, A.; Specht, E.D.; Wang, Z.L.; Tkaczyk, J.E.; Sutliff, J.A.; Deluca, J.A.

    1993-12-31

    Local texture in polycrystalline TlBa{sub 2}Ca{sub 2}Cu{sub 3}O{sub 8+x} deposits has been determined from transmission electron microscopy, electron backscatter diffraction patterns and x-ray diffraction. The small-grained deposits had excellent c-axis alignment and contained colonies of grains with similar but not identical a-axis orientations. Most grain boundaries within a colony have small misorientation angles and should not be weak links. It is proposed that long range conduction utilizes a percolative network of small angle grain boundaries at colony intersections.

  6. Synthesis and structural investigation of the compounds containing HF 2- anions: Ca(HF 2) 2, Ba 4F 4(HF 2)(PF 6) 3 and Pb 2F 2(HF 2)(PF 6)

    NASA Astrophysics Data System (ADS)

    Bunič, Tina; Tramšek, Melita; Goreshnik, Evgeny; Žemva, Boris

    2008-09-01

    Three new compounds Ca(HF 2) 2, Ba 4F 4(HF 2)(PF 6) 3 and Pb 2F 2(HF 2)(PF 6) were obtained in the system metal(II) fluoride and anhydrous HF (aHF) acidified with excessive PF 5. The obtained polymeric solids are slightly soluble in aHF and they crystallize out of their aHF solutions. Ca(HF 2) 2 was prepared by simply dissolving CaF 2 in a neutral aHF. It represents the second known compound with homoleptic HF environment of the central atom besides Ba(H 3F 4) 2. The compounds Ba 4F 4(HF 2)(PF 6) 3 and Pb 2F 2(HF 2)(PF 6) represent two additional examples of the formation of a polymeric zigzag ladder or ribbon composed of metal cation and fluoride anion (MF +) n besides PbF(AsF 6), the first isolated compound with such zigzag ladder. The obtained new compounds were characterized by X-ray single crystal diffraction method and partly by Raman spectroscopy. Ba 4F 4(HF 2)(PF 6) 3 crystallizes in a triclinic space group P1¯ with a=4.5870(2) Å, b=8.8327(3) Å, c=11.2489(3) Å, α=67.758(9)°, β=84.722(12), γ=78.283(12)°, V=413.00(3) Å 3 at 200 K, Z=1 and R=0.0588. Pb 2F 2(HF 2)(PF 6) at 200 K: space group P1¯, a=4.5722(19) Å, b=4.763(2) Å, c=8.818(4) Å, α=86.967(10)°, β=76.774(10)°, γ=83.230(12)°, V=185.55(14) Å 3, Z=1 and R=0.0937. Pb 2F 2(HF 2)(PF 6) at 293 K: space group P1¯, a=4.586(2) Å, b=4.781(3) Å, c=8.831(5) Å, α=87.106(13)°, β=76.830(13)°, γ=83.531(11)°, V=187.27(18) Å 3, Z=1 and R=0.072. Ca(HF 2) 2 crystallizes in an orthorhombic Fddd space group with a=5.5709(6) Å, b=10.1111(9) Å, c=10.5945(10) Å, V=596.77(10) Å 3 at 200 K, Z=8 and R=0.028.

  7. Host lattice materials in the system Ca3N2-AlN-Si3N4 for white light emitting diode

    NASA Astrophysics Data System (ADS)

    Uheda, K.; Hirosaki, N.; Yamamoto, H.

    2006-09-01

    New host lattice materials whose red phosphors for white LEDs have been investigated in the ternary system Ca3N2-AlN-Si3N4, just as Ca2Si5N8 and CaSiN2:Eu were found in the binary system Ca3N2-Si3N4. A new red phosphor of CaAlSiN3:Eu which is effectively excited by blue-GaN and near UV-GaInN LED chips has been synthesized at 1600 °C for 2 h and subsequently at 1800 °C for 2 h under nitrogen pressure of 1 MPa. The host-compound has an orthorhombic structure with the space group Cmc21 (No. 36), which is isotypic with LiSi2N3 and NaSi2N3. The red phosphor showed the emission peak around 650 nm which was assinged to 5d 4f of Eu2+ ion, and its color coordinates were estimated to be 0.667 and 0.327. The optimum concentration of Eu2+ ion was 1.6 mol%. The phosphor also had a high chemical stability, high quantum output, and especially a good thermal property compared to the other phosphors, Ca2Si5N8:Eu2+ and CaSiN2:Eu2+. CaAlSiN3:Eu2+ maintained 83% of the initial efficiency above 150 °C.

  8. Vitality and chemistry of roots of red spruce in forest floors of stands with a gradient of soil Al/Ca ratios in the northeastern United States

    USGS Publications Warehouse

    Wargo, P.M.; Vogt, K.; Vogt, D.; Holifield, Q.; Tilley, J.; Lawrence, G.; David, M.

    2003-01-01

    Number of living root tips per branch, percent dead roots, percent mycorrhizae and mycorrhizal morphotype, response of woody roots to wounding and colonization by fungi, and concentrations of starch, soluble sugars, phenols, percent C and N and C/N ratio, and Al Ca, Fe, K, Mg, Mn, and P were measured for 2 consecutive years in roots of red spruce (Picea rubens Sarg.) in stands in the northeastern United States (nine in 1993 and two additional in 1994) dominated by red spruce and with a gradient of forest floor exchangeable Al/Ca ratios. Root vitality was measured for nonwoody and coarse woody roots; chemical variables were measured for nonwoody (<1 mm), fine woody (1 to <2 mm), and coarse woody (2 to <5 mm) roots. There were significant differences among sites for all variables, particularly in 1993, although few were related to the Al/Ca ratio gradient. Percent mycorrhizae decreased, while some morphotypes increased or decreased as the Al/Ca ratio increased. In nonwoody roots, N increased as the Al/Ca ratio increased. Most sampled trees appeared to be in good or fair health, suggesting that an adverse response of these root variables to high Al concentrations may be apparent only after a significant change in crown health.

  9. Mechanical Properties and Fracture Behaviors of the As-Extruded Mg-5Al-3Ca Alloys Containing Yttrium at Elevated Temperature.

    PubMed

    Son, Hyeon-Taek; Kim, Yong-Ho; Kim, Taek-Soo; Lee, Seong-Hee

    2016-02-01

    Effects of yttrium (Y) addition on mechanical properties and fracture behaviors of the as-extruded Mg-Al-Ca based alloys at elevated temperature were investigated by a tensile test. After hot extrusion, the average grain size was refined by Y addition and eutectic phases were broken down into fine particles. Y addition to Mg-5Al-3Ca based alloy resulted in the improvement of strength and ductility at elevated temperature due to fine grain and suppression of grain growth by formation of thermally stable Al2Y intermetallic compound.

  10. Mechanical Properties and Fracture Behaviors of the As-Extruded Mg-5Al-3Ca Alloys Containing Yttrium at Elevated Temperature.

    PubMed

    Son, Hyeon-Taek; Kim, Yong-Ho; Kim, Taek-Soo; Lee, Seong-Hee

    2016-02-01

    Effects of yttrium (Y) addition on mechanical properties and fracture behaviors of the as-extruded Mg-Al-Ca based alloys at elevated temperature were investigated by a tensile test. After hot extrusion, the average grain size was refined by Y addition and eutectic phases were broken down into fine particles. Y addition to Mg-5Al-3Ca based alloy resulted in the improvement of strength and ductility at elevated temperature due to fine grain and suppression of grain growth by formation of thermally stable Al2Y intermetallic compound. PMID:27433675

  11. Thermodynamics of Complex Sulfide Inclusion Formation in Ca-Treated Al-Killed Structural Steel

    NASA Astrophysics Data System (ADS)

    Guo, Yin-tao; He, Sheng-ping; Chen, Gu-jun; Wang, Qian

    2016-08-01

    Controlling the morphology of the sulfide inclusion is of vital importance in enhancing the properties of structural steel. Long strip-shaped sulfides in hot-rolled steel can spherize when, instead of the inclusion of pure single-phase MnS, the guest is a complex sulfide, such as an oxide-sulfide duplex and a solid-solution sulfide particle. In this study, the inclusions in a commercial rolled structural steel were investigated. Spherical and elongated oxide-sulfide duplex as well as single-phase (Mn,Ca)S solid solution inclusions were observed in the steel. A thermodynamic equilibrium between the oxide and sulfide inclusions was proposed to understand the oxide-sulfide duplex inclusion formation. Based on the equilibrium solidification principle, thermodynamic discussions on inclusion precipitation during the solidification process were performed for both general and resulfurized structural steel. The predicted results of the present study agreed well with the experimental ones.

  12. Synthesis and characterization of phosphates in molten systems Cs 2O-P 2O 5-CaO- MIII2O 3 ( MIII—Al, Fe, Cr)

    NASA Astrophysics Data System (ADS)

    Zatovsky, Igor V.; Strutynska, Nataliya Yu.; Baumer, Vyacheslav N.; Slobodyanik, Nikolay S.; Ogorodnyk, Ivan V.; Shishkin, Oleg V.

    2011-03-01

    The crystallization of complex phosphates from the melts of Cs 2O-P 2O 5-CaO- MIII2O 3 ( MIII—Al, Fe, Cr) systems have been investigated at fixed value Cs/P molar ratios equal to 0.7, 1.0 and 1.3 and Са/Р=0.2 and Ca/ МIII=1. The fields of crystallization of CsCaP 3O 9, β-Ca 2P 2O 7, Cs 2CaP 2O 7, Cs 3CaFe(P 2O 7) 2, Ca 9MIII(PO 4) 7 ( MIII—Fe, Cr), Cs 0.63Ca 9.63Fe 0.37(PO 4) 7 and CsCa 10(PO 4) 7 were determined. Obtained phosphates were investigated using powder X-ray diffraction and FTIR spectroscopy. Novel whitlockite-related phases CsCa 10(PO 4) 7 and Cs 0.63Ca 9.63Fe 0.37(PO 4) 7 have been characterized by single crystal X-ray diffraction: space group R3c, a=10.5536(5) and 10.5221(4) Å, с=37.2283(19) and 37.2405(17) Å, respectively.

  13. High-pressure structural configuration and phase transition in celsian, BaAl2Si2O8

    NASA Astrophysics Data System (ADS)

    Curetti, Nadia; Benna, Piera; Bruno, Emiliano

    2016-10-01

    In situ high-pressure X-ray diffraction study was performed on celsian (Cls97Or3) from Jakobsberg, Sweden. A single crystal of celsian was loaded in an ETH-type diamond anvil cell, and unit-cell parameters were measured at 20 different pressures up to 6.0 GPa at room T. The evolution of the unit-cell parameters and volume as a function of pressure shows a discontinuity at P ~ 5.7 GPa indicating a displacive first-order phase transition. The P-V data were fitted by a second-order Birch-Murnaghan EoS only up to 2.55 GPa, because at higher pressures a slight change in the compressional behavior of the unit-cell volume is observed, indicating a pre-transition volume softening. The resulting EoS coefficients are V 0 = 1461.4(1) Å3 and K T0 = 88.1(6) GPa. A second crystal of celsian was loaded in the DAC cell, and single-crystal in situ HP X-ray diffraction was performed at P = 0.0001, 2.1, 4.2, 5.5, 5.9, 6.5 and 7.8 GPa. The data collections between 0 and 5.5 GPa show only a- and b-type reflections confirming the I2/c space group. The appearance of c and d-type reflections at 5.9, 6.5 and 7.8 GPa, the analysis of the systematic absence and the structural refinements define the HP phase transition as an I2/c-P21/c transition. The most significant changes with compression in celsian are the deformation in the Ba polyhedra and the variation in the T-O-T angles.

  14. Aluminum resistance in wheat involves maintenance of leaf Ca(2+) and Mg(2+) content, decreased lipid peroxidation and Al accumulation, and low photosystem II excitation pressure.

    PubMed

    Moustaka, Julietta; Ouzounidou, Georgia; Bayçu, Gülriz; Moustakas, Michael

    2016-08-01

    The phytotoxic aluminum species (Al(3+)) is considered as the primary factor limiting crop productivity in over 40 % of world's arable land that is acidic. We evaluated the responses of two wheat cultivars (Triticum aestivum L.) with differential Al resistance, cv. Yecora E (Al-resistant) and cv. Dio (Al-sensitive), exposed to 0, 37, 74 and 148 μM Al for 14 days in hydroponic culture at pH 4.5. With increasing Al concentration, leaf Ca(2+) and Mg(2+) content decreased, as well as the effective quantum yield of photosystem II (PSII) photochemistry (Φ PSII ), while a gradual increase in leaf membrane lipid peroxidation, Al accumulation, photoinhibition (estimated as F v /F m ), and PSII excitation pressure (1 - q p ) occurred. However, the Al-resistant cultivar with lower Al accumulation, retained larger concentrations of Ca(2+) and Mg(2+) in the leaves and kept a larger fraction of the PSII reaction centres (RCs) in an open configuration, i.e. a higher ratio of oxidized to reduced quinone A (QA), than plants of the Al-sensitive cultivar. Four times higher Al concentration in the nutrient solution was required for Al-resistant plants (148 μM Al) than for Al-sensitive (37 μM Al), in order to establish the same closed RCs. Yet, the decline in photosynthetic efficiency in the cultivar Dio was not only due to closure of PSII RCs but also to a decrease in the quantum yield of the open RCs. We suggest that Al(3+) toxicity may be mediated by nutrient deficiency and oxidative stress, and that Al-resistance of the wheat cultivar Yecora E, may be due at least partially, from the decreased Al accumulation that resulted to decreased reactive oxygen species (ROS) formation. However, under equal internal Al accumulation (exposure Al concentration: Dio 74 μM, Yecora E 148 μM) that resulted to the same oxidative stress, the reduced PSII excitation pressure and the better PSII functioning of the Al-resistant cultivar was probably due to the larger concentrations of Ca

  15. Chemical stabilization and high pressure synthesis of Ba-free Hg-based superconductors, (Hg,M)Sr2Ca(n-1)Cu(n)O(y)(n=1 to approximately 3)

    NASA Technical Reports Server (NTRS)

    Kishio, K.; Shimoyama, J.; Hahakura, S.; Kitazawa, K.; Yamaura, K.; Hiroi, Z.; Takano, M.

    1995-01-01

    A homologous series of new Hg-based HTSC compounds, (Hg,M)Sr2Ca(n - 1)Cu(n)P(y) with n = 1 to 3, have been synthesized. The stabilization of the pure phases have been accomplished by chemical doping of third elements such as M = Cr, Mo and Re. While the Hgl2O1(n = 1) phase was readily obtained in this way, it was necessary to simultaneously dope Y into the Ca site to stabilize the Hg1212(n = 2) phase. On the other hand, single-phase Y-free Hg1212(n = 2) and Hg1223 (n = 3) samples were synthesized only under a high pressure of 6 GPa. In sharp contrast to the Ba containing compounds, all the samples prepared in the present study have been quite stable during the synthesis and no deterioration in air has been observed after the preparation.

  16. Chemical stabilization and high pressure synthesis of Ba-free Hg-based superconductors, (Hg,M)Sr{sub 2}Ca{sub n-1}Cu{sub n}O{sub y}(N=1{approximately}3)

    SciTech Connect

    Kishio, K. |; Shimoyama, J.; Hahakura, S.

    1994-12-31

    A homologous series of new Hg-based HTSC compounds, (Hg,M)Sr{sub 2}Ca{sub n-1}Cu{sub n}O{sub y} with n=1 to 3, have been synthesized. The stabilization of the pure phases have been accomplished by chemical doping of third elements such as M=Cr, Mo and Re. While the Hg1201(n=1) phase was readily obtained in this way, it was necessary to simultaneously dope Y into the Ca site to stabilize the Hg1212(n=2) phase. On the other hand, single-phase Y-free Hg1212(n=2) and Hg1223(n=3) samples were synthesized only under a high pressure of 6 GPa. In sharp contrast to the Ba-containing compounds, all the samples prepared in the present study have been quite stable during the synthesis and no deterioration in air has been observed after the preparation.

  17. Crystal-structure and magnetic phase transformations in solid solutions of BiFeO{sub 3}-AFe{sub 0.5}Nb{sub 0.5}O{sub 3} (A = Ca, Sr, Ba, Pb)

    SciTech Connect

    Troyanchuk, I. O.; Bushinsky, M. V. Chobot, A. N.; Mantytskaya, O. S.; Pushkarev, N. V.; Szymczak, R.

    2008-08-15

    Solid solutions of Bi{sub 1-x}A{sub x}(Fe{sub 1-x/2}Nb{sub x/2})O{sub 3}, where A = Ca, Ba, and Pb, are obtained and their crystal structure and magnetic properties are investigated. It is shown that for A = Ca and x {approx} 0.15, the symmetry of the unit cell changes from rhombohedral (space group R3c) to orthorhombic (Pbnm). The transformation leads to the emergence of spontaneous magnetization due to the Dzyaloshinskii-Moriya interaction. Solid solutions with A = Pb remain rhombohedral up to a concentration of x = 0.3. Spontaneous magnetization sharply increases in the compound with x {approx} 1 at low temperatures and is due to the formation of the spin-glass component.

  18. Structure and ferroelectric studies of (Ba{sub 0.85}Ca{sub 0.15})(Ti{sub 0.9}Zr{sub 0.1})O{sub 3} piezoelectric ceramics

    SciTech Connect

    Venkata Ramana, E.; Mahajan, A.; Graça, M.P.F.; Mendiratta, S.K.; Monteiro, J.M.; Valente, M.A.

    2013-10-15

    Graphical abstract: - Highlights: • (Ba{sub 0.85}Ca{sub 0.15})(Ti{sub 0.9}Zr{sub 0.1})O{sub 3} (BCTZO) ceramic was synthesized by the ceramic method. • In situ XRD and Raman spectra showed the phase transition of BCTZO around 360 K. • The ceramics showed a tunability of 82% at 40 kV cm{sup −1} electric field. • BCTZO exhibited good quality factor of 111 at microwave frequencies. • Piezoforce microscopy studies indicated the switchability of ferroelectric domains. - Abstract: We have synthesized and studied the structural and ferroelectric properties of lead-free 0.5(Ba{sub 0.7}Ca{sub 0.3})TiO{sub 3}–0.5Ba(Zr{sub 0.2}Ti{sub 0.8})O{sub 3} ceramics in the temperature region of its ferroelectric transition. The synthesized material showed high dielectric constant, low loss and good pyroelectric figure of merit. From the temperature dependent X-ray diffraction measurements, we determined the tricritical point to be in the temperature range of 303–400 K. The dielectric measurements indicate a diffuse ferroelectric phase transition (DPT) around 360 K in agreement with the X-ray measurements. We studied the evolution of Raman spectra with temperature to understand the nature of phase transition in BaTiO{sub 3} (BTO) and the BCTZO. The results indicates that the transition of ferroelectric–paraelectric state is not sharp as in the case of BTO and the polar state persists through the paraelectric state. In general, our study indicates that there are ferroelectric domains of nanometer size beyond the commonly defined transition temperature. The observation of local piezoelectric hysteresis loop indicated the existence of intrinsic ferroelectric property of the ceramic at the nanoscale. The ceramics exhibited electric field tunable dielectric properties with a tunability of 82% at an applied DC field of 40 kV cm{sup −1}, low dielectric loss of 0.001 and room temperature pyroelectric coefficient of 6 × 10{sup −8} C cm{sup −2} K{sup −1} and the

  19. Giant magnetocaloric effect of Mn{sub 0.92}Ba{sub 0.08}As thin film grown on Al{sub 2}O{sub 3}(0001) substrate

    SciTech Connect

    Dang Duc Dung; Duong Anh Tuan; Duong Van Thiet; Shin, Yooleemi; Cho, Sunglae

    2012-04-01

    The epitaxial Mn{sub 0.92}Ba{sub 0.08}As thin film was grown on Al{sub 2}O{sub 3}(0001) substrate by molecular beam epitaxy. The Curie temperature (T{sub C}) around 350 K was enhanced with the addition of Ba, compared to that of bulk MnAs (T{sub C} {approx} 318 K). We have observed the linear resistivity versus the square of temperature and high negative magnetoresistance near Curie temperature. Moreover, the giant magnetocaloric effect was found with maximum magnetic entropy change, 65 J/kgK, around room temperature at 5 T.

  20. Photocatalytic characteristics for the nanocrystalline TiO2 on the Ag-doped CaAl2O4:(Eu,Nd) phosphor

    NASA Astrophysics Data System (ADS)

    Kim, Jung-Sik; Sung, Hyun-Je; Kim, Bum-Joon

    2015-04-01

    This study investigated the photocatalytic behavior of nanocrystalline TiO2 deposited on Ag-doped long-lasting phosphor (CaAl2O4:Eu2+,Nd3+). The CaAl2O4:Eu2+,Nd3+ phosphor powders were prepared via conventional sintering using CaCO3, Al2O3, Eu2O3, and Nd2O3 as raw materials according to the appropriate molar ratios. Silver nanoparticles were loaded on the phosphor by mixing with an aqueous Ag-dispersion solution. Nanocrystalline TiO2 was deposited on Ag-doped CaAl2O4:Eu2+,Nd3+ powders via low-pressure chemical vapor deposition (LPCVD). The TiO2 coated on the phosphor was actively photo-reactive under irradiation with visible light and showed much faster benzene degradation than pure TiO2, which is almost non-reactive. The coupling of TiO2 with phosphor may result in an energy band bending in the junction region, which then induces the TiO2 crystal at the interface to be photo-reactive under irradiation with visible light. In addition, the intermetallic compound of CaTiO3 that formed at the interface between TiO2 and the CaAl2O4:(Eu2+,Nd3+) phosphor results in the formation of oxygen vacancies and additional electrons that promote the photodecomposition of benzene gas. The addition of Ag nanoparticles enhanced the photocatalytic reactivity of the TiO2/CaAl2O4:Eu2+,Nd3+ phosphor. TiO2 on the Ag-doped phosphor presented a higher benzene gas decomposition rate than the TiO2 did on the phosphor without Ag-doping under both irradiation with ultraviolet and visible light.