The crystal chemistry and electrical properties of Fe doped Ca12Al14O33 (Mayenite)

X-ray and neutron powder diffraction have been used to study the crystal chemistry of Fe doped mayenite (Ca12Al14-xFexO33). Solid- state synthesis was used to prepare Ca12Al14-xFexO33 where x = 0, 0.1, 0.2, 0.5 and 0.6 and the citrate gel route was used to prepare Ca12Al14-xFexO33 where x = 0, 0.05, 0.1, 0.2, 0.3 and 0.4. X-ray powder diffraction data indicate that samples with the same composition but synthesized by the citrate gel route were more likely to be phase pure than samples obtained by traditional solid-state synthesis. The refined lattice parameters were observed to increase with increasing Fe concentration, irrespective of the synthesis method. Refined neutron powder data confirm that Fe is going into Al site rather than Ca site. A 2-point probe was used to measure the electrical properties of the Fe doped citrate gel synthesized samples and showed that the resistivity increases for the Fe doped samples compared to the undoped mayenite

Direct Formation and Structural Characterization of Electride C12A7

Ca12Al14O33 (C12A7 or Mayenite) is a material whose caged clathrate structure and occluded anionic species leads to significant functionality. The creation of occluded anionic vacancies leads to the injection of localized electrons at the center of the cage, converting the wide band gap insulator to a semi- or metallic conducting material. The conversion to the electride historically requires the synthesis of oxy-C12A7, consolidation, and then reduction to introduce anionic vacancies. This report develops and characterizes an electride formation procedure from three starting points: unconsolidated oxy-C12A7, heterogenous solid-state reactants (CaCO3and Al2O3), and homogenous non-carbonaceous polymer assisted sol-gel reactants. Electride-C12A7 formation is observed in a vacuum furnace where the reactants are in direct contact with a carbon source. Process time and temperature-dependent structural characterization provides insight into the source of high temperature C12A7 stability, the mechanism of anionic vacancy formation, and the magnitude of ultimate conductivity that cannot be explained by current reduction theories. A new theory is presented where mixed O- and C-occupied cages lead to high temperature stability, oxidation of C species creates anionic vacancies, and an equilibrium between the reducing power of the electride-C12A7 and of the C species leads to the ultimate conductivity achieved by the process. This represents a shift in understanding of the carbonaceous reduction process and the first report of high purity electride-C12A7 formation from heterogenous solid-state reactants and homogenous non-carbonaceous polymer assisted sol-gel reactants

Direct Formation and Structural Characterization of Electride C12A7

Ca12Al14O33 (C12A7 or Mayenite) is a material whose caged clathrate structure and occluded anionic species leads to significant functionality. The creation of occluded anionic vacancies leads to the injection of localized electrons at the center of the cage, converting the wide band gap insulator to a semi- or metallic conducting material. The conversion to the electride historically requires the synthesis of oxy-C12A7, consolidation, and then reduction to introduce anionic vacancies. This report develops and characterizes an electride formation procedure from three starting points: unconsolidated oxy-C12A7, heterogenous solid-state reactants (CaCO3 and Al2O3), and homogenous non-carbonaceous polymer assisted sol-gel reactants. Electride-C12A7 formation is observed in a vacuum furnace where the reactants are in direct contact with a carbon source. Process time and temperature-dependent structural characterization provides insight into the source of high temperature C12A7 stability, the mechanism of anionic vacancy formation, and the magnitude of ultimate conductivity that cannot be explained by current reduction theories. A new theory is presented where mixed O- and C-occupied cages lead to high temperature stability, oxidation of C species creates anionic vacancies, and an equilibrium between the reducing power of the electride-C12A7 and of the C species leads to the ultimate conductivity achieved by the process. This represents a shift in understanding of the carbonaceous reduction process and the first report of high purity electride-C12A7 formation from heterogenous solid-state reactants and homogenous non-carbonaceous polymer assisted sol-gel reactants

Development of Bulk Bi2+xSr3-yCa yCu 2O8+delta Superconductors by Partial-Melting Route for Fault Current Limiters Application

The production of bulk Bi2+xSr3-yCa yCu 2O8+delta (Bi-2212) superconductors for fault current limiter application was developed via a partial-melting route. Aiming high Ic (critical current), which is the essential superconducting characteristic for application of this material in the construction of Fault Current Limiters (FCL), the produced blocks have predominance of Bi-2212 phase (83 wt%), which characterizes with high values of zero and onset transport critical temperature of 92K and 97.5K, respectively. A relatively low transition width, deltaT, from the superconducting to the normal state of 5.5K, revealed a good intergrain connectivity. Consequently, current measurements on the blocks of Bi-2212 show promising Ic values of 230A and 850A for direct and alternate current, respectively. It is expected that further increases in the Ic values will depend on the elimination of an observed amorphous phase and further reduction of amount and grain sizes of secondary phases, still present in the blocks obtained by the proposed partial-melting route. This may be achieved by a further optimization of the partial-melting processing parameters