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      Floating Zone Growth and Characterization of (Ca 1– x Nd x ) 12Al 14O 33+6 x ( x ∼ 0.001) Single Crystals

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      ACS Omega
      American Chemical Society

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          Abstract

          Rare earth Nd 3+ ion-doped Ca 12Al 14O 33 single crystals were grown at a rate of 1 mm/h by the floating zone technique in an oxygen atmosphere. The Nd concentration in the central area of the as-grown crystals was higher than that in the peripheral area due to the highly concave growth interface shape. The average Nd concentration in the as-prepared parallelepiped slices of ∼6 × 3 × 2 mm 3 for electride fabrication was ∼0.093 ± 0.011 atom % Nd in contrast to the nominal 0.1 atom % Nd concentration. The Nd-doped C12A7:Nd single crystalline electride prepared by thermal treatment with a Ti metal at 1100 °C for 48 h induced an insulator–metal transition with the highest conductivity of approximately 1165 S/cm. These annealing conditions provide an approach to completely remove clathrated oxide ions from the crystallographic cages, leading to the formation of C12A7:Nd( e ) and C12A7: e electrides with high-density electrons (∼2.4 ± 0.2 × 10 21 and ∼1.8 ± 0.1 × 10 21 cm –3) localized in the cages. The carrier mobility at room temperature in C12A7:Nd( e ) was very similar to that in C12A7: e , even though it was very high at temperatures below ∼150 K.

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          Electride support boosts nitrogen dissociation over ruthenium catalyst and shifts the bottleneck in ammonia synthesis

          Novel approaches to efficient ammonia synthesis at an ambient pressure are actively sought out so as to reduce the cost of ammonia production and to allow for compact production facilities. It is accepted that the key is the development of a high-performance catalyst that significantly enhances dissociation of the nitrogen–nitrogen triple bond, which is generally considered a rate-determining step. Here we examine kinetics of nitrogen and hydrogen isotope exchange and hydrogen adsorption/desorption reactions for a recently discovered efficient catalyst for ammonia synthesis—ruthenium-loaded 12CaO·7Al2O3 electride (Ru/C12A7:e−)—and find that the rate controlling step of ammonia synthesis over Ru/C12A7:e− is not dissociation of the nitrogen–nitrogen triple bond but the subsequent formation of N–H n species. A mechanism of ammonia synthesis involving reversible storage and release of hydrogen atoms on the Ru/C12A7:e− surface is proposed on the basis of observed hydrogen absorption/desorption kinetics.
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            Light-induced conversion of an insulating refractory oxide into a persistent electronic conductor.

            Materials that are good electrical conductors are not in general optically transparent, yet a combination of high conductivity and transparency is desirable for many emerging opto-electronic applications. To this end, various transparent oxides composed of transition or post-transition metals (such as indium tin oxide) are rendered electrically conducting by ion doping. But such an approach does not work for the abundant transparent oxides of the main-group metals. Here we demonstrate a process by which the transparent insulating oxide 12CaO x 7Al(2)O(3) (refs 7-13) can be converted into an electrical conductor. H(-) ions are incorporated into the subnanometre-sized cages of the oxide by a thermal treatment in a hydrogen atmosphere; subsequent irradiation of the material with ultraviolet light results in a conductive state that persists after irradiation ceases. The photo-activated material exhibits moderate electrical conductivity (approximately 0.3 S cm(-1)) at room temperature, with visible light absorption losses of only one per cent for 200-nm-thick films. We suggest that this concept can be applied to other main-group metal oxides, for the direct optical writing of conducting wires in insulating transparent media and the formation of a high-density optical memory.
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              Field Emission of Electron Anions Clathrated in Subnanometer-Sized Cages in [Ca24Al28O64]4+(4e-)

                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                09 December 2016
                31 December 2016
                : 1
                : 6
                : 1157-1163
                Affiliations
                [1]Center for Crystal Science and Technology, University of Yamanashi , 7-32 Miyamae-cho, Kofu, Yamanashi 400-8511, Japan
                Author notes
                [* ]E-mail: itanaka@ 123456yamanashi.ac.jp . Phone: +81-55-220-8625. Fax: +81-55-220-8270.
                Article
                10.1021/acsomega.6b00409
                6640739
                0ff7a124-0534-4643-a084-01b83165d06d
                Copyright © 2016 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 23 November 2016
                : 30 November 2016
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                ao6b00409
                ao-2016-004097

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