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Structure and Oxygen Storage Capabilities of Heavily Oxidized Y<sub>1-x</sub>Tb<sub>x</sub>MnO<sub>3+d</sub>

ORAL

Abstract

Non-stoichiometric oxides have attracted tremendous interest for their promising potential for applications as materials with reversible oxygen storage/release capabilities. The development of oxygen storage materials is critical for the growth of new energy related technologies such as oxy-fuel and chemical looping combustion and reforming for clean coal energy and synthesis gas production.  We have recently reported superior oxygen storage/release performances displayed by rare-earth hexagonal manganites, namely RMnO3+d,(where R is a rare earth elements or Y).  These materials are capable of storing as much as 2000 μmol-O/g when annealed in air.  Large changes of oxygen content occur on cycling at unusually low but desirable temperatures between 250 and 350° C.  Tb-substituted hexagonal Y1-xTbxMnO3+d materials are singled out because of their capability to hold even more oxygen (up to 0.5 oxygen atom per unit formula) with the drastic enhancement causing significant distortions of the structural symmetry.  Neutron data enabled the determination of an elegant solution of a previously unseen superlattice which is four times larger than that of the pristine YMnO3 parent material.  Detailed discussions of the structure and materials properties will be presented.

Presenters

  • Omar Chmaissem

    Argonne National Laboratory, Northern Illinois University

Authors

  • Omar Chmaissem

    Argonne National Laboratory, Northern Illinois University

  • Elena Krivyakina

    Northern Illinois University and Argonne National Laboratory

  • Bogdan Dabrowski

    Institute of Physics, Polish Academy of Sciences, Warsaw, Poland

  • Stephan Rosenkranz

    Argonne National Laboratory, Materials Science Division, Argonne National Laboratory