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Formation of the (La0.67Sr0.33)2MnO4 Phase in La–Sr–Mn–O Thin Films by Pulsed Laser Deposition

Published online by Cambridge University Press:  31 January 2011

Y. H. Li
Affiliation:
National Science Foundation-Materials Research, Science and Engineering Center and Center for Superconductivity Research, University of Maryland, Park, Maryland 20742
L. Salamanca-Riba
Affiliation:
National Science Foundation-Materials Research, Science and Engineering Center and Center for Superconductivity Research, University of Maryland, Park, Maryland 20742
Y. Zhao
Affiliation:
National Science Foundation-Materials Research, Science and Engineering Center and Center for Superconductivity Research, University of Maryland, Park, Maryland 20742
S. B. Ogale
Affiliation:
National Science Foundation-Materials Research, Science and Engineering Center and Center for Superconductivity Research, University of Maryland, Park, Maryland 20742
R. Ramesh
Affiliation:
National Science Foundation-Materials Research, Science and Engineering Center and Center for Superconductivity Research, University of Maryland, Park, Maryland 20742
T. Venkatesan
Affiliation:
National Science Foundation-Materials Research, Science and Engineering Center and Center for Superconductivity Research, University of Maryland, Park, Maryland 20742
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Abstract

La0.67Sr0.33MnO3 thin films were grown on LaAlO3 substrate in vacuum using pulsed laser deposition to investigate the effect of changing oxygen content. Transmission electron microscopy studies showed that the epitaxial (La0.67Sr0.33)2MnO4 phase with K2NiF4 structure formed unexpectedly as a matrix with a square-shaped nanometer-sized MnO phase distributed in a regular pattern throughout the whole film like self-assembled quantum dots. The MnO phase grew epitaxially from the LaAlO3 substrate to the top of the film with no outgrowth. High-resolution image simulation indicated that Sr ions take up only positions in every other La layer in the (La0.67Sr0.33)2MnO4 structure. Basing our theory on the composition and structure of the matrix phase, we propose that it is possibly electron-doped with a mixed valence of Mn2+/Mn3+ instead of the Mn3+/Mn4+ as in the hole-doped case.

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Articles
Copyright
Copyright © Materials Research Society 2000

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