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Evolution of correlated electron behavior from the surface to the bulk in SrxCa1-xVO3

Published online by Cambridge University Press:  16 March 2015

J. Laverock
Affiliation:
Department of Physics, Boston University, 590 Commonwealth Avenue, Boston, MA 02215, U.S.A.
B. Chen
Affiliation:
Department of Physics, Boston University, 590 Commonwealth Avenue, Boston, MA 02215, U.S.A.
J. Kuyyalil
Affiliation:
Department of Physics, Boston University, 590 Commonwealth Avenue, Boston, MA 02215, U.S.A.
R. P. Singh
Affiliation:
Department of Physics, University of Warwick, Coventry CV4 7AL, United Kingdom
G. Balakrishnan
Affiliation:
Department of Physics, University of Warwick, Coventry CV4 7AL, United Kingdom
R. M. Qiao
Affiliation:
Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, U.S.A.
W. L. Yang
Affiliation:
Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, U.S.A.
J. Adell
Affiliation:
MAX-lab, Lund University, SE-221 00 Lund, Sweden
B. Karlin
Affiliation:
Materials Science and Engineering Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, U.S.A.
J. C. Woicik
Affiliation:
Materials Science and Engineering Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, U.S.A.
K. E. Smith
Affiliation:
Department of Physics, Boston University, 590 Commonwealth Avenue, Boston, MA 02215, U.S.A. School of Chemical Sciences and The MacDiarmid Institute for Advanced Materials and Nanotechnology, University of Auckland, Auckland 1142, New Zealand
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Abstract

We present a detailed depth-sensitive study of the evolution in correlated electron behavior from the surface of the prototypical correlated oxide, SrxCa1-xVO3, to its bulk. Photoemission measurements of varying surface sensitivity are employed to directly compare both the spectral weight and energetics of the correlated electron features, and resonant soft x-ray emission spectroscopy is used as a bulk-sensitive reference. The surface component, which still contributes significantly to photoemission at 2.2 keV, is characterized by a transfer of spectral weight into the incoherent lower Hubbard band and the corresponding shift of these states towards lower binding energy.

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Articles
Copyright
Copyright © Materials Research Society 2015 

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References

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