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Quantifying electronic correlation strength in a complex oxide: A combined DMFT and ARPES study of LaNiO3

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posted on 09.05.2016, 00:00 authored by EA Nowadnick, JP Ruf, H Park, PDC King, DG Schlom, KM Shen, AJ Millis
The electronic correlation strength is a basic quantity that characterizes the physical properties of materials such as transition metal oxides. Determining correlation strengths requires both precise definitions and a careful comparison between experiment and theory. In this paper, we define the correlation strength via the magnitude of the electron self-energy near the Fermi level. For the case of LaNiO3, we obtain both the experimental and theoretical mass enhancements m/m by considering high resolution angle-resolved photoemission spectroscopy (ARPES) measurements and density functional + dynamical mean field theory (DFT + DMFT) calculations. We use valence-band photoemission data to constrain the free parameters in the theory and demonstrate a quantitative agreement between the experiment and theory when both the realistic crystal structure and strong electronic correlations are taken into account. In addition, by considering DFT + DMFT calculations on epitaxially strained LaNiO3, we find a strain-induced evolution of m/m in qualitative agreement with trends derived from optics experiments. These results provide a benchmark for the accuracy of the DFT + DMFT theoretical approach, and can serve as a test case when considering other complex materials. By establishing the level of accuracy of the theory, this work also will enable better quantitative predictions when engineering new emergent properties in nickelate heterostructures.


This work was supported by the Cornell Center for Materials Research with funding from the NSF MRSEC program (DMR-1120296) and the Office of Naval Research (N00014-12-1-0791). J.P.R. acknowledges support from the NSF IGERT program (DGE-0903653). A.J.M. acknowledges support from the Basic Energy Sciences division of the Department of Energy under Grant ER-046169. H.P. gratefully acknowledges the support of start-up funds from University of Illinois at Chicago and Argonne National Laboratory. Part of the computational work was carried out at computing facilities supported by the Cornell Center for Materials Research.


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This is a copy of an article published in Physical review B: Condensed matter and materials physics © 2015 American Physical Society Publications.


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