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Depth-resolved charge reconstruction at the LaNiO3/CaMnO3 interface
Author(s) -
Ravini U. Chandrasena,
Charles Louis Flint,
Wei-Shih Yang,
Arian Arab,
Slavomír Nemšák,
Mathias Gehlmann,
V. Burak Özdöl,
F. Bisti,
Kanishka Wijesekara,
Julia Meyer-Ilse,
Eric M. Gullikson,
Elke Arenholz,
Jim Ciston,
Claus M. Schneider,
Vladimir N. Strocov,
Y. Suzuki,
A. X. Gray
Publication year - 2018
Publication title -
physical review. b./physical review. b
Language(s) - English
Resource type - Journals
eISSN - 2469-9969
pISSN - 2469-9950
DOI - 10.1103/physrevb.98.155103
Subject(s) - antiferromagnetism , superexchange , crystallography , ferromagnetism , materials science , condensed matter physics , physics , mott insulator , chemistry
Author(s): Chandrasena, RU; Flint, CL; Yang, W; Arab, A; Nemsak, S; Gehlmann, M; Ozdol, VB; Bisti, F; Wijesekara, KD; Meyer-Ilse, J; Gullikson, E; Arenholz, E; Ciston, J; Schneider, CM; Strocov, VN; Suzuki, Y; Gray, AX | Abstract: © 2018 American Physical Society. Rational design of low-dimensional electronic phenomena at oxide interfaces is currently considered to be one of the most promising schemes for realizing new energy-efficient logic and memory devices. An atomically abrupt interface between paramagnetic LaNiO3 and antiferromagnetic CaMnO3 exhibits interfacial ferromagnetism, which can be tuned via a thickness-dependent metal-insulator transition in LaNiO3. Once fully understood, such emergent functionality could turn this archetypal Mott-interface system into a key building block for the above-mentioned future devices. Here, we use depth-resolved standing-wave photoemission spectroscopy in conjunction with scanning transmission electron microscopy and x-ray absorption spectroscopy, to demonstrate a depth-dependent charge reconstruction at the LaNiO3/CaMnO3 interface. Our measurements reveal an increased concentration of Mn3+ and Ni2+ cations at the interface, which create an electronic environment favorable for the emergence of interfacial ferromagnetism mediated via the Mn4+-Mn3+ ferromagnetic double exchange and Ni2+-O-Mn4+ superexchange mechanisms. Our findings suggest a strategy for designing functional Mott oxide heterostructures by tuning the interfacial cation characteristics via controlled manipulation of thickness, strain, and ionic defect states.

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