Direct observation of ferroelectric field effect and vacancy-controlled screening at the BiFeO3/LaxSr1 - xMnO3 interface

Young Min Kim, Anna Morozovska, Eugene Eliseev, Mark P. Oxley, Rohan Mishra, Sverre M. Selbach, Tor Grande, S. T. Pantelides, Sergei V. Kalinin, Albina Y. Borisevich

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176 Scopus citations

Abstract

The development of interface-based magnetoelectric devices necessitates an understanding of polarization-mediated electronic phenomena and atomistic polarization screening mechanisms. In this work, the LSMO/BFO interface is studied on a single unit-cell level through a combination of direct order parameter mapping by scanning transmission electron microscopy and electron energy-loss spectroscopy. We demonstrate an unexpected ~5% lattice expansion for regions with negative polarization charge, with a concurrent anomalous decrease of the Mn valence and change in oxygen K-edge intensity. We interpret this behaviour as direct evidence for screening by oxygen vacancies. The vacancies are predominantly accumulated at the second atomic layer of BFO, reflecting the difference of ionic conductivity between the components. This vacancy exclusion from the interface leads to the formation of a tail-to-tail domain wall. At the same time, purely electronic screening is realized for positive polarization charge, with insignificant changes in lattice and electronic properties. These results underline the non-trivial role of electrochemical phenomena in determining the functional properties of oxide interfaces. Furthermore, these behaviours suggest that vacancy dynamics and exclusion play major roles in determining interface functionality in oxide multilayers, providing clear implications for novel functionalities in potential electronic devices.

Original languageEnglish
JournalNature Materials
Volume13
Issue number11
DOIs
StateAccepted/In press - Aug 17 2014

Funding

The work is supported in part (A.Y.B., Y-M.K., S.V.K., R.M. and S.T.P.) by the Materials Science and Engineering Division, Office of Basic Energy Sciences of the US DOE and through a user project supported by Oak Ridge National Laboratory’s Center for Nanophase Materials Sciences, which is sponsored at Oak Ridge National Laboratory by the Scientific User Facilities Division, Office of Basic Energy Sciences, US Department of Energy. M.P.O. acknowledges support from DOE grant DE-FG02-09ER46554. The authors thank P. Yu (Tsinghua University, Beijing, China), Y-H. Chu (National Chiao Tung University, Hsinchu, Taiwan) and R. Ramesh (University of California Berkeley) for providing BiFeO3 films for the study. A.M. and E.E. acknowledge support via a bilateral SFFR-NSF project, namely US National Science Foundation under NSF-DMR-1210588 and State Fund of Fundamental Research of Ukraine, grant UU48/002. This research used resources of the National Energy Research Scientific Computing Center, which is supported by the Office of Science of the US Department of Energy under Contract No. DE-AC02-05CH11231.

FundersFunder number
Oak Ridge National Laboratory
Office of Basic Energy Sciences of the US DOE
SFFR-NSF
Scientific User Facilities Division
National Science FoundationNSF-DMR-1210588
U.S. Department of EnergyDE-FG02-09ER46554
Office of ScienceDE-AC02-05CH11231
Basic Energy Sciences
Oak Ridge National Laboratory
Division of Materials Sciences and Engineering
State Fund for Fundamental Research of UkraineUU48/002

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