Abstract
Tin titanate (SnTiO3) has been notoriously impossible to prepare as a thin-film ferroelectric, probably because high-temperature annealing converts much of the Sn2+ to Sn4+. In the present paper, we show two things: first, perovskite phase SnTiO3 can be prepared by atomic-layer deposition directly onto p-type Si substrates; and second, these films exhibit ferroelectric switching at room temperature, with p-type Si acting as electrodes. X-ray diffraction measurements reveal that the film is single-phase, preferred-orientation ferroelectric perovskite SnTiO3. Our films showed well-saturated, square, and repeatable hysteresis loops of around 3μC/cm2 remnant polarization at room temperature, as detected by out-of-plane polarization versus electric field and field cycling measurements. Furthermore, photovoltaic and photoferroelectricity were found in Pt/SnTiO3/Si/SnTiO3/Pt heterostructures, the properties of which can be tuned through band-gap engineering by strain according to first-principles calculations. This is a lead-free room-temperature ferroelectric oxide of potential device application.
Original language | English |
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Article number | 054109 |
Journal | Physical Review B |
Volume | 97 |
Issue number | 5 |
DOIs | |
State | Published - Feb 20 2018 |
Funding
R.A. acknowledges receiving graduate fellowships from DOD Grant No. FA9550-16-1-0295. Work at Argonne (Y.S. and S.H., design of experiment, data analysis, and contribution to manuscript writing) and ORNL (C.S. and H.N.L., optical spectroscopy) was supported by the US Department of Energy (DOE), Office of Science, Office of Basic Energy Sciences (BES), Materials Sciences and Engineering Division. S.C., K.P., and S.M.N. are grateful for financial support from the NSF (CDMR No. 1309114), and C.G.T. acknowledges support from the NSF (CDMR No. 1309114, CBET No. 1067424, and EEC No. 1062943). S.H. acknowledges financial support via Creative Materials Discovery Program from National Research Foundation of Korea funded by the Ministry of Science and ICT (NRF-2017M3D1A1086861). A part of the work was carried out at the University of Puerto Rico with financial support provided by the DoD-AFOSR Grant No. FA95501610295. J.F.S. acknowledges his visit expenses to UPR from NSF-IFN Grant No. 1002410.