Please use this identifier to cite or link to this item: https://apo.ansto.gov.au/dspace/handle/10238/12523
Title: Defect structure and property consequence when small Li+ ions meet BaTiO3
Authors: Narayanan, N
Lou, Q
Rawal, A
Lu, T
Liu, Z
Chen, J
Langley, J
Chen, H
Hester, JR
Cox, N
Fuess, H
McIntyre, GJ
Li, G
Yu, DH
Liu, Y
Keywords: Ferroelectric materials
Antiferroelectric materials
Defects
Density
Electronic structure
Electrical properties
Oxides
Ions
Lithium
Neutron diffraction
Nuclear magnetic resonance
Electron microprobe analysis
Doped materials
Issue Date: 31-Aug-2020
Publisher: American Physical Society
Citation: Narayanan, N., Lou, Q., Rawal, A., Lu, T., Liu, Z., Chen, J., Langley, J., Chen, H., Hester, J., Cox, N., Fuess, H., McIntyre, G. J., Li, G., Yu, D., & Liu, Y. (2020). Defect structure and property consequence when small Li+ ions meet BaTiO3. Physical Review Materials, 4(8), 084412. doi:10.1103/PhysRevMaterials.4.084412
Abstract: In the present work the longstanding issue of the structure and dynamics of smaller ions in oxides and its impact on the properties was investigated on 7% Li-doped BaTiO3. The investigation combined several techniques, notably neutron powder diffraction (NPD), nuclear magnetic resonance (7Li-NMR), electron paramagnetic resonance (EPR), electron microprobe, electric polarization (EP) measurement, and electronic structure calculations based on density-functional theory (DFT). Electron microprobe confirmed multiple phases, one containing incorporated Li in the BaTiO3 host lattice and another glassy phase which breaks the host lattice due to excessive Li accumulation. While the average structure of Li in BaTiO3 could not be determined by NPD, 7Li-NMR revealed one broad “disordered” and multiple “ordered” peaks. Local structure models with different defect types involving Li+ were modeled and the corresponding chemical shifts (δ) were compared with experimental values. It is found that the closest defect model describing the ordered peaks, is with Ti4+ being replaced by four Li+ ions. The biexponential behavior of the spin-lattice relaxation of the ordered peaks each with a short and a long relaxation discloses the existence of paramagnetic ions. Finally, EPR revealed the existence of the paramagnetic ion Ti3+ as a charge-transfer defect. DFT calculations disclosed local antipolar displacements of Ti ions around both types of defect sites upon insertion of Li+. This is in accordance with the experimental observation of pinching effects of the EP in Li-doped BaTiO3. These studies demonstrate the huge impact of the local structure of the doped smaller/lighter ions on the functional properties of oxides. ©2020 American Physical Society
URI: https://doi.org/10.1103/PhysRevMaterials.4.084412
https://apo.ansto.gov.au/dspace/handle/10238/12523
ISSN: 2475-9953
Appears in Collections:Journal Articles

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