Novel optically active lead-free relaxor ferroelectric (Ba0.6Bi0.2Li0.2)TiO3. (11th May 2016)
- Record Type:
- Journal Article
- Title:
- Novel optically active lead-free relaxor ferroelectric (Ba0.6Bi0.2Li0.2)TiO3. (11th May 2016)
- Main Title:
- Novel optically active lead-free relaxor ferroelectric (Ba0.6Bi0.2Li0.2)TiO3
- Authors:
- Borkar, Hitesh
Rao, Vaibhav
Dutta, Soma
Barvat, Arun
Pal, Prabir
Tomar, M
Gupta, Vinay
Scott, J F
Kumar, Ashok - Abstract:
- Abstract: We discovered a near-room-temperature lead-free relaxor-ferroelectric (Ba0.6 Bi0.2 Li0.2 )TiO3 (BBLT) having A-site compositionally disordered ABO3 perovskite structure. Microstructure-property relations revealed that the chemical inhomogeneities and development of local polar nano-regions (PNRs) are responsible for dielectric dispersion as a function of probe frequencies and temperatures. Rietveld analysis indicates mixed crystal structure with 80% tetragonal structure (space group P4mm ) and 20% orthorhombic structure (space group Amm2 ), which is confirmed by the high resolution transmission electron diffraction (HRTEM). Dielectric constant and tangent loss dispersion with and without illumination of light obey nonlinear Vogel–Fulcher (VF) relations. The material shows slim polarization–hysteresis ( P – E ) loops and excellent displacement coefficients ( d 33 ~ 233 pm V −1 ) near room temperature, which gradually diminish near the maximum dielectric dispersion temperature ( T m ). The underlying physics for light-sensitive dielectric dispersion was probed by x-ray photon spectroscopy (XPS), which strongly suggests that mixed valence of bismuth ions, especially Bi 5+ ions, comprise most of the optically active centers. Ultraviolet photoemission measurements showed most of the Ti ions are in 4 + states and sit at the centers of the TiO6 octahedra; along with asymmetric hybridization between O 2 p and Bi 6 s orbitals, this appears to be the main driving force forAbstract: We discovered a near-room-temperature lead-free relaxor-ferroelectric (Ba0.6 Bi0.2 Li0.2 )TiO3 (BBLT) having A-site compositionally disordered ABO3 perovskite structure. Microstructure-property relations revealed that the chemical inhomogeneities and development of local polar nano-regions (PNRs) are responsible for dielectric dispersion as a function of probe frequencies and temperatures. Rietveld analysis indicates mixed crystal structure with 80% tetragonal structure (space group P4mm ) and 20% orthorhombic structure (space group Amm2 ), which is confirmed by the high resolution transmission electron diffraction (HRTEM). Dielectric constant and tangent loss dispersion with and without illumination of light obey nonlinear Vogel–Fulcher (VF) relations. The material shows slim polarization–hysteresis ( P – E ) loops and excellent displacement coefficients ( d 33 ~ 233 pm V −1 ) near room temperature, which gradually diminish near the maximum dielectric dispersion temperature ( T m ). The underlying physics for light-sensitive dielectric dispersion was probed by x-ray photon spectroscopy (XPS), which strongly suggests that mixed valence of bismuth ions, especially Bi 5+ ions, comprise most of the optically active centers. Ultraviolet photoemission measurements showed most of the Ti ions are in 4 + states and sit at the centers of the TiO6 octahedra; along with asymmetric hybridization between O 2 p and Bi 6 s orbitals, this appears to be the main driving force for net polarization. This BBLT material may open a new path for environmental friendly lead-free relaxor-ferroelectric research. … (more)
- Is Part Of:
- Journal of physics. Volume 28:Number 26(2016)
- Journal:
- Journal of physics
- Issue:
- Volume 28:Number 26(2016)
- Issue Display:
- Volume 28, Issue 26 (2016)
- Year:
- 2016
- Volume:
- 28
- Issue:
- 26
- Issue Sort Value:
- 2016-0028-0026-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-05-11
- Subjects:
- relaxor -- dielectric spectroscopy -- polar nano regions -- ferroelectric
Condensed matter -- Periodicals
Matière condensée -- Périodiques
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530.4105 - Journal URLs:
- http://www.iop.org/Journals/cm ↗
http://iopscience.iop.org/0953-8984/ ↗
http://ioppublishing.org/ ↗ - DOI:
- 10.1088/0953-8984/28/26/265901 ↗
- Languages:
- English
- ISSNs:
- 0953-8984
- Deposit Type:
- Legaldeposit
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