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Barium titanate

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Barium titanate
Barium titanate ceramics in plastic package
Polycrystalline BaTiO3 in plastic
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.031.783 Edit this at Wikidata
EC Number
  • 234-975-0
RTECS number
  • XR1437333
UNII
  • InChI=1S/2Ba.4O.Ti/q2*+2;4*-1; checkY
    Key: JRPBQTZRNDNNOP-UHFFFAOYSA-N checkY
  • InChI=1/2Ba.4O.Ti/q2*+2;4*-1;/r2Ba.O4Ti/c;;1-5(2,3)4/q2*+2;-4
    Key: JRPBQTZRNDNNOP-NXYSCRTKAD
  • [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-]
Properties
BaTiO3
Molar mass 233.192 g
Appearance white crystals
Odor odorless
Density 6.02 g/cm3, solid
Melting point 1,625 °C (2,957 °F; 1,898 K)
insoluble
Solubility slightly soluble in dilute mineral acids; dissolves in concentrated hydrofluoric acid
Band gap 3.2 eV (300 K, single crystal)[1]
no2.412; ne=2.360[2]
Structure
Tetragonal, tP5
P4mm, No. 99
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H302, H332
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Barium titanate is an inorganic compound with chemical formula BaTiO3. Barium titanate appears white as a powder and is transparent when prepared as large crystals. It is a ferroelectric ceramic material that exhibits the photorefractive effect and piezoelectric properties. It is used in capacitors, electromechanical transducers and nonlinear optics.

Structure

Main article: Perovskite (structure)
Structure of cubic BaTiO3. The red spheres are oxide centres, blue are Ti4+ cations, and the green spheres are Ba2+.

The solid exists in one of four polymorphs depending on temperature. From high to low temperature, these crystal symmetries of the four polymorphs are cubic, tetragonal, orthorhombic, and rhombohedral crystal structure. All of these phases exhibit the ferroelectric effect apart from the cubic phase. The high temperature cubic phase is easiest to describe, as it consists of regular corner-sharing octahedral TiO6 units that define a cube with O vertices and Ti-O-Ti edges. In the cubic phase, Ba2+ is located at the center of the cube, with a nominal coordination number of 12. Lower symmetry phases are stabilized at lower temperatures and involve movement of the Ti4+ to off-center positions. The remarkable properties of this material arise from the cooperative behavior of the Ti4+ distortions.[3]

Above the melting point, the liquid has a remarkably different local structure to the solid forms, with the majority of Ti4+ coordinated to four oxygen, in tetrahedral TiO4 units, which coexist with more highly coordinated units.[4]

Production and handling properties

Scanning Electron Microscopy (SEM) images showing particles of BaTiO3. The different morphologies depend on the synthesis conditions (precipitation, hydrothermal and solvothermal synthesis): size and shape can be varied by changing the concentration of precursors, the reaction temperature and the time. Color (if added) helps to emphasize the grayscale levels. In general, the synthesis of Barium titanate by precipitation from aqueous solution allows to produce particles with spherical shape with size that can be tailored from a few nanometers to several hundred nanometers by decreasing the concentration of reactants. At very low concentration the particles have the tendency to develop a dendritic-like morphology, as reported in the images.

Barium titanate can be synthesized by the relatively simple sol–hydrothermal method.[5] Barium titanate can also be manufactured by heating barium carbonate and titanium dioxide. The reaction proceeds via liquid phase sintering. Single crystals can be grown at around 1100 °C from molten potassium fluoride.[6] Other materials are often added as dopants, e.g., Sr to giveform solid solutions with strontium titanate. It reacts with nitrogen trichloride and produces a greenish or gray mixture; the ferroelectric properties of the mixture are still present in this form.

Much effort has been spent studying the relationship between particle morphology and its properties. Fully dense nanocrystalline barium titanate has 40% higher permittivity than the same material prepared in classic ways.[7] The addition of inclusions of barium titanate to tin has been shown to produce a bulk material with a higher viscoelastic stiffness than that of diamonds. Barium titanate goes through two phase transitions that change the crystal shape and volume. This phase change leads to composites where the barium titanates have a negative bulk modulus (Young's modulus), meaning that when a force acts on the inclusions, there is displacement in the opposite direction, further stiffening the composite.[8]

Like many oxides, barium titanate is insoluble in water but attacked by sulfuric acid. Its bulk room-temperature bandgap is 3.2 eV, but this increases to ~3.5 eV when the particle size is reduced from about 15 to 7 nm.[1]

Uses

Scanning transmission electron microscopy of the ferroelastic domains that form in BaTiO3 on cooling through the Curie temperature. The vertex point, where domain bundles meet, moves from the center in isometric crystals (top) to off-center in oblongs (bottom).[9]

Barium titanate is a dielectric ceramic used in capacitors, with dielectric constant values as high as 7,000. Over a narrow temperature range, values as high as 15,000 are possible; most common ceramic and polymer materials are less than 10, while others, such as titanium dioxide (TiO2), have values between 20 and 70.[10]

It is a piezoelectric material used in microphones and other transducers. The spontaneous polarization of barium titanate single crystals at room temperature range between 0.15 C/m2 in earlier studies,[11] and 0.26 C/m2 in more recent publications,[12] and its Curie temperature is between 120 and 130 °C. The differences are related to the growth technique, with earlier flux grown crystals being less pure than current crystals grown with the Czochralski process,[13] which therefore have a larger spontaneous polarization and a higher Curie temperature.

As a piezoelectric material, it has been largely replaced by lead zirconate titanate, also known as PZT. Polycrystalline barium titanate has a positive temperature coefficient of resistance, making it a useful material for thermistors and self-regulating electric heating systems.

Barium titanate crystals find use in nonlinear optics. The material has high beam-coupling gain, and can be operated at visible and near-infrared wavelengths. It has the highest reflectivity of the materials used for self-pumped phase conjugation (SPPC) applications. It can be used for continuous-wave four-wave mixing with milliwatt-range optical power. For photorefractive applications, barium titanate can be doped by various other elements, e.g. iron.[14]

Thin films of barium titanate display electrooptic modulation to frequencies over 40 GHz.[15]

The pyroelectric and ferroelectric properties of barium titanate are used in some types of uncooled sensors for thermal cameras.

High-purity barium titanate powder is reported to be a key component of new barium titanate capacitor energy storage systems for use in electric vehicles.[16]

Due to their elevated biocompatibility, barium titanate nanoparticles (BTNPs) have been recently employed as nanocarriers for drug delivery.[17]

Magnetoelectric effect of giant strengths have been reported in thin films grown on barium titanate substrates.[18][19]

Natural occurrence

Barioperovskite is a very rare natural analogue of BaTiO3, found as microinclusions in benitoite.[20]

See also

References

  1. ^ a b Suzuki, Keigo; Kijima, Kazunori (2005). "Optical Band Gap of Barium Titanate Nanoparticles Prepared by RF-plasma Chemical Vapor Deposition". Jpn. J. Appl. Phys. 44 (4A): 2081–2082. Bibcode:2005JaJAP..44.2081S. doi:10.1143/JJAP.44.2081.
  2. ^ Tong, Xingcun Colin (2013). Advanced Materials for Integrated Optical Waveguides. Springer Science & Business Media. p. 357. ISBN 978-3-319-01550-7.
  3. ^ Manuel Gaudon. Out-of-centre distortions around an octahedrally coordinated Ti4+ in BaTiO3. Polyhedron, Elsevier, 2015, 88, pp.6-10. <10.1016/j.poly.2014.12.004>. <hal-01112286>
  4. ^ Alderman O L G; Benmore C; Neuefeind J; Tamalonis A; Weber R (2019). "Molten barium titanate: a high-pressure liquid silicate analogue". Journal of Physics: Condensed Matter. 31 (20): 20LT01. doi:10.1088/1361-648X/ab0939. PMID 30790768.
  5. ^ Selvaraj, M.; Venkatachalapathy, V.; Mayandi, J.; Karazhanov, S.; Pearce, J. M. (2015). "Preparation of meta-stable phases of barium titanate by Sol-hydrothermal method". AIP Advances. 5 (11): 117119. Bibcode:2015AIPA....5k7119S. doi:10.1063/1.4935645.
  6. ^ Galasso, Francis S. (1973). Barium Titanate, BaTiO3. Vol. 14. pp. 142–143. doi:10.1002/9780470132456.ch28. ISBN 9780470132456. {{cite book}}: |journal= ignored (help)
  7. ^ Nyutu, Edward K.; Chen, Chun-Hu; Dutta, Prabir K.; Suib, Steven L. (2008). "Effect of Microwave Frequency on Hydrothermal Synthesis of Nanocrystalline Tetragonal Barium Titanate". The Journal of Physical Chemistry C. 112 (26): 9659. CiteSeerX 10.1.1.660.3769. doi:10.1021/jp7112818.
  8. ^ Jaglinski, T.; Kochmann, D.; Stone, D.; Lakes, R. S. (2007). "Composite materials with viscoelastic stiffness greater than diamond". Science. 315 (5812): 620–2. Bibcode:2007Sci...315..620J. CiteSeerX 10.1.1.1025.8289. doi:10.1126/science.1135837. PMID 17272714.
  9. ^ Scott, J. F.; Schilling, A.; Rowley, S. E.; Gregg, J. M. (2015). "Some current problems in perovskite nano-ferroelectrics and multiferroics: Kinetically-limited systems of finite lateral size". Science and Technology of Advanced Materials. 16 (3): 036001. Bibcode:2015STAdM..16c6001S. doi:10.1088/1468-6996/16/3/036001. PMC 5099849. PMID 27877812.
  10. ^ Waugh, Mark D (2010). "Design solutions for DC bias in multilayer ceramic capacitors" (PDF). Electronic Engineering Times.
  11. ^ von Hippel, A. (1950-07-01). "Ferroelectricity, Domain Structure, and Phase Transitions of Barium Titanate". Reviews of Modern Physics. 22 (3): 221–237. Bibcode:1950RvMP...22..221V. doi:10.1103/RevModPhys.22.221.
  12. ^ Shieh, J.; Yeh, J. H.; Shu, Y. C.; Yen, J. H. (2009-04-15). "Hysteresis behaviors of barium titanate single crystals based on the operation of multiple 90° switching systems". Materials Science and Engineering: B. Proceedings of the joint meeting of the 2nd International Conference on the Science and Technology for Advanced Ceramics (STAC-II) and the 1st International Conference on the Science and Technology of Solid Surfaces and Interfaces (STSI-I). 161 (1–3): 50–54. doi:10.1016/j.mseb.2008.11.046. ISSN 0921-5107.
  13. ^ Godefroy, Geneviève (1996). "Ferroélectricité". Techniques de l'Ingénieur Matériaux Pour l'Électronique et Dispositifs Associés (in French). base documentaire : TIB271DUO. (ref. article : e1870).
  14. ^ "Fe:LiNbO3 Crystal". redoptronics.com.
  15. ^ Tang, Pingsheng; Towner, D.; Hamano, T.; Meier, A.; Wessels, B. (2004). "Electrooptic modulation up to 40 GHz in a barium titanate thin film waveguide modulator". Optics Express. 12 (24): 5962–7. Bibcode:2004OExpr..12.5962T. doi:10.1364/OPEX.12.005962. PMID 19488237.
  16. ^ "Nanoparticle Compatibility: New Nanocomposite Processing Technique Creates More Powerful Capacitors". gatech.edu. April 26, 2007. Retrieved 2009-06-06.
  17. ^ Genchi, G.G.; Marino, A.; Rocca, A.; Mattoli, V.; Ciofani, G. (5 May 2016). "Barium titanate nanoparticles: Promising multitasking vectors in nanomedicine". Nanotechnology. 27 (23): 232001. Bibcode:2016Nanot..27w2001G. doi:10.1088/0957-4484/27/23/232001. ISSN 0957-4484. PMID 27145888.
  18. ^ Eerenstein, W.; Mathur, N. D.; Scott, J. F. (August 2006). "Multiferroic and magnetoelectric materials". Nature. 442 (7104): 759–765. Bibcode:2006Natur.442..759E. doi:10.1038/nature05023. ISSN 1476-4687. PMID 16915279.
  19. ^ Rafique, Mohsin (May 2017). "Giant room temperature magnetoelectric response in strain controlled nanocomposites". Applied Physics Letters. 110 (20): 202902. doi:10.1063/1.4983357.
  20. ^ Ma, Chi; Rossman, George R. (2008). "Barioperovskite, BaTiO3, a new mineral from the Benitoite Mine, California". American Mineralogist. 93 (1): 154–157. Bibcode:2008AmMin..93..154M. doi:10.2138/am.2008.2636.
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