Sodium bismuth titanate

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Sodium bismuth titanate or bismuth sodium titanium oxide (NBT or BNT) is a solid inorganic compound of sodium, bismuth, titanium and oxygen with the chemical formula of Na0.5Bi0.5TiO3 or Bi0.5Na0.5TiO3. This compound adopts the perovskite structure.

Contents

Synthesis

Na0.5Bi0.5TiO3 is not a naturally occurring mineral and several synthesis routes to obtain the compound have been developed. It can be easily prepared by solid state reaction between Na2CO3, Bi2O3 and TiO2 at temperatures around 850 °C.

Structure

The exact room-temperature crystal structure of sodium bismuth titanate has been a matter of debate for several years. Early studies in the 1960s using X-ray diffraction suggested Na0.5Bi0.5TiO3 to adopt either a pseudo-cubic or a rhombohedral crystal structure. [1] In 2010, based on the high-resolution single-crystal X-ray diffraction data, a monoclinic structure (space group Cc) was proposed. On heating, Na0.5Bi0.5TiO3 transforms at 533 ± 5 K to a tetragonal structure (space group P4bm) and above 793 ± 5 K to cubic structure (space group Pm3m). [2]

Physical properties

Na0.5Bi0.5TiO3 is a relaxor ferroelectric. Its optical band gap was reported to be in the 3.0–3.5 eV. [3]

Applications

Various solid solutions with tetragonal ferroelectric perovskites including BaTiO3, [4] Bi0.5K0.5TiO3 [5] have been developed to obtain morphotropic phase boundaries to enhance the piezoelectric properties of Na0.5Bi0.5TiO3. The extraordinarily large strain generated by a field-induced phase transition in sodium bismuth titanate-based solid solutions prompted researchers to investigate its potential as an alternative to lead zirconate titanate for actuator applications. [6]

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<span class="mw-page-title-main">Perovskite (structure)</span> Type of crystal structure

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<span class="mw-page-title-main">Strontium titanate</span> Chemical compound

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<span class="mw-page-title-main">Lead zirconate titanate</span> Chemical compound

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<span class="mw-page-title-main">Bismuth titanate</span> Chemical compound

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A polar metal, metallic ferroelectric, or ferroelectric metal is a metal that contains an electric dipole moment. Its components have an ordered electric dipole. Such metals should be unexpected, because the charge should conduct by way of the free electrons in the metal and neutralize the polarized charge. However they do exist. Probably the first report of a polar metal was in single crystals of the cuprate superconductors YBa2Cu3O7−δ,. A polarization was observed along one (001) axis by pyroelectric effect measurements, and the sign of the polarization was shown to be reversible, while its magnitude could be increased by poling with an electric field. The polarization was found to disappear in the superconducting state. The lattice distortions responsible were considered to be a result of oxygen ion displacements induced by doped charges that break inversion symmetry. The effect was utilized for fabrication of pyroelectric detectors for space applications, having the advantage of large pyroelectric coefficient and low intrinsic resistance. Another substance family that can produce a polar metal is the nickelate perovskites. One example interpreted to show polar metallic behavior is lanthanum nickelate, LaNiO3. A thin film of LaNiO3 grown on the (111) crystal face of lanthanum aluminate, (LaAlO3) was interpreted to be both conductor and a polar material at room temperature. The resistivity of this system, however, shows an upturn with decreasing temperature, hence does not strictly adhere to the definition of a metal. Also, when grown 3 or 4 unit cells thick (1-2 nm) on the (100) crystal face of LaAlO3, the LaNiO3 can be a polar insulator or polar metal depending on the atomic termination of the surface. Lithium osmate, LiOsO3 also undergoes a ferrorelectric transition when it is cooled below 140K. The point group changes from R3c to R3c losing its centrosymmetry. At room temperature and below, lithium osmate is an electric conductor, in single crystal, polycrystalline or powder forms, and the ferroelectric form only appears below 140K. Above 140K the material behaves like a normal metal. Artificial two-dimensional polar metal by charge transfer to a ferroelectric insulator has been realized in LaAlO3/Ba0.8Sr0.2TiO3/SrTiO3 complex oxide heterostructures.

<span class="mw-page-title-main">Bengt Aurivillius</span> Swedish chemist

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<span class="mw-page-title-main">Dragan Damjanovic</span> Swiss-Bosnian-Herzegovinian materials scientist

Dragan Damjanovic is a Swiss-Bosnian-Herzegovinian materials scientist. From 2008 to 2022, he was a professor of material sciences at EPFL and head of the Group for Ferroelectrics and Functional Oxides.

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References

  1. Smolenskii, G.; Isupov, V.; Agranovskaya, A.; Krainik, N. (1961). "New ferroelectrics of complex composition". Sov. Phys. Solid State. 2: 2651–2654.
  2. Zvirgzds, J.A.; Kapostin, P.P.; Zvirgzde, J.V.; Kruzina, T.V. (1982). "X-ray study of phase transitions in ferroelectric Na0.5Bi0.5TiO3". Ferroelectrics. 40 (1): 75–77. Bibcode:1982Fer....40...75Z. doi:10.1080/00150198208210600.
  3. Bousquet, M.; Duclere, J.R.; Orhan, E.; Boulle, A.; Bachelet, C.; Champeaux, C (2010). "Optical properties of an epitaxial Na0.5Bi0.5TiO3 thin film grown by laser ablation: Experimental approach and density functional theory calculations". J. Appl. Phys. 107 (10): 104107–104107–13. Bibcode:2010JAP...107j4107B. doi:10.1063/1.3400095.
  4. Takenaka, T.; Maruyama, K.-I.; Sakata, K. (1991). "(Bi1/2Na1/2)TiO3-BaTiO3 system for lead-free piezoelectric ceramics". Jpn. J. Appl. Phys. Part 1. 30 (9S): 2236–2239. Bibcode:1991JaJAP..30.2236T. doi:10.1143/JJAP.30.2236. S2CID   124093028.
  5. Sasaki, A.; Chiba, T.; Mamiya, Y.; Otsuki, E. Dielectric and piezoelectric properties of (Bi0.5Na0.5)TiO3-(Bi0.5K0.5)TiO3 systems. Jpn. J. Appl. Phys. Part 1 1999, 38, 5564–5567.
  6. Reichmann, K.; Feteira, A., Li M. (2015). "Bismuth Sodium Titanate Based Materials for Piezoelectric Actuators". Materials. 8 (12): 8467–8495. Bibcode:2015Mate....8.8467R. doi: 10.3390/ma8125469 . PMC   5458809 . PMID   28793724.{{cite journal}}: CS1 maint: multiple names: authors list (link)

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