LSAT (oxide)

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LSAT (oxide)
Names
Other names
lanthanum aluminate - strontium aluminium tantalate
Identifiers
3D model (JSmol)
PubChem CID
  • InChI=1S/10Al.3La.47H2O.4O.14Sr.7Ta/h;;;;;;;;;;;;;47*1H2;;;;;;;;;;;;;;;;;;;;;;;;;/q;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;;2*-1;14*+2;;;;;;;/p-26
    Key: HIPYJEIMBYUORH-UHFFFAOYSA-A
  • O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[O-][Ta](=O)([O-])O[Al].[Al].[Al].[Al].[Al].[Al].[Al].[Al].[Al].[Al].[Sr+2].[Sr+2].[Sr+2].[Sr+2].[Sr+2].[Sr+2].[Sr+2].[Sr+2].[Sr+2].[Sr+2].[Sr+2].[Sr+2].[Sr+2].[Sr+2].[La].[La].[La].[Ta].[Ta].[Ta].[Ta].[Ta].[Ta]
Properties
(LaAlO3)0.3(Sr2TaAlO6)0.7
Density 6.74 g/cm3
Melting point 1,840 °C (3,340 °F; 2,110 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

LSAT is the most common name for the inorganic compound lanthanum aluminate - strontium aluminium tantalate, which has the chemical formula (LaAlO3)0.3(Sr2TaAlO6)0.7 or its less common alternative: (La0.18Sr0.82)(Al0.59Ta0.41)O3. LSAT is a hard, optically transparent oxide of the elements lanthanum, aluminium, strontium and tantalum. LSAT has the perovskite crystal structure, and its most common use is as a single crystal substrate for the growth of epitaxial thin films.

Contents

Background

LSAT was originally developed as a substrate for the growth of high Tc cuprate superconductors thin films, mostly of yttrium barium copper oxide (YBCO), for microwave device applications. The motivation for its development was to create a lattice-matched substrate with a similar thermal expansion coefficient and no structural phase transition over a wide temperature range, spanning from the high temperatures used for the growth of cuprates, to the cryogenic temperatures where they are superconducting. [1]

Properties

LSAT has a Mohs hardness of 6.5, placing it between quartz and the mineral feldspar. Its relative dielectric constant is ~22 and it has a thermal expansion coefficient of 8~10×10−6/K. The thermal conductivity of LSAT is 5.1 Wm−1K−1. [2] [3] LSAT's (cubic) lattice parameter of 3.868 Å makes it compatible for the growth of a wide range of perovskite oxides with a relatively low strain.[ citation needed ]

LSAT's melting temperature of 1,840C is lower compared to similar alternative substrates, such as LaAlO3. This property enables the growth of LSAT single crystals using the Czochralski process (CZ), which has commercial advantages. [4]

Uses

An LSAT single-crystal substrate (5x5x0.5 mm) LSAT substrate.jpg
An LSAT single-crystal substrate (5x5x0.5 mm)

LSAT is primarily used in its single crystal form, typically as thin (≤1 mm) wafers. These wafers are used as a common substrate for epitaxial growth of thin films. LSAT substrates are popular for epitaxial oxides and their heterostructures, often in the study of electron correlation phenomena. Typical materials grown on LSAT substrates include strontium titanate (SrTiO3), cuprate superconductors (such as YBCO), iron-based superconductors (iron-pnictides), rare-earth manganites, rare-earth nickelates and others. Semiconductors such as gallium nitride can also be grown on LSAT. [5]

LSAT's usefulness as a substrate for the growth of such films stems from its high chemical and thermal stability, and very low electrical conductivity. The growth conditions for such epitaxial layers can cause some substrates to form high densities of defects that can alter their properties. One example is the tendency of strontium titanate to form oxygen vacancy defects under high temperatures in high vacuum. These defects result in considerable variations of its properties, including the increase of electrical conductivity and optical opacity. LSAT on the other hand, is stable in both oxidizing and fairly reducing environments in high temperatures, thus enabling a larger window for the processing and growth conditions.[ citation needed ]

See also

Related Research Articles

Unconventional superconductors are materials that display superconductivity which is not explained by the usual BCS theory or its extension, the Eliashberg theory. The pairing in unconventional superconductors may originate from some other mechanism than the electron–phonon interaction. Alternatively, a superconductor is unconventional if the superconducting order parameter transforms according to a non-trivial irreducible representation of the point group or space group of the system. Per definition, superconductors that break additional symmetries to U (1) symmetry are known as unconventional superconductors.

<span class="mw-page-title-main">High-temperature superconductivity</span> Superconductive behavior at temperatures much higher than absolute zero

High-temperature superconductivity is superconductivity in materials with a critical temperature above 77 K, the boiling point of liquid nitrogen. They are only "high-temperature" relative to previously known superconductors, which function at colder temperatures, close to absolute zero. The "high temperatures" are still far below ambient, and therefore require cooling. The first breakthrough of high-temperature superconductor was discovered in 1986 by IBM researchers Georg Bednorz and K. Alex Müller. Although the critical temperature is around 35.1 K, this new type of superconductor was readily modified by Ching-Wu Chu to make the first high-temperature superconductor with critical temperature 93 K. Bednorz and Müller were awarded the Nobel Prize in Physics in 1987 "for their important break-through in the discovery of superconductivity in ceramic materials". Most high-Tc materials are type-II superconductors.

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

A perovskite is any material of formula ABX3 with a crystal structure similar to that of the mineral perovskite, this latter consisting of calcium titanium oxide (CaTiO3). The mineral was first discovered in the Ural mountains of Russia by Gustav Rose in 1839 and named after Russian mineralogist L. A. Perovski (1792–1856). 'A' and 'B' are two positively charged ions (i.e. cations), often of very different sizes, and X is a negatively charged ion (an anion, frequently oxide) that bonds to both cations. The 'A' atoms are generally larger than the 'B' atoms. The ideal cubic structure has the B cation in 6-fold coordination, surrounded by an octahedron of anions, and the A cation in 12-fold cuboctahedral coordination. Additional perovskite forms may exist where both/either the A and B sites have a configuration of A1x-1A2x and/or B1y-1B2y and the X may deviate from the ideal coordination configuration as ions within the A and B sites undergo changes in their oxidation states.

<span class="mw-page-title-main">Yttrium barium copper oxide</span> Chemical compound

Yttrium barium copper oxide (YBCO) is a family of crystalline chemical compounds that display high-temperature superconductivity; it includes the first material ever discovered to become superconducting above the boiling point of liquid nitrogen [77 K ] at about 93 K.

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

Strontium titanate is an oxide of strontium and titanium with the chemical formula SrTiO3. At room temperature, it is a centrosymmetric paraelectric material with a perovskite structure. At low temperatures it approaches a ferroelectric phase transition with a very large dielectric constant ~104 but remains paraelectric down to the lowest temperatures measured as a result of quantum fluctuations, making it a quantum paraelectric. It was long thought to be a wholly artificial material, until 1982 when its natural counterpart—discovered in Siberia and named tausonite—was recognised by the IMA. Tausonite remains an extremely rare mineral in nature, occurring as very tiny crystals. Its most important application has been in its synthesized form wherein it is occasionally encountered as a diamond simulant, in precision optics, in varistors, and in advanced ceramics.

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

Lead zirconate titanate, also called lead zirconium titanate and commonly abbreviated as PZT, is an inorganic compound with the chemical formula Pb[ZrxTi1−x]O3(0 ≤ x ≤ 1).. It is a ceramic perovskite material that shows a marked piezoelectric effect, meaning that the compound changes shape when an electric field is applied. It is used in a number of practical applications such as ultrasonic transducers and piezoelectric resonators. It is a white to off-white solid.

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

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

<span class="mw-page-title-main">Bismuth strontium calcium copper oxide</span> Family of high-temperature superconductors

Bismuth strontium calcium copper oxide (BSCCO, pronounced bisko), is a type of cuprate superconductor having the generalized chemical formula Bi2Sr2Can−1CunO2n+4+x, with n = 2 being the most commonly studied compound (though n = 1 and n = 3 have also received significant attention). Discovered as a general class in 1988, BSCCO was the first high-temperature superconductor which did not contain a rare-earth element.

<span class="mw-page-title-main">K. Alex Müller</span> Swiss physicist and Nobel laureate (1927–2023)

Karl Alexander Müller was a Swiss physicist and Nobel laureate. He received the Nobel Prize in Physics in 1987 with Georg Bednorz for their work in superconductivity in ceramic materials.

<span class="mw-page-title-main">Lanthanum strontium manganite</span>

Lanthanum strontium manganite (LSM or LSMO) is an oxide ceramic material with the general formula La1−xSrxMnO3, where x describes the doping level.

Cuprate superconductors are a family of high-temperature superconducting materials made of layers of copper oxides (CuO2) alternating with layers of other metal oxides, which act as charge reservoirs. At ambient pressure, cuprate superconductors are the highest temperature superconductors known. However, the mechanism by which superconductivity occurs is still not understood.

<span class="mw-page-title-main">Perovskite</span> Oxide mineral

Perovskite (pronunciation: ) is a calcium titanium oxide mineral composed of calcium titanate (chemical formula CaTiO3). Its name is also applied to the class of compounds which have the same type of crystal structure as CaTiO3, known as the perovskite structure, which has a general chemical formula A2+B4+(X2−)3. Many different cations can be embedded in this structure, allowing the development of diverse engineered materials.

<span class="mw-page-title-main">Superconducting wire</span> Wires exhibiting zero resistance

Superconducting wires are electrical wires made of superconductive material. When cooled below their transition temperatures, they have zero electrical resistance. Most commonly, conventional superconductors such as niobium–titanium are used, but high-temperature superconductors such as YBCO are entering the market.

<span class="mw-page-title-main">Distrontium ruthenate</span> Chemical compound

Distrontium ruthenate, also known as strontium ruthenate, is an oxide of strontium and ruthenium with the chemical formula Sr2RuO4. It was the first reported perovskite superconductor that did not contain copper. Strontium ruthenate is structurally very similar to the high-temperature cuprate superconductors, and in particular, is almost identical to the lanthanum doped superconductor (La, Sr)2CuO4. However, the transition temperature for the superconducting phase transition is 0.93 K (about 1.5 K for the best sample), which is much lower than the corresponding value for cuprates.

<span class="mw-page-title-main">Lanthanum aluminate-strontium titanate interface</span>

The interface between lanthanum aluminate (LaAlO3) and strontium titanate (SrTiO3) is a notable materials interface because it exhibits properties not found in its constituent materials. Individually, LaAlO3 and SrTiO3 are non-magnetic insulators, yet LaAlO3/SrTiO3 interfaces can exhibit electrical metallic conductivity, superconductivity, ferromagnetism, large negative in-plane magnetoresistance, and giant persistent photoconductivity. The study of how these properties emerge at the LaAlO3/SrTiO3 interface is a growing area of research in condensed matter physics.

Lanthanum aluminate is an inorganic compound with the formula LaAlO3, often abbreviated as LAO. It is an optically transparent ceramic oxide with a distorted perovskite structure.

A complex oxide is a chemical compound that contains oxygen and at least two other elements. Complex oxide materials are notable for their wide range of magnetic and electronic properties, such as ferromagnetism, ferroelectricity, and high-temperature superconductivity. These properties often come from their strongly correlated electrons in d or f orbitals.

Lanthanum ytterbium oxide is a solid inorganic compound of lanthanum, ytterbium and oxygen with the chemical formula of LaYbO3. This compound adopts the perovskite structure.

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">Mixed conductor</span>

Mixed conductors, also known as mixed ion-electron conductors(MIEC), are a single-phase material that has significant conduction ionically and electronically. Due to the mixed conduction, a formally neutral species can transport in a solid and therefore mass storage and redistribution are enabled. Mixed conductors are well known in conjugation with high-temperature superconductivity and are able to capacitate rapid solid-state reactions.

References

  1. B.C. Chakoumakos (1998). "Thermal expansion of LaAlO3 and (La,Sr)(Al,Ta)O3 substrate materials for superconducting thin-film device applications" (PDF). Journal of Applied Physics . 83 (4): 1979–1982. Bibcode:1998JAP....83.1979C. doi:10.1063/1.366925.
  2. LSAT properties Archived 2014-06-27 at archive.today from the manufacturer Toplent Photonics Componenets
  3. LSAT properties from the manufacturer Sigma-Aldrich
  4. LSAT specs and information from the manufacturer MTI Corp.
  5. W. Wang; et al. (2013). "Growth and characterization of GaN-based LED wafers on La0.3Sr1.7AlTaO6 substrates". Journal of Materials Chemistry C . 1 (26): 4070. doi:10.1039/C3TC00916E.