Magnesium selenide

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Magnesium selenide
Names
Systematic IUPAC name
Magnesium selenide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.013.820 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 215-201-0
PubChem CID
UNII
  • InChI=1S/Mg.Se/q+2;-2
    Key: AZUPEYZKABXNLR-UHFFFAOYSA-N
  • [Mg+2].[Se-2]
Properties
MgSe
Molar mass 103.27 g/mol [1]
Density 4.21 g/cm3 (rock-salt) [2]
3.32 g/cm3 (zincblende) [1]
Melting point 1,290 °C; 2,350 °F; 1,560 K [1]
Band gap 3.9 eV (rock-salt) (300 K)
4.0 eV (zincblende) (300 K)
Structure
Rock-salt (cubic)
Zincblende (cubic)
Wurtzite (hexagonal)
a = 0.55 nm (rock-salt)
a = 0.59 nm (zincblende)
a = 0.415 nm, c = 0.672 nm (wurtzite) [2]
Related compounds
Other anions
Magnesium oxide
Magnesium sulfide
Magnesium telluride
Other cations
Cadmium selenide
Mercury selenide
Zinc selenide
Related compounds
Magnesium zinc selenide
Cadmium magnesium selenide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Magnesium selenide is an inorganic compound with the chemical formula MgSe. It contains magnesium and selenium in a 1:1 ratio. It belongs to the II-VI family of semiconductor compounds.

Contents

Structure

Three crystal structures for MgSe have been experimentally characterized. The rock-salt structure is considered to be the most stable crystal structure that has been observed in bulk samples of MgSe, and a cubic lattice constant of 0.55 nm was deduced for this structure. [2] Although attempts at preparing pure zincblende MgSe have been unsuccessful, [3] the lattice constant of zincblende MgSe has been extrapolated from epitaxial thin films of zincblende MgxZn1-xSySe1-x and MgxZn1-xSe grown on gallium arsenide, the latter of which was prepared with a high magnesium content (up to 95% Mg, i.e., Mg0.95Zn0.05Se). [3] [4] There is good agreement between these and other extrapolations that the lattice constant of pure zincblende MgSe is 0.59 nm. [1] [2] The wurtzite structure of MgSe has been observed, but it is unstable and slowly converts to the rock-salt structure. [5]

NiAs- and FeSi-type crystal structures of MgSe are predicted to form by subjecting the rock-salt crystal structure to extremely high pressures. [2]

Electronic properties

Both rock-salt and zincblende MgSe are semiconductors. On the basis of different extrapolations, a room temperature bandgap of 4.0 eV has been recommended for zincblende MgSe. [1] [2] A room temperature bandgap of 3.9 eV was determined for rock-salt MgSe. [2] [3]

Preparation

Thin films of amorphous, wurtzite and rock-salt MgSe have been prepared by vacuum deposition of Mg and Se at cryogenic temperatures, followed by heating and annealing. [5] Compound semiconductor alloys of MgSe, such as MgxZn1-xSe, have been prepared by molecular beam epitaxy. [3] [4]

Reactions

Samples of pure MgSe and Mg-rich MgxZn1-xSe (x > 0.7) readily react with water and oxidize in air. [2] [3]

Related Research Articles

<span class="mw-page-title-main">Epitaxy</span> Crystal growth process relative to the substrate

Epitaxy refers to a type of crystal growth or material deposition in which new crystalline layers are formed with one or more well-defined orientations with respect to the crystalline seed layer. The deposited crystalline film is called an epitaxial film or epitaxial layer. The relative orientation(s) of the epitaxial layer to the seed layer is defined in terms of the orientation of the crystal lattice of each material. For most epitaxial growths, the new layer is usually crystalline and each crystallographic domain of the overlayer must have a well-defined orientation relative to the substrate crystal structure. Epitaxy can involve single-crystal structures, although grain-to-grain epitaxy has been observed in granular films. For most technological applications, single-domain epitaxy, which is the growth of an overlayer crystal with one well-defined orientation with respect to the substrate crystal, is preferred. Epitaxy can also play an important role while growing superlattice structures.

<span class="mw-page-title-main">Cubic crystal system</span> Crystallographic system where the unit cell is in the shape of a cube

In crystallography, the cubiccrystal system is a crystal system where the unit cell is in the shape of a cube. This is one of the most common and simplest shapes found in crystals and minerals.

<span class="mw-page-title-main">Cadmium sulfide</span> Chemical compound

Cadmium sulfide is the inorganic compound with the formula CdS. Cadmium sulfide is a yellow salt. It occurs in nature with two different crystal structures as the rare minerals greenockite and hawleyite, but is more prevalent as an impurity substituent in the similarly structured zinc ores sphalerite and wurtzite, which are the major economic sources of cadmium. As a compound that is easy to isolate and purify, it is the principal source of cadmium for all commercial applications. Its vivid yellow color led to its adoption as a pigment for the yellow paint "cadmium yellow" in the 18th century.

<span class="mw-page-title-main">Indium antimonide</span> Chemical compound

Indium antimonide (InSb) is a crystalline compound made from the elements indium (In) and antimony (Sb). It is a narrow-gap semiconductor material from the III-V group used in infrared detectors, including thermal imaging cameras, FLIR systems, infrared homing missile guidance systems, and in infrared astronomy. Indium antimonide detectors are sensitive to infrared wavelengths between 1 and 5 μm.

<span class="mw-page-title-main">Cadmium selenide</span> Chemical compound

Cadmium selenide is an inorganic compound with the formula CdSe. It is a black to red-black solid that is classified as a II-VI semiconductor of the n-type. It is a pigment but applications are declining because of environmental concerns

<span class="mw-page-title-main">Zinc selenide</span> Chemical compound

Zinc selenide is the inorganic compound with the formula ZnSe. It is a lemon-yellow solid although most samples have a duller color due to the effects of oxidation. It is an intrinsic semiconductor with a band gap of about 2.70 eV at 25 °C (77 °F). ZnSe occurs as the rare mineral stilleite, named after Hans Stille.

Indium gallium arsenide (InGaAs) is a ternary alloy of indium arsenide (InAs) and gallium arsenide (GaAs). Indium and gallium are group III elements of the periodic table while arsenic is a group V element. Alloys made of these chemical groups are referred to as "III-V" compounds. InGaAs has properties intermediate between those of GaAs and InAs. InGaAs is a room-temperature semiconductor with applications in electronics and photonics.

<span class="mw-page-title-main">Magnesium sulfide</span> Inorganic compound generated in the production of metallic iron

Magnesium sulfide is an inorganic compound with the formula MgS. It is a white crystalline material but often is encountered in an impure form that is brown and non-crystalline powder. It is generated industrially in the production of metallic iron.

<span class="mw-page-title-main">Copper indium gallium selenide</span> Chemical compound

Copper indium gallium (di)selenide (CIGS) is a I-III-VI2 semiconductor material composed of copper, indium, gallium, and selenium. The material is a solid solution of copper indium selenide (often abbreviated "CIS") and copper gallium selenide. It has a chemical formula of CuIn1−xGaxSe2, where the value of x can vary from 0 (pure copper indium selenide) to 1 (pure copper gallium selenide). CIGS is a tetrahedrally bonded semiconductor, with the chalcopyrite crystal structure, and a bandgap varying continuously with x from about 1.0 eV (for copper indium selenide) to about 1.7 eV (for copper gallium selenide).

<span class="mw-page-title-main">Zinc telluride</span> Chemical compound

Zinc telluride is a binary chemical compound with the formula ZnTe. This solid is a semiconductor material with a direct band gap of 2.26 eV. It is usually a p-type semiconductor. Its crystal structure is cubic, like that for sphalerite and diamond.

<span class="mw-page-title-main">Mercury selenide</span> Chemical compound

Mercury selenide is a chemical compound of mercury and selenium. It is a grey-black crystalline solid semi-metal with a sphalerite structure. The lattice constant is 0.608 nm.

<span class="mw-page-title-main">Tin selenide</span> Chemical compound

Tin selenide, also known as stannous selenide, is an inorganic compound with the formula SnSe. Tin(II) selenide is a typical layered metal chalcogenide as it includes a group 16 anion (Se2−) and an electropositive element (Sn2+), and is arranged in a layered structure. Tin(II) selenide is a narrow band-gap (IV-VI) semiconductor structurally analogous to black phosphorus. It has received considerable interest for applications including low-cost photovoltaics, and memory-switching devices.

In chemistry, the Grimm–Sommerfeld rule predicts that binary compounds with covalent character that have an average of 4 electrons per atom will have structures where both atoms are tetrahedrally coordinated. Examples are silicon carbide, the III-V semiconductors indium phosphide and gallium arsenide, the II-VI semiconductors, cadmium sulfide, cadmium selenide.

Selective area epitaxy is the local growth of epitaxial layer through a patterned amorphous dielectric mask (typically SiO2 or Si3N4) deposited on a semiconductor substrate. Semiconductor growth conditions are selected to ensure epitaxial growth on the exposed substrate, but not on the dielectric mask. SAE can be executed in various epitaxial growth methods such as molecular beam epitaxy (MBE), metalorganic vapour phase epitaxy (MOVPE) and chemical beam epitaxy (CBE). By SAE, semiconductor nanostructures such as quantum dots and nanowires can be grown to their designed places.

<span class="mw-page-title-main">I-III-VI semiconductors</span> Solid semiconducting materials

I-III-VI2 semiconductors are solid semiconducting materials that contain three or more chemical elements belonging to groups I, III and VI (IUPAC groups 1/11, 13 and 16) of the periodic table. They usually involve two metals and one chalcogen. Some of these materials have a direct bandgap, Eg, of approximately 1.5 eV, which makes them efficient absorbers of sunlight and thus potential solar cell materials. A fourth element is often added to a I-III-VI2 material to tune the bandgap for maximum solar cell efficiency. A representative example is copper indium gallium selenide (CuInxGa(1–x)Se2, Eg = 1.7–1.0 eV for x = 0–1), which is used in copper indium gallium selenide solar cells.

II-VI semiconductor compounds are compounds composed of a metal from either group 2 or 12 of the periodic table and a nonmetal from group 16 . These semiconductors crystallize either in the zincblende lattice structure or the wurtzite crystal structure. They generally exhibit large band gaps, making them popular for short wavelength applications in optoelectronics.

Aluminium gallium antimonide, also known as gallium aluminium antimonide or AlGaSb (AlxGa1-xSb), is a ternary III-V semiconductor compound. It can be considered as an alloy between aluminium antimonide and gallium antimonide. The alloy can contain any ratio between aluminium and gallium. AlGaSb refers generally to any composition of the alloy.

Gallium indium antimonide, also known as indium gallium antimonide, GaInSb, or InGaSb (GaxIn1-xSb), is a ternary III-V semiconductor compound. It can be considered as an alloy between gallium antimonide and indium antimonide. The alloy can contain any ratio between gallium and indium. GaInSb refers generally to any composition of the alloy.

Aluminium arsenide antimonide, or AlAsSb (AlAs1-xSbx), is a ternary III-V semiconductor compound. It can be considered as an alloy between aluminium arsenide and aluminium antimonide. The alloy can contain any ratio between arsenic and antimony. AlAsSb refers generally to any composition of the alloy.

References

  1. 1 2 3 4 5 Adachi, S., ed. (2004). "Zincblende Magnesium Selenide (β-MgSe)". Handbook on Physical Properties of Semiconductors. Kluwer Academic Publishers. pp. 37–50. doi:10.1007/1-4020-7821-8_3. ISBN   978-1-4020-7820-0.
  2. 1 2 3 4 5 6 7 8 Madelung, O., Rössler, U., Schulz, M., eds. (1999). "Magnesium oxide (MgO) physical properties (MgSe)". II-VI and I-VII Compounds; Semimagnetic Compounds. Landolt-Börnstein - Group III Condensed Matter. Vol. 41B. Springer-Verlag. pp. 1–8. doi:10.1007/10681719_218. ISBN   978-3-540-64964-9.
  3. 1 2 3 4 5 Jobst, B., Hommel, D., Lunz, U., Gerhard, T., Landwehr, G. (1996). "E0 band-gap energy and lattice constant of ternary Zn1−xMgxSe as functions of composition". Applied Physics Letters. 69 (1): 97–99. doi:10.1063/1.118132. ISSN   1077-3118.
  4. 1 2 Okuyama, H., Nakano, K., Miyajima, T., Akimoto, K. (1992). "Epitaxial growth of ZnMgSSe on GaAs substrate by molecular beam epitaxy". Journal of Crystal Growth. 117 (1–4): 139–143. Bibcode:1992JCrGr.117..139O. doi:10.1016/0022-0248(92)90732-X. ISSN   0022-0248. S2CID   97851344.
  5. 1 2 Mittendorf, H. (1965). "Röntgenographische und optische Untersuchungen aufgedampfter Schichten aus Erdalkalichalkogeniden". Zeitschrift für Physik (in German). 183 (2): 113–129. Bibcode:1965ZPhy..183..113M. doi:10.1007/BF01380788. ISSN   1434-6001. S2CID   121137813.