Lanthanum phosphide

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Lanthanum phosphide
NaCl polyhedra.svg
Names
Other names
Phosphanylidynelanthanum
Identifiers
3D model (JSmol)
ECHA InfoCard 100.042.515 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 246-782-9
PubChem CID
  • InChI=1S/La.P
    Key: GZHCNRONBGZNAH-UHFFFAOYSA-N
  • P#[La]
Properties
LaP
Molar mass 169.88
AppearanceBlack crystals
Density 5.2 g/cm3
Reacts with water
Structure [1]
Rock salt structure
Fm3m
a = 0.6025 nm
4
Octahedral at La3+, Octahedral at P3-
Related compounds
Other anions
Lanthanum nitride
Lanthanum arsenide
Lanthanum bismuthide
Other cations
Scandium phosphide
Yttrium phosphide
Cerium phosphide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Lanthanum phosphide is an inorganic compound of lanthanum and phosphorus with the chemical formula LaP.

Contents

Synthesis

Lanthanum phosphide can be made by heating lanthanum metal with excess phosphorus in a vacuum: [2]

4 La + P4 → 4 LaP

Physical properties

Lanthanum phosphide forms black crystals of a cubic system, space group Fm3m, cell parameters a = 0.6025 nm, with number of formulas per unit cell Z = 4. [1]

The crystals are very unstable and decompose in the open air.

Electronic properties

Lanthanum phosphide is an example of a strongly correlated material, [3] complicating theoretical prediction of its properties.

According to HSE06 calculations, lanthanum phosphide has been theoretically predicted to have an indirect band gap of 0.25 eV along the Γ-X direction. [4] According to HSE06 calculations with spin-orbit coupling, the band gap is predicted to be a direct gap of 0.72 eV at the X point. [5] Using EVGGA, the compound is predicted to have a band gap of 0.56 eV along the Γ-X direction. [6] FP-LAPW has predicted an indirect gap of 0.33 eV along the Γ-X direction. [3]

Chemical properties

Lanthanum phosphide reacts with water, releasing highly toxic phosphine gas:

LaP + 3H2O → La(OH)3 + PH3

Uses

Lanthanum phosphide compound is a semiconductor used in high power, high frequency applications, and in laser diodes. [7] [8]

Lanthanum polyphosphide

In addition to the simple phosphide, LaP, lanthanum and phosphorus can also form phosphorus-rich compounds such as LaP2 [9] LaP5 [10] and LaP7. [11]

Related Research Articles

<span class="mw-page-title-main">Phosphide</span>

In chemistry, a phosphide is a compound containing the P3− ion or its equivalent. Many different phosphides are known, with widely differing structures. Most commonly encountered on the binary phosphides, i.e. those materials consisting only of phosphorus and a less electronegative element. Numerous are polyphosphides, which are solids consisting of anionic chains or clusters of phosphorus. Phosphides are known with the majority of less electronegative elements with the exception of Hg, Pb, Sb, Bi, Te, and Po. Finally, some phosphides are molecular.

The nitridoborates are chemical compounds of boron and nitrogen with metals. These compounds are typically produced at high temperature by reacting hexagonal boron nitride with metal nitrides or by metathesis reactions involving nitridoborates. A wide range of these compounds have been made involving lithium, alkaline earth metals and lanthanides, and their structures determined using crystallographic techniques such as X-ray crystallography. Structurally one of their interesting features is the presence of polyatomic anions of boron and nitrogen where the geometry and the B–N bond length have been interpreted in terms of π-bonding.

Oxyphosphides are chemical compounds formally containing the group PO, with one phosphorus and one oxygen atom. The phosphorus and oxygen are not bound together as in phosphates or phosphine oxides, instead they are bound separately to the cations (metals), and could be considered as a mixed phosphide-oxide compound. So a compound with OmPn requires cations to balance a negative charge of 2m+3n. The cations will have charges of +2 or +3. The trications are often rare earth elements or actinides. They are in the category of oxy-pnictide compounds.

The phosphidosilicates or phosphosilicides are inorganic compounds containing silicon bonded to phosphorus and one or more other kinds of elements. In the phosphosilicates each silicon atom is surrounded by four phosphorus atoms in a tetrahedron. The triphosphosilicates have a SiP3 unit, that can be a planar triangle like carbonate CO3. The phosphorus atoms can be shared to form different patterns e.g. [Si2P6]10− which forms pairs, and [Si3P7]3− which contains two-dimensional double layer sheets. [SiP4]8− with isolated tetrahedra, and [SiP2]2− with a three dimensional network with shared tetrahedron corners. SiP clusters can be joined, not only by sharing a P atom, but also by way of a P-P bond. This does not happen with nitridosilicates or plain silicates.

Hans Georg von Schnering was a German chemist and professor of inorganic chemistry at the University of Münster, honorary professor at the University of Stuttgart and director at the Max Planck Institute for Solid State Research.

The telluride phosphides are a class of mixed anion compounds containing both telluride and phosphide ions. The phosphidotelluride or telluridophosphide compounds have a [TeP]3− group in which the tellurium atom has a bond to the phosphorus atom. A formal charge of −2 is on the phosphorus and −1 on the tellurium. There is no binary compound of tellurium and phosphorus. Not many telluride phosphides are known, but they have been discovered for noble metals, actinides, and group 4 elements.

The telluride iodides are chemical compounds that contain both telluride ions (Te2−) and iodide ions (I). They are in the class of mixed anion compounds or chalcogenide halides.

A chloride nitride is a mixed anion compound containing both chloride (Cl) and nitride ions (N3−). Another name is metallochloronitrides. They are a subclass of halide nitrides or pnictide halides.

A Phosphide chloride is a mixed anion compound containing both phosphide (P3−) and chloride (Cl) ions.

Phosphide silicides or silicide phosphides or silicophosphides are compounds containing anions composed of silicide (Si4−) and phosphide (P3−). They can be considered as mixed anion compounds. They are distinct from the phosphidosilicates, which have the phosphorus bonded to the silicon. Related compounds include the phosphide carbides, germanide phosphides, nitride silicides, and antimonide silicides.

Phosphide carbides or carbide phosphides are compounds containing anions composed of carbide (C4−) and phosphide (P3−). They can be considered as mixed anion compounds. Related compounds include the phosphide silicides, germanide phosphides, arsenide carbides, nitride carbides and silicide carbides.

Phosphanides are chemicals containing the [PH2] anion. This is also known as the phosphino anion or phosphido ligand. The IUPAC name can also be dihydridophosphate(1−).

Arsenidogermanates are chemical compounds that contain anions with arsenic bonded to germanium. They are in the category of tetrelarsenides, pnictidogermanates, or tetrelpnictides.

Lithium phosphide is an inorganic compound of lithium and phosphorus with the chemical formula Li
3
P
. This dark colored compound is formally the Li+ salt of P3-. It is a hazardous to handle because of its high reactivity toward air.

Phosphide iodides or iodide phosphides are compounds containing anions composed of iodide (I) and phosphide (P3−). They can be considered as mixed anion compounds. They are in the category of pnictidehalides. Related compounds include the phosphide chlorides, arsenide iodides antimonide iodides and phosphide bromides.

Phosphide bromides or bromide phosphides are compounds containing anions composed of bromide (Br) and phosphide (P3−) anions. Usually phosphorus is covalently connected into more complex structures. They can be considered as mixed anion compounds. They are in the category of pnictidehalides. Related compounds include the phosphide chlorides, phosphide iodides, nitride bromides, arsenide bromides, and antimonide bromides.

Arsenide bromides or bromide arsenides are compounds containing anions composed of bromide (Br) and arsenide (As3−). They can be considered as mixed anion compounds. They are in the category of pnictidehalides. Related compounds include the arsenide chlorides, arsenide iodides, phosphide bromides, and antimonide bromides.

Arsenide iodides or iodide arsenides are compounds containing anions composed of iodide (I) and arsenide (As3−). They can be considered as mixed anion compounds. They are in the category of pnictidehalides. Related compounds include the arsenide chlorides, arsenide bromides, phosphide iodides, and antimonide iodides.

Antimonide bromides or bromide antimonides are compounds containing anions composed of bromide (Br) and antimonide (Sb3−). They can be considered as mixed anion compounds. They are in the category of pnictidehalides. Related compounds include the antimonide chlorides, antimonide iodides, arsenide chlorides, arsenide bromides, arsenide iodides, phosphide chlorides, phosphide bromides, and phosphide iodides. The bromoantimonates have antimony in positive oxidation states.

Caesium phosphide refers to any of several inorganic compounds with the formula CsPx. The most studied member is Cs3P7, which forms yellow crystals of tetragonal structure (P41 group), which turn brown when heated to 300 °C, and colorless when cooled with liquid nitrogen.

References

  1. 1 2 Standard X-ray Diffraction Powder Patterns (PDF). U.S. Department of Commerce, National Bureau of Standards. 1967-08-31. p. 69. Retrieved 2023-11-04.
  2. Samsonov, G.V.; Endrzheevskaya, S.N. (September 1963). "Production and Some Properties of Lanthanum Phosphide". Journal of General Chemistry of the USSR (English Translation). 33 (9). Consultants Bureau: 2729. Google books Journal index
  3. 1 2 Shoaib, M.; Murtaza, G.; Khenata, R.; Farooq, M.; Ali, Roshan (2013). "Structural, elastic, electronic and chemical bonding properties of AB (A=Sc,Y,La;B=N,P,As,Sb,Bi) from first principles". Computational Materials Science. 79. Elsevier BV: 239–246. doi:10.1016/j.commatsci.2013.06.015. ISSN   0927-0256.
  4. Yan, X. Z.; Chen, Y. M.; Kuang, X. Y.; Xiang, S. K. (2014-08-26). "Theoretical investigation of La monopnictides: Electronic properties and pressure-induced phase transition". Journal of Applied Physics. 116 (8). AIP Publishing: 083707. Bibcode:2014JAP...116h3707Y. doi:10.1063/1.4893645. ISSN   0021-8979.
  5. Zhou, Yu; Tao, Wang-Li; Zeng, Zhao-Yi; Chen, Xiang-Rong; Chen, Qi-Feng (2019-01-28). "Thermoelectric properties of topological insulator lanthanum phosphide via first-principles study". Journal of Applied Physics. 125 (4). AIP Publishing: 045107. Bibcode:2019JAP...125d5107Z. doi:10.1063/1.5043170. ISSN   0021-8979.
  6. Charifi, Z.; Reshak, Ali Hussain; Baaziz, H. (2008). "Phase transition of LaX (X = P, As, Sb and Bi) at high pressure: Theoretical investigation of the structural and electronic properties". Solid State Communications. 148 (3–4). Elsevier BV: 139–144. Bibcode:2008SSCom.148..139C. doi:10.1016/j.ssc.2008.07.038. ISSN   0038-1098.
  7. Lewis, Robert A. (30 March 2016). Hawley's Condensed Chemical Dictionary. John Wiley & Sons. ISBN   978-1-119-19372-2 . Retrieved 21 December 2021.
  8. O'Bannon, Loran (6 December 2012). Dictionary of Ceramic Science and Engineering. Springer Science & Business Media. p. 151. ISBN   978-1-4613-2655-7 . Retrieved 21 December 2021.
  9. v. Schnering, H. G.; Wichelhaus, W.; Nahrup, M. Schulze (1975). "Zur Chemie und Strukturchemie der Phosphide und Polyphosphide. XI. Lanthandiphosphid LaP2; Darstellung, Struktur und Eigenschaften". Zeitschrift für anorganische und allgemeine Chemie. 412 (3). Wiley: 193–201. doi:10.1002/zaac.19754120302. ISSN   0044-2313.
  10. Wichelhaus, W.; Schnering, H. (1976). "Zur Chemie und Strukturchemie der Phosphide und Polyphosphide. 12. Die Pentaphosphide des Lanthans und Neodyms, LaP5 und NdP5". Zeitschrift für Anorganische und Allgemeine Chemie. 419: 77–86. doi:10.1002/ZAAC.19764190113. S2CID   97289383.
  11. Raghavan, V. (2004). "Fe-La-P (iron-lanthanum-phosphorus)". Journal of Phase Equilibria and Diffusion. 25 (2). Springer Science and Business Media LLC: 172–173. doi:10.1007/s11669-004-0019-7. ISSN   1547-7037.

Further reading