Jump to content

Indium(III) sulfide

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by MSBOT (talk | contribs) at 14:23, 15 April 2012 (r2.7.3) (Robot: Modifying fa:سولفید ایندیم(III)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Indium(III) sulfide
Names
Other names
indium sesquisulfide, diindium trisulphide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.031.571 Edit this at Wikidata
  • InChI=1S/2In.3S checkY
    Key: ZOMNDSJRWSNDFL-UHFFFAOYSA-N checkY
  • InChI=1/2In.3S/rIn2S3/c3-1-5-2-4
    Key: ZOMNDSJRWSNDFL-YYMIQOPKAJ
  • S=[In]S[In]=S
Properties
In2S3
Molar mass 325.82 g/mol
Appearance red powder
Density 4.90 g/cm³, solid
Melting point 1050.0 °C
insoluble
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propaneInstability 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g. white phosphorusSpecial hazards (white): no code
3
4
2
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 ?)

Indium(III) sulfide is the inorganic compound with the formula In2S3. Three different structures ("polymorphs") are known: yellow, α-In2S3 has a defect cubic structure, red β-In2S3 has a defect spinel, tetragonal, structure, and γ-In2S3 has a layered structure. The red, β, form is considered to be the most stable form at room temperature, although the yellow form may be present depending on the method of production. Like related covalent solids, In2S3 is insoluble in all solvents. It is attacked by acids and by sulfide. It is slightly soluble in Na2S.[1]

Indium sulfide was the first indium compound ever described, being reported in 1863.[2] Reich and Richter determined the existence of indium as a new element from the sulfide precipitate.

Structure and properties

In2S3 features tetrahedral In(III) centers linked to four sulfido ligands. β-In2S3 is a diamagnetic, n-type semiconductor with an optical band gap of 2.1 eV. It has been proposed to replace the hazardous cadmium sulfide, CdS, as a buffer layer in solar cells.[3]

Production

Traditionally it was prepared in the chemical laboratory by direct combination of the elements. Production from volatile complexes of indium and sulfur for example dithiocarbamates (e.g. Et2InIIIS2CNEt2) have been explored as methods suitable for vapor deposition techniques.[4]

General references

  • WebElements
  • Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.

References

  1. ^ Indium Sulfide
  2. ^ F. Reich, Th. Richter (1863). "Vorläufige Notiz über ein neues Metall". J. Prakt. Chem. 89: 441. doi:10.1002/prac.18630890156.
  3. ^ N. Barreau, S. Marsillac, D. Albertini and J. C. Bernede (2002). "Structural, optical and electrical properties of β-In2S3-3xO3x thin films obtained by PVD". Thin Solid Films. 403: 331–334. doi:10.1016/S0040-6090(01)01512-7.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^ S. W. Haggata M Azad Malik, M. Motevalli, and P. O'Brien (1995). "Synthesis and Characterization of Some Mixed Alkyl Thiocarbamates of Gallium and Indium, Precursors for III/VI Materials: The X-ray Single-Crystal Structures of Dimethyl- and Diethylindium Diethyldithiocarbamate". Chem. Mater. 7 (4): 716–724. doi:10.1021/cm00052a017.{{cite journal}}: CS1 maint: multiple names: authors list (link)