Thallium(I) sulfide
Unit cell of thallium sulfide under standard conditions. The yellow atoms represent the sulfur anions.
Unit cell of thallium sulfide.
Names
IUPAC name
Thallium(I) sulfide
Other names
thallous sulfide, thallous sulphide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.013.865 Edit this at Wikidata
EC Number
  • 215-250-8
UNII
  • InChI=1S/S.2Tl/q-2;2*+1 checkY
    Key: BXJGLLKRUQQYTC-UHFFFAOYSA-N checkY
  • S([Tl])[Tl]
Properties
Tl2S
Molar mass 440.833 g/mol
Appearance black crystalline solid
Density 8.390 g/cm3
Melting point 448 °C (838 °F; 721 K)
Boiling point 1,367 °C (2,493 °F; 1,640 K)
−88.8·10−6 cm3/mol
Structure
Trigonal, hR81
R3, No. 146
a = 12.150(2) Å, c = 18.190(4) Å[1]
2325.57 Å3
27
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Thallium(I) sulfide, Tl2S, is a chemical compound of thallium and sulfur. It was used in some of the earliest photo-electric detectors by Theodore Case who developed the so-called thalofide (sometimes spelt thallofide) cell, used in early film projectors. Case described the detector material as consisting of thallium, oxygen and sulfur,[2] and this was incorrectly described by others as being thallium oxysulfide, which incidentally is a compound that is not known. Case's work was then built on by R.J. Cashman who recognised that the controlled oxidation of the Tl2S film was key to the operation of the cell.[3] Cashman's work culminated in the development of long wave infrared detectors used during the Second World War.[4] Reliable Tl2S detectors were also developed in Germany at the same time.[3]
Tl2S is found in nature as the mineral carlinite[5] which has the distinction of being the only sulfide mineral of thallium that does not contain at least two metals. Tl2S has a distorted anti-CdI2 structure.[6]
Tl2S can be prepared from the elements or by precipitating the sulfide from a solution of thallium(I), e.g. the sulfate or nitrate. Thin films have been deposited, produced from a mixture of citratothallium complex and thiourea. Heating the film in nitrogen at 300°C converts all the product into Tl2S [7]

References

  1. ^ Giester, G.; Lengauer, C.L.; Tillmanns, E.; Zemann, J. (2002). "Tl2S: Re-Determination of Crystal Structure and Stereochemical Discussion". Journal of Solid State Chemistry. 168 (1): 322–330. Bibcode:2002JSSCh.168..322G. doi:10.1006/jssc.2002.9711.
  2. ^ T. W. Case (1920). "Thalofide Cell"—a New Photo-Electric Substance". Phys. Rev. 15 (4): 289. Bibcode:1920PhRv...15..289C. doi:10.1103/PhysRev.15.289.
  3. ^ a b D. J. Lovell (1971). "Cashman thallous sulfide cell". Appl. Opt. 10 (5): 1003–8. Bibcode:1971ApOpt..10.1003L. doi:10.1364/AO.10.001003. PMID 20094592.
  4. ^ American patent 2448517, filed 1944, granted 1948
  5. ^ "Carlinite". webmineral. Retrieved 2009-06-06.
  6. ^ Giester, G.; Lengauer, C. L.; Tillmanns, E.; Zemann, J. (2002). "Tl2S: Re-Determination of Crystal Structure and Stereochemical Discussion". Journal of Solid State Chemistry. 168 (1): 322. Bibcode:2002JSSCh.168..322G. doi:10.1006/jssc.2002.9711.
  7. ^ V. Estrella, M. T. S. Nair and P. K. Nair (2002). "Crystalline structure of chemically deposited thallium sulfide thin films". Thin Solid Films. 414 (2): 281. Bibcode:2002TSF...414..281E. doi:10.1016/S0040-6090(02)00500-X.
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