Cadmium sulfide

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Cadmium sulfide
3D model of the structure of hawleyite
3D model of the structure of hawleyite
3D model of the structure of greenockite
3D model of the structure of greenockite
Names
Other names
cadmium(II) sulfide
greenockite
hawleyite
cadmium yellow
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.013.771 Edit this at Wikidata
EC Number
  • 215-147-8
13655
RTECS number
  • EV3150000
UNII
UN number 2570
  • InChI=1S/Cd.S/q+2;-2 checkY
    Key: FRLJSGOEGLARCA-UHFFFAOYSA-N checkY
  • InChI=1/Cd.S/q+2;-2
    Key: FRLJSGOEGLARCA-UHFFFAOYAL
  • monomer: [S-2].[Cd+2]
  • hawleyite: [SH+2]12[CdH2-2] [SH+2]3[CdH2-2] [SH+2]([CdH-2]14)[CdH-2]1[S+2]5([CdH-2]38)[Cd-2]26[SH+2]2[CdH-2]([S+2]4)[SH+2]1[CdH2-2] [SH+2]3[CdH-2]2[S+2] [CdH-2]([SH+2]6[CdH-2]([SH+2])[SH+2]68)[SH+2]([CdH2-2]6)[CdH-2]35
  • greenockite: [CdH2-2]1[S+2]47[CdH-2]2[S+2] [CdH-2]3[S+2]8([CdH2-2] [SH+2]([CdH2-2]4)[CdH2-2]6)[CdH-2]4[S+2] [CdH-2]5[S+2]6([CdH2-2]6)[Cd-2]78[S+2]78[CdH-2]([SH+2]69)[SH+2]5[CdH2-2] [SH+2]4[CdH-2]7[SH+2]3[CdH2-2] [SH+2]2[CdH-2]8[SH+2]1[CdH2-2]9
  • greenockite: [CdH2-2]1[SH+2]([CdH2-2]6)[CdH2-2] [SH+2]7[CdH-2]2[S+2] [Cd-2]3([S+2] [CdH-2]9[S+2]5)[S+2]18[Cd-2]45[S+2] [CdH-2]5[SH+2]6[Cd-2]78[S+2]78[CdH2-2] [SH+2]5[CdH2-2] [S+2]4([CdH2-2] [SH+2]9[CdH2-2]4)[CdH-2]7[S+2]34[CdH2-2] [SH+2]2[CdH2-2]8
Properties
CdS
Molar mass 144.47 g·mol−1
Appearance Yellow-orange to brown solid.
Density 4.826 g/cm3, solid.
Melting point 1,750 °C (3,180 °F; 2,020 K) 10 MPa
Boiling point 980 °C (1,800 °F; 1,250 K) (sublimation)
insoluble[1]
Solubility soluble in acid
very slightly soluble in ammonium hydroxide
Band gap 2.42 eV
-50.0·10−6 cm3/mol
2.529
Structure
Hexagonal, Cubic
Thermochemistry
65 J·mol−1·K−1[2]
−162 kJ·mol−1[2]
Hazards
GHS labelling:
GHS07: Exclamation markGHS08: Health hazard
Danger
H302, H341, H350, H361, H372, H413
P201, P202, P260, P264, P270, P273, P281, P301+P312, P308+P313, P314, P330, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
3
0
0
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
7080 mg/kg (rat, oral)
NIOSH (US health exposure limits):
PEL (Permissible)
 [1910.1027] TWA 0.005 mg/m3 (as Cd)[3]
REL (Recommended)
 Ca[3]
IDLH (Immediate danger)
 Ca [9 mg/m3 (as Cd)][3]
Safety data sheet (SDS) ICSC 0404
Related compounds
Other anions
 Cadmium oxide
Cadmium selenide
Other cations
 Zinc sulfide
Mercury sulfide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Cadmium sulfide is the inorganic compound with the formula CdS. Cadmium sulfide is a yellow salt.[4] 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.[4] Its vivid yellow color led to its adoption as a pigment for the yellow paint "cadmium yellow" in the 18th century.

Production[edit]

Cadmium sulfide can be prepared by the precipitation from soluble cadmium(II) salts with sulfide ion. This reaction has been used for gravimetric analysis and qualitative inorganic analysis.[5]
The preparative route and the subsequent treatment of the product, affects the polymorphic form that is produced (i.e., cubic vs hexagonal). It has been asserted that chemical precipitation methods result in the cubic zincblende form.[6]

Pigment production usually involves the precipitation of CdS, the washing of the solid precipitate to remove soluble cadmium salts followed by calcination (roasting) to convert it to the hexagonal form followed by milling to produce a powder.[7] When cadmium sulfide selenides are required the CdSe is co-precipitated with CdS and the cadmium sulfoselenide is created during the calcination step.[7]

Cadmium sulfide is sometimes associated with sulfate reducing bacteria.[8][9]

Routes to thin films of CdS[edit]

Special methods are used to produce films of CdS as components in some photoresistors and solar cells. In the chemical bath deposition method, thin films of CdS have been prepared using thiourea as the source of sulfide anions and an ammonium buffer solution to control pH:[10]

Cd2+ + H2O + (NH2)2CS + 2 NH3 → CdS + (NH2)2CO + 2 NH4+

Cadmium sulfide can be produced using metalorganic vapour phase epitaxy and MOCVD techniques by the reaction of dimethylcadmium with diethyl sulfide:[11]

Cd(CH3)2 + Et2S → CdS + CH3CH3 + C4H10

Other methods to produce films of CdS include

Reactions[edit]

Cadmium sulfide can be dissolved in acids.[17]

CdS + 2 HCl → CdCl2 + H2S

When solutions of sulfide containing dispersed CdS particles are irradiated with light, hydrogen gas is generated:[18]

H2S → H2 + S ΔfH = +9.4 kcal/mol

The proposed mechanism involves the electron/hole pairs created when incident light is absorbed by the cadmium sulfide[19] followed by these reacting with water and sulfide:[18]

Production of an electron–hole pair
CdS + hν → e− + h+
Reaction of electron
2e− + 2H2O → H2 + 2OH−
Reaction of hole
2h+ + S2− → S

Structure and physical properties[edit]

Cadmium sulfide has, like zinc sulfide, two crystal forms. The more stable hexagonal wurtzite structure (found in the mineral Greenockite) and the cubic zinc blende structure (found in the mineral Hawleyite). In both of these forms the cadmium and sulfur atoms are four coordinate.[20] There is also a high pressure form with the NaCl rock salt structure.[20]

Cadmium sulfide is a direct band gap semiconductor (gap 2.42 eV).[19] The proximity of its band gap to visible light wavelengths gives it a coloured appearance.[4]
As well as this obvious property other properties result:

  • the conductivity increases when irradiated,[19] (leading to uses as a photoresistor)
  • when combined with a p-type semiconductor it forms the core component of a photovoltaic (solar) cell and a CdS/Cu2S solar cell was one of the first efficient cells to be reported (1954)[21][22]
  • when doped with for example Cu+ ("activator") and Al3+ ("coactivator") CdS luminesces under electron beam excitation (cathodoluminescence) and is used as phosphor[23]
  • both polymorphs are piezoelectric and the hexagonal is also pyroelectric[24]
  • electroluminescence[25]
  • CdS crystals can act as a gain medium in solid state laser[26][27]
  • In thin-film form, CdS can be combined with other layers for use in certain types of solar cells.[28] CdS was also one of the first semiconductor materials to be used for thin-film transistors (TFTs).[29] However interest in compound semiconductors for TFTs largely waned after the emergence of amorphous silicon technology in the late 1970s.
  • Thin films of CdS can be piezoelectric and have been used as transducers which can operate at frequencies in the GHz region.
  • Nanoribbons of CdS show a net cooling due annihilation of phonons, during anti-Stokes luminescence at ~510 nm. As a result, a maximum temperature drop of 40 and 15 K has been demonstrated when the nanoribbons are pumped with a 514 or 532 nm laser.[30]

Applications[edit]

Pigment[edit]

Yellow cadmium sulfide- pigment

CdS is used as pigment in plastics, showing good thermal stability, light and weather fastness, chemical resistance and high opacity.[7] As a pigment, CdS is known as cadmium yellow (CI pigment yellow 37).[4][31] About 2000 tons are produced annually as of 1982, representing about 25% of the cadmium processed commercially.[32]

Historical use in art[edit]

The general commercial availability of cadmium sulfide from the 1840s led to its adoption by artists, notably Van Gogh, Monet (in his London series and other works) and Matisse (Bathers by a River 1916–1919).[33] The presence of cadmium in paints has been used to detect forgeries in paintings alleged to have been produced prior to the 19th century.[34]

CdS-CdSe solutions[edit]

CdS and CdSe form solid solutions with each other. Increasing amounts of cadmium selenide, gives pigments verging toward red, for example CI pigment orange 20 and CI pigment red 108.[31]
Such solid solutions are components of photoresistors (light dependent resistors) sensitive to visible and near infrared light.[citation needed]

Safety[edit]

Cadmium sulfide is toxic, especially dangerous when inhaled as dust, and cadmium compounds in general are classified as carcinogenic.[35] Problems of biocompatibility have been reported when CdS is used as colors in tattoos.[36] CdS has an LD50 of approximately 7,080 mg/kg in rats - which is higher than other cadmium compounds due to its low solubility.[37]

References[edit]

  1. ^ Lide, David R. (1998). Handbook of Chemistry and Physics (87 ed.). Boca Raton, FL: CRC Press. pp. 4–67, 1363. ISBN 978-0-8493-0594-8.
  2. ^ a b Zumdahl, Steven S. (2009). Chemical Principles 6th Ed. Houghton Mifflin Company. p. A21. ISBN 978-0-618-94690-7.
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  4. ^ a b c d Egon Wiberg, Arnold Frederick Holleman (2001) Inorganic Chemistry, Elsevier ISBN 0-12-352651-5
  5. ^ Fred Ibbotson (2007), The Chemical Analysis of Steel-Works' Materials,Read Books, ISBN 1-4067-8113-4
  6. ^ Paul Klocek (1991), Handbook of Infrared Optical Materials, CRC Press ISBN 0-8247-8468-5
  7. ^ a b c Hugh MacDonald Smith (2002). High Performance Pigments. Wiley-VCH. ISBN 978-3-527-30204-8.
  8. ^ Larry L. Barton 1995 Sulfate reducing bacteria, Springer, ISBN 0-306-44857-2
  9. ^ Sweeney, Rozamond Y.; Mao, Chuanbin; Gao, Xiaoxia; Burt, Justin L.; Belcher, Angela M.; Georgiou, George; Iverson, Brent L. (2004). "Bacterial Biosynthesis of Cadmium Sulfide Nanocrystals". Chemistry & Biology. 11 (11): 1553–9. doi:10.1016/j.chembiol.2004.08.022. PMID 15556006.
  10. ^ Oladeji, I.O.; Chow, L. (1997). "Optimization of Chemical Bath Deposited Cadmium Sulfide". J. Electrochem. Soc. 144 (7): 7. CiteSeerX 10.1.1.563.1643. doi:10.1149/1.1837815.
  11. ^ Uda, H; Yonezawa, H; Ohtsubo, Y; Kosaka, M; Sonomura, H (2003). "Thin CdS films prepared by metalorganic chemical vapor deposition". Solar Energy Materials and Solar Cells. 75 (1–2): 219. doi:10.1016/S0927-0248(02)00163-0.
  12. ^ Reisfeld, R (2002). "Nanosized semiconductor particles in glasses prepared by the sol–gel method: their optical properties and potential uses". Journal of Alloys and Compounds. 341 (1–2): 56. doi:10.1016/S0925-8388(02)00059-2.
  13. ^ Moon, B; Lee, J; Jung, H (2006). "Comparative studies of the properties of CdS films deposited on different substrates by R.F. sputtering". Thin Solid Films. 511–512: 299. Bibcode:2006TSF...511..299M. doi:10.1016/j.tsf.2005.11.080.
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  22. ^ Reynolds, D.; Leies, G.; Antes, L.; Marburger, R. (1954). "Photovoltaic Effect in Cadmium Sulfide". Physical Review. 96 (2): 533. Bibcode:1954PhRv...96..533R. doi:10.1103/PhysRev.96.533.
  23. ^ C. Fouassier,(1994), Luminescence in Encyclopedia of Inorganic Chemistry, John Wiley & Sons ISBN 0-471-93620-0
  24. ^ Minkus, Wilfred (1965). "Temperature Dependence of the Pyroelectric Effect in Cadmium Sulfide". Physical Review. 138 (4A): A1277–A1287. Bibcode:1965PhRv..138.1277M. doi:10.1103/PhysRev.138.A1277.
  25. ^ Smith, Roland (1957). "Low-Field Electroluminescence in Insulating Crystals of Cadmium Sulfide". Physical Review. 105 (3): 900. Bibcode:1957PhRv..105..900S. doi:10.1103/PhysRev.105.900.
  26. ^ Akimov, Yu A; Burov, A A; Drozhbin, Yu A; Kovalenko, V A; Kozlov, S E; Kryukova, I V; Rodichenko, G V; Stepanov, B M; Yakovlev, V A (1972). "KGP-2: An Electron-Beam-Pumped Cadmium Sulfide Laser". Soviet Journal of Quantum Electronics. 2 (3): 284. Bibcode:1972QuEle...2..284A. doi:10.1070/QE1972v002n03ABEH004443.
  27. ^ Agarwal, Ritesh; Barrelet, Carl J.; Lieber, Charles M. (2005). "Lasing in Single Cadmium Sulfide Nanowire Optical Cavities". Nano Letters. 5 (5): 917–920. arXiv:cond-mat/0412144v1. Bibcode:2005NanoL...5..917A. doi:10.1021/nl050440u. PMID 15884894. S2CID 651903.
  28. ^ Zhao, H.; Farah, Alvi; Morel, D.; Ferekides, C.S. (2009). "The effect of impurities on the doping and VOC of Cd Te/CDS thin film solar cells". Thin Solid Films. 517 (7): 2365–2369. Bibcode:2009TSF...517.2365Z. doi:10.1016/j.tsf.2008.11.041.
  29. ^ Weimer, Paul (1962). "The TFT A New Thin-Film Transistor". Proceedings of the IRE. 50 (6): 1462–1469. doi:10.1109/JRPROC.1962.288190. S2CID 51650159.
  30. ^ Zhang, Jun (24 January 2013). "Laser cooling of a semiconductor by 40 kelvin". Nature. 493 (7433): 504–508. Bibcode:2013Natur.493..504Z. doi:10.1038/nature11721. PMID 23344360. S2CID 4426843.
  31. ^ a b R. M. Christie 2001 Colour Chemistry, p. 155 Royal Society of Chemistry ISBN 0-85404-573-2
  32. ^ Karl-Heinz Schulte-Schrepping, Magnus Piscator "Cadmium and Cadmium Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, 2007 Wiley-VCH, Weinheim. doi:10.1002/14356007.a04_499.
  33. ^ Sidney Perkowitz, 1998, Empire of Light: A History of Discovery in Science and Art Joseph Henry Press, ISBN 0-309-06556-9
  34. ^ W. Stanley Taft, James W. Mayer, Richard Newman, Peter Kuniholm, Dusan Stulik (2000) The Science of Paintings, Springer, ISBN 0-387-98722-3
  35. ^ "CDC - CADMIUM SULFIDE - International Chemical Safety Cards - NIOSH". June 26, 2018. Archived from the original on 2018-06-26.
  36. ^ Bjornberg, A (Sep 1963). "Reactions to light in yellow tattoos from cadmium sulfide". Arch Dermatol. 88 (3): 267–71. doi:10.1001/archderm.1963.01590210025003. PMID 14043617.
  37. ^ "Sicherheitsdatenblatt" (PDF). Archived from the original (PDF) on 24 July 2015.

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