ZnS powders containing different concentrations of sulfur vacancies
|Molar mass||97.474 g/mol|
|Melting point||1,850 °C (3,360 °F; 2,120 K) (sublime)|
|Band gap||3.54 eV (cubic, 300 K)
3.91 eV (hexagonal, 300 K)
Std enthalpy of
|Safety data sheet||ICSC 1627|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Zinc sulfide (or zinc sulphide) is an inorganic compound with the chemical formula of ZnS. This is the main form of zinc found in nature, where it mainly occurs as the mineral sphalerite. Although this mineral is usually black because of various impurities, the pure material is white, and it is widely used as a pigment. In its dense synthetic form, zinc sulfide can be transparent, and it is used as a window for visible optics and infrared optics.
ZnS exists in two main crystalline forms, and this dualism is often a salient example of polymorphism. In each form, the coordination geometry at Zn and S is tetrahedral. The more stable cubic form is known also as zinc blende or sphalerite. The hexagonal form is known as the mineral wurtzite, although it also can be produced synthetically. The transition from the sphalerite form to the wurtzite form occurs at around 1020 celsius. A tetragonal form is also known as the very rare mineral called polhemusite, with the formula (Zn,Hg)S.
Zinc sulfide, with addition of few ppm of suitable activator, is used as phosphor in many applications, from cathode ray tubes through X-ray screens to glow in the dark products. When silver is used as activator, the resulting color is bright blue, with maximum at 450 nanometers. Using manganese yields an orange-red color at around 590 nanometers. Copper gives long-time glow, and it has the familiar greenish glow-in-the-dark. Copper-doped zinc sulfide ("ZnS plus Cu") is used also in electroluminescent panels. It also exhibits phosphorescence due to impurities on illumination with blue or ultraviolet light.
Zinc sulfide is also used as an infrared optical material, transmitting from visible wavelengths to just over 12 micrometers. It can be used planar as an optical window or shaped into a lens. It is made as microcrystalline sheets by the synthesis from hydrogen sulfide gas and zinc vapour, and this is sold as FLIR-grade (Forward Looking IR), where the zinc sulfide is in a milky-yellow, opaque form. This material when hot isostatically pressed (HIPed) can be converted to a water-clear form known as Cleartran (trademark). Early commercial forms were marketed as Irtran-2 but this designation is now obsolete.
Fine ZnS powder is an efficient photocatalyst, which produces hydrogen gas from water upon illumination. Sulfur vacancies can be introduced in ZnS during its synthesis; this gradually turns the white-yellowish ZnS into a brown powder, and boosts the photocatalytic activity through enhanced light absorption.
Both sphalerite and wurtzite are intrinsic, wide-bandgap semiconductors. These are prototypical II-VI semiconductors, and they adopt structures related to many of the other semiconductors, such as gallium arsenide. The cubic form of ZnS has a band gap of about 3.54 electron volts at 300 kelvin, but the hexagonal form has a band gap of about 3.91 electron volts. ZnS can be doped as either an n-type semiconductor or a p-type semiconductor.
The phosphorescence of ZnS was first reported by the French chemist Théodore Sidot in 1866. His findings were presented by A. E. Becquerel, who was renowned for the research on luminescence. ZnS was used by Ernest Rutherford and others in the early years of nuclear physics as a scintillation detector, because it emits light upon excitation by x-rays or electron beam, making it useful for X-ray screens and cathode ray tubes. This property made zinc sulfide useful in the dials of radium watches.
Zinc sulfide is usually produced from waste materials from other applications. Typical sources include smelter, slag, and pickle liquors. It is also a by-product of the synthesis of ammonia from methane where zinc oxide is used to scavenge hydrogen sulfide impurities in the natural gas:
- ZnO + H2S → ZnS + H2O
It is easily produced by igniting a mixture of zinc and sulfur. Since zinc sulfide is insoluble in water, it can also be produced in a precipitation reaction. Solutions containing Zn2+ salts readily form a precipitate ZnS in the presence of sulfide ions (e.g., from H2S).
- Zn2+ + S2− → ZnS
- Wang, Gang; Huang, Baibiao; Li, Zhujie; Lou, Zaizhu; Wang, Zeyan; Dai, Ying; Whangbo, Myung-Hwan (2015). "Synthesis and characterization of ZnS with controlled amount of S vacancies for photocatalytic H2 production under visible light". Scientific Reports. 5: 8544. Bibcode:2015NatSR...5E8544W. doi:10.1038/srep08544. PMC . PMID 25712901.
- Wells, A. F. (1984), Structural Inorganic Chemistry (5th ed.), Oxford: Clarendon Press, ISBN 0-19-855370-6
- Karl A. Franz, Wolfgang G. Kehr, Alfred Siggel, Jürgen Wieczoreck, and Waldemar Adam "Luminescent Materials" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. doi:10.1002/14356007.a15_519
- Gerhard Auer, Peter Woditsch, Axel Westerhaus, Jürgen Kischkewitz, Wolf-Dieter Griebler and Marcel Liedekerke "Pigments, Inorganic, 2. White Pigments" in Ullmann's Encyclopedia of Industrial Chemistry 2009, Wiley-VCH, Weinheim. doi: 10.1002/14356007.n20_n01
- Sidot, T. (1866). ". Sur les propriétés de la blende hexagonale". Compt. Rend. 63: 188–189.
- Greenwood, Norman N.; Earnshaw, Alan (1984). Chemistry of the Elements. Oxford: Pergamon Press. p. 1405. ISBN 0-08-022057-6.
- Sur un nouveau procédé de préparation – du sulfure de zinc phosphorescent" by R. Coustal, F. Prevet, 1929
- Mendham, J.; Denney, R. C.; Barnes, J. D.; Thomas, M. J. K. (2000), Vogel's Quantitative Chemical Analysis (6th ed.), New York: Prentice Hall, ISBN 0-582-22628-7
|Wikimedia Commons has media related to Zinc sulfide.|
- Zinc and Sulfur at The Periodic Table of Videos (University of Nottingham)
- Composition of CRT phosphors
- University of Reading, Infrared Multilayer Laboratory optical data
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