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Zinc nitride

From Wikipedia, the free encyclopedia
Zinc nitride
Identifiers
3D model (JSmol)
ECHA InfoCard100.013.826Edit this at Wikidata
EC Number
  • 215-207-3
UNII
  • InChI=1S/2N.3Zn/q2*-1;;;+2
    Key: AKJVMGQSGCSQBU-UHFFFAOYSA-N
  • [N-]=[Zn].[N-]=[Zn].[Zn+2]
Properties
Zn3N2
Molar mass224.154 g/mol
Appearanceblue-gray cubic crystals[1]
Density6.22 g/cm3, solid[1]
Melting pointdecomposes 700°C[1]
insoluble, reacts
Structure
Cubic,cI80
Ia-3, No. 206[2]
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H315,H319
P264,P280,P302+P352,P305+P351+P338,P321,P332+P313,P337+P313,P362
NFPA 704 (fire diamond)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound

Zinc nitride (Zn3N2) is aninorganic compound ofzinc andnitrogen, usually obtained as (blue)grey crystals. It is a semiconductor. In pure form, it has the anti-bixbyite structure.

Chemical properties

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Zinc nitride can be obtained bythermally decomposing zincamide (zinc diamine)[3] in ananaerobic environment, at temperatures in excess of 200°C. The by-product of the reaction isammonia.[4]

3 Zn(NH2)2 → Zn3N2 + 4NH3

It can also be formed by heating zinc to 600°C in a current of ammonia; the by-product ishydrogen gas.[3][5]

3Zn + 2NH3 → Zn3N2 + 3H2

The decomposition of Zinc Nitride into the elements at the same temperature is a competing reaction.[6] At 700 °C Zinc Nitride decomposes.[1] It has also been made by producing an electric discharge between zinc electrodes in a nitrogen atmosphere.[6][7] Thin films have been produced bychemical vapour deposition of Bis(bis(trimethylsilyl)amido]zinc with ammonia gas onto silica or ZnO coated alumina at 275 to 410 °C.[8]

The crystal structure is anti-isomorphous withManganese(III) oxide. (bixbyite).[2][7] The heat of formation is c. 24 kilocalories (100 kJ) per mol.[7] It is a semiconductor with a reported bandgap of c. 3.2eV,[9] however, a thin zinc nitride film prepared by electrolysis of molten salt mixture containing Li3N with a zinc electrode showed a band-gap of 1.01 eV.[10]

Zinc nitride reacts violently withwater to form ammonia andzinc oxide.[3][4]

Zn3N2 + 3H2O → 3ZnO + 2NH3

Zinc nitride reacts with lithium (produced in an electrochemical cell) by insertion. The initial reaction is the irreversible conversion into LiZn in a matrix ofbeta-Li3N. These products then can be converted reversibly and electrochemically into LiZnN and metallic Zn.[11][12]

See also

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References

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  1. ^abcdCRC Handbook of Chemistry and Physics (96 ed.), §4-100 Physical Constants of Inorganic Compounds
  2. ^abPartin, D. E.; Williams, D. J.; O'Keeffe, M. (1997). "The Crystal Structures of Mg3N2 and Zn3N2".Journal of Solid State Chemistry.132 (1):56–59.Bibcode:1997JSSCh.132...56P.doi:10.1006/jssc.1997.7407.
  3. ^abcRoscoe, H. E.;Schorlemmer, C. (1907) [1878].A Treatise on Chemistry: Volume II, The Metals (4th ed.). London:Macmillan. pp. 650–651. Retrieved2007-11-01.
  4. ^abBloxam, C. L. (1903).Chemistry, Inorganic and Organic (9th ed.). Philadelphia: P. Blakiston's Son & Co. p. 380. Retrieved2007-10-31.
  5. ^Lowry, M. T. (1922).Inorganic Chemistry.Macmillan. p. 872. Retrieved2007-11-01.
  6. ^abMaxtead, E.B. (1921),Ammonia and the Nitrides, pp. 69–20
  7. ^abcMellor, J.W. (1964),A Comprehensive Treatise on Inorganic and Theoretical Chemistry, vol. 8, Part 1, pp. 160–161
  8. ^Maile, E.; Fischer, R. A. (Oct 2005), "MOCVD of the Cubic Zinc Nitride Phase, Zn3N2, Using Zn[N(SiMe3)2]2 and Ammonia as Precursors",Chemical Vapor Deposition,11 (10):409–414,doi:10.1002/cvde.200506383
  9. ^Ebru, S.T.; Ramazan, E.; Hamide, K. (2007),"Structural and Optical Properties of Zinc Nitride Films Prepared by Pulsed Filtered Cathodic Vacuum Arc Deposition"(PDF),Chin. Phys. Lett.,24 (12): 3477,Bibcode:2007ChPhL..24.3477S,doi:10.1088/0256-307x/24/12/051,S2CID 123496085, archived fromthe original(PDF) on 2016-03-24, retrieved2016-03-17
  10. ^Toyoura, Kazuaki; Tsujimura, Hiroyuki; Goto, Takuya; Hachiya, Kan; Hagiwara, Rika; Ito, Yasuhiko (2005), "Optical properties of zinc nitride formed by molten salt electrochemical process",Thin Solid Films,492 (1–2):88–92,Bibcode:2005TSF...492...88T,doi:10.1016/j.tsf.2005.06.057
  11. ^Amatucci, G. G.; Pereira, N. (2004)."Nitride and Silicide Negative Electrodes". In Nazri, G.-A.; Pistoia, G. (eds.).Lithium Batteries: Science and Technology.Kluwer Academic Publishers. p. 256.ISBN 978-1-4020-7628-2. Retrieved2007-11-01.
  12. ^Pereiraa, N.; Klein, L.C.; Amatuccia, G.G. (2002), "The Electrochemistry of Zn3 N 2 and LiZnN - A Lithium Reaction Mechanism for Metal Nitride Electrodes",Journal of the Electrochemical Society,149 (3): A262,Bibcode:2002JElS..149A.262P,doi:10.1149/1.1446079

Further reading

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External links

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Zinc(I)
Organozinc(I) compounds
Zinc(II)
Organozinc(II) compounds
Salts and covalent derivatives of thenitride ion
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