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Cobalt(II,III) oxide

From Wikipedia, the free encyclopedia
Cobalt(II,III) oxide[1]
Cobalt(II,III) oxide
Cobalt(II,III) oxide
Ball-and-stick model of the unit cell of Co3O4
Ball-and-stick model of the unit cell of Co3O4
Names
IUPAC name
cobalt(II) dicobalt(III) oxide
Other names
  • Cobalt oxide
  • Cobalt(II,III) oxide
  • Cobaltosic oxide
  • Tricobalt tetroxide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.013.780 Edit this at Wikidata
EC Number
  • 215-157-2
RTECS number
  • GG2500000
UNII
  • InChI=1S/3Co.4O checkY
    Key: LBFUKZWYPLNNJC-UHFFFAOYSA-N checkY
  • InChI=1/3Co.4O/rCo2O3.CoO/c3-1-5-2-4;1-2
    Key: LBFUKZWYPLNNJC-PMPQCLQHAA
  • [Co]=O.O=[Co]O[Co]=O
Properties
Co3O4
CoO·Co2O3
Molar mass 240.80 g/mol
Appearance black solid
Density 6.07 g/cm3[2]
Melting point 895 °C (1,643 °F; 1,168 K)
Boiling point 900 °C (1,650 °F; 1,170 K) (decomposes)
Insoluble
Solubility soluble (with degradation) in acids and alkalis
+7380·10−6 cm3/mol
Structure
cubic
Fd3m, No. 227[3]
Hazards
GHS labelling:
GHS09: Environmental hazardGHS08: Health hazard
Danger
H317, H334, H350, H411
P261, P273, P284, P304+P340, P342+P311
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 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
2
0
0
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 ?)

Cobalt(II,III) oxide is an inorganic compound with the formula Co3O4. Along with cobalt(II) oxide, it is one of two well characterized and stable cobalt oxides.[4] It is a black antiferromagnetic solid. As a mixed valence compound, its formula is sometimes written as CoIICoIII2O4 and sometimes as CoO•Co2O3.[5] It occurs naturally as the rare mineral guite which is named in honor of Prof. Xiangping Gu (1964-). [6]

Structure

[edit]

Co3O4 adopts the normal spinel structure, with Co2+ ions in tetrahedral interstices and Co3+ ions in the octahedral interstices of the cubic close-packed lattice of oxide anions.[5]

tetrahedral coordination geometry of Co(II) distorted octahedral coordination geometry of Co(III) distorted tetrahedral coordination geometry of O

Synthesis

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Cobalt(II) oxide, CoO, converts to Co3O4 upon heating at around 600–700 °C in air.[5] Above 900 °C, CoO is stable.[5][7] These reactions are described by the following equilibrium:

2 Co3O4 ⇌ 6 CoO + O2

Applications

[edit]

Cobalt(II,III) oxide is used as a blue coloring agent for pottery enamel and glass, as an alternative to cobalt(II) oxide.[8]

Cobalt(II,III) oxide is used as an electrode in some lithium-ion batteries, possibly in the form of cobalt oxide nanoparticles.

Cobalt(III) fluoride can be prepared from cobalt(II,III) oxide by sequential treatment with hydrogen fluoride and then fluorine gas, producing a mixture of cobalt(II) fluoride and cobalt oxyfluoride as intermediates, with overall stoichiometry:[4]

Co3O4 + 4 HFCoF2 + 2 CoOF + 2 H2O
2CoF2 + 4 CoOF + 5 F2 → 6 CoF3 + 2 O2

See also

[edit]

References

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  1. ^ "Cobalt(II,III) oxide 203114". Sigma-Aldrich.
  2. ^ Lide, David R., ed. (2006). CRC Handbook of Chemistry and Physics (87th ed.). Boca Raton, Florida: CRC Press. ISBN 0-8493-0487-3.
  3. ^ "mp-18748: Co3O4 (cubic, Fd-3m, 227)". materialsproject.org. Retrieved 2019-12-20.
  4. ^ a b Vilakazi, B. M.; Wagener, J. B.; van der Merwe, E. M. (2020). "A thermogravimetric investigation into the synthesis of CoF3 from Co3O4". Journal of Fluorine Chemistry. 240. doi:10.1016/j.jfluchem.2020.109638.
  5. ^ a b c d Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 1118. doi:10.1016/C2009-0-30414-6. ISBN 978-0-08-037941-8.
  6. ^ mindat.org https://www.mindat.org/min-52593.html. Retrieved 2026-03-24. {{cite web}}: Missing or empty |title= (help)
  7. ^ Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. p. 1520.
  8. ^ Frank Hamer, Janet Hamer (2004): The Potter's Dictionary of Materials and Techniques. University of Pennsylvania Press; 437 pp. ISBN 0812238109