Copper(I) oxide

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Copper(I) oxide
Copper(I) oxide
Copper(I) oxide unit cell
IUPAC name
Copper(I) oxide
Other names
Cuprous oxide
Dicopper oxide
Red copper oxide
1317-39-1 YesY
ChemSpider 8488659 YesY
EC number 215-270-7
Jmol-3D images Image
KEGG C18714 YesY
PubChem 10313194
RTECS number GL8050000
Molar mass 143.09 g/mol
Appearance brownish-red solid
Density 6.0 g/cm3
Melting point 1,232 °C (2,250 °F; 1,505 K)
Boiling point 1,800 °C (3,270 °F; 2,070 K)
Solubility in acid Soluble
Band gap 2.137 eV
93 J·mol−1·K−1
−170 kJ·mol−1
Safety data sheet
EU classification Harmful (Xn)
Dangerous for the environment (N)
R-phrases R22, R50/53
S-phrases (S2), S22, S60, S61
NFPA 704
Flammability code 0: Will not burn. E.g., water Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g., calcium Special hazards (white): no codeNFPA 704 four-colored diamond
US health exposure limits (NIOSH):
TWA 1 mg/m3 (as Cu)[1]
TWA 1 mg/m3 (as Cu)[1]
TWA 100 mg/m3 (as Cu)[1]
Related compounds
Other anions
Copper(I) sulfide
Copper(II) sulfide
Copper(I) selenide
Other cations
Copper(II) oxide
Silver(I) oxide
Nickel(II) oxide
Zinc oxide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Copper(I) oxide or cuprous oxide is the inorganic compound with the formula Cu2O. It is one of the principal oxides of copper. This red-coloured solid is a component of some antifouling paints. The compound can appear either yellow or red, depending on the size of the particles.[2] Copper(I) oxide is found as the reddish mineral cuprite.


Copper(I) oxide may be produced by several methods.[3] Most straightforwardly, it arises via the oxidation of copper metal:

4 Cu + O2 → 2 Cu2O

Additives such as water and acids affect the rate of this process as well as the further oxidation to copper(II) oxides. It is also produced commercially by reduction of copper(II) solutions with sulfur dioxide. Aqueous cuprous chloride solutions react with base to give the same material. In all cases, the color is highly sensitive to the procedural details.

Formation of copper(I) oxide is the basis of the Fehling's test and Benedict's test for reducing sugars. These sugars reduce an alkaline solution of a copper(II) salt, giving a bright red precipitate of Cu2O.

It forms on silver-plated copper parts exposed to moisture when the silver layer is porous or damaged. This kind of corrosion is known as red plague.

Little evidence exists for cuprous hydroxide, which is expected to rapidly undergo dehydration. A similar situation applies to the hydroxides of gold(I) and silver(I).

Copper(I) oxide can also be prepared by reacting a copper-ammonia complex with hydrogen peroxide.


The solid is diamagnetic. In terms of their coordination spheres, copper centres are 2-coordinated and the oxides are tetrahedral. The structure thus resembles in some sense the main polymorphs of SiO2, and both structures feature interpenetrated lattices.

Copper(I) oxide dissolves in concentrated ammonia solution to form the colourless complex [Cu(NH3)2]+, which is easily oxidized in air to the blue [Cu(NH3)4(H2O)2]2+. It dissolves in hydrochloric acid to give solutions of CuCl2. Dilute sulfuric acid and nitric acid produce copper(II) sulfate and copper(II) nitrate, respectively.[4]

Cu2O degrades to copper(II) oxide in moist air.


Cu2O crystallizes in a cubic structure with a lattice constant al=4.2696 Å. The Cu atoms arrange in a fcc sublattice, the O atoms in a bcc sublattice. One sublattice is shifted by a quarter of the body diagonal. The space group is \scriptstyle Pn\bar{3}m, which includes the point group with full octahedral symmetry.

Semiconducting properties[edit]

In the history of semiconductor physics, Cu2O is one of the most studied materials, and many experimental observations and semiconductor applications have been demonstrated first in this material:

Today, it is still under investigation in semiconductor optics. In particular, researchers are attempting to create a Bose–Einstein condensate of excitons in Cu2O.[6]

The lowest excitons in Cu2O are extremely long lived; absorption lineshapes have been demonstrated with neV linewidths, which is the narrowest bulk exciton resonance ever observed.[9] The associated quadrupole polaritons have low group velocity approaching the speed of sound. Thus, light moves almost as slowly as sound in this medium, which results in high polariton densities. Another unusual feature of the ground state excitons is that all primary scattering mechanisms are known quantitatively.[10] Cu2O was the first substance where an entirely parameter-free model of absorption linewidth broadening by temperature could be established, allowing the corresponding absorption coefficient to be deduced. It can be shown using Cu2O that the Kramers–Kronig relations do not apply to polaritons.[6]


Cuprous oxide is commonly used as a pigment, a fungicide, and an antifouling agent for marine paints. Rectifier diodes based on this material have been used industrially as early as 1924, long before silicon became the standard. Copper(I) oxide is also responsible for the pink color in a positive Benedict's Test.

See also[edit]


  1. ^ a b c "NIOSH Pocket Guide to Chemical Hazards #0150". National Institute for Occupational Safety and Health (NIOSH). 
  2. ^ N. N. Greenwood, A. Earnshaw, Chemistry of the Elements, 2nd ed., Butterworth-Heinemann, Oxford, UK, 1997.
  3. ^ H. Wayne Richardson "Copper Compounds in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. doi:10.1002/14356007.a07_567
  4. ^ D. Nicholls, Complexes and First-Row Transition Elements, Macmillan Press, London, 1973.
  5. ^ L. O. Grondahl, Unidirectional current carrying device, Patent, 1927
  6. ^ a b c d e C. F. Klingshirn, Semiconductor Optics, 3rd ed., Springer, 2006, ISBN 354038345X
  7. ^ L. Hanke, D. Fröhlich, A.L. Ivanov, P.B. Littlewood, and H. Stolz "LA-Phonoritons in Cu2O" Phys. Rev. Lett. 83 (1999), 4365.
  8. ^ L. Brillouin: Wave Propagation and Group Velocity, Academic Press, New York, 1960.
  9. ^ J. Brandt, D. Fröhlich, C. Sandfort, M. Bayer, H. Stolz, and N. Naka, Ultranarrow absorption and two-phonon excitation spectroscopy of Cu2O paraexcitons in a high magnetic field, Phys. Rev. Lett. 99, 217403 (2007). doi:10.1103/PhysRevLett.99.217403
  10. ^ J. P. Wolfe and A. Mysyrowicz: Excitonic Matter, Scientific American 250 (1984), No. 3, 98.

External links[edit]