Erbium(III) oxide

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Erbium oxide[1]
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Template:Longitem Er2O3
Molar mass 382.56 g/mol
Appearance pink crystals
Density 8.64 g/cm3
Melting point Template:Chembox CalcTemperatures
Boiling point Template:Chembox CalcTemperatures
Template:Longitem +73,920·10−6 cm3/mol
Template:Longitem Cubic, cI80
Template:Longitem Ia-3, No. 206
Template:Longitem 108.5 J·mol−1·K−1
Template:Longitem 155.6 J·mol−1·K−1
Template:Longitem −1897.9 kJ·mol−1
Template:Longitem Erbium(III) chloride
Template:Longitem Holmium(III) oxide, Thulium(III) oxide

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Erbium(III) oxide is the inorganic compound with the formula Template:Chem2. It is a pink paramagnetic solid. It finds uses in various optical materials.[2]

Structure

Erbium(III) oxide has a cubic structure resembling the bixbyite motif. The Er3+ centers are octahedral.[2]

Reactions

Erbium oxide is produced by burning erbium metal.[3] Erbium oxide is insoluble in water but soluble in mineral acids. Er2O3 does not readily absorb moisture and carbon dioxide from the atmosphere. It can react with acids to form the corresponding erbium(III) salts. For example, with hydrochloric acid, the oxide follows the following idealized reaction leading to erbium chloride:

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In practice, such simple acid-base reactions are accompanied by hydration:

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Properties

One interesting property of erbium oxides is their ability to up convert photons. Photon upconversion takes place when infrared or visible radiation, low energy light, is converted to ultraviolet or violet radiation higher energy light via multiple transfer or absorption of energy.[4] Erbium oxide nanoparticles also possess photoluminescence properties. Erbium oxide nanoparticles can be formed by applying ultrasound (20 kHz, 29 W·cm−2) in the presence of multiwall carbon nanotubes. The erbium oxide nanoparticles that have been produced using ultrasound are erbium carboxioxide, hexagonal and spherical geometry erbium oxide. Each ultrasonically formed erbium oxide exhibits photoluminescence in the visible region of the electromagnetic spectrum under excitation of wavelength 379 nm in water. Hexagonal erbium oxide photoluminescence is long-lived and allows higher energy transitions (4S3/24I15/2). Spherical erbium oxide does not undergo 4S3/24I15/2 energy transitions.[5]

Uses

The applications of Er2O3 are varied due to their electrical, optical and photoluminescence properties. Nanoscale materials doped with Er3+ are of much interest because they have special particle-size-dependent optical and electrical properties.[6] Erbium oxide doped nanoparticle materials can be dispersed in glass or plastic for display purposes, such as display monitors. The spectroscopy of Er3+ electronic transitions in host crystals latticesScript error: No such module "Unsubst".Template:Category handlerTemplate:Category handler[<span title="Script error: No such module "string".">words missing?]Script error: No such module "Check for unknown parameters". of nanoparticles combined with ultrasonically formed geometries in aqueous solution of carbon nanotubes is of great interest for synthesis of photoluminescence nanoparticles in "green" chemistry.[5]

Erbium oxide is widely used in interferometers that require high-power lasers.[7] These interferometers often employ erbium-doped fiber amplifiers (EDFAs) to enhance the power of the laser beams.[8] EDFAs, which utilize erbium ions, provide low noise and high gain, making them ideal for long-distance signal transmission and high-resolution measurements in interferometry.[9]

Erbium oxide is among the most important rare earth metals used in biomedicine.[10] The photoluminescence property of erbium oxide nanoparticles on carbon nanotubes makes them useful in biomedical applications. For example, erbium oxide nanoparticles can be surface modified for distribution into aqueous and non-aqueous media for bioimaging.[6] Erbium oxides are also used as gate dielectrics in semiconductor devices since it has a high dielectric constant (10–14) and a large band gap. Erbium is sometimes used as a coloring for glasses,[1] and erbium oxide can also be used as a burnable neutron poison for nuclear fuel.

History

Impure erbium(III) oxide was isolated by Carl Gustaf Mosander in 1843, and first obtained in pure form in 1905 by Georges Urbain and Charles James.[11]

References

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