Erbium(III) oxide

Last updated
Erbium oxide [1]
Tl2O3structure.jpg
ErOPulver.jpg
Names
Other names
Erbium oxide, erbia
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.031.847 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 235-045-7
PubChem CID
  • InChI=1S/2Er.3O Yes check.svgY
    Key: VQCBHWLJZDBHOS-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/2Er.3O/rEr2O3/c3-1-5-2-4
    Key: VQCBHWLJZDBHOS-YMHUIQTEAQ
  • O=[Er]O[Er]=O
  • ionic:[O-2].[Er+3].[O-2].[Er+3].[O-2]
Properties
Er2O3
Molar mass 382.56 g/mol
Appearancepink crystals
Density 8.64 g/cm3
Melting point 2,344 °C (4,251 °F; 2,617 K)
Boiling point 3,290 °C (5,950 °F; 3,560 K)
insoluble in water
+73,920·10−6 cm3/mol
Structure
Cubic, cI80
Ia-3, No. 206
Thermochemistry
108.5 J·mol−1·K−1
Std molar
entropy
(S298)
155.6 J·mol−1·K−1
−1897.9 kJ·mol−1
Related compounds
Other anions
Erbium(III) chloride
Other cations
Holmium(III) oxide, Thulium(III) oxide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

Erbium(III) oxide is the inorganic compound with the formula Er2O3. It is a pink paramagnetic solid. It finds uses in various optical materials. [2]

Contents

Structure

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

Reactions

The formation of erbium oxide is accomplished by burning erbium metal. [3] Erbium oxide is insoluble in water and 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:

Er2O3 + 6 HCl → 2 ErCl3 + 3 H2O

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

ErCl3 + 9 H2O → [Er(H2O)9]Cl3

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 successfully made by employing ultrasound are erbium carboxioxide, hexagonal and spherical geometry erbium oxide. Each ultrasonically formed erbium oxide is photoluminescence in the visible region of the electromagnetic spectrum under excitation of 379 nm in water. Hexagonal erbium oxide photoluminescence is long lived and allows higher energy transitions (4S3/2 - 4I15/2). Spherical erbium oxide does not experience 4S3/2 - 4I15/2 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 lattices 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 among the most important rare earth metals used in biomedicine. [7] 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 semi conductor devices since it has a high dielectric constant (10–14) and a large band gap. Erbium is sometimes used as a coloring for glasses [8] 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. [9]

Related Research Articles

<span class="mw-page-title-main">Erbium</span> Chemical element, symbol Er and atomic number 68

Erbium is a chemical element; it has symbol Er and atomic number 68. A silvery-white solid metal when artificially isolated, natural erbium is always found in chemical combination with other elements. It is a lanthanide, a rare-earth element, originally found in the gadolinite mine in Ytterby, Sweden, which is the source of the element's name.

<span class="mw-page-title-main">Praseodymium</span> Chemical element, symbol Pr and atomic number 59

Praseodymium is a chemical element; it has symbol Pr and the atomic number 59. It is the third member of the lanthanide series and is considered one of the rare-earth metals. It is a soft, silvery, malleable and ductile metal, valued for its magnetic, electrical, chemical, and optical properties. It is too reactive to be found in native form, and pure praseodymium metal slowly develops a green oxide coating when exposed to air.

Iron(III) chloride describes the inorganic compounds with the formula FeCl3(H2O)x. Also called ferric chloride, these compounds are some of the most important and commonplace compounds of iron. They are available both in anhydrous and in hydrated forms which are both hygroscopic. They feature iron in its +3 oxidation state. The anhydrous derivative is a Lewis acid, while all forms are mild oxidizing agent. It is used as a water cleaner and as an etchant for metals.

Neodymium(III) chloride or neodymium trichloride is a chemical compound of neodymium and chlorine with the formula NdCl3. This anhydrous compound is a mauve-colored solid that rapidly absorbs water on exposure to air to form a purple-colored hexahydrate, NdCl3·6H2O. Neodymium(III) chloride is produced from minerals monazite and bastnäsite using a complex multistage extraction process. The chloride has several important applications as an intermediate chemical for production of neodymium metal and neodymium-based lasers and optical fibers. Other applications include a catalyst in organic synthesis and in decomposition of waste water contamination, corrosion protection of aluminium and its alloys, and fluorescent labeling of organic molecules (DNA).

<span class="mw-page-title-main">Gold(III) chloride</span> Chemical compound

Gold(III) chloride, traditionally called auric chloride, is an inorganic compound of gold and chlorine with the molecular formula Au2Cl6. The "III" in the name indicates that the gold has an oxidation state of +3, typical for many gold compounds. It has two forms, the monohydrate (AuCl3·H2O) and the anhydrous form, which are both hygroscopic and light-sensitive solids. This compound is a dimer of AuCl3. This compound has a few uses, such as an oxidizing agent and for catalyzing various organic reactions.

<span class="mw-page-title-main">Ytterbium(III) oxide</span> Chemical compound

Ytterbium(III) oxide is the chemical compound with the formula Yb2O3. It is one of the more commonly encountered compounds of ytterbium. It occurs naturally in trace amounts in the mineral gadolinite. It was first isolated from this in 1878 by Jean Charles Galissard de Marignac.

<span class="mw-page-title-main">Erbium(III) chloride</span> Chemical compound

Erbium(III) chloride is a violet solid with the formula ErCl3. It is used in the preparation of erbium metal.

<span class="mw-page-title-main">Holmium(III) oxide</span> Chemical compound

Holmium(III) oxide, or holmium oxide is a chemical compound of a rare-earth element holmium and oxygen with the formula Ho2O3. Together with dysprosium(III) oxide (Dy2O3), holmium oxide is one of the most powerfully paramagnetic substances known. The oxide, also called holmia, occurs as a component of the related erbium oxide mineral called erbia. Typically, the oxides of the trivalent lanthanides coexist in nature, and separation of these components requires specialized methods. Holmium oxide is used in making specialty colored glasses. Glass containing holmium oxide and holmium oxide solutions have a series of sharp optical absorption peaks in the visible spectral range. They are therefore traditionally used as a convenient calibration standard for optical spectrophotometers.

<span class="mw-page-title-main">Lanthanum oxide</span> Chemical compound

Lanthanum(III) oxide, also known as lanthana, chemical formula La2O3, is an inorganic compound containing the rare earth element lanthanum and oxygen. It is used in some ferroelectric materials, as a component of optical materials, and is a feedstock for certain catalysts, among other uses.

<span class="mw-page-title-main">Tantalum pentoxide</span> Chemical compound

Tantalum pentoxide, also known as tantalum(V) oxide, is the inorganic compound with the formula Ta
2
O
5
. It is a white solid that is insoluble in all solvents but is attacked by strong bases and hydrofluoric acid. Ta
2
O
5
is an inert material with a high refractive index and low absorption, which makes it useful for coatings. It is also extensively used in the production of capacitors, due to its high dielectric constant.

<span class="mw-page-title-main">Transparent conducting film</span> Optically transparent and electrically conductive material

Transparent conducting films (TCFs) are thin films of optically transparent and electrically conductive material. They are an important component in a number of electronic devices including liquid-crystal displays, OLEDs, touchscreens and photovoltaics. While indium tin oxide (ITO) is the most widely used, alternatives include wider-spectrum transparent conductive oxides (TCOs), conductive polymers, metal grids and random metallic networks, carbon nanotubes (CNT), graphene, nanowire meshes and ultra thin metal films.

<span class="mw-page-title-main">Photon upconversion</span> Optical process

Photon upconversion (UC) is a process in which the sequential absorption of two or more photons leads to the emission of light at shorter wavelength than the excitation wavelength. It is an anti-Stokes type emission. An example is the conversion of infrared light to visible light. Upconversion can take place in both organic and inorganic materials, through a number of different mechanisms. Organic molecules that can achieve photon upconversion through triplet-triplet annihilation are typically polycyclic aromatic hydrocarbons (PAHs). Inorganic materials capable of photon upconversion often contain ions of d-block or f-block elements. Examples of these ions are Ln3+, Ti2+, Ni2+, Mo3+, Re4+, Os4+, and so on.

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<span class="mw-page-title-main">Carbon quantum dot</span>

Carbon quantum dots also commonly called carbon nano dots are carbon nanoparticles which are less than 10 nm in size and have some form of surface passivation.

Upconverting nanoparticles (UCNPs) are nanoscale particles that exhibit photon upconversion. In photon upconversion, two or more incident photons of relatively low energy are absorbed and converted into one emitted photon with higher energy. Generally, absorption occurs in the infrared, while emission occurs in the visible or ultraviolet regions of the electromagnetic spectrum. UCNPs are usually composed of rare-earth based lanthanide- or actinide-doped transition metals and are of particular interest for their applications in in vivo bio-imaging, bio-sensing, and nanomedicine because of their highly efficient cellular uptake and high optical penetrating power with little background noise in the deep tissue level. They also have potential applications in photovoltaics and security, such as infrared detection of hazardous materials.

<span class="mw-page-title-main">Erbium(III) hydroxide</span> Chemical compound

Erbium(III) hydroxide is an inorganic compound with chemical formula Er(OH)3.

<span class="mw-page-title-main">Erbium(III) acetate</span> Chemical compound

Erbium(III) acetate is the acetate salt of erbium, with the proposed chemical formula of Er(CH3COO)3. It can be used to synthesize some optical materials.

<span class="mw-page-title-main">Terbium compounds</span> Chemical compounds with at least one terbium atom

Terbium compounds are compounds formed by the lanthanide metal terbium (Tb). Terbium generally exhibits the +3 oxidation state in these compounds, such as in TbCl3, Tb(NO3)3 and Tb(CH3COO)3. Compounds with terbium in the +4 oxidation state are also known, such as TbO2 and BaTbF6. Terbium can also form compounds in the 0, +1 and +2 oxidation states.

Erbium compounds are compounds containing the element erbium (Er). These compounds are usually dominated by erbium in the +3 oxidation state, although the +2, +1 and 0 oxidation states have also been reported.

<span class="mw-page-title-main">Erbium(III) selenate</span> Chemical compound

Erbium(III) selenate is an inorganic compound, with the chemical formula Er2(SeO4)3. It exists as an anhydrate or an octahydrate.

References

  1. Lide, David R. (1998). Handbook of Chemistry and Physics (87 ed.). Boca Raton, FL: CRC Press. pp. 4–57. ISBN   978-0-8493-0594-8.
  2. 1 2 Adachi, Gin-ya; Imanaka, Nobuhito (1998). "The Binary Rare Earth Oxides". Chemical Reviews. 98 (4): 1479–1514. doi:10.1021/cr940055h. PMID   11848940.
  3. Emsley, John (2001). "Erbium" Nature's Building Blocks: An A-Z Guide to Elements. Oxford, England, Uk: Oxford University Press. pp.  136–139. ISBN   978-0-19-850340-8.
  4. "Rare-earth-doped nanoparticles prove illuminating". SPIE. Retrieved April 10, 2012.
  5. 1 2 Radziuk, Darya; Andre Skirtach; Andre Geßner; Michael U. Kumke; Wei Zhang; Helmuth M€ohwald; Dmitry Shchukin (24 October 2011). "Ultrasonic Approach for Formation of Erbium Oxide Nanoparticles with Variable Geometries". Langmuir. 27 (23): 14472–14480. doi:10.1021/la203622u. PMID   22022886.
  6. 1 2 Richard, Scheps (12 February 1996). "Upconversion laser processes". Progress in Quantum Electronics. 20 (4): 271–358. Bibcode:1996PQE....20..271S. doi:10.1016/0079-6727(95)00007-0.
  7. Andre, Skirtach; Almudena Javier; Oliver Kref; Karen Kohler; Alicia Alberola; Helmuth Mohwald; Wolfgang Parak; Gleb Sukhorukov (2006). "Laser-Induced Release of Encapsulated Materials inside Living Cells" (PDF). Angew. Chem. Int. Ed. 38 (28): 4612–4617. doi:10.1002/anie.200504599. PMID   16791887 . Retrieved April 15, 2012.
  8. Lide, David (1998). Handbook of Chemistry and Physics. Boca, Raton Fl: CRC Press. pp. 4–57. ISBN   978-0849305948.
  9. Aaron John Ihde (1984). The development of modern chemistry. Courier Dover Publications. pp. 378–379. ISBN   978-0-486-64235-2.