Ruthenium(IV) oxide

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Ruthenium(IV) oxide
Ruthenium(IV)-oxide-unit-cell-3D-vdW.png
Names
IUPAC name
Ruthenium(IV) oxide
Other names
Ruthenium dioxide
Identifiers
3D model (JSmol)
ECHA InfoCard 100.031.660 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 234-840-6
PubChem CID
  • InChI=1S/2O.Ru
  • O=[Ru]=O
Properties
RuO2
Molar mass 133.0688 g/mol
Appearanceblue-black solid
Density 6.97 g/cm3
Boiling point 1,200 °C (2,190 °F; 1,470 K) sublimates
insoluble
+162.0·10−6 cm3/mol
Structure
Rutile (tetragonal), tP6
P42/mnm, No. 136
Octahedral (RuIV); trigonal planar (O2−)
Hazards
Flash point Non-flammable
Related compounds
Other anions
Ruthenium disulfide
Other cations
Osmium(IV) oxide
Related ruthenium oxides
Ruthenium tetroxide
Supplementary data page
Ruthenium(IV) oxide (data page)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Ruthenium(IV) oxide is the inorganic compound with the formula Ru O2. This black solid is the most common oxide of ruthenium. It is widely used as an electrocatalyst for producing chlorine, chlorine oxides, and O2. [1] Like many dioxides, RuO2 adopts the rutile structure. [2] [3]

Contents

Preparation

It is usually prepared by oxidation of ruthenium trichloride. Nearly stoichiometric single crystals of RuO2 can be obtained by chemical vapor transport, using O2 as the transport agent: [4] [5]

RuO2 + O2 RuO4

Films of RuO2 can be prepared by chemical vapor deposition (CVD) from volatile ruthenium compounds. [6] RuO2 can also be prepared through electroplating from a solution of ruthenium trichloride. [7]

Electrostatically stabilized hydrosols of pristine ruthenium dioxide hydrate have been prepared by exploiting the autocatalytic reduction of ruthenium tetroxide in aqueous solution. The resulting particle populations may be controlled to comprise substantially monodisperse, uniform spheres with diameters in the range 40nm - 160nm. [8]

Uses

Ruthenium(IV) oxide is being used as the main component in the catalyst of the Sumitomo-Deacon process which produces chlorine by the oxidation of hydrogen chloride. [9] [10]

RuO2 can be used as catalyst in many other situations. Noteworthy reactions are the Fischer–Tropsch process, Haber–Bosch process, and various manifestations of fuel cells.

Aspirational and niche applications

RuO2 is extensively used for the coating of titanium anodes for the electrolytic production of chlorine and for the preparation of resistors or integrated circuits. [11] [12] Ruthenium oxide resistors can be used as sensitive thermometers in the temperature range .02 < T < 4 K. It can be also used as active material in supercapacitor because it has very high charge transfer capability. Ruthenium oxide has great capacity to store charge when used in aqueous solutions. [13] Average capacities of ruthenium(IV) oxide have reached 650 F/g when in H2SO4 solution and annealed at temperatures lower than 200 °C. [14] In attempts to optimise its capacitive properties, prior work has looked at the hydration of ruthenium oxide, its crystallinity and particle size.

Related Research Articles

<span class="mw-page-title-main">Oxide</span> Chemical compound where oxygen atoms are combined with atoms of other elements

An oxide is a chemical compound containing at least one oxygen atom and one other element in its chemical formula. "Oxide" itself is the dianion of oxygen, an O2– ion with oxygen in the oxidation state of −2. Most of the Earth's crust consists of oxides. Even materials considered pure elements often develop an oxide coating. For example, aluminium foil develops a thin skin of Al2O3 that protects the foil from further oxidation.

<span class="mw-page-title-main">Ruthenium</span> Chemical element, symbol Ru and atomic number 44

Ruthenium is a chemical element with the symbol Ru and atomic number 44. It is a rare transition metal belonging to the platinum group of the periodic table. Like the other metals of the platinum group, ruthenium is inert to most other chemicals. Russian-born scientist of Baltic-German ancestry Karl Ernst Claus discovered the element in 1844 at Kazan State University and named ruthenium in honor of Russia. Ruthenium is usually found as a minor component of platinum ores; the annual production has risen from about 19 tonnes in 2009 to some 35.5 tonnes in 2017. Most ruthenium produced is used in wear-resistant electrical contacts and thick-film resistors. A minor application for ruthenium is in platinum alloys and as a chemistry catalyst. A new application of ruthenium is as the capping layer for extreme ultraviolet photomasks. Ruthenium is generally found in ores with the other platinum group metals in the Ural Mountains and in North and South America. Small but commercially important quantities are also found in pentlandite extracted from Sudbury, Ontario, and in pyroxenite deposits in South Africa.

<span class="mw-page-title-main">Osmium tetroxide</span> Chemical compound

Osmium tetroxide (also osmium(VIII) oxide) is the chemical compound with the formula OsO4. The compound is noteworthy for its many uses, despite its toxicity and the rarity of osmium. It also has a number of unusual properties, one being that the solid is volatile. The compound is colourless, but most samples appear yellow. This is most likely due to the presence of the impurity OsO2, which is yellow-brown in colour. In biology, its property of binding to lipids has made it a widely-used stain in electron microscopy.

<span class="mw-page-title-main">Manganese dioxide</span> Chemical compound

Manganese dioxide is the inorganic compound with the formula MnO
2
. This blackish or brown solid occurs naturally as the mineral pyrolusite, which is the main ore of manganese and a component of manganese nodules. The principal use for MnO
2
is for dry-cell batteries, such as the alkaline battery and the zinc–carbon battery. MnO
2
is also used as a pigment and as a precursor to other manganese compounds, such as KMnO
4
. It is used as a reagent in organic synthesis, for example, for the oxidation of allylic alcohols. MnO
2
has an α-polymorph that can incorporate a variety of atoms in the "tunnels" or "channels" between the manganese oxide octahedra. There is considerable interest in α-MnO
2
as a possible cathode for lithium-ion batteries.

<span class="mw-page-title-main">Titanium tetrachloride</span> Inorganic chemical compound

Titanium tetrachloride is the inorganic compound with the formula TiCl4. It is an important intermediate in the production of titanium metal and the pigment titanium dioxide. TiCl4 is a volatile liquid. Upon contact with humid air, it forms thick clouds of titanium dioxide and hydrochloric acid, a reaction that was formerly exploited for use in smoke machines. It is sometimes referred to as "tickle" or "tickle 4" due to the phonetic resemblance of its molecular formula to the word.

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

Rhodium(III) chloride refers to inorganic compounds with the formula RhCl3(H2O)n, where n varies from 0 to 3. These are diamagnetic solids featuring octahedral Rh(III) centres. Depending on the value of n, the material is either a dense brown solid or a soluble reddish salt. The soluble trihydrated (n = 3) salt is widely used to prepare compounds used in homogeneous catalysis, notably for the industrial production of acetic acid and hydroformylation.

Selenic acid is the inorganic compound with the formula H2SeO4. It is an oxoacid of selenium, and its structure is more accurately described as O2Se(OH)2. It is a colorless compound. Although it has few uses, one of its salts, sodium selenate is used in the production of glass and animal feeds.

In chemistry, a plumbate often refers to compounds that can be viewed as derivatives of the hypothetical PbO2−3 anion. The term also refers to any anion of lead or any salt thereof. So the term is vague and somewhat archaic.

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

Ruthenium(III) chloride is the chemical compound with the formula RuCl3. "Ruthenium(III) chloride" more commonly refers to the hydrate RuCl3·xH2O. Both the anhydrous and hydrated species are dark brown or black solids. The hydrate, with a varying proportion of water of crystallization, often approximating to a trihydrate, is a commonly used starting material in ruthenium chemistry.

Ruthenium tetroxide is the inorganic compound with the formula RuO4. It is a yellow volatile solid that melts near room temperature. It has the odor of ozone. Samples are typically black due to impurities. The analogous OsO4 is more widely used and better known. It is also the anhydride of hyperruthenic acid (H2RuO5). One of the few solvents in which RuO4 forms stable solutions is CCl4.

<span class="mw-page-title-main">Nickel(II) iodide</span> Chemical compound

Nickel(II) iodide is an inorganic compound with the formula NiI2. This paramagnetic black solid dissolves readily in water to give bluish-green solutions, from which crystallizes the aquo complex [Ni(H2O)6]I2 (image above). This bluish-green colour is typical of hydrated nickel(II) compounds. Nickel iodides find some applications in homogeneous catalysis.

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

Tungsten(IV) oxide is the chemical compound with the formula WO2. The bronze-colored solid crystallizes in a monoclinic cell. The rutile-like structure features distorted octahedral WO6 centers with alternate short W–W bonds (248 pm). Each tungsten center has the d2 configuration, which gives the material a high electrical conductivity.

Osmium compounds are compounds containing the element osmium (Os). Osmium forms compounds with oxidation states ranging from −2 to +8. The most common oxidation states are +2, +3, +4, and +8. The +8 oxidation state is notable for being the highest attained by any chemical element aside from iridium's +9 and is encountered only in xenon, ruthenium, hassium, iridium, and plutonium. The oxidation states −1 and −2 represented by the two reactive compounds Na
2
[Os
4
(CO)
13
]
and Na
2
[Os(CO)
4
]
are used in the synthesis of osmium cluster compounds.

The transition metal ruthenium forms several compounds, with oxidation states of ruthenium ranging from 0 to +8, and −2. The properties of ruthenium and osmium compounds are often similar. The +2, +3, and +4 states are the most common. The most prevalent precursor is ruthenium trichloride, a red solid that is poorly defined chemically but versatile synthetically.

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

Iridium(IV) oxide, IrO2, is the only well-characterised oxide of iridium. It is a blue-black solid. The compound adopts the TiO2 rutile structure, featuring six coordinate iridium and three coordinate oxygen.

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

Rhenium(IV) oxide or rhenium dioxide is the inorganic compound with the formula ReO2. This gray to black crystalline solid is a laboratory reagent that can be used as a catalyst. It adopts the rutile structure.

<span class="mw-page-title-main">Osmium dioxide</span> Chemical compound

Osmium dioxide is an inorganic compound with the formula OsO2. It exists as brown to black crystalline powder, but single crystals are golden and exhibit metallic conductivity. The compound crystallizes in the rutile structural motif, i.e. the connectivity is very similar to that in the mineral rutile.

<span class="mw-page-title-main">Dichlorotris(triphenylphosphine)ruthenium(II)</span> Chemical compound

Dichlorotris(triphenylphosphine)ruthenium(II) is a coordination complex of ruthenium. It is a chocolate brown solid that is soluble in organic solvents such as benzene. The compound is used as a precursor to other complexes including those used in homogeneous catalysis.

Water oxidation is one of the half reactions of water splitting:

Iridium compounds are compounds containing the element iridium (Ir). Iridium forms compounds in oxidation states between −3 and +9, but the most common oxidation states are +1, +3, and +4. Well-characterized compounds containing iridium in the +6 oxidation state include IrF6 and the oxides Sr2MgIrO6 and Sr2CaIrO6. iridium(VIII) oxide was generated under matrix isolation conditions at 6 K in argon. The highest oxidation state (+9), which is also the highest recorded for any element, is found in gaseous [IrO4]+.

References

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  7. Lee, S. (2003). "Electrochromism of amorphous ruthenium oxide thin films". Solid State Ionics. 165 (1–4): 217–221. doi:10.1016/j.ssi.2003.08.035.
  8. McMurray, H. N. (1993). "Uniform colloids of ruthenium dioxide hydrate evolved by the surface-catalyzed reduction of ruthenium tetroxide". The Journal of Physical Chemistry. 97 (30): 8039–8045. doi:10.1021/j100132a038.
  9. Vogt, Helmut; Balej, Jan; Bennett, John E.; Wintzer, Peter; Sheikh, Saeed Akbar; Gallone, Patrizio (2000-06-15), "Chlorine Oxides and Chlorine Oxygen Acids", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, doi:10.1002/14356007.a06_483, ISBN   3527306730
  10. Seki, Kohei (2010-05-29). "Development of RuO2/Rutile-TiO2 Catalyst for Industrial HCl Oxidation Process". Catalysis Surveys from Asia. Springer Science and Business Media LLC. 14 (3–4): 168–175. doi:10.1007/s10563-010-9091-7. ISSN   1571-1013. S2CID   93115959.
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