Misplaced Pages

Ruthenium(IV) oxide

Names
IUPAC name Ruthenium(IV) oxide
Other names Ruthenium dioxide
Identifiers
CAS Number	12036-10-1
3D model (JSmol)	Interactive image
ECHA InfoCard	100.031.660
EC Number	234-840-6
PubChem CID	82848
CompTox Dashboard (EPA)	DTXSID0065193
InChI InChI=1S/2O.Ru
SMILES O==O
Properties
Chemical formula	RuO2
Molar mass	133.0688 g/mol
Appearance	blue-black solid
Density	6.97 g/cm
Boiling point	1,200 °C (2,190 °F; 1,470 K) sublimates
Solubility in water	insoluble
Magnetic susceptibility (χ)	+162.0·10 cm/mol
Structure
Crystal structure	Rutile (tetragonal), tP6
Space group	P42/mnm, No. 136
Coordination geometry	Octahedral (Ru); trigonal planar (O)
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 , 100 kPa). N verify (what is  ?) Infobox references

Ruthenium(IV) oxide is the inorganic compound with the formula RuO₂. This black solid is the most common oxide of ruthenium. It is widely used as an electrocatalyst for producing chlorine, chlorine oxides, and O₂. Like many dioxides, RuO₂ adopts the rutile structure.

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:

RuO₂ + O₂ ⇌ RuO₄

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

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.

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.

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. 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. Average capacities of ruthenium(IV) oxide have reached 650 F/g when in sulfuric acid and annealed at temperatures lower than 200 °C. In attempts to optimise its capacitive properties, prior work has looked at the hydration, crystallinity and particle size of ruthenium oxide.

References

1. Mills, Andrew (1989). "Heterogeneous redox catalysts for oxygen and chlorine evolution". Chemical Society Reviews. 18. Royal Society of Chemistry (RSC): 285. doi:10.1039/cs9891800285. ISSN 0306-0012.
2. Wyckoff, R.W.G.. Crystal Structures, Vol. 1. Interscience, John Wiley & Sons: 1963.
3. Wells, A. F. (1975), Structural Inorganic Chemistry (4th ed.), Oxford: Clarendon Press
4. Schäfer, Harald; Schneidereit, Gerd; Gerhardt, Wilfried (1963). "Zur Chemie der Platinmetalle. RuO2 Chemischer Transport, Eigenschaften, thermischer Zerfall". Zeitschrift für anorganische und allgemeine Chemie (in German). 319 (5–6). Wiley: 327–336. doi:10.1002/zaac.19633190514. ISSN 0044-2313.
5. Rogers, D. B.; Butler, S. R.; Shannon, R. D. (1972). "Single Crystals of Transition-Metal Dioxides". Inorganic Syntheses. Vol. XIII. pp. 135–145. doi:10.1002/9780470132449.ch27. ISBN 9780470132449.
6. Pizzini, S.; Buzzanca, G.; Mari, C.; Rossi, L.; Torchio, S. (1972). "Preparation, structure and electrical properties of thick ruthenium dioxide films". Materials Research Bulletin. 7 (5). Elsevier BV: 449–462. doi:10.1016/0025-5408(72)90147-x. ISSN 0025-5408.
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. 14 (3–4). Springer Science and Business Media LLC: 168–175. doi:10.1007/s10563-010-9091-7. ISSN 1571-1013. S2CID 93115959.
11. De Nora, O. (1970). "Anwendung maßbeständiger aktivierter Titan-Anoden bei der Chloralkali-Elektrolyse". Chemie Ingenieur Technik. 42 (4). Wiley: 222–226. doi:10.1002/cite.330420417. ISSN 0009-286X.
12. Iles, G.S. (1967). "Ruthenium Oxide Glaze Resistors". Platinum Metals Review. 11 (4): 126.
13. Matthey, Johnson (2002). "Nanocrystalline Ruthenium Supercapacitor Material". Platinum Metals Review. 46 (3): 105. Archived from the original on 2015-09-24. Retrieved 2013-09-16.
14. Kim,Il-Hwan; Kim, Kwang-Bum; Electrochem. Solid-State Lett., 2001, 4, 5,A62-A64

External links

• Los Alamos National Laboratory – Ruthenium Archived 2007-04-05 at the Wayback Machine

• Ruthenium(IV) compounds
• Transition metal oxides