Osmium borides

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Structure of orthorhombic OsB2. Green atoms are Os, pink - boron OsB2structure.JPG
Structure of orthorhombic OsB2. Green atoms are Os, pink – boron

Osmium borides are compounds of osmium and boron. Their most remarkable property is potentially high hardness. It is thought that a combination of high electron density of osmium with the strength of boron-osmium covalent bonds will make osmium borides superhard materials, however this has not been demonstrated yet. For example, OsB2 is hard (hardness comparable to that of sapphire), but not superhard. [1]

Contents

Synthesis

Osmium borides are produced in vacuum or inert atmosphere to prevent formation of osmium tetroxide, which is a hazardous compound. Synthesis occurs at high temperatures (~1000 °C) from a mixture of MgB2 and OsCl3. [1]

Structure

Three osmium borides are known: OsB, Os2B3 and OsB2. The first two have hexagonal structure, [2] similar to that of rhenium diboride. Osmium diboride was first also sought as hexagonal, [3] but one of its phases was later reassigned to orthorhombic. [1] [4] In recent methods of synthesis, it has also been found that a hexagonal phase of OsB2 exists with a similar structure to ReB2. [5]

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<span class="mw-page-title-main">Boron</span> Chemical element, symbol B and atomic number 5

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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.

<span class="mw-page-title-main">Rhenium diboride</span> Chemical compound

Rhenium diboride (ReB2) is a synthetic superhard material. It was first synthesized in 1962  and re-emerged recently due to hopes of achieving high hardness comparable to that of diamond. The reported ultrahigh hardness has been questioned, although this is a matter of definition as in the initial test rhenium diboride was able to scratch diamond.

<span class="mw-page-title-main">Aluminium diboride</span> Chemical compound

Aluminium diboride (AlB2) is a chemical compound made from the metal aluminium and the metalloid boron. It is one of two compounds of aluminium and boron, the other being AlB12, which are both commonly referred to as aluminium boride.

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Aluminium magnesium boride or Al3Mg3B56, colloqually known as BAM, is a chemical compound of aluminium, magnesium and boron. Whereas its nominal formula is AlMgB14, the chemical composition is closer to Al0.75Mg0.75B14. It is a ceramic alloy that is highly resistive to wear and has an extremely low coefficient of sliding friction, reaching a record value of 0.04 in unlubricated and 0.02 in lubricated AlMgB14−TiB2 composites. First reported in 1970, BAM has an orthorhombic structure with four icosahedral B12 units per unit cell. This ultrahard material has a coefficient of thermal expansion comparable to that of other widely used materials such as steel and concrete.

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<span class="mw-page-title-main">Ruthenium boride</span>

Ruthenium borides are compounds of ruthenium and boron. Their most remarkable property is potentially high hardness. Vickers hardness HV = 50 GPa was reported for thin films composed of RuB2 and Ru2B3 phases. This value is significantly higher than those of bulk RuB2 or Ru2B3, but it has to be confirmed independently, as measurements on superhard materials are intrinsically difficult. For example, note that the initial report on extreme hardness of related material rhenium diboride was probably too optimistic.

<span class="mw-page-title-main">Tantalum boride</span>

Tantalum borides are compounds of tantalum and boron most remarkable for their extreme hardness.

<span class="mw-page-title-main">Tungsten borides</span>

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<span class="mw-page-title-main">Allotropes of boron</span> Materials made only out of boron

Boron can be prepared in several crystalline and amorphous forms. Well known crystalline forms are α-rhombohedral (α-R), β-rhombohedral (β-R), and β-tetragonal (β-T). In special circumstances, boron can also be synthesized in the form of its α-tetragonal (α-T) and γ-orthorhombic (γ) allotropes. Two amorphous forms, one a finely divided powder and the other a glassy solid, are also known. Although at least 14 more allotropes have been reported, these other forms are based on tenuous evidence or have not been experimentally confirmed, or are thought to represent mixed allotropes, or boron frameworks stabilized by impurities. Whereas the β-rhombohedral phase is the most stable and the others are metastable, the transformation rate is negligible at room temperature, and thus all five phases can exist at ambient conditions. Amorphous powder boron and polycrystalline β-rhombohedral boron are the most common forms. The latter allotrope is a very hard grey material, about ten percent lighter than aluminium and with a melting point (2080 °C) several hundred degrees higher than that of steel.

Diboride may refer to:

Ultra-high-temperature ceramics (UHTCs) are a type of refractory ceramics that that can withstand extremely high temperatures without degrading, often above 2,000 °C. They also often have high thermal conductivities and are highly resistant to thermal shock, meaning they can withstand sudden and extreme changes in temperature without cracking or breaking. Chemically, they are usually borides, carbides, nitrides, and oxides of early transition metals.

Francis Pettit Bundy was an American physicist, known as a member of General Electric's team of researchers that in December 1954 created diamond chips by applying ultra high pressure to graphite with iron sulfide as a catalyst.

References

  1. 1 2 3 Cumberland, Robert W.; et al. (April 27, 2005). "Osmium Diboride, An Ultra-Incompressible, Hard Material". Journal of the American Chemical Society. 127 (20): 7264–5. doi:10.1021/ja043806y. PMID   15898746.
  2. M. Hebbache; et al. (2006). "A new superhard material: Osmium diboride OsB2". Solid State Communications. 139 (5): 227–231. Bibcode:2006SSCom.139..227H. doi:10.1016/j.ssc.2006.05.041.
  3. Kempter, C. P.; Fries, R. J. (1961). "Crystallography of the Ru-B and Os-B Systems". The Journal of Chemical Physics. 34 (6): 1994. Bibcode:1961JChPh..34.1994K. doi:10.1063/1.1731807.
  4. Roof, R. B.; Kempter, C. P. (1962). "New Orthorhombic Phase in the Ru-B and Os-B Systems". The Journal of Chemical Physics. 37 (7): 1473. Bibcode:1962JChPh..37.1473R. doi:10.1063/1.1733309.
  5. Xie, Zhilin; Blair, Richard G.; Orlovskaya, Nina; Cullen, David A.; Andrew Payzant, E. (2014-11-01). "Thermal stability of hexagonal OsB2". Journal of Solid State Chemistry. 219: 210–219. Bibcode:2014JSSCh.219..210X. doi: 10.1016/j.jssc.2014.07.035 .