Graphane

 Graphane is a two-dimensional polymer of carbon and hydrogen with the formula unit (CH)n where n is large.[1] Partial hydrogenation is then hydrogenated graphene.[2]

Graphane
Graphane.png
Identifiers
CAS Number
  • 1221743-01-6 ☒
ChemSpider
  • none
Properties
Chemical formula
(CH)n
Molar massVariable
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

SynthesisEdit

Its preparation was reported in 2009. Graphane can be formed by electrolytic hydrogenation of graphene, few-layer graphene or high-oriented pyrolytic graphite. In the last case mechanical exfoliation of hydrogenated top layers can be used.[3]

StructureEdit

The first theoretical description of graphane was reported in 2003.[4] The structure was found, using a cluster expansion method, as the most stable of all the possible hydrogenation ratios of graphene in 2003.[5] In 2007, researchers found that the compound is more stable than other compounds containing carbon and hydrogen, such as benzenecyclohexane and polyethylene.[6] This group named the predicted compound graphane, because it is the fully saturated version of graphene. The compound is an insulator. Chemical functionalization of graphene with hydrogen may be a suitable method to open a band gap in graphene.[6]

P-doped graphane is proposed to be a high-temperature BCS theory superconductor with a Tc above 90 K.[7]

Any disorder in hydrogenation conformation tends to contract the lattice constant by about 2.0%.[8]

VariantsEdit

Partial hydrogenation leads to hydrogenated graphene rather than (fully hydrogenated) graphane.[2] Such compounds are usually named as "graphane-like" structures. Graphane and graphane-like structures can be formed by electrolytic hydrogenation of graphene or few-layer graphene or high-oriented pyrolytic graphite. In the last case mechanical exfoliation of hydrogenated top layers can be used.[9]

Hydrogenation of graphene on substrate affects only one side, preserving hexagonal symmetry. One-sided hydrogenation of graphene is possible due to the existence of ripplings. Because the latter are distributed randomly, the obtained material is disordered in contrast to two-sided graphane.[2] Annealing allows the hydrogen to disperse, reverting to graphene.[10] Simulations revealed the underlying kinetic mechanism.[11]

Density functional theory calculations suggested that hydrogenated and fluorinated forms of other group IV (SiGe and Snnanosheets present properties similar to graphane.[12]

Potential applicationsEdit

p-Doped graphane is postulated to be a high-temperature BCS theory superconductor with a Tc above 90 K.[13]

Graphane has been proposed for hydrogen storage.[6] Hydrogenation decreases the dependence of the lattice constant on temperature, which indicates a possible application in precision instruments.[8]

Note

This article uses material from the Wikipedia article
 Metasyntactic variable, which is released under the 
Creative Commons
Attribution-ShareAlike 3.0 Unported License
.