Graphane

Not to be confused with Grapheme, Graphene, or Graphyne.
Graphane
Identifiers
1221743-01-6 N
Properties
(CH)n
Molar mass Variable
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

Graphane is a two-dimensional polymer of carbon and hydrogen with the formula unit (CH)n where n is large. Graphane should not be confused with graphene, a two-dimensional form of carbon alone. Graphane is a form of hydrogenated graphene. Graphane's carbon bonds are in sp3 configuration, as opposed to graphene's sp2 bond configuration, thus graphane is a two-dimensional analog of cubic diamond.

Structure

The structure was found, using a cluster expansion method, as the most stable of all the possible hydrogenations ratios of graphene in 2003.[1] In 2007, researchers found that the compound is more stable than other compounds containing carbon and hydrogen, such as benzene, cyclohexane and polyethylene.[2] 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.[2]

P-doped graphane is proposed to be a high-temperature BCS theory superconductor with a Tc above 90 K.[3]

Any disorder in hydrogenation conformation tends to contract the lattice constant by about 2.0%.[4]

Variants

Partial hydrogenation leads to hydrogenated graphene rather than (fully hydrogenated) graphane.[5] 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.[6]

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.[5] Annealing allows the hydrogen to disperse, reverting to graphene.[7] Simulations revealed the underlying kinetic mechanism.[8]

Density functional theory calculations suggested that hydrogenated and fluorinated forms of other group IV (Si, Ge and Sn) nanosheets present properties similar to graphane.[9]

Potential applications

This compound has been proposed for hydrogen storage.[2] Hydrogenation decreases the dependence of the lattice constant on temperature, which indicates a possible application in precision instruments.[4]

References

  1. ↑ Sluiter, Marcel; Kawazoe, Yoshiyuki (2003). "Cluster expansion method for adsorption: Application to hydrogen chemisorption on graphene". Physical Review B. 68 (8): 085410. Bibcode:2003PhRvB..68h5410S. doi:10.1103/PhysRevB.68.085410.
  2. 1 2 3 Sofo, Jorge O.; et al. (2007). "Graphane: A two-dimensional hydrocarbon". Physical Review B. 75 (15): 153401–4. arXiv:cond-mat/0606704Freely accessible. Bibcode:2007PhRvB..75o3401S. doi:10.1103/PhysRevB.75.153401.
  3. ↑ G. Savini; et al. (2010). "Doped graphane: a prototype high-Tc electron-phonon superconductor". Phys Rev Lett. 105. arXiv:1002.0653v1Freely accessible.
  4. 1 2 L. F. Huang; et al. (2013). "Lattice dynamics and disorder-induced contraction in functionalized graphene". J. Appl. Phys. 113: 083524. Bibcode:2013JAP...113h3524F. doi:10.1063/1.4793790.
  5. 1 2 D. C. Elias; et al. (2009). "Control of Graphene's Properties by Reversible Hydrogenation: Evidence for Graphane". Science. 323 (5914): 610–3. arXiv:0810.4706Freely accessible. Bibcode:2009Sci...323..610E. doi:10.1126/science.1167130. PMID 19179524.
  6. ↑ A. M. Ilyin; et al. (2011). "Computer simulation and experimental study of graphane-like structures formed by electrolytic hydrogenation". Physica E. 43 (6): 1262–65. Bibcode:2011PhyE...43.1262I. doi:10.1016/j.physe.2011.02.012.
  7. ↑ Konstantin Novoselov. "Beyond the wonder material". Physics World August 2009, 27-30.
  8. ↑ L. F. Huang; et al. (2011). "Understanding the Band Gap, Magnetism, and Kinetics of Graphene Nanostripes in Graphane". J. Phys. Chem. C. 115: 21088. doi:10.1021/jp208067y.
  9. ↑ J. C. Garcia; D. B. de Lima; L. V. C. Assali; J. F. Justo (2011). "Group IV Graphene- and Graphane-Like Nanosheets". J. Phys. Chem. C. 115: 13242. arXiv:1204.2875Freely accessible. doi:10.1021/jp203657w.
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