Graphyne

Source: Wikipedia, the free encyclopedia.
Not to be confused with Graphene, Grapheme, or Graphane.
Graphyne

Chemical structure of graphyne-1
Identifiers
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Graphyne-n varieties, where n indicates the number of carbon–carbon triple bonds in a link between two adjacent hexagons. Graphyne is graphyne-1; graphdiyne is graphyne-2.

Graphyne is an

sp2-bonded carbon atoms arranged in crystal lattice. It can be seen as a lattice of benzene rings connected by acetylene bonds. The material is called graphyne-n when benzene rings are connected by n sequential acetylene molecules, and graphdiyne for a particular case of n = 2 (diacetylene
links).

Depending on the content of acetylene groups, graphyne can be considered a mixed hybridization, spk, where k can be 1 or 2,[1][2] and thus differs from the hybridization of graphene (considered pure sp2) and diamond (pure sp3).

First-principles calculations showed that periodic graphyne structures and their boron nitride analogues are stable. The calculations used phonon dispersion curves and ab-initio finite temperature, quantum mechanical molecular dynamics simulations.[3]

History

Graphyne was first theoretically proposed by Baughman et al. in 1987.[4] In 2010, Li et al. developed the first successful methodology for creating graphdiyne films using the Glaser–Hay cross-coupling reaction with hexaethynylbenzene.[5] The proposed approach makes it possible to synthesize nanometer-scale graphdiyne and graphtetrayne, which lack long-range order. In 2019, Cui and co-workers reported on a mechanochemical technique for obtaining graphyne using benzene and calcium carbide.[6] Although a gram-scale graphyne can be obtained using this approach, graphynes with long-range crystallinity over a large area remain elusive.

Although disputed, researchers used alkyne metathesis, while controlling thermodynamics and kinetics, to synthesize graphyne in 2022.[7][8] Various analytical methods indicate its excellent chemical and thermal stability. A wide-angle X-ray scattering characterization of the obtained graphyne product suggests a unified crystalline structure.[9]

In 2022, the first scalable synthesis of multi-layered γ‑graphyne was successfully performed through the polymerization of 1,3,5-tribromo-2,4,6-triethynylbenzene under

bandgap as 0.48 ± 0.05 eV, which agrees with the theoretical prediction for graphyne-based materials.[10][11]

Structure

Through the use of computer models scientists have predicted several properties of the substance on assumed geometries of the lattice. Its proposed structures are derived from inserting acetylene bonds in place of

hexagonal lattice structure and a rectangular lattice structure.[13]
Out of the theorized structures the rectangular lattice of 6,6,12-graphyne may hold the most potential for future applications.

Properties

Models predict that graphyne has the potential for

valence bands meet in a linear fashion at a single point in the Fermi level. The advantage of this scheme is that electrons behave as if they have no mass, resulting in energies that are proportional to the momentum of the electrons. Like in graphene, hexagonal graphyne has electric properties that are direction independent. However, due to the symmetry of the proposed rectangular 6,6,12-graphyne the electric properties would change along different directions in the plane of the material.[13] This unique feature of its symmetry allows graphyne to self-dope meaning that it has two different Dirac cones lying slightly above and below the Fermi level.[13] The self-doping effect of 6,6,12-graphyne can be effectively tuned by applying in-plane external strain.[14]
Graphyne samples synthesized to date have shown a melting point of 250-300 °C, low reactivity in decomposition reactions with oxygen, heat and light.[12]

Potential applications

It has been hypothesized that graphyne is preferable to graphene for specific applications owing to its particular energy structure, namely direction-dependent Dirac cones.[15][16] The directional dependency of 6,6,12-graphyne could allow for electrical grating on the nanoscale.[17] This could lead to the development of faster transistors and nanoscale electronic devices.[13][18][19] Recently it was demonstrated that photoinduced electron transfer from electron-donating partners to γ-graphyne is favorable and occurs on nano to sub-picosecond time scale.[20]

References

  1. doi:10.1016/S0008-6223(97)82794-7
    .
  2. S2CID 125591804
    .
  3. S2CID 44136901
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  4. doi:10.1063/1.453405
    .
  5. PMID 20442882
    .
  6. S2CID 104431102
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  7. ^ Hu, Yiming; Wu, Chenyu; Pan, Qingyan; Jin, Yinghua; Lyu, Rui; Martinez, Vikina; Huang, Shaofeng; Wu, Jingyi; Wayment, Lacey J.; Clark, Noel A.; Raschke, Markus B.; Zhao, Yingjie; Zhang, Wei (9 May 2022). "Synthesis of γ-graphyne using dynamic covalent chemistry".
  8. S2CID 248686420
    .
  9. ^ Leytham-Powell, Cay; Boulder, University of Colorado at. "Long-hypothesized 'next generation wonder material' created for first time". phys.org. Retrieved 2022-05-23.
  10. S2CID 252438218
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  11. PMID 29663794
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  12. ^
    S2CID 119288235
    .
  13. ^ a b c d Dumé, Belle (1 March 2012). "Could graphynes be better than graphene?". Physics World. Institute of Physics.
  14. doi:10.1063/1.4880635
    .
  15. PMID 22463556
    .
  16. doi:10.1103/Physics.5.24
    .
  17. ^ Bardhan, Debjyoti (2 March 2012). "Novel new material graphyne can be a serious competitor to graphene". techie-buzz.com.
  18. ^ Cartwright, J. (1 March 2012). "Graphyne could be better than graphene". news.sciencemag.org. Archived from the original on 2 October 2012.
  19. ^ "Graphyne Better Than Graphene?". Materials Today. 5 March 2012.
  20. S2CID 254961210
    .

External links

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