AI Article Synopsis

  • CuNi alloy foils are effective substrates for synthesizing large area single-crystalline graphene due to their high carbon catalyst activity, leading to fast growth rates and low nucleation density.
  • The reduction in nucleation density is attributed to carbon atom dissolution, which passivates the surface and raises the nucleation barrier, combined with suppressed diffusion caused by the alloy's inhomogeneous structure.
  • The study highlights that increased Ni content above a certain threshold enhances carbon diffusion into the bulk, offering valuable insights for designing catalysts for graphene and other 2D material synthesis.

Article Abstract

CuNi alloy foils are demonstrated to be one of the best substrates for synthesizing large area single-crystalline graphene because a very fast growth rate and low nucleation density can be simultaneously achieved. The fast growth rate is understood to be due the abundance of carbon precursor supply, as a result of the high catalytic activity of Ni atoms. However, a theoretical understanding of the low nucleation density remains controversial because it is known that a high carbon precursor concentration on the surface normally leads to a high nucleation density. Here, the graphene nucleation on the CuNi alloy surfaces is systematically explored and it is revealed that: i) carbon atom dissolution into the CuNi alloy passivates the alloy surface, thereby drastically increasing the graphene nucleation barrier; ii) carbon atom diffusion on the CuNi alloy surface is greatly suppressed by the inhomogeneous atomic structure of the surface; and iii) a prominent increase in the rate of carbon diffusion into the bulk occurs when the Ni composition is higher than the percolation threshold. This study reveals the key mechanism for graphene nucleation on CuNi alloy surfaces and provides a guideline for the catalyst design for the synthesis of graphene and other 2D materials.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010776PMC
http://dx.doi.org/10.1002/advs.201700961DOI Listing

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