4.8 Article

Oxygen Intercalation of Graphene on Transition Metal Substrate: An Edge-Limited Mechanism

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 6, Issue 20, Pages 4099-4105

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.5b01841

Keywords

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Funding

  1. NBRP [2011CB302004]
  2. NSFC [21173040, 21373045]
  3. NSF of Jiangsu [BK20130016]
  4. SRFDP of China [20130092110029]
  5. National Science Foundation (NSF) through the Nebraska Materials Research Science and Engineering Center (MRSEC) [DMR-1420645]

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Oxygen intercalation has been proven to be an efficient experimental approach to decouple chemical vapor deposition grown graphene from metal substrate with mild damage, thereby enabling graphene transfer. However, the mechanism of oxygen intercalation and associated rate-limiting step are still unclear on the molecular level. Here, by using density functional theory, we evaluate the thermodynamics stability of graphene edge on transition metal surface in the context of oxygen and explore various reaction pathways and energy barriers, from which we can identify the key steps as well as the roles of metal passivated graphene edges during the oxygen intercalation. Our calculations suggest that in well-controlled experimental conditions, oxygen atoms can be easily intercalated through either zigzag or armchair graphene edges on metal surface, whereas the unwanted graphene oxidation etching can be suppressed. Oxygen intercalation is, thus, an efficient and low-damage way to decouple graphene from a metal substrate while it allows reusing metal substrate for graphene growth.

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