Self-healing kinetics in monolayer graphene following very low energy ion irradiation

Monolayer graphene subjected to 13 and 90 eV Ar ion irradiation was probed by in-situ Raman spectroscopy. At 90 eV ion irradiation, a simple damage accumulation is seen. However, at 13 eV, immediately after damage formation, significant graphene self-healing is observed in real time. We argue that energy deposition through very-low-energy ion collisions can create vacancies and carbon adatoms which can diffuse easily on the surface and recombine afterward. The self-healing kinetics exhibit a fast (∼10 s) and a slow regime (∼30 min), which cannot result only from adatom-vacancy recombination. Based on a defect kinetic model, self-healing efficiency is revealed to be limited by dimer formation. Yet, the interplay between Stone-Wales defects and adatoms enables progressive release of the latter, and subsequent graphene self-healing on a longer time scale.

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Publication Details

Journal
Carbon
Published
2024-11-22
DOI
https://doi.org/10.1016/j.carbon.2024.119852
Citations
3
Primary Topic
Graphene research and applications
Type
article
Field-Weighted Citation Impact
0.35

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article

Self-healing kinetics in monolayer graphene following very low energy ion irradiation

Luc Stafford, S. Roorda, F. Schiettekatte, Satoshi Hamaguchi et al.
3 citations
Carbon
Graphene research and applications
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article

Self-healing kinetics in monolayer graphene following very low energy ion irradiation

Luc Stafford, S. Roorda, F. Schiettekatte, Satoshi Hamaguchi, Pierre Vinchon
article en
3 citations

Abstract

Monolayer graphene subjected to 13 and 90 eV Ar ion irradiation was probed by in-situ Raman spectroscopy. At 90 eV ion irradiation, a simple damage accumulation is seen. However, at 13 eV, immediately after damage formation, significant graphene self-healing is observed in real time. We argue that energy deposition through very-low-energy ion collisions can create vacancies and carbon adatoms which can diffuse easily on the surface and recombine afterward. The self-healing kinetics exhibit a fast (∼10 s) and a slow regime (∼30 min), which cannot result only from adatom-vacancy recombination. Based on a defect kinetic model, self-healing efficiency is revealed to be limited by dimer formation. Yet, the interplay between Stone-Wales defects and adatoms enables progressive release of the latter, and subsequent graphene self-healing on a longer time scale.

CarbonVol. 233
Université de Montréal (CA), The University of Osaka (JP)
Canada Foundation for Innovation, Fonds Québécois de la Recherche sur la Nature et les Technologies, Natural Sciences and Engineering Research Council of Canada, Japan Society for the Promotion of Science, Fonds de recherche du Québec – Nature et technologies, Science and Engineering Research Council
Affordable and clean energy
Openalex Percentile: Top 43%
Graphene research and applications
0.35
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