| Autor: |
Rein, Valentina, Gao, Hao, Heenen, Hendrik H., Sghaier, Wissal, Manikas, Anastasios C., Saedi, Mehdi, Margraf, Johannes T., Galiotis, Costas, Renaud, Gilles, Konovalov, Oleg V., Groot, Irene M. N., Reuter, Karsten, Jankowski, Maciej |
| Rok vydání: |
2023 |
| Předmět: |
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| Zdroj: |
ACS Nano 2024 |
| Druh dokumentu: |
Working Paper |
| DOI: |
10.1021/acsnano.4c02070 |
| Popis: |
In recent years, liquid metal catalysts have emerged as a compelling choice for the controllable, large-scale, and high-quality synthesis of two-dimensional materials. At present, there is little mechanistic understanding of the intricate catalytic process, though, of its governing factors or what renders it superior to growth at the corresponding solid catalysts. Here, we report on a combined experimental and computational study of the kinetics of graphene growth during chemical vapor deposition on a liquid copper catalyst. By monitoring the growing graphene flakes in real time using in situ radiation-mode optical microscopy, we explore the growth morphology and kinetics over a wide range of CH4-to-H2 pressure ratios and deposition temperatures. Constant growth rates of the flakes' radius indicate a growth mode limited by precursor attachment, whereas methane-flux-dependent flake shapes point to limited precursor availability. Large-scale free energy simulations enabled by an efficient machine-learning moment tensor potential trained to density-functional theory data provide quantitative barriers for key atomic-scale growth processes. The wealth of experimental and theoretical data can be consistently combined into a microkinetic model that reveals mixed growth kinetics that, in contrast to the situation at solid Cu, is partly controlled by precursor attachment alongside precursor availability. Key mechanistic aspects that directly point toward the improved graphene quality are a largely suppressed carbon dimer attachment due to the facile incorporation of this precursor species into the liquid surface and a low-barrier ring-opening process that self-heals 5-membered rings resulting from remaining dimer attachments. |
| Databáze: |
arXiv |
| Externí odkaz: |
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