石墨烯
金属
材料科学
催化作用
蚀刻(微加工)
碳纤维
化学工程
纳米技术
无机化学
冶金
复合材料
化学
有机化学
复合数
工程类
图层(电子)
作者
Guangjun Cheng,Irene Calizo,Angela R. Hight Walker
出处
期刊:Carbon
[Elsevier]
日期:2015-01-01
卷期号:81: 678-687
被引量:21
标识
DOI:10.1016/j.carbon.2014.10.005
摘要
Abstract We present a comparative investigation on the etching of graphene catalyzed by Fe and Cu. When Fe or Cu thin film deposited on graphene is rapidly annealed in either N2 or forming gas (10% H2/90% N2), particles are produced due to the dewetting of thin films. Low-voltage scanning electron microscopy reveals different morphology for Fe and Cu particles and their strikingly different catalytic etching behaviors. For the Fe thin film on graphene annealed at 950 °C in either gas environment, graphene is severely damaged, suggesting that the etching could occur through catalytic carbon hydrogenation or carbon dissolution into Fe due to the strong Fe–C interactions. In contrast, while no etching takes place for Cu particles on graphene at 1050 °C in N2, Cu particles catalytically etch channels in graphene in forming gas through carbon hydrogenation, and the width of the channel is much narrower than the diameter of Cu particle due to the non-wetting behavior of Cu on graphene. The weak interactions between Cu and graphene, along with the low solubility of carbon in Cu, make Cu particles ideal for tracking their etching paths on graphene. This work provides new insights into the metal-catalyzed etching of graphene.
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