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High-temperature scanning tunneling microscopy study of the ordering transition of an amorphous carbon layer into graphene on ruthenium(0001)

机译:钌上无定形碳层向石墨烯的有序转变的高温扫描隧道显微镜研究(0001)

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The ordering transition of an amorphous carbon layer into graphene was investigated by high-temperature scanning tunneling microscopy. A disordered C layer was prepared on a Ru(0001) surface by chemical vapor deposition of ethylene molecules at ~660 K. The carbon layer grows in the form of dendritic islands that have almost the same density as graphene. Upon annealing of the fully covered surface, residual hydrogen desorbs and a coherent but still disordered carbon layer forms, with almost the same carbon coverage as in graphene. The ordering of this layer into graphene at 920 to 950 K was monitored as a function of time. A unique mechanism was observed that involves small topographic holes in the carbon layer. The holes are mobile, and on the trajectories of the holes the disordered carbon layer is transformed into graphene. The transport of C atoms across the holes or along the hole edges provides a low-energy pathway for the ordering transition. This mechanism is prohibited in a dense graphene layer, which offers an explanation for the difficulty of removing defects from graphene synthesized by chemical methods.
机译:通过高温扫描隧道显微镜研究了非晶碳层向石墨烯的有序过渡。通过在约660 K的乙烯分子化学气相沉积,在Ru(0001)表面上制备了无序的C层。碳层以树枝状岛的形式生长,其密度几乎与石墨烯相同。在完全覆盖的表面退火后,残留的氢会解吸,形成连贯但仍无序的碳层,其碳覆盖率几乎与石墨烯相同。随时间监测该层在920至950 K下成石墨烯的顺序。观察到一种独特的机理,该机理涉及碳层中的小形貌形洞。孔是可移动的,并且在孔的轨迹上,无序的碳层转化为石墨烯。 C原子跨孔或沿孔边缘的传输为有序跃迁提供了低能途径。在致密的石墨烯层中禁止这种机理,这为从化学方法合成的石墨烯中去除缺陷的难度提供了解释。

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