石墨烯
方向错误
材料科学
微晶
成核
外延
化学气相沉积
基质(水族馆)
单晶
氧化石墨烯纸
化学工程
Crystal(编程语言)
纳米技术
光电子学
化学物理
结晶学
晶界
微观结构
复合材料
化学
冶金
图层(电子)
工程类
有机化学
地质学
程序设计语言
海洋学
计算机科学
作者
Luzhao Sun,Buhang Chen,Wendong Wang,Yanglizhi Li,Xiongzhi Zeng,Haiyang Liu,Yu Liang,Zhenyong Zhao,Ali Cai,Rui Zhang,Yeshu Zhu,Yuechen Wang,Yuqing Song,Qingjie Ding,Xuan Gao,Hailin Peng,Zhenyu Li,Li Lin,Zhongfan Liu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2021-12-29
卷期号:16 (1): 285-294
被引量:95
标识
DOI:10.1021/acsnano.1c06285
摘要
The epitaxial growth of single-crystal thin films relies on the availability of a single-crystal substrate and a strong interaction between epilayer and substrate. Previous studies have reported the roles of the substrate (e.g., symmetry and lattice constant) in determining the orientations of chemical vapor deposition (CVD)-grown graphene, and Cu(111) is considered as the most promising substrate for epitaxial growth of graphene single crystals. However, the roles of gas-phase reactants and graphene–substrate interaction in determining the graphene orientation are still unclear. Here, we find that trace amounts of oxygen is capable of enhancing the interaction between graphene edges and Cu(111) substrate and, therefore, eliminating the misoriented graphene domains in the nucleation stage. A modified anomalous grain growth method is developed to improve the size of the as-obtained Cu(111) single crystal, relying on strongly textured polycrystalline Cu foils. The batch-to-batch production of A3-size (∼0.42 × 0.3 m2) single-crystal graphene films is achieved on Cu(111) foils relying on a self-designed pilot-scale CVD system. The as-grown graphene exhibits ultrahigh carrier mobilities of 68 000 cm2 V–1 s–1 at room temperature and 210 000 cm2 V–1 s–1 at 2.2 K. The findings and strategies provided in our work would accelerate the mass production of high-quality misorientation-free graphene films.
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