Capabilities of transition metals in retarding the bonding of carbon atoms to minimize dendritic graphene. Issue 39 (28th September 2017)

• Record Type: Journal Article
• Authors: Zhu, Zhenwei; Zhan, Linjie; Wan, Wen; Zhao, Zhijuan; Shih, Tien-Mo; Cai, Weiwei
• Is Part Of: Nanoscale. Volume 9:Issue 39(2017)
• Page Start: 14804
• Page End: 14808
• Publication Date: 2017-09-28
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c7nr05253g
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : We have synthesized zigzag-edged hexagonal graphene domains by transition-metal-driven catalytic assistance via low pressure CVD. Abstract : The avoidance of growing dendritic graphene on the copper substrate during the chemical vapor deposition process is greatly desired. Here we have identified a mechanism, in which (1) transition metal plates placed inside the copper pockets reduce the majority of active carbon atoms to eventually suppress the graphene growth rate, and (2) transition metals etch graphene C–C bonds along defective edges to grow into zigzag-edge ending domains with higher priorities. Via isotopic labeling of the methane method, we have observed bright-dark-alternating hexagonal-shaped rings, which are shown in Raman mapping images. Under a hydrogen atmosphere, we are capable of acquiring hexagonal openings within graphene domains by means of transition-metal-driven catalytic etching. This methodology may work as a simple and convenient way to determine graphene size and crystal orientation, and may enable the etching of graphene into smooth and ordered zigzag edge nanoribbons without compromising the quality of graphene.