Exploring the effect of the covalent functionalization in graphene-antimonene heterostructures

被引:1
|
作者
Fickert, M. [1 ]
Martinez-Haya, R. [2 ]
Ruiz, A. M. [2 ]
Baldovi, J. J. [2 ]
Abellan, G. [2 ]
机构
[1] Friedrich Alexander Univ Erlangen Nurnberg FAU, Joint Inst Adv Mat & Proc ZMP, Dept Chem & Pharm, D-90762 Furth, Germany
[2] Univ Valencia, Inst Ciencia Mol ICMol, Valencia 46980, Spain
基金
欧洲研究理事会;
关键词
TEMPERATURE-DEPENDENT RAMAN; HIGHLY EFFICIENT; REACTIVITY; GRAPHITE; DISORDER;
D O I
10.1039/d4ra01029a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The growing field of two-dimensional (2D) materials has recently witnessed the emergence of heterostructures, however those combining monoelemental layered materials remain relatively unexplored. In this study, we present the chemical fabrication and characterization of a heterostructure formed by graphene and hexagonal antimonene. The interaction between these 2D materials is thoroughly examined through Raman spectroscopy and first-principles calculations, revealing that this can be considered as a van der Waals heterostructure. Furthermore, we have explored the influence of the antimonene 2D material on the reactivity of graphene by studying the laser-induced covalent functionalization of the graphene surface. Our findings indicate distinct degrees of functionalization based on the underlying material, SiO2 being more reactive than antimonene, opening the door for the development of controlled patterning in devices based on these heterostructures. This covalent functionalization implies a high control over the chemical information that can be stored but also removed on graphene surfaces, and its use as a patterned heterostructure based on antimonene and graphene. This research provides valuable insights into the antimonene-graphene interactions and their impact on the chemical reactivity during graphene covalent functionalization. van der Waals heterostructure preparation based on hexagonal Sb and graphene, and its subsequent patterning through functionalization with benzyl substituents.
引用
收藏
页码:13758 / 13768
页数:11
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