Raman Spectroscopy of Graphene Edges

被引:921
作者
Casiraghi, C. [1 ]
Hartschuh, A. [2 ,3 ]
Qian, H. [2 ,3 ]
Piscanec, S. [1 ]
Georgi, C. [2 ,3 ]
Fasoli, A. [1 ]
Novoselov, K. S. [4 ]
Basko, D. M. [5 ,6 ]
Ferrari, A. C. [1 ]
机构
[1] Univ Cambridge, Dept Engn, Cambridge CB2 1PZ, England
[2] Univ Munich, Dept Chem & Biochem, Munich, Germany
[3] Univ Munich, CeNS, Munich, Germany
[4] Univ Manchester, Dept Phys & Astron, Manchester M13 9PL, Lancs, England
[5] Univ Grenoble 1, Lab Phys & Modelisat Mileux Condenses, Grenoble, France
[6] CNRS, Grenoble, France
基金
欧洲研究理事会;
关键词
GRAPHITE; ELECTRON; SCATTERING; SPECTRUM; STATE;
D O I
10.1021/nl8032697
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphene edges are of particular interest since their orientation determines the electronic properties. Here we present a detailed Raman investigation of graphene flakes with edges oriented at different crystallographic directions. We also develop a real space theory for Raman scattering to analyze the general case of disordered edges. The position, width, and intensity of G and D peaks are studied as a function of the incident light polarization. The D-band is strongest for polarization parallel to the edge and minimum for perpendicular. Raman mapping shows that the D peak is localized in proximity of the edge. For ideal edges, the D peak is zero for zigzag orientation and large for armchair, allowing in principle the use of Raman spectroscopy as a sensitive tool for edge orientation. However, for real samples, the D to G ratio does not always show a significant dependence on edge orientation. Thus, even though edges can appear macroscopically smooth and oriented at well-defined angles, they are not necessarily microscopically ordered.
引用
收藏
页码:1433 / 1441
页数:9
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