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Electronic Structure and Structural Evolutions of Hydrogenated Graphene Probed by Raman Spectroscopy

2010/09/01 by Zhiqiang Luo, Luo, Zhiqiang, Ting Yu +15
Materials Science · Physics and Astronomy · #Diamond and Carbon-based Materials Research #FOS: Physical sciences #Graphene research and applications #Materials Science (cond-mat.mtrl-sci) #Supercapacitor Materials and Fabrication #cond-mat.mtrl-sci

paper · pdf · doi:10.48550/arxiv.1009.0091

15 pages, 4 figures, 1 table

openalex publication_date 2010/09/01 · arxiv created 2010/12/03 · arxiv updated 2010/12/06 · openalex created_date 2019/06/27 · openalex updated_date 2026/07/28

Abstract

The electronic structure and structural evolution of hydrogenated graphene are investigated by Raman spectroscopy with multiple excitations. The excitation energy dependent saturation effect on the ratio of integrated intensities of D and G modes (ID/IG) is revealed and further developed as a quick method for estimation of inter-defect distance and defect density in hydrogenated graphene. At low hydrogen coverage, the chemisorbed H atoms behave like defects in sp2 C=C matrix; while for a high hydrogen coverage, the sp3 C-H bonds become coalescent clusters, resulting in confinement effect on the sp2 C domains. Electronic structure changes caused by varying hydrogen coverage are evidenced by excitation energy dependent red shift of D and 2D bands. Our results provide a useful guide for developing applications of hydrogenated graphene, as well as using Raman spectroscopy as quick metrology of the defect density in further exploring other kinds of graphene derivatives.

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