拉曼光谱
材料科学
石墨烯
氧化物
衍射
G波段
D波段
结晶学
分析化学(期刊)
光谱学
纳米技术
光学
化学
物理
色谱法
量子力学
冶金
作者
Neakanshika Chadha,Rahul Sharma,Parveen Saini
出处
期刊:Carbon letters
[Springer Science+Business Media]
日期:2021-04-07
卷期号:31 (6): 1125-1131
被引量:19
标识
DOI:10.1007/s42823-021-00234-5
摘要
Lately, Raman spectroscopy has become powerful tool for quality assessment of graphene analogues with identification of intensity ratio of Raman active D-band and G-band (ID/IG ratio) as a vital parameter for quantification of defects. However, during chemical reduction of graphitic oxide (GrO) to reduced GrO (RGrO), the increased ID/IG ratio is often wrongly recognized as defect augmentation, with “formation of more numerous yet smaller size sp2 domains” as its explanation. Herein, by giving due attention to normalized peak height, full-width half-maxima and integrated peak area of Raman D- and G-bands, and compliment the findings by XRD data, we have shown that in-plane size of sp2 domains actually increases upon chemical reduction. Particularly, contrary to increased ID/IG ratio, the calculated decrease in integrated peak area ratio (AD/AG ratio) in conjunction with narrowing of D-band and broadening of G-band, evinced the decrease in in-plane defects. Finally, as duly supported by reduction induced broadening of interlayer-spacing characteristic XRD peak and narrowing of ~ 43° centered XRD hump, we have also shown that the sp2 domains actually expands in size and the observed increase in ID/IG ratio is indeed due to increase in across-plane defects, formed via along-the-layer slicing of graphitic domains.
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