Abstract
To address the environmental concerns, a relatively simple, innovative and low-cost procedure has been suggested for synthesis of graphene nanosheets (GNSs). The procedure utilized here for synthesizing GNSs is derived from aqueous suspension of graphene oxide (GO). Ficus carica (FC) is known to be remarkable antioxidant. It is regarded as suitable biocompatible alternative to hazardous and toxic chemicals. This method ensures non-hazardous nature of the deoxygenating agent (FC) as well as their oxidized outcomes. Structural and morphological characterization indicates the absence of oxygen-bearing groups from graphene oxide. Characterization was done by standard techniques such as X-ray crystallography, FTIR, RAMAN, DLS, and UV–Vis spectrophotometry. Morphological investigation of resulting material was also undertaken through standard techniques by FESEM, TEM, HRTEM with SAED pattern. Thermal stability of FC derived graphene was also investigated. The investigation may initiate new routes for preparing GNSs at large scale facilitating a better research and commercial utilization.Graphical abstract
Highlights
Graphene, the wonder material, has become popular among nanomaterial investigators
Synthesis of graphene nanosheets (GNSs) based on Ficus carica (FC) extract reduction
The peaks at ~ 1728, ~ 1590, and ~ 1011 cm−1 are believed to be due to presence of ketone (C=O), epoxide (C–O–C) and carboxyl (COOH and/or H2O) groups, respectively [47, 48], but in the context of GNSs, a remarkable reduction is observed in the intensities of ketonic group along with increase of carbon–carbon double bond
Summary
The wonder material, has become popular among nanomaterial investigators. The path-breaking discovery of graphene was made by Geim and co-workers [1]. Keywords Green synthesis · Graphene oxide · Graphene nanosheets · Ficus carica extract Chemical reduction of graphene oxide (GO) is considered as a superior method for large scale production. The fresh extract was used immediately for reduction of graphene oxide.
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