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A mixed-solvent strategy for facile and green preparation of graphene by liquid-phase exfoliation of graphite
A versatile and scalable mixed-solvent strategy, by which two mediocre solvents could be combined into good solvents for exfoliating graphite, is demonstrated for facile and green preparation of graphene by liquid-phase exfoliation of graphite. Mild sonication of crystal graphite powder in a mixture...
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Published in: | Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology 2012-08, Vol.14 (8), p.1-9, Article 1003 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A versatile and scalable mixed-solvent strategy, by which two mediocre solvents could be combined into good solvents for exfoliating graphite, is demonstrated for facile and green preparation of graphene by liquid-phase exfoliation of graphite. Mild sonication of crystal graphite powder in a mixture of water and alcohol could yield graphene nanosheets, which formed a highly stable suspension in the mixed solvents. The graphene yield was estimated as ~10 wt%. The optimum mass fraction of ethanol in water–ethanol mixtures and isopropanol in water–isopropanol mixtures was experimentally determined as ~40 and ~55 % respectively, which could be roughly predicted by the theory of Hansen solubility parameters. Statistics based on atomic force microscopic analysis show that up to ~86 % of the prepared nanosheets were less than 10-layer thick with a monolayer fraction of ~8 %. High resolution transmission electron microscopy, infrared spectroscopy, X-ray diffraction, and Raman spectrum analysis of the vacuum-filtered films suggest the graphene sheets to be largely free of defects and oxides. The proposed mixed-solvent strategy here extends the scope for liquid-phase processing graphene and gives researchers great freedom in designing ideal solvent systems for specific applications. |
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ISSN: | 1388-0764 1572-896X |
DOI: | 10.1007/s11051-012-1003-5 |