Continuous Production of Functionalized Graphene Inks by Soft Solution Processing

• Published in: Nanomaterials (Basel, Switzerland) Vol. 13; no. 14; p. 2043
• Main Authors: Rao, Kodepelly Sanjeeva, Senthilnathan, Jaganathan, Ting, Jyh-Ming, Yoshimura, Masahiro
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 11.07.2023; MDPI
• Subjects: Acetonitrile; Aqueous solutions; Azobisisobutyronitrile; Batteries; Carbon; Catalysis; Centrifugation; Chemical vapor deposition; Continuous production; Dimethylformamide; Dispersants; Dispersion; Electrochemistry; Energy storage; Ethylene glycol; Functional groups; functionalized graphene; Glass substrates; Glycine; Graphene; Graphite; Green chemistry; Inks; Insertion; Methods; Nitrogen; NMR; Nuclear magnetic resonance; Photoelectrons; Printing-ink; Raman spectra; Raman spectroscopy; solution processing; Solvents; Spectrum analysis; Taiwan; functionalized graphene; solution processing; continuous production; inks
• ISSN: 2079-4991; 2079-4991
• DOI: 10.3390/nano13142043

The continuous production of high-quality, few-layer graphene nanosheets (GNSs) functionalized with nitrogen-containing groups was achieved via a two-stage reaction method. The initial stage produces few-layer GNSs by utilizing our recently developed glycine-bisulfate ionic complex-assisted electrochemical exfoliation of graphite. The second stage, developed here, uses a radical initiator and nitrogen precursor (azobisisobutyronitrile) under microwave conditions in an aqueous solution for the efficient nitrogen functionalization of the initially formed GNSs. These nitrile radical reactions have great advantages in green chemistry and soft processing. Raman spectra confirm the insertion of nitrogen functional groups into nitrogen-functionalized graphene (N-FG), whose disorder is higher than that of GNSs. X-ray photoelectron spectra confirm the insertion of edge/surface nitrogen functional groups. The insertion of nitrogen functional groups is further confirmed by the enhanced dispersibility of N-FG in dimethyl formamide, ethylene glycol, acetonitrile, and water. Indeed, after the synthesis of N-FG in solution, it is possible to disperse N-FG in these liquid dispersants just by a simple washing-centrifugation separation-dispersion sequence. Therefore, without any drying, milling, and redispersion into liquid again, we can produce N-FG ink with only solution processing. Thus, the present work demonstrates the 'continuous solution processing' of N-FG inks without complicated post-processing conditions. Furthermore, the formation mechanism of N-FG is presented.