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The interlayer space of 2D materials can be a slit reactor where transformations not typical for the gas phase occur. We report redox reactions involving acetonitrile and nitrogen oxide guests in galleries of fluorinated graphite. Fluorinated graphite intercalation compounds with acetonitrile are treated with dinitrogen tetraoxide and the synthesis products are studied by a set of experimental methods. Data analysis reveals that N2O4 dissociates in fluorinated graphite matrices to form nitrogen-containing species NO3, NO2, NO, and N2. The interaction of NO3 with acetonitrile yields HNO3, which predominates as a guest in the synthesis products independently of the fluorination degree of the matrix. This reaction is accompanied by the removal of fluorine atoms weakly bonded to the graphite layers, leading to partial defluorination of the matrices. Our work demonstrates the possibility of using fluorinated graphite as a test nanoreactor whose dimension can be controlled by fluorination of the layers.

N-doped graphene based on graphene oxide and 3,3',4,4'-tetraaminodiphenyl oxide (TADPO) was obtained using a one-step hydrothermal process. The resulting materials were fully characterized using elemental analysis, infrared spectroscopy, Raman spectroscopy, thermogravimetric analysis, X-ray diffraction, scanning electron micrographs, and transmission electron microscopy. The findings reveal that benzimidazole rings were formed during the reaction, and the mass content of nitrogen in the obtained material varied from 12.3% to 14.7%, depending on the initial concentration of TADPO. Owing to the redox activity of benzimidazole rings, the new N-doped graphene materials demonstrated a high specific capacitance, reaching 340 F g -1 at 0.1 A g -1 , which was significantly higher than that of the sample of reduced graphene oxide obtained under similar conditions without the use of TADPO (169 F g -1 at 0.1 A g -1 ). The resulting material also exhibited good cyclic stability after 5000 cycles.

Microwave (MW) irradiation is often used in preparation of nanomaterials. Here, we investigate MW exfoliation patterns of intercalated fluorinated graphite (C 2 F) depending on the nature of the "guest". The resulting highly exfoliated graphites (multi-layer graphenes) show advantageous characteristics, as compared to the products of convective heating.

The applications of multilayered graphenes (MLGs), nanocomposites "MLG-decontaminant" and polydicarbonfluoride intercalation compounds for the localization and deactivation of toxic spills and gaseous emissions under technogenic accidents are investigated in this paper. The intercalation compounds contain oxidizers as intercalants, and MLGs are formed destructively by thermolysis of polydicarbonfluoride intercalation compounds. The sorptive capacity of MLGs (about 240 ml of liquid phase per 1 g of MLG) is much higher than in well-known expanded graphites (EGs) obtained from graphite oxide or graphite acid salts. Our investigation revealed the possibility of the production of the "MLG-decontaminant" nanocomposites with the neutralizator content >95% due to the extremely low (down to 0.4 g/l) apparent density of MLG and its high specific surface (about 370 m 2 /g). The use of these nanocomposites for the acid-base or redox neutralization of contaminants does not result in the overheating, sputtering or evaporation of liquid phases, because their neutralization products sorb into MLGs. It prevents the soil mineralization by liquid or solid deactivated spills. We revealed that polydicarbonfluoride intercalation compounds with oxidizers (ClF 3 , HNO 3 , N 2 O 4 ) can be efficiently used for the deactivation of spills and gaseous emissions of nitrogen-containing base compounds.

The influence of dimensional effects on the compositions and properties of polydicarbonfluoride (C2 F)n prepared from multilayered graphenes was investigated. Multilayered graphenes were produced by destructive thermal decomposition of intercalation compounds of "idealized" (C2 F)n that were obtained by reaction of gaseous ClF3 with natural graphite at a room temperature. The precursors of multilayered graphenes have a common formula (C2 F⋅xR)n where R is an organic or inorganic component. It was shown that polydicarbonfluoride prepared from multilayered graphene does not form stable intercalation compound with ClF3 , in contrast to polydicarbonfluoride prepared from graphite, that forms its intercalation compound with ClF3 during fluorination of initial graphite in the ClF3 excess. Investigations of polydicarbonfluoride prepared from multilayered graphene showed that it cannot form intercalation compounds with different classes of organic and inorganic compounds as polydicarbonfluoride prepared from graphite can do. The absence of such intercalation activity for polydicarbonfluoride prepared from multilayered graphene can be explained by high exfoliation degree of multilayered graphene (3-4 nm) along the c-axis that results in the presence of two-dimensional (2D) structure properties in multilayered graphene. Dimensional effects transformed the chemical properties of polydicarbonfluoride prepared from multilayered graphene and lowered its decomposition temperature by 150 K in comparison with polydicarbonfluoride prepared from graphite., (© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Thin graphene/polymer sheet composites were fabricated using easily soluble expanded graphite (ESEG), and their field emission (FE) parameters were examined. Due to the high dispersability of ESEG, a stable graphene suspension was prepared by ultrasonication in toluene without the need for a surfactant. The suspension consisted of exfoliated graphene sheets with a thickness of 1 - 2 nm. Using a calendering process, the solution was further shear mixed with ethyl cellulose to obtain a well-dispersed graphene/polymer composite. The composite was screen printed onto a conducing substrate to fabricate the FE cathode layers. The FE measurements were taken in a diode configuration at an applied electrostatic field and inter-electrode distance of 1.7 to 6 V/microm and approximately 200 microm, respectively. The threshold turn-on-field was approximately 3.5 V/microm at a current density of approximately 10 microA/cm2 with a corresponding mean field enhancement factor of 1350 +/- 50. Emission occurred mainly from the edges and bends of the graphene layers. The luminescence uniformity of the composite cathode layers was examined using a phosphor-coated anode.

We have fluorinated few-layer graphene (FLG) by using a low-temperature fluorination route with gaseous ClF3. The treatment process resulted in a new graphene derivative with a finite approximate composition of C2F. TEM studies showed that the product consisted of thin transparent sheets with no more than 10 fluorographene layers stacked together. Spectroscopic methods revealed a predominantly covalent nature of the C-F bonds in the as-synthesized product and we found no evidence for the existence of so-called "semi-ionic" C-F bonds, as observed in bulk C(x)F. In contrast to the case of graphite and typical (thick) expanded graphites, fluorination of FLG did not lead to the intercalation of ClF3 molecules, owing to the lack of a 3D layered structure. The approximate "critical" number of graphene layers that were necessary to form a phase of intercalated compound was estimated to be more than 12, thus providing a "chemical proof" of the difference between the properties of few-layered graphenes and bulk graphites. Fluorographene C2F was successfully delaminated into thinner layers in organic solvents, which is an important property for its integration into electronic devices, nanohybrids, etc., (Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Easily soluble expanded graphite is synthesized in a one-step exfoliation process that can be used for the lowcost mass production of graphene for various applications because of the simplicity and speed of the process. The graphene obtained is sufficiently expanded to be dispersed in aqueous solutions with an ordinary surfactant and in organic solvents., (Copyright © 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim.)