Fluorographene with High Fluorine/Carbon Ratio: A Nanofiller for Preparing Low‑κ Polyimide Hybrid Films

Sufficient amounts of fluorographene sheets with different sheet-size and fluorine/carbon ratio were synthesized for preparing of fluorographene/polyimide hybrids in order to explore the effect of fluorographene on the dielectric properties of hybrid materials. It is found that the fluorine/carbon ratio, width of band gap, and sheet-size of fluorographene play the important roles in determining the final dielectric properties of hybrids. The fluorographene with high fluorine/carbon ratio (F/C ≈ 1) presents broaden band gap, enhanced hydrophobicity, good dispersity and thermal stability, etc. Even at a very low filling, only 1 wt %, its polyimide hybrids exhibited drastically reduced dielectric constants as low as 2.1 without sacrificing thermal stability, improved mechanical properties obviously and decreased water absorption by about 120% to 1.0 wt %. This provides a novel route for improving the dielectric properties of materials and a new thought to carry out the application of fluorographene as an advanced material

High-Yield Production of Highly Fluorinated Graphene by Direct Heating Fluorination of Graphene-oxide

By employing honeycomb GO with large surface area as the starting materials and using elemental fluorine, we developed a novel, straightforward topotactic route toward highly fluorinated graphene in really large quantities at low temperature. The value of F/C molar ratio approaches to 1.02. Few-layer fluorinated graphene sheets are obtained, among which the yield of monolayered FG sheet is about 10% and the number of layers is mainly in the range of 2–5. Variations in morphology and chemical structure of fluorinated graphene were explored, and some physical properties were reported

Preparing Highly Fluorinated Multiwall Carbon Nanotube by Direct Heating-Fluorination during the Elimination of Oxygen-Related Groups

Pristine and oxidized multiwalled carbon nanotubes (MWCNTs) were separately prepared and directly fluorinated with F₂ through two different routes: heating-fluorination and isothermal-fluorination. The amount of fluorine atoms (hereinafter referred to as “F-content”) bonding to the fluorinated samples was largely dependent on the modifing route and chemical bonding of MWCNTs. The F-content of heating-fluorinated pristine and oxidized MWCNTs was 3.2% and 9.2% respectively, which were about 8 times and 18 times that of the corresponding isothermal-fluorinated MWCNTs. According to structural analysis of samples before and after fluorination, it was found that thermal elimination of oxygen-related groups bonding to MWCNTs contributed to the formation of strongly covalent C–F bonds during heating-fluorination. It was considered that the oxygen-related groups provided reactive sites for the fluorination. The fluorination reaction took place at an sp³ carbon linking with the oxygen-related groups and did not increase the density of defect on MWCNTs. A radical-mediated mechanism is accepted for this reaction. Thus, MWCNTs could be first oxidized to increase the number of oxygen-related groups and then heating-fluorinated by F₂ directly to get highly fluorinated MWCNTs with stable C–F bonds