Graphene quantum dots (GQDs) with tunable photoluminescence (PL) and hydrophobicity were synthesized from an abundant natural carbon source containing nitrogen, sulfur, and oxygen heteroatoms. Asphaltene and its oxidized and reduced derivatives were used as precursors to produce GQDs in organic solvents (i.e., methanol, toluene, and chloroform) using a facile ultrasonication technique. Asphaltene surface chemistry was tuned by sequential oxidation and reduction to investigate the surface effects on GQD properties. Spectroscopic characterizations confirmed the presence of N, S, and O heteroatoms and different electron-donating and electron-withdrawing groups. Microscopic characterizations revealed that these crystalline carbon nanomaterials have mono-layered or multi-layered structures with lateral sizes in the range of ∼5–15 nm. The asphaltene-derived GQDs exhibit tunable PL with emission colors ranging from blue to orange, depending on the carbon precursor and the organic solvent. Solvent exchange studies also revealed that asphaltene and its derivatives contain hydrophilic and hydrophobic fractions, resulting in varied hydrophobicity of the synthesized GQDs. Adding to the appeal of the present work, PL quenching of GQD-silica hybrid materials upon exposure to nitro-aromatics confirms that these GQDs can be incorporated to different host materials for advanced sensing or optoelectronic applications.

Phosphorus-containing graphene-based hybrids are materials with outstanding properties for diverse applications. In this work, an easy route to produce phosphorus-graphene oxide hybrid materials is described, involving the use of variable amounts of H₃PO₄ and H₂SO₄ during the reaction of oxidation of a graphitic precursor. The physical and chemical features of the hybrids change significantly with the variation in the acid amounts used in the syntheses. XPS and solid-state ¹³C and ³¹P NMR results show that the hybrids contain large amounts of oxygen functional groups, with the phosphorus incorporation proceeding mostly through the formation of phosphate-like linkages and other functions with C–O–P bonds. The experimental findings are supported by DFT calculations, which allow the assessment of the energetics and the geometry of the interaction between phosphate groups and graphene-based models; these calculations are also used to predict the chemical shifts in the ³¹P and ¹³C NMR spectra of the models, which show good agreement with the experimentally observed solid-state NMR spectra.

In this paper, we report for the first time, to the best of our knowledge, the experimental generation of dark pulses in the 1.5 µm band from a passively $Q$-switched fiber laser employing graphite oxide as the saturable absorber, generating tunable microsecond pulses with kHz repetition rates. The graphite oxide samples were obtained by recycling the graphite present in Li-ion batteries used in cell phones through a chemical separation and oxidation process. Sample characterization employing x-ray diffraction, solid-state $ ^{{13}}{\rm C} $ nuclear magnetic resonance, and Raman spectroscopy showed that the produced graphite oxide exhibited a homogeneously oxidized structure. Dark pulse emission could be observed at a relatively low pump threshold of 35 mW in a short 20 m laser cavity, indicating that the graphite oxide acted as a saturable absorber, significantly enhancing the nonlinearity of the laser cavity. Additionally, dark pulse operation was demonstrated at a high stability with a signal-to-noise ratio of 56 dB and a pulse-to-pulse timing jitter of 159.84 fs.