Graphene-based materials are elective materials for a number of technologies due to their unique properties. Also, semiconductor nanocrystals have been extensively explored due to their size-dependent properties that make them useful for several applications. By coupling both types of materials, new applications are envisaged that explore the synergistic properties in such hybrid nanostructures. This research reports a general wet chemistry method to prepare graphene oxide (GO) sheets decorated with nanophases of semiconductor metal sulfides. This method allows the in situ growth of metal sulfides onto GO by using metal dialkyldithiocarbamate complexes as single-molecule precursors. In particular, the role of GO as heterogeneous substrate for the growth of semiconductor nanocrystals was investigated by using Raman spectroscopic and imaging methods. The method was further extended to other graphene-based materials, which are easily prepared in a larger scale, such as exfoliated graphite oxide (EGO).

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Graphene oxide (GO) has been widely explored as a platform for producing hybrid materials exhibiting synergistic properties of interest in heterogeneous (photo)catalysis. However, there has been less emphasis in demonstrating that such properties are intrinsic to the nature of the hybrid material, which to some extent can be attributed to the lack of straightforward screening techniques. In this work, we demonstrate that surface-enhanced Raman scattering can be easily explored to probe certain regions of GO sheets decorated with a semiconductor (ZnS). In particular, our studies reveal an enhancement of the Raman signal of 4-mercaptopyridine (4-MPy), which was used as a molecular probe, upon adsorption on ZnS@GO materials when compared to adsorption on the separated parent ZnS powders or GO flakes. The GO sheets in the composite play an important role in the enhancement of the Raman signal observed for this molecular probe because they create energy levels within the ZnS energy gap. This hypothesis was further confirmed by electronic density functional theory calculations employed to investigate the adsorption mechanism of 4-MPy on both ZnS and ZnS@GO substrates. The calculated results are in accordance with the experimental data, predicting the adsorption mode on both S and Zn surface sites, with preference toward the sulfur atom due to the influence of GO.

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Herein, S‐doped graphene flakes‐based composites with Fe3O4 and/or CuS nanoparticles (NPs) are reported as photo‐Fenton catalysts for the 4‐nitrophenol (4‐NP) degradation. The S‐doped graphene flakes (S‐GF) were prepared using a thermal treatment approach, and the nanocomposites by the in situ growth of Fe3O4 and/or CuS onto the S‐GF scaffold. The characterization methods confirmed the formation of two‐ and three‐components nanocomposites. The Fe3O4 NPs presented a cubic inverse spinel structure and the CuS phases a covellite structure, both with smaller crystallite sizes in the nanocomposites. The new nanocomposites showed higher ability to catalyze the photo‐Fenton 4‐NP degradation than the individual components. The S‐GF@CuS−Fe3O4 nanocomposite exhibited the best catalytic activity: 95.2 % of 4‐NP degradation, a kinetic of pseudo‐first order (k=0.016 min−1), high photo‐Fenton catalytic stability and catalyst's composition/structure preservation. The CuS NPs showed an important role in the photo‐Fenton‐like catalytic activity improvement.

SiO2@TiO2 core-shell nanoparticles were successfully synthesized via a simple, reproducible, and low-cost method and tested for methylene blue adsorption and UV photodegradation, with a view to their application in wastewater treatment. The monodisperse SiO2 core was obtained by the classical Stöber method and then coated with a thin layer of TiO2, followed by calcination or hydrothermal treatments. The properties of SiO2@TiO2 core-shell NPs resulted from the synergy between the photocatalytic properties of TiO2 and the adsorptive properties of SiO2. The synthesized NPs were characterized using FT-IR spectroscopy, HR-TEM, FE–SEM, and EDS. Zeta potential, specific surface area, and porosity were also determined. The results show that the synthesized SiO2@TiO2 NPs that are hydrothermally treated have similar behaviors and properties regardless of the hydrothermal treatment type and synthesis scale and better performance compared to the SiO2@TiO2 calcined and TiO2 reference samples. The generation of reactive species was determined by EPR, and the photocatalytic activity was evaluated by the methylene blue (MB) removal in aqueous solution under UV light. Hydrothermally treated SiO2@TiO2 showed the highest adsorption capacity and photocatalytic removal of almost 100% of MB after 15 min in UV light, 55 and 89% higher compared to SiO2 and TiO2 reference samples, respectively, while the SiO2@TiO2 calcined sample showed 80%. It was also observed that the SiO2-containing samples showed a considerable adsorption capacity compared to the TiO2 reference sample, which improved the MB removal. These results demonstrate the efficient synergy effect between SiO2 and TiO2, which enhances both the adsorption and photocatalytic properties of the nanomaterial. A possible photocatalytic mechanism was also proposed. Also noteworthy is that the performance of the upscaled HT1 sample was similar to one of the lab-scale synthesized samples, demonstrating the potentiality of this synthesis methodology in producing candidate nanomaterials for the removal of contaminants from wastewater.

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