Recent studies have shown that the composite of semiconductor photocatalytic materials and g-C₃N₄ can effectively inhibit photocatalytic carrier recombination and enhance the adsorption performance of the composite photocatalytic materials, so that the composite photocatalyst has stronger photocatalytic activity. In this paper, three kinds of graphitic carbon nitride photocatalyst g-C₃N₄ with different morphologies were prepared using the same precursor system by the chemical cracking method. After characterization and application, the sample with the most significant photocatalytic activity was selected and the g-C₃N₄/BiVO₄ heterostructure was synthesized by the simple solvent evaporation method, then the photocatalytic experiment was carried out. The results show that, when the content of BiVO₄ in the composite sample is 1%, the photocatalytic activity of RhB was the highest, and the degradation rate could reach 90.4%. The kinetic results showed that the degradation of RhB was consistent with the quasi-primary degradation kinetic model. The results of the photocatalytic cycle experiment show that the photocatalytic performance remains unchanged and stable after four photocatalytic cycles. The existence of a g-C₃N₄/BiVO₄ binary heterojunction was confirmed by UV/Visible diffuse reflection (UV-DRS) and photoluminescence (PL) experiments. Owing to the Z-type charge process between BiVO₄ and g-C₃N₄, efficient carrier separation was achieved, thus enhancing the photocatalytic capacity. This work provides a new idea for the study of heterojunction photocatalytic materials based on g-C₃N₄.

The purpose of this study is to explore the possibility of using graphene–zinc oxide–hydroxyapatite (GO/ZnO/nHAp) composite microspheres as bone regeneration materials by making use of the complementary advantages of nanocomposites, so as to provide reference for the clinical application of preventing and solving bacterial infection after implantation of synthetic materials. Firstly, GO/ZnO composites and hydroxyapatite nanoparticles were synthesized using the hydrothermal method, and then GO/ZnO/nHAp composite microspheres were prepared via high-temperature sintering. The graphene–zinc oxide–calcium phosphate composite microspheres were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), energy dispersion spectroscopy (EDS), water contact angle measurement, degradation and pH determination, and differential thermal analysis (DiamondTG/DTA). The biocompatibility, osteogenic activity, and antibacterial activity of GO/ZnO/nHAp composite microspheres were further studied. The results of the cell experiment and antibacterial experiment showed that 0.5% and 1% GO-ZnO-nHAp composite microspheres not only had good biocompatibility and osteogenic ability but also inhibited Escherichia coli and Staphylococcus aureus by more than 45% and 70%. Therefore, GO/ZnO/nHAp composite microspheres have good physical and chemical properties and show good osteogenic induction and antibacterial activity, and this material has the possibility of being used as a bone regeneration material.

In this study, GO/ZnO/Ag nanocomposites were prepared by a hydrothermal method in one step. The microstructure and surface morphology of the material were analyzed by x-ray diffraction and a scanning electron microscope. The chemical interactions between the available oxygen functional groups of reduced graphene oxide and the inorganic parts (Ag and ZnO) were analyzed by XPS and FTIR. The synergistic antibacterial activity of the nanocomposites against Streptococcus mutans was investigated. It was confirmed that GO/ZnO/Ag could inhibit the growth of S. mutans. The minimal inhibitory concentration and minimum bactericidal concentration of GO/ZnO/Ag on the surface structure of S. mutans were 62.5 and 125 µg/ml, respectively. The material was added to a dental dentin binder, and the modified dentin binder specimens with GO/ZnO/Ag had a significant antibacterial effect against Streptococcus mutans. The results showed that a low dose of GO/ZnO/Ag did not affect the shear bond strength of the dentin binder (P > 0.05), while a high dose of GO/ZnO/Ag decreased the shear bond strength of the dentin binder (P < 0.05). With an increase in GO/ZnO/Ag, the contact angle of the modified dentin binder specimens decreased and the hydrophilicity increased. The nanocomposites can not only be used as antibacterial agents but also have potential applications in biomedical fields.

N- and S-doped CQDs were prepared using L-cysteine as a precursor. Different NS-CQDs/g-C₃N₄ composite photocatalysts were formed by modifying graphite-phase carbon nitride with different contents of NS-CQDs using a hydrothermal method. The morphology, constituent elements and functional groups of the composite photocatalysts were analyzed by SEM, EDS, TEM, Mapping, XRD and FT-IR as a proof of its successful preparation. Meanwhile, it was characterized by PL, UV-Vis DRS and electrochemical impedance, which proved that the CQDs could be used as an electronic memory in the composite system to accelerate the electron transfer induced by the photo-excitation of g-C₃N₄ and effectively inhibit the recombination of e⁻-h⁺ improvement of the photocatalytic activity of g-C₃N₄. The stability of the composite photocatalysts under different conditions and the photodegradation activity of Rh B under visible light were investigated. It was found that the photocatalytic degradation efficiency of rhodamine B by NS-CQDS-modified g-C₃N₄ was significantly higher than that of pure g-C₃N₄, which could reach 90.82%, and its degradation rate was 3.5 times higher than that of pure g-C₃N₄. It was demonstrated by free radical trapping experiments that ·OH and ·O₂⁻ were the main active species in the photocatalytic degradation process, in which ·O₂⁻ played a guiding role.

In this work, a CdTe quantum dot-based fluorescent probe was synthesized to determine felodipine (FEL). The synthesis conditions, structure, and interaction conditions with FEL of CdTe quantum dots were analysed by fluorescence spectrophotometry, Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), UV–visible spectroscopy, and TEM. The CdTe QD concentration was 2.0 × 10⁻⁴ mol/L. The amount of quantum dots controlled in the experiment was 0.8 mL. The controlled feeding ratio of N (Cd²⁺):N (Te²⁻):N (TGA) was 2:1:4, the heating temperature was 140 °C, the heating time was 60 min, and the pH of the QD precursor was adjusted to 11 for subsequent experiments. The UV–visible spectrum showed that the emission wavelength of CdTe quantum dots at 545 nm was the strongest and symmetric. The particle size of the synthesized quantum dots was approximately 5 nm. In the interaction of CdTe quantum dots with FEL, the FEL dosage was 1.0 mL, the optimal pH value of Tris-HCl buffer was 8.2, the amount of buffer was 1.5 mL, and the reaction time was 20 min. The standard curve of FEL was determined under the optimal synthesis conditions of CdTe quantum dots and reaction of CdTe quantum dots with FEL. The linear equation was Y = 3.9448x + 50.068, the correlation coefficient R2 was 0.9986, and the linear range was 5 × 10⁻⁶–1.1 × 10⁻⁴ mol/L. A CdTe quantum dot-based fluorescent probe was successfully constructed and could be used to determine the FEL tablet content.

A cerium/silver/zinc oxide (Ce/Ag/ZnO) inorganic nanocomposite was synthesized through a homogeneous precipitation method. The characterization and photocatalysis procedures were carried out by Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflection spectroscopy, and photocatalytic performance. The characteristic absorption peak of ZnO was near 432 cm ⁻¹ , no absorption was observed peak near 1,083 cm ⁻¹ for CeO ₂ and ZnO, the absorption peak near 721 cm ⁻¹ was generated by the vibration of CeO ₂ , and the absorption peak had an obvious blue shift. The XRD results showed a strong interfacial interaction among Ag, CeO ₂ and ZnO to form a core–shell structure. The SEM image showed that the Ce/Ag/ZnO samples are approximately 25 nm. The XPS spectra showed that the Ce/Ag/ZnO nanocomposite powders were successfully prepared. The UV-Vis diffuse reflection spectra showed that the Ce/Ag/ZnO nanocomposites reduced the band gap and increased the ability of visible light response. The addition of rare earth Ce could inhibit the recombination of ZnO photoelectron pairs and improve the photocatalytic effect. Therefore, Ce/Ag/ZnO exhibited good characteristics of nanocomposite materials and good photocatalytic ability.