This study synthesized graphene oxide (GO)/zinc oxide (ZnO)/silver (Ag) composite materials and investigated their photocatalytic degradation performance for ciprofloxacin (CIP) under visible light irradiation. GO/ZnO/Ag composites with different ratios were prepared via an impregnation and chemical reduction method and characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FT-IR), and X-ray photoelectron spectroscopy (XPS). The results demonstrated that under optimal conditions (20 mg/L CIP concentration, 15 mg catalyst dosage, GO/ZnO-3%/Ag-doping ratio, and pH 5), the GO/ZnO/Ag composite exhibited the highest photocatalytic activity, achieving a maximum degradation rate of 82.13%. This catalyst effectively degraded ciprofloxacin under light irradiation, showing promising potential for water purification applications.

Using an ultrasound-assisted chemical technique, ZnO quantum dot and ZnO composites were created. The optical characteristics and structural details of these composites were examined using TEM, XRD, XPS, FT-IR, UV-vis, and BET. The results revealed that both the ZnO quantum dot composite and ZnO composite exhibited outstanding optical properties, making them suitable for photocatalytic reactions. In order to analyze the photocatalytic performance, a degradation experiment was conducted using Rhodamine B solution as the simulation dye wastewater. The experiment demonstrated that the degradation of Rhodamine B followed the first-order reaction kinetics equation when combined with the photocatalytic reaction kinetics. Moreover, through cyclic stability testing, it was determined that the ZnO QDs-GO-g-C₃N₄ composite sample showed good stability and could be reused. The degradation rates of Rhodamine B solution using ZnO-GO-g-C₃N₄ and ZnO QDs-GO-g-C₃N₄ reached 95.25% and 97.16%, respectively. Furthermore, free-radical-trapping experiments confirmed that ·O²⁻ was the main active species in the catalytic system and its photocatalytic mechanism was elucidated. The photocatalytic oxidation of ZnO quantum dots in this study has important reference value and provides a new idea for the subsequent research.

With the unprecedented progress of biomedical nanotechnology in the past few decades, traditional drug delivery systems (DDSs) have been incorporated into intelligent DDSs with stimulus responsive characteristics. Graphene oxide (GO) and Chitosan (CS) have excellent physical, chemical, mechanical, and optical properties, and their synergistic effects have attracted widespread attention in the biomedical field. In this review, we focus on the physicochemical characteristics of GO, CS, and GO/CS composites, as well as the research progress of DDS types based on GO/CS.

Against the background of the vigorous development of materials science and the deep cross-infiltration in many fields, a new medicine food homology, carbon dots (herein combined and abbreviated as MFH-CDs), has sprung up, showing great potential. This review used ChatGPT 4.0 to collect background information related to carbon dots, focusing on the common rich medicinal and food resources such as Lycium barbarum, Chinese yam, honeysuckle, and Ganoderma lucidum. These carbon dots are synthesized by hydrothermal synthesis, microwave radiation, and pyrolysis, which have the advantages of small particle size, high quantum yield, and low cytotoxicity. Recent studies have found that MFH-CDs have great application potential in biosensors, biological imaging, and drug delivery. In this paper, the characteristics of preparing carbon dots from different medicinal and edible resources and their applications in biology in recent years are reviewed, which provides in-depth guidance for the research and application of carbon dots from medicinal and edible biomass, helps it shine in multidisciplinary fields, and opens a brand-new journey from traditional medicinal and edible culture to cutting-edge technology application.

To address challenges in antibiotic wastewater treatment, we synthesized a series of graphitic carbon nitride (g-C₃N₄)-based photocatalysts (BCN, PCN, TCN, BTCN, and TCNE-modified PTCN) via defect engineering. TCNE modification disrupted the triazine ring-bridging amino network in PTCN, forming a porous structure with enhanced specific surface area validated by SEM/TEM while retaining the graphene-like framework confirmed by XRD/FTIR. Photoluminescence (PL) analysis revealed prolonged photogenerated carrier lifetime and improved separation efficiency in PTCN, achieving 89.10% degradation of chlortetracycline hydrochloride under visible light—1.65-fold higher than pristine g-C₃N₄. Mechanistic studies identified superoxide radicals (•O₂⁻) as dominant active species, generated via O₂ activation at defect sites and efficient electron-hole utilization. Optimized conditions enabled PTCN to maintain high activity across a broad pH range and retain 82.59% efficiency after five cycles. This work advances defect-engineered photocatalyst design for adaptable, high-performance antibiotic degradation, offering practical insights for wastewater remediation.

Sulfur hexafluoride (SF₆), the strongest greenhouse gas, has great challenges in degradation because of its stable structure, posing significant environmental concerns. Photocatalysis offers an environmentally friendly, low-energy solution, but the fluoride deposition on catalysts reduces their activity, thus limiting their large-scale application. To prevent catalyst fluoride poisoning, we report a thin-layer graphitic carbon nitride (CN) material loaded with MoO_x (CNM) that resists fluoride deposition for long-term SF₆ degradation. By combining molecular structure design and nanostructure regulation, we construct a photocatalyst with enhanced charge carrier mobility and reduced transport distances. We find that the CNM exhibits a high specific surface area, increased contact between reactants and active sites, and efficient electron–hole separation due to the Mo-N bonds, achieving an SF₆ degradation efficiency of 1.73 mmol/g after one day due to the prolonged catalytic durability of the catalyst, which is eight times higher than pristine g-C₃N₄ (0.21 mmol/g). We demonstrate the potential of CNMs for low-energy, high-efficiency SF₆ degradation, offering a new approach to mitigate the environmental impact of this potent greenhouse gas. We envision that this study will inspire further research into advanced photocatalytic materials for environmental remediation, contributing to global efforts in combating climate change.