In the last decade, carbon dots (C-dots, CDs) or carbon quantum dots (CQDs) have attracted a considerable amount of attention from the scientific community as a low cost and biocompatible alternative to semiconductor quantum dots. In particular, doped C-dots have excellent fluorescent properties that have been successfully utilized for numerous applications. In this minireview, we overview the recent advances on the synthesis of doped C-dots derived from carbon-rich sources and their potential applications for biomedical and sensing applications. In addition, we will also discuss some challenges and outline some future perspectives of this exciting material.

Rare-earth phosphors are commonly used in display panels, security printing, and fluorescent lamps, and have potential applications in lasers and bioimaging. In the present study, Eu3+- and Dy3+-codoped uniform-shaped Y2O3 submicron particles were prepared using the urea homogeneous precipitation method. The structure and morphology of the resulting particles were characterized by X-ray diffraction, field emission scanning electron microscope, and field emission transmission electron microscope, whereas their optical properties were monitored by photoluminescence spectroscopy. The room-temperature luminescence color emission of the synthesized particles can be tuned from red to yellow by switching the excitation wavelength from 254 to 350 nm. The luminescence intensities of red and yellow emissions could be altered by varying the dopant concentration. Strong quenching was observed at high Eu3+ and Dy3+ concentrations in the Y2O3 host lattice.

The rapid growth in the global population has led to increased environmental pollution and energy demands, exacerbating the issue of environmental contamination. This contamination is significantly impacted by various types of pesticides found in water sources, which pose serious health risks to humans, animals, and aquatic ecosystems. In response, extensive research into water treatment technologies has been conducted, focusing on efficient methods to remove these pollutants, with advanced oxidation processes and the utilization of tungsten trioxide (WO₃) as a photocatalyst showing promising results. This paper aims to review WO₃-based photocatalytic processes for pesticide degradation, highlighting the potential of modified WO₃ structures to improve photocatalytic efficiency and address current environmental challenges. Different WO₃ synthesis routes and methods for modification have been discussed. The synthesis of WO₃-based photocatalysts encompasses various methods that significantly affect their morphologies, sizes, structures, and thus catalytic performance, cost-effectiveness, and environmental sustainability. Techniques like hydrothermal, solvothermal, co-precipitation, sol-gel, and green synthesis and physical deposition techniques are elaborated, highlighting their unique advantages in producing nanostructures with desired physical and chemical properties. Moreover, enhancement methods aimed at optimizing the photocatalytic activity of WO₃ under visible light for pollutant degradation have been discussed. Evaluation of WO₃-based photocatalytic systems for pesticide treatment, emphasizing the effectiveness of various catalysts in degrading pesticides including organochlorines, organophosphorus, and chloropyridines have been conducted.

To date, Ag-based nanomaterials have demonstrated a high potential to overcome antibiotic resistance issues. However, bare Ag nanomaterials are prone to agglomeration in the biological environment, which results in a loss of antibacterial activity over time. Furthermore, it is still challenging to collect small-sized Ag nanomaterials right after the synthesis process. In this study, spherical-shaped Ag nanoparticles (NPs) (~6–10 nm) were attached on the surface of cetyltrimethylammonium bromide (CTAB)-loaded mesoporous silica nanoparticles (MSNs) (~100–110 nm). Antibacterial activity tests suggested that the obtained nanocomposite can be used as a highly efficient antibacterial agent against both Gram-negative and Gram-positive bacterial strains. The minimum inhibitory concentration (MIC) recalculated to pure Ag weight in nanocomposite was found to be ~1.84 µg/mL (for Escherichia coli) and ~0.92 µg/mL (for Staphylococcus aureus)—significantly smaller compared to values reported to date. The improved antibacterial activity of the prepared nanocomposite can be attributed to the even distribution of non-aggregated Ag NPs per volume unit and the presence of CTAB in the nanocomposite pores.

Perovskite solar cells (PSCs) with a standard sandwich structure suffer from optical transmission losses due to the substrate and its active layers. Developing strategies for compensating for the losses in light harvesting is of significant importance to achieving a further enhancement in device efficiencies. In this work, the down-conversion effect of carbon quantum dots (CQDs) was employed to convert the UV fraction of the incident light into visible light. For this, thin films of poly(methyl methacrylate) with embedded carbon quantum dots (CQD@PMMA) were deposited on the illumination side of PSCs. Analysis of the device performances before and after application of CQD@PMMA photoactive functional film on PSCs revealed that the devices with the coating showed an improved photocurrent and fill factor, resulting in higher device efficiency.