Pharmaceuticals are increasingly significant contaminants in the environmental ecosystem, prompting the exploration of photocatalysis as a promising method for removing their pollutants. However, the application of semiconductor metal oxides as photocatalysts has been limited by issues such as rapid photocarrier recombination and high band gap energy. One emerging strategy to enhance the photocatalytic performance of metal oxides involves integrating them with carbon dots, which offer advantages including low toxicity, aqueous stability, increased surface area, cost effectiveness, biocompatibility, and chemical inertness. In this study, we conducted a critical review focusing on the nanocomposite development of metal oxide/carbon dots for the photocatalytic removal of pharmaceutical pollutants. Our study highlights that carbon dots can significantly enhance the photocatalytic efficiency of these metal oxides as photocatalytic materials by improving the adsorption of organic pollutants and enhancing light absorption in the visible spectrum. This review aims to provide insights for future research aimed at advancing the development of enhanced photocatalytic metal oxide/carbon dot nanocomposites.

The nanocomposites of activated-carbon-decorated silicon nanocrystals (ACAC) were synchronously derived in a single step from biomass rice husks, through the simple route of the calcination method together with the magnesiothermic reduction process. The final product, ACAC, exhibited an aggregated structure of activated-carbon-encapsulated nanocrystalline silicon spheres, and reveals a high specific surface area (498.5 m²/g). Owing to the mutualization of advantages from both silicon nanocrystals (i.e., low discharge potential and high specific capacity) and activated carbon (i.e., high porosity and good electrical conductivity), the ACAC nanocomposites are able to play a substantial role as an anodic source material for the lithium-ion battery (LIB). Namely, a high coulombic efficiency (97.5%), a high discharge capacity (716 mAh/g), and a high reversible specific capacity (429 mAh/g after 100 cycles) were accomplished when using ACAC as an LIB anode. The results advocate that the simultaneous synthesis of biomass-derived ACAC is beneficial for green energy-storage device applications.

Aiming at materializing an excellent anodic source material of the high-performance sodium-ion battery (SIB), we fabricated the biomass carbon-silicon (C-Si) nanocomposites by the one-pot synthesis of facile magnesiothermic reduction using brown rice husk ashes. The C-Si nanocomposites displayed an aggregated morphology, where the spherical Si nanoparticles (9 nm on average) and the C nanoflakes were encapsulated and decorated with each other. When utilizing the nanocomposites as an SIB anode, a high initial discharge capacity (i.e., 378 mAh/g at 100 mA/g) and a high reversible capacity (i.e., 122 mAh/g at 200 mA/g) were achieved owing to their enhanced electronic and ionic conductivities. Moreover, the SIB device exhibited a high cyclic stability in its Coulombic efficiency (i.e., 98% after 100 charge-discharge cycles at 200 mA/g). These outstanding results depict that the one-pot synthesized biomass C-Si nanocomposites are beneficial for future green energy-storage technology.