BACKGROUND: Nanozymes, a new class of nanomaterials, have emerged as promising substitutes for enzymes in biosensor design due to their exceptional stability, affordability, and ready availability. While nanozymes address many limitations of natural enzymes, they still face challenges, particularly in achieving the catalytic activity levels of their natural counterparts. This indicates the need for enhancing the sensitivity of biosensors based on nanozymes. The catalytic activity of nanozyme can be significantly improved by regulating its size, morphology, and surface composition of nanomaterial.
RESULTS: In this work, a kind of hollow core-shell structure was designed to enhance the catalytic activity of nanozymes. The hollow core-shell structure material consists of a nanozymes core layer, a hollow layer, and a MOF shell layer. Taking the classic peroxidase like Fe3O4 as an example, the development of a novel nanozyme@MOF, specifically p-Fe3O4@PDA@ZIF-67, is detailed, showcasing its application in enhancing the sensitivity of sensors based on Fe3O4 nanozymes. This innovative nanocomposite, featuring that MOF layer was designed to adsorb the signal molecules of the sensor to improve the utilization rate of reactive oxygen species generated by the nanozymes catalyzed reactions and the hollow layer was designed to prevent the active sites of nanozymes from being cover by the MOF layer. The manuscript emphasizes the nanocomposite\'s remarkable sensitivity in detecting hydrogen peroxide (H2O2), coupled with high specificity and reproducibility, even in complex environments like milk samples.
UNASSIGNED: This work firstly proposed and proved that Fe3O4 nanozyme@MOF with hollow layer structure was designed to improve the catalytic activity of the Fe3O4 nanozyme and the sensitivity of the sensors based on Fe3O4 nanozyme. This research marks a significant advancement in nanozyme technology, demonstrating the potential of structural innovation in creating high-performance, sensitive, and stable biosensors for various applications.

The work aimed to synthesize three heterojunction photocatalysts (Eg = 2.65-2.78 eV) via in-situ encapsulation of 5% zinc doped titanium oxynitride (Zn0.05TiOxNy) catalyst into MOF-5 and bulk (BCN)/sulfur-doped (SCN) g-C3N4 supports using a microwave method. The prepared photocatalysts were characterized and utilized to purify textile industrial wastewater from the organic dye (e.g., methylene blue, MB) and microbial (e.g., E. coli, S. aureus, and C. albicans) contaminants under dark, visible, and solar lights. The output data confirmed the higher activity of Zn0.05TiOxNy@SCN and Zn0.05TiOxNy@MOF-5 for photo-induced microbial growth inactivation (> 90%) under visible light, with photo-biocidal efficiency of 0.91-1.69 mCFU/Einstein. Such a phenomenon is ascribed to the synergism between the high antimicrobial capacity of supports and photoactivity of Zn0.05TiOxNy. Also, Zn0.05TiOxNy@SCN exhibited far superiority to mineralize MB dye (Kphoto of 2.73 × 10-2 min-1) under direct sunlight due to its high photonic (ζ% of 4.4-8.3%)/quantum (QE of 0.56-0.54%) efficiencies for the generation of hydroxyl and superoxide (-•O2/•OH) oxidative species. As a practical case study, all heterojunction photocatalysts also demonstrated high-performance stability (5 cycles) for real textile wastewater treatment under sunlight (efficiency = 76.1-84.6%).