Search

Per‐ and polyfluoroalkyl substances (PFAS) pose significant environmental and health risks due to their ubiquitous presence and persistence in water systems. Herein, the efficacy of piezocatalysis using barium titanate nanoparticles under ultrasound irradiation for the degradation and defluorination of perfluorooctane sulfonate (PFOS) in water is investigated. The research demonstrates a substantial 90.5% degradation and 29% defluorination of PFOS after 6 h of treatment, highlighting the potential of piezocatalysis as a promising approach for PFAS degradation. Additionally, the quantification of degradation products elucidates the transformation pathways of PFOS, suggesting a stepwise chain‐shortening mechanism. The findings underscore the importance of continued research in optimizing piezocatalytic processes and exploring synergistic approaches with other advanced oxidation methods to effectively address PFAS contamination challenges. These efforts are essential for advancing sustainable water treatment strategies and mitigating the environmental and health hazards associated with PFAS contamination. [ABSTRACT FROM AUTHOR]

Covalent Organic Frameworks (COFs) emerged as versatile materials with promising potential in biomedicine. Their customizable functionalities and tunable pore structures make them valuable for various biomedical applications such as biosensing, bioimaging, antimicrobial activity, and targeted drug delivery. Despite efforts made to create nanoscale COFs (nCOFs) to enhance their interaction with biological systems, a comprehensive understanding of their inherent biological activities remains a significant challenge. In this study, a thorough investigation is conducted into the biocompatibility and anti‐neoplastic properties of two distinct imine‐based nCOFs. The approach involved an in‐depth analysis of these nCOFs through in vitro experiments with various cell types and in vivo assessments using murine models. These findings revealed significant cytotoxic effects on tumor cells. Moreover, the activation of multiple cellular death pathways, including apoptosis, necroptosis, and ferroptosis is determined, supported by evidence at the molecular level. In vivo evaluations exhibited marked inhibition of tumor growth, associated with the elevated spontaneous accumulation of nCOFs in tumor tissues and the modulation of cell death‐related protein expression. The research contributes to developing a roadmap for the characterization of the intricate interactions between nCOFs and biological systems and opens new avenues for exploiting their therapeutic potential in advanced biomedical applications. [ABSTRACT FROM AUTHOR]

Iron oxide nanoparticles hold great potential for future biomedical applications but, to date, usually suffer from reduced magnetic properties compared to their bulk counterparts. The replacement of Fe(III) ions with Zn(II) ions can enhance their magnetic properties while keeping their biocompatibility characteristics. Yet, common synthesis methods for these highly magnetic particles require using environmentally harmful solvents, multiple steps, and postfunctionalization, all while being affected by poor scalability and high polydispersity. To address these challenges, in this study, a single‐step coprecipitation‐based method is developed to fabricate gelatin‐coated, zinc‐substituted, sub‐10 nm‐sized iron oxide nanoparticles exhibiting high saturation magnetization. This single‐step synthesis benefits from simplicity and robustness, capable of yielding large amounts of highly magnetic nanoparticles without the utilization of environmentally harmful or highly toxic reagents. Furthermore, in situ gelatin coating during the synthesis ensures particle stability in aqueous solutions over a wide range of pH and enhances cell compatibility. Systematic investigations show a direct correlation between the particles' magnetization and the concentrations of Zn(II) and NaOH, where particles with a zinc‐to‐iron ratio of Zn:Fe = 0.18:2.82 reach a maximum saturation magnetization of 91.2 emu g−1. Thus, these particles are promising candidates for biomedical applications. [ABSTRACT FROM AUTHOR]

Piezocatalysis has gradually come into the limelight due to its great potential for solving energy shortages and environmental pollution problems. However, limited piezocatalytic efficiency is a severe bottleneck for its practical applications. Here, well‐defined BaTiO3 nanosheets with highly exposed {001} polar facets are successfully synthesized to enhance the piezocatalytic activity. The [001] piezoelectric polarization can drive the carriers to migrate to the surface along the out‐of‐plane direction. The polar surface provides abundant active sites for the piezocatalytic reaction. As a result, a superior piezocatalytic degradation ratio of organic pollutants is obtained with a high first‐order rate constant k of 0.0835 min−1, which is 2.7 times higher than the BaTiO3 nanoparticles. Furthermore, BaTiO3 nanosheets display an outstanding H2 production capability, with the rate of 305 µmol g−1 h–1, which is almost two times higher than that of BaTiO3 nanoparticles. This work thus provides a novel and comprehensive strategy for designing high‐performance piezocatalysts with an out‐of‐plane polarization, and also provides novel insights for the optimization of the piezocatalytic activity by regulating the polar facet of piezocatalysts. [ABSTRACT FROM AUTHOR]

Electric fields are increasingly recognized for their role as 'smart reagents' that can trigger or accelerate chemical reactions. Expanding upon this concept, our research introduces an innovative method that exploits electric fields induced by ultrasound on piezoelectric nanoparticles to facilitate the azide-alkyne Huisgen cycloaddition in nonaqueous environments. The intense electric field generated around the BaTiO 3 nanoparticles, as supported by density functional theory calculations, provides the suitable conditions necessary to trigger the cycloaddition of the alkyne-functionalized nanoparticles and the azide present in the solution. To quantitatively assess the occurrence of the click cycloaddition reaction at the nanoparticle surface interface, we tacked the azide with either an electroactive ferrocene moiety or with gold nanoparticles, which act as surface Raman enhancers. These experiments not only provide experimental validation of our approach, but also highlights the potential of piezoelectrostatic catalysts in enhancing the scalability of electrostatic catalysis.