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Wastewater treatments using photocatalysts and metal-organic frameworks (MOFs) have gained increasing importance due to their catalytic reactions leading to the decomposition of dyes and organic pollutants without generating secondary pollutants. This work aims at developing an advanced photocatalytic fabric by conceiving a heterojunction of NH-MIL-88B (Fe/Co) (n-type) and AgPO (p-type) and increasing the electrical conductivity to facilitate charge transfer at the heterojunction. Of particular interest is the design of a conductive Z-scheme heterophotocatalytic fabric by implementing polypyrrole (PPy) between the heterocatalysts and to investigate the role of the heterojunction and increased conductivity in the generation of reactive species and the photocatalytic mechanism. The electrochemical characterization evinces that the enhanced photocatalytic reaction by the conductive heterojunction is attributed to the efficient electron-hole separation and the increased redox power by the Z-scheme construction. Notably, the implementation of PPy not only accelerated the photocatalytic reactivity by the promoted charge mobility but also improved the structural stability of the catalysts by gluing them on the fabric substrate. The developed photocatalytic system demonstrated significantly enhanced purification performance compared with a single photocatalytic system and showed consistent performance with repeated use cycles. The result of this study implicates that electrical conductivity in a photocatalytic system plays a crucial role in the photocatalytic mechanism, charge mobility, and photocatalytic reactivity.
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http://dx.doi.org/10.1021/acsomega.3c09625 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
Hefei National Research Center for Physical Sciences at the Microscale, School of Chemistry and Materials Science, State Key Laboratory of Precision and Intelligent Chemistry, National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, Anhui, 230026, China.
The construction of C─N bonds from simple precursors under ambient conditions is a fundamental challenge in green chemistry, especially when it comes to avoiding energy-intensive protocols. Here, we present a continuous flow photocatalytic platform that enables the efficient coupling of C─N bonds between methanol and ammonia at ambient temperature and pressure. By synergistically engineering a Pd clusters-decorated TiO photocatalyst (1Pd/TiO) and a mass transfer-enhanced gas-liquid-solid Taylor flow reactor, the system achieves a remarkable formamide productivity of 256.
View Article and Find Full Text PDFInt J Phytoremediation
September 2025
Innovative Food Technologies Development Application and Research Center, Gölköy Campus Bolu, Bioenvironment and Green Synthesis Research Group, Bolu Abant İzzet Baysal University, Bolu, Türkiye.
This study presents an eco-friendly approach for the green synthesis of manganese oxide nanoparticles (MnONPs) using () (einkorn wheat) seed extract as a reducing and stabilizing agent. The synthesized MnONPs were characterized by UV-Vis, XRD, FTIR, SEM-EDX, BET, and zeta potential analyses, which confirmed their crystalline nature, spherical morphology, and mesoporous structure with a surface area of 41.50 m/g.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
College of Smart Materials and Future Energy, Fudan University, Songhu Road 2005, Shanghai, 200438, P.R. China.
Solar-driven photocatalytic oxygen reduction reaction using covalent organic frameworks (COFs) offers a promising approach for sustainable hydrogen peroxide (HO) production. Despite their advantages, the reported COFs-based photocatalysts suffer insufficient photocatalytic HO efficiency due to the mismatched electron-proton dynamics. Herein, we report three one-dimensional (1D) COF photocatalysts for efficient HO production via the hydrogen radical (H•) mediated concerted electron-proton transfer (CEPT) process.
View Article and Find Full Text PDFChempluschem
September 2025
Academy of Scientific and Innovative Research (ACSIR), Ghaziabad, 201002, India.
Photoreforming of biomass presents a promising approach for sustainable H production by utilizing renewable solar energy under ambient conditions. However, its application is often limited by the poor solubility of biomass-derived substrates. Herein, this challenge is addressed by synthesizing hydrophilic, electron-rich pyridine-based glycopolymers via reversible addition-fragmentation chain transfer polymerization, followed by deacetylation of glucose- and maltose-based segments.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Department of Chemistry, Roy and Diana Vagelos Laboratories, University of Pennsylvania, Philadelphia, Pennsylvania 19014, United States.
Phenol overoxidation has severely hindered the advancement and synthetic utility of oxidative phenol coupling for over two decades, preventing the development of general catalytic methods. Electron-deficient phenols resist selective coupling due to their high oxidation potential, while monosubstituted phenols undergo uncontrolled overoxidation, making their selective transformation highly challenging. We present a strategy that harnesses biphenol-boron complexation to suppress overoxidation, unlocking the selective catalytic oxidative coupling of both electron-deficient and monosubstituted phenols.
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