Facing the constraints of critical agglomeration and poor reusability of CuFeO in catalytic applications, the feasibility of synthesizing a composite catalyst using carbon coating technology for efficient TC removal with enhanced PDS activity was investigated. The composite catalyst (CuFeO@C) can stimulate both radical (SO and HO•) and non-radical (O) pathways to dominate the catalytic reaction for removing 95.7% of the TC in 60 min. Meanwhile, the defective structure of the external carbon layer protected the internal CuFeO from excessive oxidation, allowing the CuFeO@C to maintain over 90% TC removal after 5 cycles with less interference from inorganic anions, demonstrating significant catalytic performance and satisfactory reusability. Finally, the DFT calculations and TEST evaluation were performed to discuss the structural properties of TC and its toxicity assessment during the whole degradation process, while three possible degradation pathways were proposed. Significantly, the carbon-coated composite catalysts of potential universal applicability for multi-pathway PDS activation offered an attractive new strategy for the effective degradation of antibiotic wastewater.
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http://dx.doi.org/10.1016/j.jhazmat.2023.132417 | DOI Listing |
Inorg Chem
January 2025
School of Materials Science and Engineering, China University of Petroleum, Qingdao 266580, PR China.
Mismatched electron and proton transport rates impede the manifestation of effective performance of the electrocatalytic oxygen evolution reaction (OER), thereby limiting its industrial applications. Inspired by the natural protein cluster in PS-II, different organic-inorganic hybrid electrocatalysts were synthesized via a hydrothermal method. -Toluidine (PT), benzoic acid (BA), and -aminobenzoic acid (PABA) were successfully intercalated into NiFe-LDH.
View Article and Find Full Text PDFACS Nano
January 2025
Dto. de Física de Materiales, Universidad Complutense de Madrid, 28040 Madrid, Spain.
We experimentally observe quantum confinement states in bulk MoS by using angle-resolved photoemission spectroscopy (ARPES). The band structure at the Γ̅ point reveals quantum well states (QWSs) linked to vertical quantum confinement of the electrons, confirmed by the absence of dispersion in and a strong intensity modulation with the photon energy. Notably, the binding energy dependence of the QWSs versus does not follow the quadratic dependence of a two-dimensional electron gas.
View Article and Find Full Text PDFInorg Chem
January 2025
NIMS-CNRS-Saint-Gobain International Collaboration Center, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki 305-0044, Japan.
In this study, we investigate structural disorder and its implications in metal cluster (MC)-based compounds, specifically focusing on Cs[{MoX}X] (X = Cl and Br). Utilizing synchrotron radiation X-ray diffraction, Fourier transform infrared spectroscopy, and luminescence measurements, we examined the incorporation of water molecules into these compounds and their effects on the crystal structure and optical properties. Our findings reveal that the presence of water molecules induces the lattice disorder, particularly the displacement of Cs atoms.
View Article and Find Full Text PDFJ Org Chem
January 2025
Universität Rostock, Institut für Chemie, A.-Einstein-Str. 3a, 18059 Rostock, Germany.
Novel π-expanded and N-doped fluoranthenes were synthesized and thoroughly investigated. These eight unsubstituted compounds are obtained in a multistep synthesis with CH activation as the last key reaction step. The structures vary in their position of π-expansion on the fluoranthene scaffold and the location of the pyridinic nitrogen atom.
View Article and Find Full Text PDFSmall
January 2025
Advanced Catalytic Materials (ACM), KAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Photo-thermal catalysis, leveraging both thermal and non-thermal solar contributions, emerges as a sustainable approach for fuel and chemical synthesis. In this study, an Fe-based catalyst derived from a metal-organic framework is presented for efficient photo-thermal ammonia (NH) decomposition. Optimal conditions, under light irradiation without external heating, result in a notable 55% NH conversion.
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